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J. Funct. Biomater., Volume 15, Issue 4 (April 2024) – 32 articles

Cover Story (view full-size image): This work uses finite element analysis (FEA) to combine biomimetic Voronoi lattice structures that simulate the cancellous bone of the human jaw to advance dental implant designs. It utilizes nTOP 4.17.3 and Creo Parametric 8.0 to accurately mimic the trabecular bone's complicated porosity and biomechanical properties. The research presented improves the biomechanical performance of dental implants during dynamic mastication by varying pore diameters from 1.0 to 2.5 mm. These findings indicate the ideal pore size, which is consistent with natural bone mechanics, thereby significantly improving osseointegration and stability. Indeed, this is an important step in the development of long-lasting, patient-specific implants, thus laying the foundations for the next generation of dental treatments. View this paper
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11 pages, 3878 KiB  
Article
Deferoxamine-Loaded Chitosan-Based Hydrogel on Bone Implants Showing Enhanced Bond Strength and Pro-Angiogenic Effects
by Huan Liu, Kai Li, Deliang Yi, Yi Ding, Yanfeng Gao and Xuebin Zheng
J. Funct. Biomater. 2024, 15(4), 112; https://doi.org/10.3390/jfb15040112 - 22 Apr 2024
Cited by 2 | Viewed by 2070
Abstract
Angiogenesis is vital for bone fracture healing and plays a significant role in the fate of orthopedic implants. The growth and maintenance of new blood vessels at the fracture site of patients is essential, which promotes the clinical outcome of plasma sprayed Ti [...] Read more.
Angiogenesis is vital for bone fracture healing and plays a significant role in the fate of orthopedic implants. The growth and maintenance of new blood vessels at the fracture site of patients is essential, which promotes the clinical outcome of plasma sprayed Ti (PST) coated orthopedic implants. In order to endow the PST coating with pro-angiogenic effects, deferoxamine-loaded chitosan-based hydrogel was fabricated on the coating surface. Polydopamine-modified chitosan (CS/PDA) hydrogel exhibited enhanced bonding strength to PST coatings as evidenced by scratch test. The deferoxamine-loaded CS/PDA (CS/PDA-DFO) exhibited a sustained drug-release property, and the cumulative concentration of released DFO reached 20.21 μg/mL on day 7. PST-CS/PDA with higher wettability and active group quantity enhanced the viability and adhesion characteristics of human umbilical vein endothelial cells (HUVECs) and upregulated the secretion level of nitric oxide and vascular endothelial growth factor. Moreover, the introduction of DFO in PST-CS/PDA further enhanced the pro-angiogenic effects. Above all, this study offers a novel approach for developing hydrogel coating on orthopedic implants showing enhanced bonding strength and pro-angiogenic effects. Full article
(This article belongs to the Section Bone Biomaterials)
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Figure 1

Figure 1
<p>(<b>A</b>) The FE-SEM images of PST and PST-CS/PDA. (<b>B</b>) Pore size distribution of CS/PDA hydrogel. (<b>C</b>) FTIR spectra of CS, PDA, and CS/PDA. (<b>D</b>) XPS spectra with peak fitting analysis for C 1s and N 1s of PST-CS/PDA and PST-CS/PDA-DFO. (<b>E</b>) Water contact angle of PST, PST-CS/PDA, and PST-CS/PDA coatings. (<b>F</b>) The acoustic signal and friction coefficient of PST-CS and PST-CS/PDA. (<b>G</b>) Degradation behavior of the PST-CS and PST-CS/PDA.</p>
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<p>(<b>A</b>) Cumulative DFO release of PST-CS/PDA-DFO coating in PBS. (<b>B</b>) The cumulative release concentration of DFO.</p>
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<p>The CCK-8 assay of HUVECs incubated on each group for 1, 4, and 7 days, <span class="html-italic">n</span> = 3, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>HUVECs cultured on PST, PST-CS/PDA, and PST-CS/PDA-DFO. (<b>A</b>) FE-SEM and (<b>B</b>) CLSM observation of cell adhesion morphology. (<b>C</b>) Quantitative analysis of cell spreading area, <span class="html-italic">n</span> = 3, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>(<b>A</b>) NO secretion and (<b>B</b>) VEGF secretion of HUVECs cultured on PST, PST-CS/PDA, and PST-CS/PDA-DFO for 3 days, <span class="html-italic">n</span> = 3, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
Full article ">Scheme 1
<p>Schematic illustration for the fabrication of the preparation of CS/PDA-DFO hydrogel on the PST coating.</p>
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17 pages, 3600 KiB  
Article
Natural Biomolecule Ovomucin–Chitosan Oligosaccharide Self-Assembly Nanogel for Lutein Application Enhancement: Characterization, Environmental Stability and Bioavailability
by Qi Xu, Haoye Teng, Xuanchen Li, Zhenqing Zhang, Yumeng Han and Haixin Sun
J. Funct. Biomater. 2024, 15(4), 111; https://doi.org/10.3390/jfb15040111 - 21 Apr 2024
Cited by 3 | Viewed by 1632
Abstract
As an essential nutrient, lutein (LUT) has the ability to aid in the prevention of eye diseases, cardiovascular diseases, and cancer. However, the application of LUT is largely restricted by its poor solubility and susceptibility to oxidative degradation. Thus, in this study, LUT-loaded [...] Read more.
As an essential nutrient, lutein (LUT) has the ability to aid in the prevention of eye diseases, cardiovascular diseases, and cancer. However, the application of LUT is largely restricted by its poor solubility and susceptibility to oxidative degradation. Thus, in this study, LUT-loaded nanogel (OVM-COS-LUT) was prepared by a self-assembly of ovomucin (OVM) and chitosan oligosaccharide (COS) to enhance the effective protection and bioavailability of LUT. The nanogel had excellent dispersion (PDI = 0.25) and an 89.96% LUT encapsulation rate. XRD crystal structure analysis confirmed that the encapsulated LUT maintained an amorphous morphology. In addition, the nanogel showed satisfactory stability with pH levels ranging from 2 to 9 and high ionic strengths (>100 mM). Even under long-term storage, the nanogel maintained an optimistic stabilization and protection capacity; its effective retention rates could reach 96.54%. In vitro, digestion simulation showed that the bioaccessibility and sustained release of OVM-COS-LUT nanogel was superior to that of free LUT. The nanogel provided significant antioxidant activity, and no significant harmful effects were detected in cytotoxicity analyses at higher concentrations. In summary, OVM-COS-LUT can be utilized as a potential safe oral and functional carrier for encapsulating LUT. Full article
(This article belongs to the Special Issue State of the Art in Biomaterials for Drug Delivery)
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Figure 1

Figure 1
<p>Optical pictures of LUT and OVM-COS-LUT (<b>a</b>). UV–Vis spectrum of OVM-COS and OVM-COS-LUT, ranging 300–700 nm (<b>b</b>). TEM image (scale bar = 100/500 nm) of OVM-COS-LUT (<b>c</b>).</p>
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<p>Circular dichroism (CD) spectra (<b>a</b>) and fluorescence spectra (<b>b</b>) of OVM, OVM-COS, and OVM-COS-LUT.</p>
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<p>FT-IR spectra (<b>a</b>) and XRD spectra (<b>b</b>) of COS, LUT, OVM, OVM-COS, and OVM-COS-LUT.</p>
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<p>Particle size, PDI of OVM-COS-LUT at pH 2–9 (<b>a</b>). Optical image of OVM-COS-LUT at pH = 4.5 (<b>b</b>). Optical images of OVM-COS-LUT at different pH 2–9 (<b>c</b>).</p>
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<p>Particle size and PDI of OVM-COS-LUT (<b>a</b>). Particle size and solution state changes in OVM (<b>b</b>). Optical images of OVM-COS-LUT under different NaCl concentrations (0–500 mM) (<b>c</b>).</p>
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<p>UV–Vis spectrum (<b>a</b>); particle size and PDI (<b>b</b>); optical images (<b>c</b>) of OVM-COS-LUT during 30-day storage.</p>
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<p>DPPH scavenging activity of LUT, OVM-COS, and OVM-COS-LUT at different lutein concentrations (***: <span class="html-italic">p</span> &lt; 0.001) (<b>a</b>). Release behavior of LUT and OVM-COS-LUT nanogel in a simulated medium (<b>b</b>). Bioaccessibility of LUT and OVM-COS-LUT in simulated gastrointestinal digestion (***: <span class="html-italic">p</span> &lt; 0.001) (<b>c</b>). Size changes in OVM-COS-LUT in successive gastrointestinal digestion (<b>d</b>). Schematic diagram of the simulated release of free lutein and OVM-COS-LUT nanogel (In the schematic structure of OVM-COS-LUT nanogel, the blue line represents OVM, and the gradient red line represents COS.) (<b>e</b>). Parts of <a href="#jfb-15-00111-f007" class="html-fig">Figure 7</a>e were drawn using pictures from Server Medical Art. Servier Medical Art by Servier is licensed under Creative Commons Attribution 4.0. <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a> (accessed on 15 November 2023).</p>
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<p>Effect of different concentrations of OVM-COS-LUT nanogel on cell viability (control: no nanogel was added).</p>
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34 pages, 23488 KiB  
Article
Performance of Austenitic High-Nitrogen Steels under Gross Slip Fretting Corrosion in Bovine Serum
by Alfons Fischer, Philipe Telouk, Christian Beckmann, Saskia Heermant, Adrian Wittrock, Jörg Debus and Markus A. Wimmer
J. Funct. Biomater. 2024, 15(4), 110; https://doi.org/10.3390/jfb15040110 - 18 Apr 2024
Cited by 1 | Viewed by 1499
Abstract
Modular artificial hip joints are a clinical standard today. However, the release of wear products from the head–taper interface, which includes wear particles in the nm size range, as well as metal ions, have raised concerns. Depending on the loading of such taper [...] Read more.
Modular artificial hip joints are a clinical standard today. However, the release of wear products from the head–taper interface, which includes wear particles in the nm size range, as well as metal ions, have raised concerns. Depending on the loading of such taper joints, a wide variety of different mechanisms have been found by retrieval analyses. From these, this paper concentrates on analyzing the contribution of gross slip fretting corrosion at ultra-mild wear rates using a bovine calf serum solution (BCS) as the lubricant. The parameters were chosen based on biomechanical considerations, producing wear rates of some ng/m wear path. In parallel, the evolution of tribomaterial (third bodies) was analyzed as to its constituents and generation rates. It has already been shown earlier that, by an advantageous combination of wear mechanisms and submechanisms, certain constituents of the tribomaterial remain inside the contact area and act like extreme-pressure lubricant additives. For the known wear and corrosion resistance of austenitic high-nitrogen steels (AHNSs), which outperform CoCrMo alloys even under inflammatory conditions, we hypothesized that such steels will generate ultra-mild wear rates under gross slip fretting. While testing AHNSs against commercially available biomedical-grade materials of CoCrMo and TiAlV alloys, as well as zirconia-toughened alumina (ZTA) and against itself, it was found that AHNSs in combination with a Ti6Al4V alloy generated the smallest wear rate under gross slip fretting corrosion. This paper then discusses the wear behavior on the basis of ex situ analyses of the worn surfaces as to the acting wear mechanisms and submechanisms, as well as to the tribological reaction products. Full article
(This article belongs to the Special Issue Metallic Biomaterials for Medical Applications)
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Figure 1
<p>Microstructures of the investigated austenitic high-nitrogen steels. (<b>a</b>) FeCN0.9; (<b>b</b>) FeCN0.6.</p>
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<p>(<b>a</b>) Scheme of the fretting test rig. (<b>b</b>) Elements of the tribological system and loading parameters.</p>
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<p>Mean frictional work of experiments with FeCN0.9 runs against (<b>a</b>,<b>b</b>) fluted Ti6Al4V and (<b>c</b>,<b>d</b>) fluted FeCN0.6.</p>
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<p>OCP over the entire duration of the fretting experiments for different pin materials against FL-FeCN0.6.</p>
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<p>Wear appearances on a fluted Ti6Al4V cylinder (<b>a</b>,<b>b</b>) after 40,000 cycles against FeCN0.6 (<b>c</b>,<b>d</b>). The samples have been sonicated in ethanol.</p>
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<p>EDS scans of a contact ridge and grainy debris on fluted Ti6Al4V cylinder. The samples have been sonicated in ethanol.</p>
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<p>Pile of grainy debris (areas and spectra 19 and 21) within a valley (areas and spectra 20 and 22) of a fluted Ti6Al4V cylinder after the fretting test against polished FeCN0.9. The samples have been sonicated in ethanol. Blank cells within this and all further EDS tables mean “not detected”.</p>
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<p>EDS scans of a contact ridge and grainy debris on the FeCN0.6 pin. The samples have been sonicated in ethanol.</p>
Full article ">Figure 8 Cont.
<p>EDS scans of a contact ridge and grainy debris on the FeCN0.6 pin. The samples have been sonicated in ethanol.</p>
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<p>Wear appearances on a fluted CoC0.06 cylinder (<b>a</b>,<b>b</b>) after 40,000 cycles against polished FeCN0.6 pins (<b>c</b>,<b>d</b>). The samples have been sonicated in ethanol.</p>
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<p>EDS scans of a contact ridge and grainy debris on a fluted CoC0.06 cylinder. The samples have been sonicated in ethanol.</p>
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<p>EDS scans of grainy debris between the wear grooves on the FeCN0.6 pin. The samples have been sonicated in ethanol.</p>
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<p>Wear appearances on a fluted FeCN0.6 cylinder (<b>a</b>,<b>b</b>) after 40,000 cycles against CoC0.06 pins (<b>c</b>,<b>d</b>). The samples have been sonicated in ethanol.</p>
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<p>EDS scans of a contact ridge and grainy debris on a fluted FeCN0.6 cylinder. The samples have been sonicated in ethanol.</p>
Full article ">Figure 13 Cont.
<p>EDS scans of a contact ridge and grainy debris on a fluted FeCN0.6 cylinder. The samples have been sonicated in ethanol.</p>
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<p>EDS scans of grainy debris on a polished CoC0.06 pin. The samples have been sonicated in ethanol.</p>
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<p>Wear appearances on a fluted FeCN0.6 cylinder (<b>a</b>,<b>b</b>) after 40,000 cycles against polished FeCN0.9 pins (<b>c</b>,<b>d</b>). The samples have been sonicated in ethanol.</p>
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<p>EDS scans of the debris pushed out to both sides of the contact area of the fluted FeCN0.6 cylinder. The samples have been sonicated in ethanol.</p>
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<p>EDS scans of grainy debris on a polished FeCN0.9 pin. The samples have been sonicated in ethanol.</p>
Full article ">Figure 17 Cont.
<p>EDS scans of grainy debris on a polished FeCN0.9 pin. The samples have been sonicated in ethanol.</p>
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<p>Wear appearances on a fluted FeCN0.6 cylinder (<b>a</b>,<b>b</b>) after 40,000 cycles against ZTA (<b>c</b>,<b>d</b>). The samples have been sonicated in ethanol.</p>
Full article ">Figure 18 Cont.
<p>Wear appearances on a fluted FeCN0.6 cylinder (<b>a</b>,<b>b</b>) after 40,000 cycles against ZTA (<b>c</b>,<b>d</b>). The samples have been sonicated in ethanol.</p>
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<p>EDS scans of a contact ridge and grainy debris on fluted FeCN0.6 cylinder. The samples have been sonicated in ethanol.</p>
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<p>The graded structure of sliding interfaces according to reference [<a href="#B30-jfb-15-00110" class="html-bibr">30</a>].</p>
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<p>Accumulated frictional work per wear path W<sub>acc/l</sub> in mNm/m of the different combinations of materials. (<b>a</b>) W<sub>acc/l</sub> of the fluted couples, this work; (<b>b</b>) W<sub>acc/l</sub> of all couples tested [<a href="#B20-jfb-15-00110" class="html-bibr">20</a>,<a href="#B39-jfb-15-00110" class="html-bibr">39</a>,<a href="#B44-jfb-15-00110" class="html-bibr">44</a>].</p>
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<p>Normalized gross MML generation rate g<sub>MML</sub> in ng/m and the ΔOCP in V of the different combinations of materials (* ZTA/metal couples). (<b>a</b>) This work; (<b>b</b>) This and former work [<a href="#B20-jfb-15-00110" class="html-bibr">20</a>,<a href="#B39-jfb-15-00110" class="html-bibr">39</a>,<a href="#B44-jfb-15-00110" class="html-bibr">44</a>].</p>
Full article ">Figure 23
<p>Normalized gross wear rate w<sub>FC</sub> vs. the normalized gross MML generate rate g<sub>MML</sub> of the different combinations of materials (* ZTA/metal couples). (<b>a</b>) This work; (<b>b</b>) This and former work [<a href="#B20-jfb-15-00110" class="html-bibr">20</a>,<a href="#B39-jfb-15-00110" class="html-bibr">39</a>,<a href="#B44-jfb-15-00110" class="html-bibr">44</a>].</p>
Full article ">
16 pages, 5700 KiB  
Article
3D Printing of a Porous Zn-1Mg-0.1Sr Alloy Scaffold: A Study on Mechanical Properties, Degradability, and Biosafety
by Xiangyu Cao, Xinguang Wang, Jiazheng Chen, Xiao Geng and Hua Tian
J. Funct. Biomater. 2024, 15(4), 109; https://doi.org/10.3390/jfb15040109 - 18 Apr 2024
Cited by 1 | Viewed by 2174
Abstract
In recent years, the use of zinc (Zn) alloys as degradable metal materials has attracted considerable attention in the field of biomedical bone implant materials. This study investigates the fabrication of porous scaffolds using a Zn-1Mg-0.1Sr alloy through a three-dimensional (3D) printing technique, [...] Read more.
In recent years, the use of zinc (Zn) alloys as degradable metal materials has attracted considerable attention in the field of biomedical bone implant materials. This study investigates the fabrication of porous scaffolds using a Zn-1Mg-0.1Sr alloy through a three-dimensional (3D) printing technique, selective laser melting (SLM). The results showed that the porous Zn-1Mg-0.1Sr alloy scaffold featured a microporous structure and exhibited a compressive strength (CS) of 33.71 ± 2.51 MPa, a yield strength (YS) of 27.88 ± 1.58 MPa, and an elastic modulus (E) of 2.3 ± 0.8 GPa. During the immersion experiments, the immersion solution showed a concentration of 2.14 ± 0.82 mg/L for Zn2+ and 0.34 ± 0.14 mg/L for Sr2+, with an average pH of 7.61 ± 0.09. The porous Zn-1Mg-0.1Sr alloy demonstrated a weight loss of 12.82 ± 0.55% and a corrosion degradation rate of 0.36 ± 0.01 mm/year in 14 days. The Cell Counting Kit-8 (CCK-8) assay was used to check the viability of the cells. The results showed that the 10% and 20% extracts significantly increased the activity of osteoblast precursor cells (MC3T3-E1), with a cytotoxicity grade of 0, which indicates safety and non-toxicity. In summary, the porous Zn-1Mg-0.1Sr alloy scaffold exhibits outstanding mechanical properties, an appropriate degradation rate, and favorable biosafety, making it an ideal candidate for degradable metal bone implants. Full article
(This article belongs to the Special Issue Advanced 3D Printing Biomaterials)
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Figure 1

Figure 1
<p>Morphology of the porous Zn-1Mg-0.1Sr alloy scaffold: (<b>a</b>) gyroid model; (<b>b</b>) microscopic morphology; (<b>c</b>) micro-CT image; and (<b>d</b>) SEM image.</p>
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<p>EDS and XRD analysis of the porous Zn-1Mg-0.1Sr alloy scaffold: (<b>a</b>,<b>b</b>) EDS analysis image; (<b>c</b>) XRD pattern.</p>
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<p>Compression tests: (<b>a</b>) stress–strain curves of porous Zn-1Mg-0.1Sr and pure Zn alloy scaffolds; (<b>b</b>) compressive strength of porous Zn-1Mg-0.1Sr and pure Zn alloy scaffolds.</p>
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<p>SEM images, EDS analysis, and XRD analysis of the porous Zn-1Mg-0.1Sr alloy scaffold after immersion in SBF for various durations: (<b>a</b>) SEM images; (<b>b</b>,<b>c</b>) EDS analysis images; and (<b>d</b>) XRD pattern.</p>
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<p>Porous Zn-1Mg-0.1Sr alloy scaffold in SBF over time: (<b>a</b>) Zn<sup>2+</sup> amount; (<b>b</b>) Sr<sup>2+</sup> amount. (<b>c</b>) pH value variation curves; (<b>d</b>) corrosion degradation weight loss percentage and corrosion degradation rate.</p>
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<p>Optical density (OD) and relative growth rate (RGR%) of MC3T3-E1 cells in each experimental group: (<b>a</b>) optical density (OD); (<b>b</b>) relative growth rate (RGR%).</p>
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<p>Live/dead fluorescence staining of MC3T3-E1 cells exposed to different concentrations of extracts and for different culture periods.</p>
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16 pages, 4806 KiB  
Article
Biological and Mechanical Performance of Dual-Setting Brushite–Silica Gel Cements
by Valentin C. Steinacker, Tobias Renner, Ib Holzmeister, Sebastian Gubik, Urs Müller-Richter, Niko Breitenbücher, Andreas Fuchs, Anton Straub, Mario Scheurer, Alexander C. Kübler and Uwe Gbureck
J. Funct. Biomater. 2024, 15(4), 108; https://doi.org/10.3390/jfb15040108 - 18 Apr 2024
Viewed by 1608
Abstract
Bone defects resulting from trauma, diseases, or surgical procedures pose significant challenges in the field of oral and maxillofacial surgery. The development of effective bone substitute materials that promote bone healing and regeneration is crucial for successful clinical outcomes. Calcium phosphate cements (CPCs) [...] Read more.
Bone defects resulting from trauma, diseases, or surgical procedures pose significant challenges in the field of oral and maxillofacial surgery. The development of effective bone substitute materials that promote bone healing and regeneration is crucial for successful clinical outcomes. Calcium phosphate cements (CPCs) have emerged as promising candidates for bone replacement due to their biocompatibility, bioactivity, and ability to integrate with host tissues. However, there is a continuous demand for further improvements in the mechanical properties, biodegradability, and bioactivity of these materials. Dual setting of cements is one way to improve the performance of CPCs. Therefore, silicate matrices can be incorporated in these cements. Silicate-based materials have shown great potential in various biomedical applications, including tissue engineering and drug delivery systems. In the context of bone regeneration, silicate matrices offer unique advantages such as improved mechanical stability, controlled release of bioactive ions, and enhanced cellular responses. Comprehensive assessments of both the material properties and biological responses of our samples were conducted. Cytocompatibility was assessed through in vitro testing using osteoblastic (MG-63) and osteoclastic (RAW 264.7) cell lines. Cell activity on the surfaces was quantified, and scanning electron microscopy (SEM) was employed to capture images of the RAW cells. In our study, incorporation of tetraethyl orthosilicate (TEOS) in dual-curing cements significantly enhanced physical properties, attributed to increased crosslinking density and reduced pore size. Higher alkoxysilyl group concentration improved biocompatibility by facilitating greater crosslinking. Additionally, our findings suggest citrate’s potential as an alternative retarder due to its positive interaction with the silicate matrix, offering insights for future dental material research. This paper aims to provide an overview of the importance of silicate matrices as modifiers for calcium phosphate cements, focusing on their impact on the mechanical properties, setting behaviour, and biocompatibility of the resulting composites. Full article
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Figure 1
<p>Diffraction pattern of the phase composition of brushite and BCB cements as reference and as dual-setting cements (TEOS and TEOS-OC) (b brushite ICDD #09-0077, m monetite ICDD #09-0080, β β-TCP ICDD #09-0169, B baghdadite ICDD #54-0710). The patterns were calculated using TOPAS 4.2 software (Bruker AXS, Karlsruhe, Germany).</p>
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<p>pH profile of the washing solution (<span class="html-italic">n</span> = 3) in which the cements of brushite (<b>a</b>) with TEOS or TEOS-OC; and BCB (<b>b</b>) with TEOS or TEOS-OC were placed. Each washing cycle took 1 h. The error bars represent the standard deviation.</p>
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<p>Initial setting times as determined by the Gillmore needle test of brushite (<b>a</b>) with TEOS or TEOS-OC; and BCB (<b>b</b>) with TEOS or TEOS-OC. The error bars represent the standard deviation (<span class="html-italic">n</span> = 8).</p>
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<p>Compressive strength of cuboid brushite (<b>a</b>) and BCB (<b>b</b>) specimens with different formulations of silicate matrices ∗ = <span class="html-italic">p</span> &lt; 0.05; ∗∗ = <span class="html-italic">p</span> &lt; 0.005; the error bars represent the standard deviation (<span class="html-italic">n</span> = 8).</p>
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<p>Cell activity (<b>a</b>) and cell number (100% at 50,000 cells) (<b>b</b>) of MG-63 on brushite specimens with regard to different compositions of silicate matrices. WST-1 activity and cell proliferation in comparison to the brushite reference ∗ = <span class="html-italic">p</span> &lt; 0.05; ∗∗ = <span class="html-italic">p</span> &lt; 0.005; the error bars represent the standard deviation (<span class="html-italic">n</span> = 4).</p>
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<p>Cell activity (<b>a</b>) and cell number (100% at 50,000 cells) (<b>b</b>) of MG-63 on brushite and BCB specimens with regard to different compositions of silicate matrices. WST-1 activity and cell proliferation in comparison to the brushite reference ∗ = <span class="html-italic">p</span> &lt; 0.05; the error bars represent the standard deviation (<span class="html-italic">n</span> = 4).</p>
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<p>TRAP activity of RAW 264.7 cells incubated with 50 ng/mL RANKL on brushite cements with and without silicate matrices over 15 d. TRAP activity in comparison to the brushite reference; the error bars represent the standard deviation (<span class="html-italic">n</span> = 4).</p>
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<p>DNA concentration of RAW 264.7 cells incubated with 50 ng/mL RANKL on brushite cements with and without silicate matrices over 15 d. DNA-concentration in comparison to the brushite reference ∗ = <span class="html-italic">p</span> &lt; 0.05; the error bars represent the standard deviation (<span class="html-italic">n</span> = 4).</p>
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<p>SEM images of RAW 264.7 differentiated with RANKL on the surface of the various calcium phosphate cements with and without TEOS-OC at day 6, 10 and 15. The images were made at 1000× magnification and given with a scale of 20 μm.</p>
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<p>Cumulative Ca<sup>2+</sup> ion concentration due to their release by passive, total, and active resorption of calcium phosphate cements for 15 d. The specimens were incubated without cells for passive resorption and with cells for total resorption, and the difference between those two was formed for active resorption. The error bars represent the standard deviation (<span class="html-italic">n</span> = 4).</p>
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<p>Cumulative Si<sup>4+</sup> ion concentration due to their release by passive, total, and active resorption of calcium phosphate cements for 15 d. The specimens were incubated without cells for passive resorption and with cells for total resorption, and the difference between those two was formed for active resorption. The error bars represent the standard deviation (<span class="html-italic">n</span> = 4).</p>
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<p>Cumulative PO<sub>4</sub><sup>3−</sup> ion concentration due to their release by passive, total, and active resorption of calcium phosphate cements for 15 d. The specimens were incubated without cells for passive resorption and with cells for total resorption, and the difference between those two was formed for active resorption. The error bars represent the standard deviation (<span class="html-italic">n</span> = 4).</p>
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<p>Diffraction pattern of the phase composition of brushite cement as reference and dual-setting cement TEOS-OC (b brushite, m monetite, β β-TCP, a hydroxyapatite). The patterns were calculated using TOPAS 4.2 software (Bruker AXS, Karlsruhe, Germany).</p>
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4 pages, 178 KiB  
Editorial
Functional Biomaterials and Digital Technologies in Dentistry: From Bench to Bedside
by Ping Li, Guojiang Wan, Shulan Xu and An Li
J. Funct. Biomater. 2024, 15(4), 107; https://doi.org/10.3390/jfb15040107 - 17 Apr 2024
Viewed by 1810
Abstract
This Special Issue, “Functional Biomaterials and Digital Technologies in Dentistry: From Bench to Bedside”, highlights the integration of advanced materials science and digital technologies in dental and maxillofacial applications [...] Full article
12 pages, 978 KiB  
Article
Effects of Erythropoietin-Promoted Fracture Healing on Bone Turnover Markers in Cats
by Radina Vasileva, Tsvetan Chaprazov and Aneliya Milanova
J. Funct. Biomater. 2024, 15(4), 106; https://doi.org/10.3390/jfb15040106 - 17 Apr 2024
Viewed by 1774
Abstract
In orthopaedics, erythropoietin (EPO) is applied in the preoperative management of anaemic patients, but also as a stimulating factor to assist bone regeneration due to its angiogenic and osteoinductive potential. Since orthopaedists mainly rely on their clinical experience to assess bone healing, additional [...] Read more.
In orthopaedics, erythropoietin (EPO) is applied in the preoperative management of anaemic patients, but also as a stimulating factor to assist bone regeneration due to its angiogenic and osteoinductive potential. Since orthopaedists mainly rely on their clinical experience to assess bone healing, additional and more objective methods such as studying the dynamics of bone markers are needed. Therefore, the aim of this study was to investigate the plasma activity of bone-specific alkaline phosphatase (BALP), the N-terminal propeptide of type I collagen (PINP), the C-terminal telopeptide of type I collagen (CTX), and deoxypyridinoline (DPD) during the first 2 months of healing of comminuted fractures in cats, either non-stimulated or locally stimulated with recombinant human erythropoietin (rhEPO). The study included twelve cats of mixed breeds, aged 7.2 ± 4 months, weighing 2.11 ± 1.1 kg, with comminuted diaphyseal fractures of the femur. Surgical treatment with plate osteosynthesis was performed in all animals. The cats were randomly divided into two groups—a control (n = 6) and an EPO group (n = 6). The locally applied EPO leads to the increased activity of bone formation markers (BALP and PINP) during the second week after the osteosynthesis, preceding the peaks in the control group by two weeks. The studied bone resorption markers (DPD, CTX) varied insignificantly during the studied period. In conclusion, erythropoietin could serve as a promoter of bone healing in comminuted fractures in cats. Full article
(This article belongs to the Special Issue Advances in Bone Substitute Biomaterials)
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<p>Changes in the blood levels of bone-specific alkaline phosphatase (BALP, ng/mL) in the cats from both groups.</p>
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<p>Changes in the blood levels of the N-terminal propeptide of type I collagen (PINP, ng/mL) in the cats from both groups.</p>
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<p>Changes in the blood levels of deoxypyridinoline (DPD, ng/mL) in the cats from both groups.</p>
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<p>Changes in the blood levels of the C-terminal telopeptide of type I collagen (CTX, ng/mL) in the cats from both groups.</p>
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13 pages, 14329 KiB  
Article
Strontium-Doped Bioglass-Laden Gelatin Methacryloyl Hydrogels for Vital Pulp Therapy
by Sepideh Aminmansour, Ana Beatriz Gomes de Carvalho, Lais Medeiros Cardoso, Caroline Anselmi, Maedeh Rahimnejad, Renan Dal-Fabbro, Erika Benavides, Tiago Moreira Bastos Campos, Alexandre Luiz Souto Borges and Marco C. Bottino
J. Funct. Biomater. 2024, 15(4), 105; https://doi.org/10.3390/jfb15040105 - 17 Apr 2024
Cited by 2 | Viewed by 1942
Abstract
This study aimed to develop gelatin methacryloyl (GelMA)-injectable hydrogels incorporated with 58S bioactive glass/BG-doped with strontium for vital pulp therapy applications. GelMA hydrogels containing 0% (control), 5%, 10%, and 20% BG (w/v) were prepared. Their morphological and chemical properties [...] Read more.
This study aimed to develop gelatin methacryloyl (GelMA)-injectable hydrogels incorporated with 58S bioactive glass/BG-doped with strontium for vital pulp therapy applications. GelMA hydrogels containing 0% (control), 5%, 10%, and 20% BG (w/v) were prepared. Their morphological and chemical properties were evaluated by scanning electron microscopy/SEM, energy dispersive spectroscopy/EDS, and Fourier transform infrared spectroscopy/FTIR (n = 3). Their swelling capacity and degradation ratio were also measured (n = 4). Cell viability (n = 8), mineralized matrix formation, cell adhesion, and spreading (n = 6) on DPSCs were evaluated. Data were analyzed using ANOVA/post hoc tests (α = 5%). SEM and EDS characterization confirmed the incorporation of BG particles into the hydrogel matrix, showing GelMA’s (C, O) and BG’s (Si, Cl, Na, Sr) chemical elements. FTIR revealed the main chemical groups of GelMA and BG, as ~1000 cm−1 corresponds to Si-O and ~1440 cm−1 to C-H. All the formulations were degraded by day 12, with a lower degradation ratio observed for GelMA+BG20%. Increasing the concentration of BG resulted in a lower mass swelling ratio. Biologically, all the groups were compatible with cells (p > 0.6196), and cell adhesion increased over time, irrespective of BG concentration, indicating great biocompatibility. GelMA+BG5% demonstrated a higher deposition of mineral nodules over 21 days (p < 0.0001), evidencing the osteogenic potential of hydrogels. GelMA hydrogels incorporated with BG present great cytocompatibility, support cell adhesion, and have a clinically relevant degradation profile and suitable mineralization potential, supporting their therapeutic potential as promising biomaterials for pulp capping. Full article
(This article belongs to the Section Dental Biomaterials)
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<p>Morphological characterization by SEM pictures at 250×, 500×, and 1 k× magnifications of GelMA hydrogels incorporated with varying BG concentrations. Yellow arrows show the BG particles dispersed inside the hydrogel matrix.</p>
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<p>(<b>A</b>) Chemical characterization by EDS spectrum of GelMA hydrogels and (<b>B</b>) chemical characterization by EDS spectrum of GelMA+BG 20%.</p>
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<p>(<b>A</b>) Fourier transform infrared spectroscopy graph according to the different concentrations of BG incorporated into GelMA and 58S BG powder. (<b>B</b>) RAMAN spectrum for BG powder.</p>
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<p>Mechanical properties of GelMA- and BG-incorporated hydrogels. Results are presented as mean and SD. Different capital letters indicate significant differences between groups within each condition. Different lower-case letters demonstrate significant differences between conditions within each group. Two-way ANOVA/Sidak’s post hoc test (n = 8; α = 0.05).</p>
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<p>(<b>A</b>) Mass swelling ratio (%) for GelMA and different concentrations of BG. ANOVA/Games–Howell (n = 3; α = 0.05); (<b>B</b>) remaining mass (%) for hydrogels after different time points. Results are presented as mean and confidence interval (CI). (<b>C</b>) Cell viability (% of control) after 1, 3, and 7 days. The percentage of cell viability was normalized by the fluorescence of the negative control (NC) group. Welch’s ANOVA/Games–Howell (n = 8; α = 0.05). (<b>D</b>) Mineralized matrix formation (% of control for each period). Two-way ANOVA/Sidak’s post hoc test (n = 6; α = 0.05). Results are presented as mean and SD for bar graphs. Different capital letters indicate significant differences between groups within each time point. Different lower-case letters demonstrate significant differences between time points within each group.</p>
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<p>Cell adhesion and spreading for the analyzed groups for different time points (12, 24, and 48 h). Actin filaments (red) were stained with ActinRed 555 reagent, and cell nuclei (blue) were labeled with DAPI.</p>
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12 pages, 4067 KiB  
Article
Binary Mixtures of Meloxicam and L-Tartaric Acid for Oral Bioavailability Modulation of Pharmaceutical Dosage Forms
by Cristina Macasoi, Viorica Meltzer, Ioana Stanculescu, Cosmin Romanitan and Elena Pincu
J. Funct. Biomater. 2024, 15(4), 104; https://doi.org/10.3390/jfb15040104 - 16 Apr 2024
Viewed by 1541
Abstract
Binary mixtures of active pharmaceutical ingredients (API) are researched to improve the oral bioavailability of pharmaceutical dosage forms. The purpose of this study was to obtain mixtures of meloxicam and L-tartaric acid because tartaric acid improves intestinal absorption and meloxicam is more soluble [...] Read more.
Binary mixtures of active pharmaceutical ingredients (API) are researched to improve the oral bioavailability of pharmaceutical dosage forms. The purpose of this study was to obtain mixtures of meloxicam and L-tartaric acid because tartaric acid improves intestinal absorption and meloxicam is more soluble in a weakly basic environment. The mixtures in the 0–1 molar fraction range, obtained from solvent-assisted mechanosynthesis, were investigated by differential scanning calorimetry (DSC), Fourier Transform Infrared (FTIR) spectroscopy, Fourier Transform Raman spectroscopy (FT-Raman), X-ray powder diffraction (XRD) and solubility tests. The physicochemical characteristics of the compounds obtained from DSC data reveal, for the first time, the formation of a co-crystal at meloxicam molar fraction of 0.5. FTIR spectroscopy data show the existence of hydrogen bonds between the co-crystal components meloxicam and L-tartaric acid. FT-Raman spectroscopy was used complementary with FT-IR spectroscopy to analyze the pure APIs and their mixtures, to emphasize the appearance/disappearance and the shifts of the position/intensity of vibrational bands, following the formation of hydrogen-bonded structures or van der Waals interactions, and to especially monitor the crystal lattice vibrations below 400 cm−1. The experimental results obtained by X-ray powder diffraction confirmed the formation of the co-crystal by the loss and, respectively, the apparition of peaks from the single components in the co-crystal diffractogram. The solubility tests showed that the co-crystal product has a lower aqueous solubility due to the acidic character of the other component, tartaric acid. However, when the solubility tests were performed in buffer solution of pH 7.4, the solubility of meloxicam from the co-crystal mixture was increased by 57% compared to that of pure meloxicam. In conclusion, the studied API mixtures may be considered potential biomaterials for improved drug release molecular solids. Full article
(This article belongs to the Special Issue Biomaterials for Translational Medicine)
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<p>Schematic representation of the co-crystallization of the components by solvent-assisted mechanosynthesis.</p>
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<p>Thermal study of binary mixtures (<b>a</b>) DSC curves; (<b>b</b>) Phase diagram for binary mixtures meloxicam—tartaric acid: ideal behaviour—empty triangles and real behaviour (eutectic points are shown as filled squares, liquidus points as filled triangles and co-crystal decomposition as filled circles. I–V are the region of coexistence of different phases).</p>
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<p>Thermal study of binary mixtures (<b>a</b>) DSC curves; (<b>b</b>) Phase diagram for binary mixtures meloxicam—tartaric acid: ideal behaviour—empty triangles and real behaviour (eutectic points are shown as filled squares, liquidus points as filled triangles and co-crystal decomposition as filled circles. I–V are the region of coexistence of different phases).</p>
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<p>(<b>a</b>) TG curves; (<b>b</b>) the decomposition enthalpy of the co-crystal.</p>
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<p>Chemical structure of meloxicam (<b>a</b>) and L-tartaric acid ((2R,3R)-2,3-dihydroxybutanedioic acid) (<b>b</b>).</p>
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<p>FTIR spectra of meloxicam (A), tartaric acid (B) and their equimolar mixture (C).</p>
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<p>FT-Raman of pure meloxicam (red line), tartaric acid (black line) and their equimolar mixture (blue line).</p>
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<p>PXRD patterns of tartaric acid (A), meloxicam (B) and their co-crystal (C). (new diffraction peaks are marked with *).</p>
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29 pages, 4486 KiB  
Review
Zinc Oxide-Based Nanomaterials for Microbiostatic Activities: A Review
by Alemtsehay Tesfay Reda, Jae Yeon Park and Yong Tae Park
J. Funct. Biomater. 2024, 15(4), 103; https://doi.org/10.3390/jfb15040103 - 15 Apr 2024
Cited by 2 | Viewed by 3669
Abstract
The world is fighting infectious diseases. Therefore, effective antimicrobials are required to prevent the spread of microbes and protect human health. Zinc oxide (ZnO) nano-materials are known for their antimicrobial activities. Because of their distinctive physical and chemical characteristics, they can be used [...] Read more.
The world is fighting infectious diseases. Therefore, effective antimicrobials are required to prevent the spread of microbes and protect human health. Zinc oxide (ZnO) nano-materials are known for their antimicrobial activities. Because of their distinctive physical and chemical characteristics, they can be used in medical and environmental applications. ZnO-based composites are among the leading sources of antimicrobial research. They are effective at killing (microbicidal) and inhibiting the growth (microbiostatic) of numerous microorganisms, such as bacteria, viruses, and fungi. Although most studies have focused on the microbicidal features, there is a lack of reviews on their microbiostatic effects. This review provides a detailed overview of available reports on the microbiostatic activities of ZnO-based nano-materials against different microorganisms. Additionally, the factors that affect the efficacy of these materials, their time course, and a comparison of the available antimicrobials are highlighted in this review. The basic properties of ZnO, challenges of working with microorganisms, and working mechanisms of microbiostatic activities are also examined. This review underscores the importance of further research to better understand ZnO-based nano-materials for controlling microbial growth. Full article
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<p>Mechanisms of antimicrobial resistance in molecular level. Reprinted from Ref. [<a href="#B115-jfb-15-00103" class="html-bibr">115</a>].</p>
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<p>Antimicrobial activity mechanism of ZnO nanostructures. Reprinted from Ref. [<a href="#B129-jfb-15-00103" class="html-bibr">129</a>].</p>
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<p>(<b>A</b>) Response of <span class="html-italic">P. putida</span> microbe to nano-ZnO. Reprinted from Ref. [<a href="#B133-jfb-15-00103" class="html-bibr">133</a>]. (<b>B</b>) Effect of size of ZnO NPs on growth of methicillin-sensitive <span class="html-italic">S. aureus</span> strain. Reprinted with permission from Ref. [<a href="#B135-jfb-15-00103" class="html-bibr">135</a>]. Copyright 2011 American Chemical Society.</p>
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<p>Growth inhibition studies of ZnO+PBS, ZnO+IL1, ZnO+IL2, IL1, IL2, and gentamicin at the concentration range of 50−120 μg/mL in (<b>a</b>) <span class="html-italic">E. coli</span>, (<b>b</b>) <span class="html-italic">B. subtilis</span>, (<b>c</b>) <span class="html-italic">K. pneumoniae</span>, and (<b>d</b>) <span class="html-italic">S. epidermidis</span>. PBS-treated cells were treated as a negative control. Error bars represent standard error with respect to the mean of three biological replicates. ** <span class="html-italic">p</span> &lt; 0.001, *** <span class="html-italic">p</span> &lt; 0.0001. Reprinted with permission from Ref. [<a href="#B147-jfb-15-00103" class="html-bibr">147</a>]. Copyright 2018 American Chemical Society.</p>
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<p>Growth curve (<b>A</b>) and inhibition efficiency (<b>B</b>) of <span class="html-italic">E. coli</span> and <span class="html-italic">S. aureus</span> exposed to the ethylcellulose/gelatin fibers with and without UV light. Reprinted with permission from Ref. [<a href="#B144-jfb-15-00103" class="html-bibr">144</a>]. Copyright 2018 American Chemical Society.</p>
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<p>Change in the band energy gap for metal/oxide-modified ZnO NPs and their antimicrobial mechanisms. Reprinted from Ref. [<a href="#B143-jfb-15-00103" class="html-bibr">143</a>].</p>
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<p>Antibacterial effect of different ZnO samples against <span class="html-italic">E. coli</span> and <span class="html-italic">S. aureus</span> and under different incubation times in vitro. ZnO samples co-cultured with bacteria for 6 h (<b>A</b>,<b>C</b>) and 24 h (<b>B</b>,<b>D</b>). * <span class="html-italic">p</span> &gt; 0.05, ** 0.01 &lt; <span class="html-italic">p</span> &lt; 0.05, and *** 0.001 &lt; <span class="html-italic">p</span> &lt; 0.0. Reprinted with permission from Ref. [<a href="#B175-jfb-15-00103" class="html-bibr">175</a>]. Copyright 2020 American Chemical Society.</p>
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18 pages, 19905 KiB  
Article
A Novel Method for Fabricating the Undulating Structures at Dermal—Epidermal Junction by Composite Molding Process
by Hao Qiao, Chuang Gao, Chunxiang Lu, Huazhen Liu, Yi Zhang, Aoxiang Jin, Qiqi Dai, Shihmo Yang, Bing Zhang and Yuanyuan Liu
J. Funct. Biomater. 2024, 15(4), 102; https://doi.org/10.3390/jfb15040102 - 15 Apr 2024
Viewed by 1568
Abstract
The dermal–epidermal junction (DEJ), located between the dermal–epidermal layers in human skin tissue, plays a significant role in its function. However, the limitations of biomaterial properties and microstructure fabrication methods mean that most current tissue engineered skin models do not consider the existence [...] Read more.
The dermal–epidermal junction (DEJ), located between the dermal–epidermal layers in human skin tissue, plays a significant role in its function. However, the limitations of biomaterial properties and microstructure fabrication methods mean that most current tissue engineered skin models do not consider the existence of DEJ. In this study, a nanofiber membrane that simulates the fluctuating structure of skin DEJ was prepared by the composite molding process. Electrospinning is a technique for the production of nanofibers, which can customize the physical and biological properties of biomaterials. At present, electrospinning technology is widely used in the simulation of customized natural skin DEJ. In this study, four different concentration ratios of poly (lactic-co-glycolic acid) (PLGA) and polycaprolactone (PCL) nanofiber membranes were prepared based on electrospinning technology. We selected a 15%PLGA + 5%PCL nanofiber membrane with mechanical properties, dimensional stability, hydrophilicity, and biocompatibility after physical properties and biological characterization. Then, the array-based microstructure model was prepared by three-dimensional (3D) printing. Subsequently, the microstructure was created on a 15%PLGA + 5%PCL membrane by the micro-imprinting process. Finally, the cell proliferation and live/dead tests of keratinocytes (HaCaTs) and fibroblasts (HSFs) were measured on the microstructural membrane and flat membrane. The results showed that 15%PLGA + 5%PCL microstructure membrane was more beneficial to promote the adhesion and proliferation of HaCaTs and HSFs than a flat membrane. Full article
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<p>Preparation process of microstructured nanofiber membrane.</p>
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<p>SEM images and diameter distribution of PLGA-PCL nanofiber membranes with different concentration ratios. (<b>A</b>–<b>D</b>) Micromorphology of PLGA-PCL nanofiber membrane magnified by 2000 times (×2000). (<b>A<sub>1</sub></b>–<b>D<sub>1</sub></b>) The microscopic morphology of PLGA-PCL membrane at 5000 times magnification (×5000). (<b>A<sub>2</sub></b>–<b>D<sub>2</sub></b>) Diameter distribution of PLGA-PCL nanofibers.</p>
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<p>Investigation of the FTIR test, shrinkage characteristics, and hydrophilicity of PLGA-PCL nanofibers. (<b>A</b>) Functional group analysis of PLGA-PCL nanofiber membranes using FTIR. (<b>B</b>) Shrinkage behavior. (<b>C</b>) Hydrophilicity; ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Investigation of the mechanical properties of PLGA-PCL nanofibers. (<b>A</b>) Stress–strain curves. (<b>B</b>) Tensile strength. (<b>C</b>) Elongation at break. (<b>D</b>) Tensile modulus; ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Evaluation of the biocompatibility of PLGA-PCL membranes for HaCaTs. (<b>A</b>) Live/dead staining of HaCaTs on nanofiber membranes. (<b>B</b>) Quantitative analysis of HaCaTs proliferation; ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Evaluation of the biocompatibility of PLGA-PCL nanofiber membranes for HSFs. (<b>A</b>) Live/dead staining of HSFs. (<b>B</b>) Quantitative analysis of HSFs proliferation on various nanofiber membranes; ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Evaluation of microstructured nanofiber membranes. (<b>A</b>) The 3D model of microstructured molds. (<b>B</b>) Light-curing printed molds. (<b>C</b>) 15%PLGA + 5%PCL membranes prepared. (<b>D</b>,<b>E</b>) Microstructured nanofiber membranes at different magnifications. (<b>F</b>) Micromorphology within the microstructured regions of the nanofibers (×1000).</p>
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<p>Assessment of biocompatibility of 15%PLGA + 5%PCL microstructure membrane for HaCaTs. (<b>A</b>) Live/dead staining of HaCaTs after 3 days of culture. (<b>B</b>) Confocal images displaying live/dead staining of HaCaTs. (<b>C</b>) Quantitative analysis of HaCaTs proliferation on microstructure membrane and flat membrane; ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Evaluation of the viability and proliferation of HSFs on 15%PLGA + 5%PCL microstructure membranes. (<b>A</b>) Live/dead staining of HSFs. (<b>B</b>) Confocal images showing live/dead staining of HSFs on microstructure membranes. (<b>C</b>) Quantitative analysis of HSFs proliferation on microstructure membrane and flat membrane; ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05.</p>
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13 pages, 2376 KiB  
Article
One-Piece Mini Dental Implant-Retained Mandibular Overdentures: 10-Year Clinical and Radiological Outcomes of a Non-Comparative Longitudinal Observational Study
by Nicole Schenk, Hristina Bukvic, Martin Schimmel, Samir Abou-Ayash and Norbert Enkling
J. Funct. Biomater. 2024, 15(4), 99; https://doi.org/10.3390/jfb15040099 - 11 Apr 2024
Cited by 1 | Viewed by 1998
Abstract
This study presents the first 10-year follow-up investigation of the implant survival and peri-implant outcomes of one-piece mini dental implants (MDIs) retaining mandibular implant overdentures (IODs), including marginal bone level alterations (ΔMBLs), clinical peri-implant parameters, and complications. Twenty participants with horizontally atrophied mandibles [...] Read more.
This study presents the first 10-year follow-up investigation of the implant survival and peri-implant outcomes of one-piece mini dental implants (MDIs) retaining mandibular implant overdentures (IODs), including marginal bone level alterations (ΔMBLs), clinical peri-implant parameters, and complications. Twenty participants with horizontally atrophied mandibles received complete dentures and four MDIs (diameter 1.8 mm) at baseline. The dentures were converted into IODs with O-ring attachments. The 10-year follow-up comprised a radiological assessment of ΔMBLs, peri-implant parameters, as well as biological and technical complications. Results from a 10-year follow-up of 14 participants showed a 100% implant survival rate for all 56 implants. The mean ΔMBL after 10 years was −1.12 ± 0.80 mm, with 49 implants classified as successful (ΔMBL < 2 mm) and 7 implants with satisfactory survival (ΔMBL 2–4 mm). Time after implant placement significantly influenced ΔMBL, with stable MBLs after 5 years. The prosthetic survival rate after 10 years was 93%. ΔMBLs were not influenced by implant position or gender but were significantly smaller in subjects older than 65 years. Conclusively, one-piece MDIs with O-ring attachments offer a reliable treatment option for horizontally atrophied mandibles after 10 years, with high implant and prosthetic survival rates, potentially benefiting from advanced age regarding peri-implant bone stability. Full article
(This article belongs to the Special Issue Advanced Biomaterials and Oral Implantology—2nd Edition)
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<p>Overview of a patient case: (<b>a</b>,<b>b</b>) occlusal view of the mandible with four mini dental implants (MDIs) during surgery, demonstrating the horizontally atrophied mandible with a knife-edge ridge; (<b>c</b>) MDIs at the 10-year follow-up examination; and (<b>d</b>) radiological evaluation of marginal bone levels (MBLs) at regions 42 and 44 at the 10-year follow-up. The blue lines represent the 1.8 mm diameter balls that were used to calibrate the subsequent measurements; the yellow lines represent the measured distances (MBLs) along the implant contours.</p>
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<p>Schematic drawing of an MDI implant with the corresponding attachment system.</p>
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<p>View of a radiological splint: (<b>a</b>) basal view of a radiological splint, including MH2 matrices and O-rings, and (<b>b</b>) clinical set-up for standardized radiograph recording.</p>
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<p>Distribution of marginal bone level alterations (ΔMBL) of all implants (<span class="html-italic">n</span> = 56) per age group.</p>
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14 pages, 3275 KiB  
Article
Biomechanical Effects of Ti-Base Abutment Height on the Dental Implant System: A Finite Element Analysis
by Miguel Beltrán-Guijarro, Esteban Pérez-Pevida, David Chávarri-Prado, Alejandro Estrada-Martínez, Markel Diéguez-Pereira, Fernando Sánchez-Lasheras and Aritza Brizuela-Velasco
J. Funct. Biomater. 2024, 15(4), 101; https://doi.org/10.3390/jfb15040101 - 11 Apr 2024
Cited by 1 | Viewed by 1666
Abstract
This study aims to analyse, using a finite element analysis, the effects of Ti-base abutment height on the distribution and magnitude of transferred load and the resulting bone microstrain in the bone-implant system. A three-dimensional bone model of the mandibular premolar section was [...] Read more.
This study aims to analyse, using a finite element analysis, the effects of Ti-base abutment height on the distribution and magnitude of transferred load and the resulting bone microstrain in the bone-implant system. A three-dimensional bone model of the mandibular premolar section was created with an implant placed in a juxta-osseous position. Three prosthetic models were designed: a 1 mm-high titanium-base (Ti-base) abutment with an 8 mm-high cemented monolithic zirconia crown was designed for model A, a 2 mm-high Ti-base abutment with a 7 mm-high crown for model B, and a 3 mm-high abutment with a 6 mm-high crown for model C. A static load of 150 N was applied to the central fossa at a six-degree angle with respect to the axial axis of the implant to evaluate the magnitude and distribution of load transfer and microstrain. The results showed a trend towards a direct linear association between the increase in the height of the Ti-base abutments and the increase in the transferred stress and the resulting microstrain to both the prosthetic elements and the bone/implant system. An increase in transferred stress and deformation of all elements of the system, within physiological ranges, was observed as the size of the Ti-base abutment increased. Full article
(This article belongs to the Special Issue Biomaterials and Biomechanics Modelling in Dental Implantology)
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<p>(<b>a</b>) Cortical bone 2 mm thick. (<b>b</b>) Medullary bone 21 mm high and 10 mm thick.</p>
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<p>Vega implant system, 4 mm in diameter and 10 mm in length.</p>
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<p>Three-dimensional models of the Ti-base with different transgingival heights.</p>
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<p>Three-dimensional models of the crowns with 8 mm (<b>a</b>), 7 mm (<b>b</b>) and 6 mm (<b>c</b>) height, respectively, with a thickness of 4 mm, and 3D model of the 7.97 mm long, 2.2 mm diameter prosthetic screw (<b>d</b>).</p>
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<p>Three-dimensional study models with their corresponding abutments and crowns. (Model <b>A</b>) with a 1 mm abutment and an 8 mm crown, (Model <b>B</b>) with a 2 mm abutment and a 7 mm crown and (Model <b>C</b>) with a 3 mm abutment and a 6 mm crown.</p>
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<p>The image shows the application of 150 N of force (B) in the central fossa with an angulation of six degrees with respect to the axial axis and fixed support (A).</p>
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<p>Three-dimensional study models, (Model <b>A</b>) with 1mm height abutment and 8mm height crown, (Model <b>B</b>) with 2 mm height abutment and 7 mm height crown and (Model <b>C</b>) with 3mm height abutment and 6mm height crown, with their corresponding von Mises stress location point expressed in MPa scaled to 150 MPa.</p>
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<p>Three-dimensional study models, (Model <b>A</b>) with 1 mm height abutment and 8mm height crown, (Model <b>B</b>) with 2 mm height abutment and 7 mm height crown and (Model <b>C</b>) with 3 mm height abutment and 6mm height crown, with their corresponding deformation.</p>
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13 pages, 2750 KiB  
Article
Antibacterial Properties of an Experimental Dental Resin Loaded with Gold Nanoshells for Photothermal Therapy Applications
by Shayan Darvish, Dana-Gabriela Budala and Ancuta Goriuc
J. Funct. Biomater. 2024, 15(4), 100; https://doi.org/10.3390/jfb15040100 - 11 Apr 2024
Cited by 6 | Viewed by 1500
Abstract
This study explored the chemical and antibacterial properties of a dental resin loaded with gold nanoshells (AuNPs) in conjunction with photothermal therapy (PTT) as a novel method against Streptococcus mutans (S. mutans) to prevent secondary caries. First, a 20-h minimum inhibitory [...] Read more.
This study explored the chemical and antibacterial properties of a dental resin loaded with gold nanoshells (AuNPs) in conjunction with photothermal therapy (PTT) as a novel method against Streptococcus mutans (S. mutans) to prevent secondary caries. First, a 20-h minimum inhibitory concentration (MIC) assay was performed on solutions of AuNPs with planktonic S. mutans under an LED device and laser at 660 nm. Next, resin blends containing 0, 1 × 1010, or 2 × 1010 AuNPs/mL were fabricated, and the degree of conversion (DC) was measured using an FTIR spectroscopy. Lastly, a colony forming unit (CFU) count was performed following 24 h growth of S. mutans on 6 mm diameter resin disks with different light treatments of an LED device and a laser at 660 nm. The MIC results only showed a reduction in S. mutans at AuNP concentrations less than 3.12 µg/mL under a laser illumination level of 95.5 J/cm2 compared to the dark treatment (p < 0.010 for each). CFU and DC results showed no significant dependence on any light treatment studied. The AuNPs expressed antibacterial effects following PPT against planktonic S. mutans but not in a polymerized dental adhesive resin. Future studies should focus on different shapes, structure, and concentrations of AuNPs loaded in a resin blend. Full article
(This article belongs to the Special Issue Recent Advances in Dental Resin Composites)
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<p>Degree of conversion for resin blends as a function of AuNP concentration. (Results are presented as mean ± one standard deviation (n = 6). Statistically different means are assigned different letters (<span class="html-italic">p</span> &lt; 0.05)).</p>
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<p>OD600 readings for <span class="html-italic">S. mutans</span> inhibitory responses to low AuNP concentration as a function of light treatment. Data are reported as average ± one standard deviation (n = 9). * Indicates significant difference from the dark treatment. Error bars presented in percentages.</p>
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<p>CFU count following application of 675 nm red LEDs. The base resin blend was prepared with Scientific Polymer Products BisEMA (RB_SPP). Data are reported as an average ± one standard deviation (n = 9). Different letters (a, b) indicate statistically different means (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>CFU count following application of a 660 nm red laser. The base resin blend was prepared with Scientific Polymer Products BisEMA (RB_SPP). Data are reported as an average ± one standard deviation (n = 9). Different letters (a, b) indicate statistically different means (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>CFU count following application of a 660 nm red laser. The base resin blend was prepared with Esstech Incorporated BisEMA (RB_EI). Data are reported as an average ± one standard deviation (n = 9). Different letters (a, b) indicate statistically different means (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>UV-Vis of (<b>left</b>): blends made with SPP-sourced BisEMA and (<b>right</b>): blends made with EI-sourced BisEMA as a function of AuNP absorbance peak at 660 nm. Data are reported as an average ± one standard deviation (n = 9). Different letters (a, b) indicate statistically different means (<span class="html-italic">p</span> &lt; 0.05).</p>
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14 pages, 4119 KiB  
Article
Plasma Gel Matrix as a Promising Carrier of Epigallocatechin Gallate for Regenerative Medicine
by Takashi Ushiki, Tomoharu Mochizuki, Mami Osawa, Katsuya Suzuki, Tetsuhiro Tsujino, Taisuke Watanabe, Carlos Fernando Mourão and Tomoyuki Kawase
J. Funct. Biomater. 2024, 15(4), 98; https://doi.org/10.3390/jfb15040098 - 10 Apr 2024
Viewed by 1696
Abstract
Plasma gel (PG) is a protein matrix prepared from platelet-poor plasma and can be utilized as a drug carrier for controlled release. We previously demonstrated its applicability as a carrier of polyphosphate. Epigallocatechin-3-gallate (EGCG) is the main flavonoid found in green tea and [...] Read more.
Plasma gel (PG) is a protein matrix prepared from platelet-poor plasma and can be utilized as a drug carrier for controlled release. We previously demonstrated its applicability as a carrier of polyphosphate. Epigallocatechin-3-gallate (EGCG) is the main flavonoid found in green tea and functions as a strong antioxidant. To explore the applicability of PG as an EGCG carrier, we examined the release of EGCG from the PG matrix using an in vitro system. Pooled platelet-poor plasma (PPP) was prepared from four healthy adult male donors, mixed with EGCG, and heated at 75 °C for 10 or 20 min to prepare the PG matrix. The PG–EGCG matrix was incubated in PBS at 37 °C, and the EGCG released into PBS was determined using spectrophotometry. The antioxidant capacity was determined based on the principle of the iodine decolorization reaction. EGCG precipitated and incorporated into the PG matrix during thermal preparation. Trypsin, used to simulate the in vivo degradation of PG, released EGCG from the PG matrix over time. The released EGCG maintained its antioxidant capacity during incubation. These results indicate that thermally prepared PG matrices can be utilized as a promising EGCG carrier in the fields of tissue engineering and regenerative medicine. Full article
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<p>The absorption spectra of PBS containing epigallocatechin gallate (EGCG) in the absence (<b>a</b>) and presence of 10% platelet-poor plasma (PPP) (<b>b</b>). The absorption of the sample without (black lines) and with 10 μM EGCG (grey lines) was examined in the range of 250 to 500 nm.</p>
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<p>The standard curves for epigallocatechin gallate (EGCG) in PBS containing 1% (<b>b</b>) and 10% (<span class="html-italic">v</span>/<span class="html-italic">v</span>) (<b>c</b>) platelet-poor plasma (PPP). In the control (<b>a</b>), PPP was not added to PBS. Plasma gel was not used for this quantitative analysis. Each point represents the average of duplicate determination.</p>
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<p>The scanning electron microscopy images of freshly prepared plasma gel (PG) matrices containing approximately 10% (<b>b</b>) and 15% (<span class="html-italic">v</span>/<span class="html-italic">v</span>) (<b>c</b>) of 20 mM epigallocatechin gallate (EGCG) in platelet-poor plasma. The PG shown in (<b>a</b>) contained no EGCG. The cross-sections of the individual PG matrices were examined. The microstructures, which were not detected in the control, are marked in light yellow in (<b>b</b>,<b>c</b>). Similar findings were obtained from three independent experiments.</p>
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<p>The time-course of changes in plasma gel (PG) matrices containing epigallocatechin gallate (EGCG) in PBS in the presence of 0.025% (<span class="html-italic">v</span>/<span class="html-italic">v</span>) trypsin at 37 °C. (<b>a</b>) Just after mixing, (<b>b</b>) day 1, (<b>c</b>) day 3, and (<b>d</b>) day 7 of incubation. Similar findings were obtained from three independent experiments.</p>
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<p>Time-course changes in the levels of EGCG released from the PG matrix into the PBS. (<b>a</b>) In the PG matrices containing low EGCG levels, trypsin significantly increased EGCG release on and after day 4. * <span class="html-italic">p</span> &lt; 0.05 (n = 6) compared with the control on day 1. (<b>b</b>) To evaluate the net EGCG antioxidant capacity (see <a href="#jfb-15-00098-f006" class="html-fig">Figure 6</a>), the preparation protocol for the PG–EGCG matrix was modified as described in the Materials and Methods section. In the PG matrices containing high EGCG levels, trypsin significantly increased EGCG release on and after day 5. * <span class="html-italic">p</span> &lt; 0.05 (n = 6) compared with the control on day 1. ** <span class="html-italic">p</span> &lt; 0.05 (n = 6) compared with the PG-EGCG with trypsin group at the same time points.</p>
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<p>Standard curve of iodine decolorization (<b>a</b>), antioxidant capacity of PBS samples (<b>b</b>,<b>c</b>), and pH of PBS samples (<b>d</b>). (<b>a</b>) Linearity was obtained in this range of the standard curve using an authentic EGCG reagent. Data are representative of three independent experiments. (<b>b</b>) Time-course changes in the antioxidant capacity of the PG matrix alone, PG matrix with trypsin, EGCG-containing PG matrix without trypsin, and EGCG-containing PG matrix with trypsin were recorded in 500 μL PBS at 37 °C. * <span class="html-italic">p</span> &lt; 0.05 (n = 6) compared with the corresponding group on day 1. (<b>c</b>) Time-course changes in the net antioxidant capacities of EGCG and PG calculated from the data in panel (<b>b</b>). * <span class="html-italic">p</span> &lt; 0.05 (n = 6) compared with the counterpart at the same time points. (<b>d</b>) The effects of the anticoagulant, ACD-A, and other additives on the pH of the PBS samples. The data are representative of the data from repeated experiments.</p>
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15 pages, 4307 KiB  
Article
Functionalization of PCL-Based Fiber Scaffolds with Different Sources of Calcium and Phosphate and Odontogenic Potential on Human Dental Pulp Cells
by Caroline Anselmi, Igor Paulino Mendes Soares, Rafaella Lara Maia Mota, Maria Luísa Leite, Rafael Antonio de Oliveira Ribeiro, Lídia de Oliveira Fernandes, Marco C. Bottino, Carlos Alberto de Souza Costa and Josimeri Hebling
J. Funct. Biomater. 2024, 15(4), 97; https://doi.org/10.3390/jfb15040097 - 10 Apr 2024
Cited by 1 | Viewed by 1564
Abstract
This study investigated the incorporation of sources of calcium, phosphate, or both into electrospun scaffolds and evaluated their bioactivity on human dental pulp cells (HDPCs). Additionally, scaffolds incorporated with calcium hydroxide (CH) were characterized for degradation, calcium release, and odontogenic differentiation by HDPCs. [...] Read more.
This study investigated the incorporation of sources of calcium, phosphate, or both into electrospun scaffolds and evaluated their bioactivity on human dental pulp cells (HDPCs). Additionally, scaffolds incorporated with calcium hydroxide (CH) were characterized for degradation, calcium release, and odontogenic differentiation by HDPCs. Polycaprolactone (PCL) was electrospun with or without 0.5% w/v of calcium hydroxide (PCL + CH), nano-hydroxyapatite (PCL + nHA), or β-glycerophosphate (PCL + βGP). SEM/EDS analysis confirmed fibrillar morphology and particle incorporation. HDPCs were cultured on the scaffolds to assess cell viability, adhesion, spreading, and mineralized matrix formation. PCL + CH was also evaluated for gene expression of odontogenic markers (RT-qPCR). Data were submitted to ANOVA and Student’s t-test (α = 5%). Added CH increased fiber diameter and interfibrillar spacing, whereas βGP decreased both. PCL + CH and PCL + nHA improved HDPC viability, adhesion, and proliferation. Mineralization was increased eightfold with PCL + CH. Scaffolds containing CH gradually degraded over six months, with calcium release within the first 140 days. CH incorporation upregulated DSPP and DMP1 expression after 7 and 14 days. In conclusion, CH- and nHA-laden PCL fiber scaffolds were cytocompatible and promoted HDPC adhesion, proliferation, and mineralized matrix deposition. PCL + CH scaffolds exhibit a slow degradation profile, providing sustained calcium release and stimulating HDPCs to upregulate odontogenesis marker genes. Full article
(This article belongs to the Special Issue Biomaterials for Dental Pulp Tissue)
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<p>(<b>a</b>) Primary culture isolation of human dental pulp cells from third molars: Pulp tissue was collected and subjected to enzymatic digestion (type 1 collagenase solution; 3 mg/mL). Adherent cells were subcultured and pooled in the third passage for phenotypic characterization. (<b>b</b>) Immunofluorescence images (10×) for labeling antigens present on multipotent cells (STRO-1 and CD146) present in the established culture. Green fluorescence (FITC) indicates antibody labeling and blue fluorescence marks the nuclei (Hoescht). Negative FITC is the secondary antibody control. Scale bar: 100 µm.</p>
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<p>(<b>a</b>) SEM images (2000×) of the scaffold surfaces. (<b>b</b>) In EDS plots, the incorporation of the inorganic particles was detected by spectra compatible with the elements Ca, P, and Na (pointers and inserts). Signals for the elements Au and Al represent the gold coating of the specimens and aluminum foil under the scaffolds, respectively. The graphs represent (<b>c</b>) fiber diameter and (<b>d</b>) percentage of interfibrillar spaces. Mean and standard deviation. Different letters indicate statistical differences (ANOVA and Welch’s ANOVA, Games–Howell, and Tukey post-hoc testing, n = 16, α = 5%).</p>
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<p>Direct fluorescence images (10×) of cell adhesion and spreading assay at 1, 3, and 7 days of HDPC culture on PCL, PCL + CH, PCL + nHA, and PCL + βGP scaffold formulations. Red fluorescence marks the actin filaments in the cell cytoskeleton. Blue fluorescence marks the cell nuclei. Scale bar: 100 µm.</p>
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<p>(<b>a</b>) Direct fluorescence images (10×) of the cell viability assay (Live/Dead) at 1, 7, and 14 days of HDPC culture on PCL, PCL + CH, PCL + nHA, and PCL + βGP scaffold formulations. Green fluorescence marks viable cells and red fluorescence marks cells in the process of death. Scale bar: 100 µm. (<b>b</b>) Viability of HDPCs over 1, 7, and 14 days of culture on the scaffold surface. Mean and standard deviation. Percent cell viability calculated based on control (PCL) values at 1 day. Uppercase letters compare the main effects of the ‘time point’ factor, and lowercase letters compare the ‘formulations’ factor. Different letters indicate statistical differences (Repeated measures ANOVA, Sidak post hoc; n = 8; α = 5%).</p>
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<p>(<b>a</b>) Representative images of scaffolds stained with Alizarin red. No cells (background), cells cultured with differentiation media, and basal media. Scale bar: 1 mm. (<b>b</b>) Deposition of mineralized matrix (% relative to control) after 21 days of HDPC cultivation on scaffold formulations using a basal or osteogenic medium. Mean and standard deviation. Uppercase letters compare the main effects of the ‘formulation’ factor, and lowercase letters compare the ‘media condition’ factor. Different letters indicate statistical differences (Two-way ANOVA, Sidak post hoc; n = 8; α = 5%).</p>
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<p>Line graph showing (<b>a</b>) mass change in scaffolds, with or without 0.5% CH (<span class="html-italic">w</span>/<span class="html-italic">v</span>), stored in deionized water for up to 6 months; (<b>b</b>) accumulated calcium release from the scaffolds, with or without 0.5% CH (<span class="html-italic">w</span>/<span class="html-italic">v</span>), storage medium (ultrapure water). Mean values and confidence intervals (n = 8; 95% CI).</p>
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<p>Gene expression of <span class="html-italic">COL1A1</span>, <span class="html-italic">ALPL</span>, <span class="html-italic">DSPP</span>, <span class="html-italic">DMP1</span>, <span class="html-italic">OPN</span>, and <span class="html-italic">OCN</span> by HDPCs cultured on scaffolds with or without 0.5% CH for 7 and 14 days of culture. Mean and standard deviation. ns = absence of statistical significance between groups (Student’s <span class="html-italic">t</span>-test, n = 6, α = 5%).</p>
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15 pages, 8413 KiB  
Article
Dental Implant Abutment Screw Loss: Presentation of 10 Cases
by Maryam Soleimani, Jarosław Żmudzki, Wojciech Pakieła, Anna Jaśkowska and Kornel Krasny
J. Funct. Biomater. 2024, 15(4), 96; https://doi.org/10.3390/jfb15040096 - 9 Apr 2024
Viewed by 2151
Abstract
Re-tightening the loosened dental implant abutment screw is an accepted procedure, however the evidence that such screw will hold sufficiently is weak. The purpose of this study was material analysis of lost dental implant abutment screws made of the TiAlV alloy from various [...] Read more.
Re-tightening the loosened dental implant abutment screw is an accepted procedure, however the evidence that such screw will hold sufficiently is weak. The purpose of this study was material analysis of lost dental implant abutment screws made of the TiAlV alloy from various manufacturers, which became lost due to unscrewing or damaged when checking if unscrewed; undamaged screws could be safely re-tightened. Among 13 failed screws retrieved from 10 cases, 10 screws were removed due to untightening and 3 were broken but without mechanical damage at the threads. Advanced corrosion was found on nine screws after 2 years of working time on all surfaces, also not mechanically loaded. Sediments observed especially in the thread area did not affect the corrosion process because of no pit densification around sediments. Pitting corrosion visible in all long-used screws raises the question of whether the screws should be replaced after a certain period during service, even if they are well-tightened. This requires further research on the influence of the degree of corrosion on the loss of the load-bearing ability of the screw. Full article
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<p>Service of broken screw exemplary case.</p>
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<p>X-ray exemplary imaging of the screw failures: left X-ray, loose/broken screw in the upper left premolar CsNo8; upper-right X-ray, broken screws in implants 21 and 23 and loosened screws in implants 24 and 25 CsNo2; lower-right X-ray, broken hex in implant 46, both screws in 44 and 46 were loose in CSNo7.</p>
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<p>Pitting corrosion, crack on the shank below screw head, and brownish/white sediments shown in order: CsNo1, CsNo8 (TiNc), CsNo2, CsNo4.</p>
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<p>Pits on the shank of CsNo2 implant abutment screw and visible traces at the bottom of the pit.</p>
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<p>Examples of the deepest pitting corrosion found on the thread and the beginnings of dissolution of machining tips at thread root in cross-sectional micrographs of a CsNo2 implant screw.</p>
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<p>Roughness profile for implant screw CsNo2 with visible uniform traces of machining and clear dimensions of deposits, and an example of wide pitting corrosion with its depth. Region between 0 and 1 related to bottom and the edge of the pits respectively.</p>
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<p>Fractures in the two broken screws among four implants which supported denture in case CsNo2.</p>
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<p>SEM EDS of brownish and white sediments.</p>
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<p>SEM EDS map around a corrosion pit on the CsNo8 implant screw with TiN coating.</p>
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<p>SEM EDS map around a corrosion pit on the CsNo8 implant screw with TiN coating.</p>
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24 pages, 3189 KiB  
Article
Green Synthesis of Gold Nanoparticles Using Liquiritin and Other Phenolics from Glycyrrhiza glabra and Their Anti-Inflammatory Activity
by Ali O. E. Eltahir, Kim L. Lategan, Oladipupo M. David, Edmund J. Pool, Robert C. Luckay and Ahmed A. Hussein
J. Funct. Biomater. 2024, 15(4), 95; https://doi.org/10.3390/jfb15040095 - 6 Apr 2024
Viewed by 2617
Abstract
Phenolic compounds are the main phytochemical constituents of many higher plants. They play an important role in synthesizing metal nanoparticles using green technology due to their ability to reduce metal salts and stabilize them through physical interaction/conjugation to the metal surface. Six pure [...] Read more.
Phenolic compounds are the main phytochemical constituents of many higher plants. They play an important role in synthesizing metal nanoparticles using green technology due to their ability to reduce metal salts and stabilize them through physical interaction/conjugation to the metal surface. Six pure phenolic compounds were isolated from licorice (Glycyrrhiza glabra) and employed in synthesizing gold nanoparticles (AuNPs). The isolated compounds were identified as liquiritin (1), isoliquiritin (2), neoisoliquiritin (3), isoliquiritin apioside (4), liquiritin apioside (5), and glabridin (6). The synthesized AuNPs were characterized using UV, zeta sizer, HRTEM, and IR and tested for their stability in different biological media. The phenolic isolates and their corresponding synthesized NP conjugates were tested for their potential in vitro cytotoxicity. The anti-inflammatory effects were investigated in both normal and inflammation-induced settings, where inflammatory biomarkers were stimulated using lipopolysaccharides (LPSs) in the RAW 264.7 macrophage cell line. LPS, functioning as a mitogen, promotes cell growth by reducing apoptosis, potentially contributing to observed outcomes. Results indicated that all six pure phenolic isolates inhibited cell proliferation. The AuNP conjugates of all the phenolic isolates, except liquiritin apioside (5), inhibited cell viability. LPS initiates inflammatory markers by binding to cell receptors and setting off a cascade of events leading to inflammation. All the pure phenolic isolates, except isoliquiritin, neoisoliquiritin, and isoliquiritin apioside inhibited the inflammatory activity of RAW cells in vitro. Full article
(This article belongs to the Special Issue Nanoparticles: Fabrication, Properties and Biomedical Application)
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<p>The chemical structures of the isolated compounds (<b>1</b>–<b>6</b>) from licorice.</p>
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<p>The chemical structures of the isolated compounds (<b>1</b>–<b>6</b>) from licorice.</p>
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<p>The assessment of RAW 264.7 cell viability and NO after 24 h exposure to various AuNPs, TE, and compounds in either the presence or absence of LPS. Cells were treated with the following: (<b>a</b>,<b>b</b>) compound <b>1</b>; (<b>c</b>,<b>d</b>) compound <b>2</b>; (<b>e</b>,<b>f</b>) compound <b>3</b>; (<b>g</b>,<b>h</b>) compound <b>4</b>; (<b>i</b>) compound <b>5</b>; (<b>j</b>,<b>k</b>) compound <b>6</b>; (<b>l</b>,<b>m</b>) TE. Data are presented as mean ± SEM, where the <span class="html-italic">p</span>-value indicates statistical significance against the relevant control, using one-way ANOVA. * <span class="html-italic">p</span> &lt; 0.001, *** <span class="html-italic">p</span> = 0.003, and **** <span class="html-italic">p</span> = 0.005. Sample X + LPS and green should be Sample X + AuNPs + LPS.</p>
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<p>The assessment of RAW 264.7 cell viability and NO after 24 h exposure to various AuNPs, TE, and compounds in either the presence or absence of LPS. Cells were treated with the following: (<b>a</b>,<b>b</b>) compound <b>1</b>; (<b>c</b>,<b>d</b>) compound <b>2</b>; (<b>e</b>,<b>f</b>) compound <b>3</b>; (<b>g</b>,<b>h</b>) compound <b>4</b>; (<b>i</b>) compound <b>5</b>; (<b>j</b>,<b>k</b>) compound <b>6</b>; (<b>l</b>,<b>m</b>) TE. Data are presented as mean ± SEM, where the <span class="html-italic">p</span>-value indicates statistical significance against the relevant control, using one-way ANOVA. * <span class="html-italic">p</span> &lt; 0.001, *** <span class="html-italic">p</span> = 0.003, and **** <span class="html-italic">p</span> = 0.005. Sample X + LPS and green should be Sample X + AuNPs + LPS.</p>
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<p>The assessment of RAW 264.7 cell viability and NO after 24 h exposure to various AuNPs, TE, and compounds in either the presence or absence of LPS. Cells were treated with the following: (<b>a</b>,<b>b</b>) compound <b>1</b>; (<b>c</b>,<b>d</b>) compound <b>2</b>; (<b>e</b>,<b>f</b>) compound <b>3</b>; (<b>g</b>,<b>h</b>) compound <b>4</b>; (<b>i</b>) compound <b>5</b>; (<b>j</b>,<b>k</b>) compound <b>6</b>; (<b>l</b>,<b>m</b>) TE. Data are presented as mean ± SEM, where the <span class="html-italic">p</span>-value indicates statistical significance against the relevant control, using one-way ANOVA. * <span class="html-italic">p</span> &lt; 0.001, *** <span class="html-italic">p</span> = 0.003, and **** <span class="html-italic">p</span> = 0.005. Sample X + LPS and green should be Sample X + AuNPs + LPS.</p>
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<p>A proposed mechanism for the reduction and capping of chalcones isolated in this study (represented by compound <b>3</b>). The reduction process includes the loss of an electron and this step is pH-dependent. The second step is the capping process where the compound forming a shell may be two or three layers around the metal NPs.</p>
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<p>Schematic diagram for the isolation and purification of the major compounds from licorice, Fr(s). = Fraction(s).</p>
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22 pages, 14658 KiB  
Article
Advancing 3D Dental Implant Finite Element Analysis: Incorporating Biomimetic Trabecular Bone with Varied Pore Sizes in Voronoi Lattices
by Dawit Bogale Alemayehu, Masahiro Todoh and Song-Jeng Huang
J. Funct. Biomater. 2024, 15(4), 94; https://doi.org/10.3390/jfb15040094 - 4 Apr 2024
Cited by 3 | Viewed by 2886
Abstract
The human mandible’s cancellous bone, which is characterized by its unique porosity and directional sensitivity to external forces, is crucial for sustaining biting stress. Traditional computer- aided design (CAD) models fail to fully represent the bone’s anisotropic structure and thus depend on simple [...] Read more.
The human mandible’s cancellous bone, which is characterized by its unique porosity and directional sensitivity to external forces, is crucial for sustaining biting stress. Traditional computer- aided design (CAD) models fail to fully represent the bone’s anisotropic structure and thus depend on simple isotropic assumptions. For our research, we use the latest versions of nTOP 4.17.3 and Creo Parametric 8.0 software to make biomimetic Voronoi lattice models that accurately reflect the complex geometry and mechanical properties of trabecular bone. The porosity of human cancellous bone is accurately modeled in this work using biomimetic Voronoi lattice models. The porosities range from 70% to 95%, which can be achieved by changing the pore sizes to 1.0 mm, 1.5 mm, 2.0 mm, and 2.5 mm. Finite element analysis (FEA) was used to examine the displacements, stresses, and strains acting on dental implants with a buttress thread, abutment, retaining screw, and biting load surface. The results show that the Voronoi model accurately depicts the complex anatomy of the trabecular bone in the human jaw, compared to standard solid block models. The ideal pore size for biomimetic Voronoi lattice trabecular bone models is 2 mm, taking in to account both the von Mises stress distribution over the dental implant, screw retention, cortical bone, cancellous bone, and micromotions. This pore size displayed balanced performance by successfully matching natural bone’s mechanical characteristics. Advanced FEA improves the biomechanical understanding of how bones and implants interact by creating more accurate models of biological problems and dynamic loading situations. This makes biomechanical engineering better. Full article
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<p>Two-dimensional drawing of dental implant assembly in creo parametric: front, side, and top views with detailed dimensions (mm).</p>
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<p>Comparative analysis of biomimetic Voronoi latticed spongy bone structures with four distinct pore sizes, (<b>a</b>) 1.0 mm, (<b>b</b>) 1.5 mm, (<b>c</b>) 2.0 mm, and (<b>d</b>) 2.5 mm, designed using nTopology (nTop 4.17.3) software.</p>
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<p>Biomimetic Voronoi-latticed trabecular bone constructed in nTopology featuring the following: (<b>a</b>) open-cell randomized lattice graph, (<b>b</b>) truncated thicken lattice graph, (<b>c</b>) finite element (FE) volume mesh, (<b>d</b>) FE boundary configuration utilizing body nodes. Each red squares with blue arros are the zoomed and detailed view for clarity purpose of images from (<b>a</b>–<b>d</b>).</p>
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<p>Components of the dental implant system, including the following: (<b>a</b>) application of dynamic explicit oblique loading at the load reference point with the MPC constraint, (<b>b</b>) 3D model components designed for finite element analysis.</p>
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<p>Detailed meshing of dental implant components and Voronoi lattice biomimetic bone, with an emphasis on the mesh configuration, as illustrated in the zoomed section.</p>
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<p>Relative density and porosity of biomimetic Voronoi lattice trabecular bone across various pore sizes.</p>
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<p>An equivalent oblique dynamic load distribution on the dental implant crown during mastication, a multidirectional analysis over 0.5 s cycle.</p>
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<p>Maximum von Mises stress distribution in double-sliced assembled implant parts for four biomimetic Voronoi-latticed trabecular bones: (<b>a</b>) VTB10, (<b>b</b>) VTB15, (<b>c</b>) VTB20, and (<b>d</b>) VTB25.</p>
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<p>Contour von Mises stress distribution in dental implants and retaining screws across biomimetic Voronoi-latticed trabecular bone pore sizes: (<b>a</b>) VTB10, (<b>b</b>) VTB15, (<b>c</b>) VTB20, (<b>d</b>) VTB25 for implants, and (<b>e</b>) VTB10, (<b>f</b>) VTB15, (<b>g</b>) VTB20, (<b>h</b>) VTB25 for retaining screws.</p>
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<p>Maximum von Mises stresses in biomimetic Voronoi lattice trabecular and cortical bones for (<b>a</b>) VTB10, (<b>b</b>) VTB15, (<b>c</b>) VTB20, and (<b>d</b>) VTB25.</p>
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<p>Contour plots of the magnitude of displacements in biomimetic Voronoi lattice trabecular bone for pore sizes: (<b>a</b>) VTB10, (<b>b</b>) VTB15, (<b>c</b>) VTB20, (<b>d</b>) VTB25.</p>
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<p>Maximum displacement response in axial, mesiodistal, and buccolingual directions for biomimetic Voronoi lattice trabecular bones: (<b>a</b>) VTB10, (<b>b</b>) VTB15, (<b>c</b>) VTB20, and (<b>d</b>) VTB25.</p>
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<p>Dynamic reaction forces in dental implant assemblies across biomimetic Voronoi-latticed trabecular bone pore sizes: (<b>a</b>) VTB10, (<b>b</b>) VTB15, (<b>c</b>) VTB20, and (<b>d</b>) VTB25.</p>
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33 pages, 4014 KiB  
Review
Advancements in Hybrid Cellulose-Based Films: Innovations and Applications in 2D Nano-Delivery Systems
by Ghazaleh Ramezani, Ion Stiharu, Theo G. M. van de Ven and Vahe Nerguizian
J. Funct. Biomater. 2024, 15(4), 93; https://doi.org/10.3390/jfb15040093 - 4 Apr 2024
Cited by 3 | Viewed by 2132
Abstract
This review paper delves into the realm of hybrid cellulose-based materials and their applications in 2D nano-delivery systems. Cellulose, recognized for its biocompatibility, versatility, and renewability, serves as the core matrix for these nanomaterials. The paper offers a comprehensive overview of the latest [...] Read more.
This review paper delves into the realm of hybrid cellulose-based materials and their applications in 2D nano-delivery systems. Cellulose, recognized for its biocompatibility, versatility, and renewability, serves as the core matrix for these nanomaterials. The paper offers a comprehensive overview of the latest advancements in the creation, analysis, and application of these materials, emphasizing their significance in nanotechnology and biomedical domains. It further illuminates the integration of nanomaterials and advanced synthesis techniques that have significantly improved the mechanical, chemical, and biological properties of hybrid cellulose-based materials. Full article
(This article belongs to the Special Issue Feature Review Papers on Functional Biomaterials)
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<p>Schematic representation of cellulose structures from resources to molecular level [<a href="#B1-jfb-15-00093" class="html-bibr">1</a>]. Copyright with permission [A Review on Surface-Functionalized Cellulosic Nanostructures as Biocompatible Antibacterial Materials|Nano-Micro Letters (<a href="http://www.springer.com" target="_blank">www.springer.com</a>)].</p>
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<p>Schematic illustration of the synthesis of the conventional cellulose nanocrystalline from cellulose nanofibrils under acid hydrolysis [<a href="#B39-jfb-15-00093" class="html-bibr">39</a>]. Copyright with permission [Biotemplated Hollow Mesoporous Silica Particles as Efficient Carriers for Drug Delivery|ACS Applied Bio Materials].</p>
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<p>(<b>a</b>) Representative images of different stages of the gel formation. (<b>b</b>) Schematic of the reaction of carboxymethyl cellulose fiber and epichlorohydrin to form the gel [<a href="#B40-jfb-15-00093" class="html-bibr">40</a>]. Copyright with permission [Highly Absorbent Antibacterial and Biofilm-Disrupting Hydrogels from Cellulose for Wound Dressing Applications|ACS Applied Materials &amp; Interfaces].</p>
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<p>Schematic of cellulose reaction with sodium periodate to produce dialdehyde-modified cellulose (DAMC), followed by reaction with sodium chlorite to synthesize dialdehyde-dicarboxylate-modified nanofibrils, and finally BHNC isolation through heat treatment [<a href="#B6-jfb-15-00093" class="html-bibr">6</a>]. Copyright with permission [Antibacterial Pickering emulsions stabilized by bifunctional hairy nanocellulose—ScienceDirect].</p>
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<p>(<b>a</b>) Applications of MOF/cellulose composite as antibacterial material and for protein immobilization. (<b>a-1</b>) Schematics of the fabrication of MOF wood composite materials and their antibacterial mechanism. (<b>a-2</b>) Illustration of antibody or enzyme immobilized by MOF on fabric substrate. (<b>b</b>) MOF/cellulose hydrogel exhibited a color transition upon sensing histamine (HI) vapor and the truth table of the logic analytical device for HI monitoring. (<b>c</b>) Photograph of a CNF@c-MOF double-layer supercapacitor device and an LED powered by devices in series under different deformations. Copyright with permission [Review on design strategies and applications of metal-organic framework-cellulose composites—ScienceDirect].</p>
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<p>In vivo photothermal cancer therapy. (<b>a</b>) Graphic depiction of laser illumination and temperature at 0, 1, 2, 3, 4, and 5 min. (<b>b</b>) Temperature augmentation during laser illumination. (<b>c</b>) Tumor volumes during the observation period. (<b>d</b>) Tumor weights measured at day 15. Unpaired <span class="html-italic">t</span> test, <span class="html-italic">n</span> = 5, *** <span class="html-italic">p</span> &lt; 0.001, ns stands for nonsignificant. Data are mean ± SD. (<b>e</b>) Representative images of tumors for each group. (<b>f</b>) Body weights of mice during different therapies. (<b>g</b>) Graphical representation of PTT/chemotherapy therapy. Intratumoral injection of cellulose/MXene/DOX hydrogels into mice followed by four steps: (1) cellulose/MXene/DOX hydrogels injected into the tumor site; (2) NIR irradiation on (PTT and chemotherapy); (3) NIR irradiation off (adjuvant chemotherapy); (4) degradation of the cellulose hydrogel platform [<a href="#B141-jfb-15-00093" class="html-bibr">141</a>]. Copyright with permission [Two-Dimensional MXene (Ti3C2)-Integrated Cellulose Hydrogels: Toward Smart Three-Dimensional Network Nanoplatforms Exhibiting Light-Induced Swelling and Bimodal Photothermal/Chemotherapy Anticancer Activity|ACS Applied Materials &amp; Interfaces].</p>
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11 pages, 2449 KiB  
Article
Nitric Oxide Photorelease from Silicone Films Doped with N-Nitroso BODIPY
by Natalia A. Virts, Tatyana Yu. Karogodina, Mikhail A. Panfilov, Alexey Yu. Vorob’ev and Alexander E. Moskalensky
J. Funct. Biomater. 2024, 15(4), 92; https://doi.org/10.3390/jfb15040092 - 2 Apr 2024
Cited by 3 | Viewed by 1668
Abstract
Nitric oxide (NO) is a unique biochemical mediator involved in the regulation of vital processes. Light-controllable NO releasers show promise in the development of smart therapies. Here, we present a novel biocompatible material based on polydimethylsiloxane (PDMS) doped with BODIPY derivatives containing an [...] Read more.
Nitric oxide (NO) is a unique biochemical mediator involved in the regulation of vital processes. Light-controllable NO releasers show promise in the development of smart therapies. Here, we present a novel biocompatible material based on polydimethylsiloxane (PDMS) doped with BODIPY derivatives containing an N-nitroso moiety that is capable of the photoinduced generation of NO. We study the green-light-induced NO-release properties with the following three methods: electrochemical gas-phase sensor, liquid-phase sensor, and the Griess assay. Prolonged release of NO from the polymer films after short irradiation by narrow-band LED light sources and a laser beam is demonstrated. Importantly, this was accompanied by no or little release of the parent compound (BODIPY-based photodonor). Silicone films with the capability of controllable and clean NO release can potentially be used as a highly portable NO delivery system for different therapeutic applications. Full article
(This article belongs to the Special Issue Advanced Biomaterials for Drug Delivery)
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<p>BODIPY-doped PDMS films fabrication process (<b>A</b>); and photo (<b>B</b>).</p>
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<p>(<b>A</b>,<b>B</b>) absorption spectra in EtOH and PDMS of <b>B1</b> and <b>B0</b>, respectively; (<b>C</b>,<b>D</b>) changes in the absorption spectra of <b>B1</b> during photolysis; (<b>E</b>) example of the decomposition of absorption spectra to the spectra of the initial and final products (photolysis in EtOH for 2 min); and (<b>F</b>) kinetics of the transition from initial to final product in EtOH and PDMS.</p>
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<p>(<b>A</b>) Photo of the laser beam passing through <b>B1</b>-doped PDMS film; (<b>B</b>) Griess assay showing the increase in nitrite concentration in a sample after irradiation of PDMS films by green light; (<b>C</b>) dynamics of gas-phase NO release from PDMS film monitored with selective NO-B4 sensor; (<b>D</b>) scheme of experimental setup for measuring laser-induced NO release into aqueous solution; and (<b>E</b>) prolonged light-induced, power-dependent release of NO into the aqueous solution monitored by an electrochemical sensor.</p>
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<p>(<b>A</b>) Absorption spectra of cuvettes with DMSO (red line) and PBS (black line) after incubation of PDMS film doped with the dye <b>B0</b>; and (<b>B</b>) time dependance of the dye leaking into PBS.</p>
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<p>The structure of the photodonor.</p>
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11 pages, 533 KiB  
Review
Comparison of Zirconia Implant Surface Modifications for Optimal Osseointegration
by Hyun Woo Jin, Sammy Noumbissi and Thomas G. Wiedemann
J. Funct. Biomater. 2024, 15(4), 91; https://doi.org/10.3390/jfb15040091 - 2 Apr 2024
Cited by 3 | Viewed by 2435
Abstract
Zirconia ceramic implants are commercially available from a rapidly growing number of manufacturers. Macroscopic and microscopic surface design and characteristics are considered to be key determining factors in the success of the osseointegration process. It is, therefore, crucial to assess which surface modification [...] Read more.
Zirconia ceramic implants are commercially available from a rapidly growing number of manufacturers. Macroscopic and microscopic surface design and characteristics are considered to be key determining factors in the success of the osseointegration process. It is, therefore, crucial to assess which surface modification promotes the most favorable biological response. The purpose of this study was to conduct a comparison of modern surface modifications that are featured in the most common commercially available zirconia ceramic implant systems. A review of the currently available literature on zirconia implant surface topography and the associated bio-physical factors was conducted, with a focus on the osseointegration of zirconia surfaces. After a review of the selected articles for this study, commercially available zirconia implant surfaces were all modified using subtractive protocols. Commercially available ceramic implant surfaces were modified or enhanced using sandblasting, acid etching, laser etching, or combinations of the aforementioned. From our literature review, laser-modified surfaces emerged as the ones with the highest surface roughness and bone–implant contact (BIC). It was also found that surface roughness could be controlled to achieve optimal roughness by modifying the laser output power during manufacturing. Furthermore, laser surface modification induced a very low amount of preload microcracks in the zirconia. Osteopontin (OPN), an early–late osteogenic differentiation marker, was significantly upregulated in laser-treated surfaces. Moreover, surface wettability was highest in laser-treated surfaces, indicating favorable hydrophilicity and thus promoting early bone forming, cell adhesion, and subsequent maturation. Sandblasting followed by laser modification and sandblasting followed by acid etching and post-milling heat treatment (SE-H) surfaces featured comparable results, with favorable biological responses around zirconia implants. Full article
(This article belongs to the Special Issue Surface Properties and Modifications of Zirconia)
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<p>Schematic workflow.</p>
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14 pages, 6661 KiB  
Article
Synthesis of Alginate/Collagen Bioink for Bioprinting Respiratory Tissue Models
by Amanda Zimmerling, Yan Zhou and Xiongbiao Chen
J. Funct. Biomater. 2024, 15(4), 90; https://doi.org/10.3390/jfb15040090 - 1 Apr 2024
Cited by 4 | Viewed by 2409
Abstract
Synthesis of bioinks for bioprinting of respiratory tissue requires considerations related to immunogenicity, mechanical properties, printability, and cellular compatibility. Biomaterials can be tailored to provide the appropriate combination of these properties through the synergy of materials with individual pros and cons. Sodium alginate, [...] Read more.
Synthesis of bioinks for bioprinting of respiratory tissue requires considerations related to immunogenicity, mechanical properties, printability, and cellular compatibility. Biomaterials can be tailored to provide the appropriate combination of these properties through the synergy of materials with individual pros and cons. Sodium alginate, a water-soluble polymer derived from seaweed, is a cheap yet printable biomaterial with good structural properties; however, it lacks physiological relevance and cell binding sites. Collagen, a common component in the extra cellular matrix of many tissues, is expensive and lacks printability; however, it is highly biocompatible and exhibits sites for cellular binding. This paper presents our study on the synthesis of bioinks from alginate and collagen for use in bioprinting respiratory tissue models. Bioinks were synthesized from 40 mg/mL (4%) alginate and 3 mg/mL (0.3%) collagen in varying ratios (1:0, 4:1, 3:1, 2:1, and 1:1); then examined in terms of rheological properties, printability, compressive, and tensile properties and cellular compatibility. The results illustrate that the ratio of alginate to collagen has a profound impact on bioink performance and that, among the examined ratios, the 3:1 ratio is the most appropriate for use in bioprinting respiratory tissue scaffolds. Full article
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<p>Comparison of rheological flow properties of 4% alginate, 4:1 alginate: collagen, 3:1 alginate: collagen, 2:1 alginate: collagen, and 1:1 alginate: collagen when undergoing a shear rate sweep from 10 to 500 rad/s at 25 °C.</p>
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<p>Rheological properties determined by a shear stress sweep from 10–500 rad/second at temperatures of 25, 35, and 45 °C for various materials: (<b>a</b>) 4% alginate; (<b>b</b>) 4:1 alginate: collagen; (<b>c</b>) 3:1 alginate: collagen; (<b>d</b>) 2:1 alginate: collagen.</p>
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<p>Printability assessment of various material ratios: (<b>a</b>) 4% alginate; (<b>b</b>) 4:1; (<b>c</b>) 3:1; (<b>d</b>) 2:1 alginate: collagen.</p>
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<p>Compressive stress–strain curve of 4% alginate, used to calculate the static compressive modulus.</p>
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<p>Compressive modulus of the various bulk materials (* indicates <span class="html-italic">p</span> &lt; 0.05, *** indicates <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>A representative stress–strain curve obtained from 3:1 alginate: collagen.</p>
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<p>Young’s modulus of various material concentrations.</p>
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<p>Ultimate tensile strength of various material concentrations.</p>
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<p>Absorbance measurements of live cell staining of various ratio materials at timepoints of 1, 3, 5, 7, 10, and 14 days.</p>
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17 pages, 3630 KiB  
Article
A New Hyaluronic Emulgel of Hesperetin for Topical Application—An In Vitro Evaluation
by Raquel Taléns-Visconti, Yousra Belarbi, Octavio Díez-Sales, Jesus Vicente de Julián-Ortiz, Ofelia Vila-Busó and Amparo Nácher
J. Funct. Biomater. 2024, 15(4), 89; https://doi.org/10.3390/jfb15040089 - 1 Apr 2024
Viewed by 1772
Abstract
The present study aimed to formulate and characterize a hesperetin formulation to achieve adequate deposition and retention of hesperetin in the epidermis as a target for some cosmetic/dermatological actions. To derive the final emulgel, various formulations incorporating different proportions of Polysorbate 80 and [...] Read more.
The present study aimed to formulate and characterize a hesperetin formulation to achieve adequate deposition and retention of hesperetin in the epidermis as a target for some cosmetic/dermatological actions. To derive the final emulgel, various formulations incorporating different proportions of Polysorbate 80 and hyaluronic acid underwent testing through a Box–Behnken experimental design. Nine formulations were created until the targeted emulgel properties were achieved. This systematic approach, following the principles of a design of experiment (DoE) methodology, adheres to a quality-by-design (QbD) paradigm, ensuring a robust and purposeful formulation and highlighting the commitment to a quality-driven design approach. The emulsions were developed using the phase inversion method, optimizing the emulgel with the incorporation of hyaluronic acid. Physically stable optimized emulgels were evaluated for their globule size, surface charge, viscosity, pH, electrical conductivity, and hesperetin content. These assays, along with the temperature swing test, were used to select the optimal formulation. It was characterized by a droplet size, d[4,3], of 4.02 μm, a Z-potential of −27.8 mV, an O/W sign, a pH of 5.2, and a creamy texture and proved to be stable for at least 2 months at room temperature. Additionally, in vitro release kinetics from the selected emulgel exhibited a sustained release profile of hesperetin. Skin assays revealed adequate retention of hesperetin in the human epidermis with minimum permeation. Altogether, these results corroborate the promising future of the proposed emulgel in cosmetic or dermatological use on healthy or diseased skin. Full article
(This article belongs to the Topic Advanced Manufacturing and Surface Technology)
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<p>Chemical structure and some properties of hesperetin. Reprinted from Ref. [<a href="#B18-jfb-15-00089" class="html-bibr">18</a>].</p>
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<p>Representative images of results of centrifugation assays (3500 rpm/30 min) in different formulations (F4, showing phase separation; F1, F6, and F7, showing stability).</p>
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<p>Representative image of emulgel formula F7 obtained using Carl Zeiss stereo microscope model GSZ at 25× (<b>a</b>) and 40× (<b>b</b>).</p>
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<p>Drop size distribution (d[4,3]) in accelerated temperature tests (NS: no significant difference; ***: <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>Representative image of Z-potential determination Zetasizer nano-S (Malvern Instruments, Worcestershire, UK).</p>
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<p>Distribution of droplet size (d[4,3]) as a function of time (NS: no significant differences).</p>
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<p>Results of (<b>a</b>) pH, (<b>b</b>) Z—potential, (<b>c</b>) conductivity, and (<b>d</b>) percent of hesperetin with respect to the time (NS: no significant differences; **: <span class="html-italic">p</span> &lt; 0.01).</p>
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<p>Percentage of hesperetin released as a function of time (h) for the emulgel (<span class="html-italic">n</span> = 4).</p>
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<p>Distribution of hesperetin (%) after 24 h human epidermis permeation experiments after application of a solution and an emulgel, respectively.</p>
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<p>Cumulative amount of hesperetin across human skin. (<b>a</b>) Semi-Solid Vehicle. (<b>b</b>) Solution (Control).</p>
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17 pages, 1389 KiB  
Article
Influence of Magnesium Degradation on Schwannoma Cell Responses to Nerve Injury Using an In Vitro Injury Model
by Krathika Bhat, Lisa Hanke, Heike Helmholz, Eckhard Quandt, Sarah Pixley and Regine Willumeit-Römer
J. Funct. Biomater. 2024, 15(4), 88; https://doi.org/10.3390/jfb15040088 - 31 Mar 2024
Viewed by 1944
Abstract
Nerve guidance conduits for peripheral nerve injuries can be improved using bioactive materials such as magnesium (Mg) and its alloys, which could provide both structural and trophic support. Therefore, we investigated whether exposure to Mg and Mg-1.6wt%Li thin films (Mg/Mg-1.6Li) would alter acute [...] Read more.
Nerve guidance conduits for peripheral nerve injuries can be improved using bioactive materials such as magnesium (Mg) and its alloys, which could provide both structural and trophic support. Therefore, we investigated whether exposure to Mg and Mg-1.6wt%Li thin films (Mg/Mg-1.6Li) would alter acute Schwann cell responses to injury. Using the RT4-D6P2T Schwannoma cell line (SCs), we tested extracts from freeze-killed cells (FKC) and nerves (FKN) as in vitro injury stimulants. Both FKC and FKN induced SC release of the macrophage chemoattractant protein 1 (MCP-1), a marker of the repair SC phenotype after injury. Next, FKC-stimulated cells exposed to Mg/Mg-1.6Li reduced MCP-1 release by 30%, suggesting that these materials could have anti-inflammatory effects. Exposing FKC-treated cells to Mg/Mg-1.6Li reduced the gene expression of the nerve growth factor (NGF), glial cell line-derived neurotrophic factor (GDNF), and myelin protein zero (MPZ), but not the p75 neurotrophin receptor. In the absence of FKC, Mg/Mg-1.6Li treatment increased the expression of NGF, p75, and MPZ, which can be beneficial to nerve regeneration. Thus, the presence of Mg can differentially alter SCs, depending on the microenvironment. These results demonstrate the applicability of this in vitro nerve injury model, and that Mg has wide-ranging effects on the repair SC phenotype. Full article
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<p>(<b>A</b>) Effect of Mg and Mg-1.6Li thin film degradation on RT4-D6P2T cell proliferation. The cell proliferation was measured by an MTT assay and is depicted relative to the untreated control. Significant differences were analyzed using one-way ANOVA (<span class="html-italic">p</span> = 0.0057). (<b>B</b>) Concentrations of Mg and Li in the supernatant resulting from Mg and Mg-1.6Li thin film degradation. The concentrations were measured by ICP-OES. Significant differences were analyzed using two-way ANOVA (1B, Mg concentrations, <span class="html-italic">p</span> &lt; 0.001) or a <span class="html-italic">t</span>-test (1B, Li concentrations (<span class="html-italic">p</span> &lt; 0.001). Following the ANOVAs, significance in the Sidak’s post hoc tests is indicated at <span class="html-italic">p</span> &lt; 0.05 (*), <span class="html-italic">p</span> &lt; 0.01 (**), <span class="html-italic">p</span> &lt; 0.001 (***). Graphs show the mean ± SD of <span class="html-italic">n</span> = 9 data points (three replicates from three independent experiments).</p>
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<p>MCP-1 release induced by FKC and FKN in RT4-D6P2T cells. The concentration of MCP-1 was measured by ELISA. Untreated cells served as the negative control, and cells treated with LPS (1 µg/mL) were used as the positive control. Significant differences were identified by a two-way ANOVA (<span class="html-italic">p</span> &lt; 0.001), and significance in the post hoc tests is shown for <span class="html-italic">p</span> &lt; 0.05 (+, #, *). Graphs show mean ± SD of <span class="html-italic">n</span> = 6 data points (three replicates from two independent experiments). Symbols: +, compared to negative control; #, compared to positive control; *, comparisons between concentrations and time.</p>
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<p>Effect of Mg and Mg-1.6Li thin film degradation on MCP-1 release induced by FKC in RT4-D6P2T cells. The concentration of MCP-1 was measured by ELISA. (<b>A</b>) After 24 h; (<b>B</b>) After 48 h. Significant differences were analyzed by one-way ANOVAs (<span class="html-italic">p</span> &lt; 0.001, each for 24 and 48 h), with post hoc test significance levels indicated at <span class="html-italic">p</span> &lt; 0.001 (***). Graphs show mean ± SD of <span class="html-italic">n</span> = 9 data points (three replicates from three independent experiments).</p>
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<p>Effect of Mg and Mg-1.6Li thin film degradation on the expression of neurotrophin-related genes as measured by RT-qPCR. (<b>A</b>) NGF; (<b>B</b>) GDNF; (<b>C</b>) p75. Graphs show mean ± SD of <span class="html-italic">n</span> = 5–9 data points (three replicates from three independent experiments, outliers excluded). The dotted line represents the control. Significant differences were identified by one-way ANOVAs (<span class="html-italic">p</span> &lt; 0.001 for each gene), and significance in the post hoc tests is indicated at <span class="html-italic">p</span> &lt; 0.05 (*); <span class="html-italic">p</span> &lt; 0.01 (**); <span class="html-italic">p</span> &lt; 0.001 (***).</p>
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<p>Effect of Mg and Mg-1.6Li thin film degradation on the expression of myelin protein genes as measured by RT-qPCR. (<b>A</b>) MPZ; (<b>B</b>) PMP22. Graphs show mean ± SD of <span class="html-italic">n</span> = 5–9 data points (three replicates from three independent experiments, outliers excluded). The dotted line represents the control. Significant differences were identified by a one-way ANOVA (<span class="html-italic">p</span> &lt; 0.001 for each gene), and significance in the post hoc test is indicated at <span class="html-italic">p</span> &lt; 0.05 (*); <span class="html-italic">p</span> &lt; 0.01 (**); <span class="html-italic">p</span> &lt; 0.001 (***).</p>
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<p>The possible mechanisms of action of Mg and Li on the repair pathways in injury stimulated SCs, as inferred from the literature. Only the mechanisms relevant to the observations in this study are depicted.</p>
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18 pages, 5731 KiB  
Article
A Novel Viscoelastic Deformation Mechanism Uncovered during Vickers Hardness Study of Bone
by Ahmed Ibrahim, Zhenting Jiang, Khosro Shirvani, Alireza Dalili and Z. Abdel Hamid
J. Funct. Biomater. 2024, 15(4), 87; https://doi.org/10.3390/jfb15040087 - 31 Mar 2024
Cited by 1 | Viewed by 1680
Abstract
This study investigates the viscoelastic deformation mechanisms of bone as a response to Vickers hardness indentation. We utilized advanced high-resolution scanning electron microscopy (SEM) to investigate a distinct deformation pattern that originates from the indentation site within the bone matrix. The focus of [...] Read more.
This study investigates the viscoelastic deformation mechanisms of bone as a response to Vickers hardness indentation. We utilized advanced high-resolution scanning electron microscopy (SEM) to investigate a distinct deformation pattern that originates from the indentation site within the bone matrix. The focus of our research was to analyze a unique deformation mechanism observed in bone tissue, which has been colloquially termed as “screw-like” due to its resemblance to a screw thread when viewed under an optical microscope. The primary goals of this research are to investigate the distinctive characteristics of the “screw-like” deformation pattern and to determine how the microstructure of bone influences the initiation and control of this mechanism. These patterns, emerging during the dwell period of indentation, underscore the viscoelastic nature of bone, indicating its propensity for energy dissipation and microstructural reconfiguration under load. This study uncovered a direct correlation between the length of the “screw-like” deformation and the duration of the indentation dwell time, providing quantifiable evidence of the bone’s viscoelastic behavior. This finding is pivotal in understanding the mechanical properties of bone, including its fracture toughness, as it relates to the complex interplay of factors such as energy dissipation, microstructural reinforcement, and stress distribution. Furthermore, this study discusses the implications of viscoelastic properties on the bone’s ability to resist mechanical challenges, underscoring the significance of viscoelasticity in bone research. Full article
(This article belongs to the Section Bone Biomaterials)
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<p>Vickers hardness test [<a href="#B22-jfb-15-00087" class="html-bibr">22</a>].</p>
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<p>(<b>a</b>) Hardness test sites on deer tibia: a cross-sectional analysis; (<b>b</b>) microscopic detail of induced “screw-like” deformation from Vickers hardness testing.</p>
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<p>Vickers hardness indentation produced “Bone Deformation” seen in optical microscope as a screw thread.</p>
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<p>High-resolution SEM shows the screw-like deformation seen in <a href="#jfb-15-00087-f003" class="html-fig">Figure 3</a>.</p>
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<p>Consistent viscoelastic dynamics in proximal indentations.</p>
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<p>Viscoelastic deformation during Vickers indentation at osteon convergence.</p>
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<p>Extended viscoelastic deformation during Vickers indentation.</p>
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<p>(<b>a</b>) SEM of “Screw-like” deformation deflected at the osteon cement lines. (<b>b</b>) Macroscopic image of “Screw-like” deformation deflected at the osteon cement lines.</p>
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22 pages, 11621 KiB  
Article
A Finite Element Method Study on a Simulation of the Thermal Behaviour of Four Methods for the Restoration of Class II Cavities
by Adela Nicoleta Staicu, Mihaela Jana Țuculină, Cristian Niky Cumpătă, Ana Maria Rîcă, Maria Cristina Beznă, Dragoș Laurențiu Popa, Alexandru Dan Popescu and Oana Andreea Diaconu
J. Funct. Biomater. 2024, 15(4), 86; https://doi.org/10.3390/jfb15040086 - 30 Mar 2024
Viewed by 1487
Abstract
The possibility of dental pulp damage during dental procedures is well known. According to studies, during finishing and polishing without cooling, temperatures of up to 140 °C or more can be generated. There are many studies that have analysed the influence of the [...] Read more.
The possibility of dental pulp damage during dental procedures is well known. According to studies, during finishing and polishing without cooling, temperatures of up to 140 °C or more can be generated. There are many studies that have analysed the influence of the finishing and polishing of fillings on the mechanical parameters, but the analysis of thermal parameters has led to uncertain results due to the difficulty of performing this in vivo. Background: We set out to conduct a study, using the finite element method, to determine the extent to which the type of class II cavity and the volume of the composite filling influence the duration of heat transfer to the pulp during finishing and polishing without cooling. Materials and Methods: A virtual model of an upper primary molar was used, with a caries process located on the distal aspect, in which four types of cavities were digitally prepared: direct access, horizontal slot, vertical slot and occlusal–proximal. All four cavity types were filled using a Filtek Supreme XT nanocomposite. Results: The study showed that the filling volume almost inversely proportionally influences the time at which the dental pulp reaches the critical temperature of irreversible damage. The lowest duration occurred in occlusal–distal restorations and the highest in direct access restorations. Conclusions: based on the results of the study, a working protocol can be issued so that finishing and polishing restorations without cooling are safe for pulpal health. Full article
(This article belongs to the Special Issue Biomaterials in Conservative Dentistry and Prosthodontics)
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<p>Specific operations of three-dimensional molar scanning.</p>
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<p>Obtaining the integral molar model.</p>
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<p>(<b>a</b>) Direct access cavity; (<b>b</b>) distal–occlusal cavity; (<b>c</b>) vertical slot cavity; (<b>d</b>) horizontal slot cavity.</p>
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<p>Alignment of the three models (views with different degrees of transparency).</p>
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<p>The two models in SolidWorks.</p>
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<p>(<b>a</b>) Composite-filling model in direct access cavity situation; (<b>b</b>) model of composite filling for the occlusal–distal cavity; (<b>c</b>) model of the composite layer for the vertical slot cavity; (<b>d</b>) composite layer model for the horizontal slot cavity.</p>
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<p>Model of the filled molar for: (<b>a</b>) direct access cavity; (<b>b</b>) occlusal–distal cavity; (<b>c</b>) vertical slot cavity; (<b>d</b>) horizontal slot cavity.</p>
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<p>Temperature evolution during the virtual experiment.</p>
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<p>Finite element structure of the analysed system.</p>
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<p>The surface that was subjected to the temperature source, and the surface to which convection was applied.</p>
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<p>Temperature map for direct access cavity restoration.</p>
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<p>Temperature evolution in the dental pulp and limit temperature of 42.5 °C.</p>
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<p>Approximating the curve with a straight line. Temperature evolution in the dental pulp (coloured in orange) and limit temperature of 42.5 °C (coloured in blue).</p>
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<p>Temperature evolution in dental structures.</p>
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<p>Temperature map for occlusal–distal cavity restoration.</p>
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<p>Temperature evolution in the dental pulp.</p>
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<p>Temperature evolution in the components of the analysed dental system.</p>
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<p>Temperature map for vertical slot cavity restoration.</p>
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<p>Temperature evolution in the dental pulp.</p>
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<p>Temperature evolution in the components of the analysed dental system.</p>
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<p>Temperature map for horizontal slot cavity restoration.</p>
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<p>Temperature evolution in the dental pulp.</p>
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<p>Temperature evolution in the analysed system components.</p>
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<p>Evolution of the temperatures in the dental pulp.</p>
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<p>Maximum temperatures in the dental pulp.</p>
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<p>Diagram of composite volumes.</p>
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<p>Time limit diagram.</p>
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13 pages, 8355 KiB  
Article
Assessment of the Cyclic Fatigue Performance of the Novel Protaper Ultimate File System Used in Different Kinematics: An In Vitro Study
by Cezar Tiberiu Diaconu, Anca Elena Diaconu, Mihaela Jana Tuculina, Laurența Lelia Mihai, Mircea Gheorghiță, Lelia Mihaela Gheorghiță, Petre Mărășescu, Alexandru Gliga and Oana Andreea Diaconu
J. Funct. Biomater. 2024, 15(4), 85; https://doi.org/10.3390/jfb15040085 - 29 Mar 2024
Cited by 2 | Viewed by 1607
Abstract
This in vitro study aims to assess the cyclic fatigue resistance of the Protaper Ultimate (PTU) files compared to the Protaper Gold (PTG) and the M3 UDG (M3) files using various motion kinematics in simulated canals. As far as the authors are aware, [...] Read more.
This in vitro study aims to assess the cyclic fatigue resistance of the Protaper Ultimate (PTU) files compared to the Protaper Gold (PTG) and the M3 UDG (M3) files using various motion kinematics in simulated canals. As far as the authors are aware, no study has previously compared the three file systems before this current investigation. Therefore, closing this information gap is the goal of the current research. Methods: A total of (60 new endodontic files were randomly divided into 6 groups (10 files per group); groups 1, 3, and 5 used continuous rotation (CR), while groups 2, 4, and 6 used forward reciprocating motion (FRM). A manufactured stainless-steel artificial canal was used to perform the cyclic fatigue testing. The results were analyzed using Student’s t-test and two-way ANOVA. All pairwise comparisons revealed statistically significant differences in the time to failure (TTF) for every study group (p < 0.001), with the exception of the PTG and M3 files, which performed similarly using both CR and FRM. Conclusions: The PTU files performed better than the PTG and M3 files in terms of the TTF and number of cycles to failure (NCF) using both CR and FRM. Full article
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<p>Testing unit: (<b>A</b>) artificial canal made of stainless steel using a CNC machine, (<b>B</b>) polycarbonate cover, (<b>C</b>) artificial canal with polycarbonate cover.</p>
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<p>Testing device. (<b>A</b>) Global view of the testing device and (<b>B</b>) specially designed jig, which held the endodontic motor in a repeatable position with an instrument inserted in the testing unit.</p>
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<p>Dental surgical microscope photographs ((<b>A</b>) PTU, (<b>B</b>) PTG, (<b>C</b>) M3) of the instruments before cyclic fatigue testing.</p>
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<p>Example of photomicrographs of the fractured surface from the PTU F2 file.</p>
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<p>Example of X-ray fluorescence analysis from the PTU files.</p>
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<p>Stereomicroscope photographs of the fractured surface ((<b>A</b>) PTU, (<b>B</b>) PTG, (<b>C</b>) M3). Cracked surfaces marked by arrows.</p>
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<p>Descriptive X-ray fluorescence analysis of the key elements in the tested instruments.</p>
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35 pages, 8310 KiB  
Review
Biomaterials for Regenerative Cranioplasty: Current State of Clinical Application and Future Challenges
by Lizhe He
J. Funct. Biomater. 2024, 15(4), 84; https://doi.org/10.3390/jfb15040084 - 28 Mar 2024
Cited by 1 | Viewed by 2801
Abstract
Acquired cranial defects are a prevalent condition in neurosurgery and call for cranioplasty, where the missing or defective cranium is replaced by an implant. Nevertheless, the biomaterials in current clinical applications are hardly exempt from long-term safety and comfort concerns. An appealing solution [...] Read more.
Acquired cranial defects are a prevalent condition in neurosurgery and call for cranioplasty, where the missing or defective cranium is replaced by an implant. Nevertheless, the biomaterials in current clinical applications are hardly exempt from long-term safety and comfort concerns. An appealing solution is regenerative cranioplasty, where biomaterials with/without cells and bioactive molecules are applied to induce the regeneration of the cranium and ultimately repair the cranial defects. This review examines the current state of research, development, and translational application of regenerative cranioplasty biomaterials and discusses the efforts required in future research. The first section briefly introduced the regenerative capacity of the cranium, including the spontaneous bone regeneration bioactivities and the presence of pluripotent skeletal stem cells in the cranial suture. Then, three major types of biomaterials for regenerative cranioplasty, namely the calcium phosphate/titanium (CaP/Ti) composites, mineralised collagen, and 3D-printed polycaprolactone (PCL) composites, are reviewed for their composition, material properties, and findings from clinical trials. The third part discusses perspectives on future research and development of regenerative cranioplasty biomaterials, with a considerable portion based on issues identified in clinical trials. This review aims to facilitate the development of biomaterials that ultimately contribute to a safer and more effective healing of cranial defects. Full article
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<p>(<b>A</b>) Spatial distribution of Prx1+ cells in calvarial sutures of PRX1-creER-EGFP+/− mice at different ages. Dashes indicate the border of calvarial sutures [<a href="#B39-jfb-15-00084" class="html-bibr">39</a>]; (<b>B</b>) spatial distribution of Prx1+ cells in sagittal sutures of PRX1-creER-EGFP+/− adult mice (2-month-old) (I) before and (II) 7 days after mechanical expansion. Dash lines demarcate the rims of sagittal suture (S.S.) that separates left parietal bone (L.P.) and right parietal bone (R.P.) Dashes indicate the border of calvarial sutures [<a href="#B29-jfb-15-00084" class="html-bibr">29</a>]; (<b>C</b>) micro-CT image, 3D reconstruction model, and histological sections of sagittal suture (green dashed lines, with magnified view) and cranial defects (blue dashed lines, with magnified view) 60 days after craniectomy in control and suture expansion groups, showing increased number of Prx1+ cells in expanded suture [<a href="#B29-jfb-15-00084" class="html-bibr">29</a>]; (<b>D</b>) CT images of a patient’s (female, 20 years old) cranium taken pre-operatively (I), POD 3 (II), POW 7 (III), and POW 23 (IV), showing spontaneous cranial regeneration [<a href="#B47-jfb-15-00084" class="html-bibr">47</a>]; (<b>E</b>) three-dimensional reconstruction of a patient’s (female, 7 years old) cranium at POD 0 (I), POM 10 (II), POM 16 (III), and POM 26 (IV), showing progressive cranial regeneration [<a href="#B48-jfb-15-00084" class="html-bibr">48</a>]; (<b>F</b>) CT images of a patient’s (male, 64 years old) cranium taken pre-operatively (I), POD 145 (II), POD 171 (III), and POM 23 (IV), showing progressive cranial regeneration [<a href="#B49-jfb-15-00084" class="html-bibr">49</a>]; (<b>G</b>) photographs of the 64-year-old patient taken at POM 23 [<a href="#B49-jfb-15-00084" class="html-bibr">49</a>]. Reprinted from Refs. [<a href="#B29-jfb-15-00084" class="html-bibr">29</a>,<a href="#B39-jfb-15-00084" class="html-bibr">39</a>,<a href="#B47-jfb-15-00084" class="html-bibr">47</a>,<a href="#B49-jfb-15-00084" class="html-bibr">49</a>]. Reprinted with permission from Ref. [<a href="#B48-jfb-15-00084" class="html-bibr">48</a>]. Copyright 2024, Elsevier, Amsterdam, The Netherlands.</p>
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<p>(<b>A</b>,<b>B</b>) Demonstration of OssDsign<sup>®</sup> PSI showing the titanium backbone covered by CaP (BioCer) tiles and a schematic view after implantation [<a href="#B60-jfb-15-00084" class="html-bibr">60</a>]; (<b>C</b>) photographs showing the inlay implantation of an OssDsign<sup>®</sup> PSI [<a href="#B60-jfb-15-00084" class="html-bibr">60</a>]; (<b>D</b>) CT images of two planes and the corresponding 3D reconstruction from a clinical case. Resorption of CaP tiles occurred mainly on the pericranium/scalp side, while new bone formation was evident on the dural side [<a href="#B63-jfb-15-00084" class="html-bibr">63</a>]. (<b>E</b>,<b>F</b>) CT images show a honeycomb-like titanium framework (white in E, black areas in F), as well as new bone (* in (<b>E</b>), pale brown in (<b>F</b>)) formation bridging and over the CaP tiles (# in (<b>E</b>), grey areas in (<b>F</b>)) 31 months post-operatively [<a href="#B63-jfb-15-00084" class="html-bibr">63</a>]. (<b>G</b>) Compositional change in mineral phases of CaP tiles before and after 31 months on a shelf or in vivo, demonstrating the formation of hydroxyapatite (HA) [<a href="#B63-jfb-15-00084" class="html-bibr">63</a>]; (<b>H,I</b>) histological staining of new bone (red) formation in three regions of the cranioplasty implant retrieved at POM 21. Black parts are titanium backbone of the implant [<a href="#B25-jfb-15-00084" class="html-bibr">25</a>]. (<b>J</b>) Toluidine blue staining of an implant retrieved 21 months post-operatively shows the deposition of new bone (NOB)-containing blood vessels (BVs) over the surface of CaP (BioCer) [<a href="#B25-jfb-15-00084" class="html-bibr">25</a>]. Reprinted from Refs. [<a href="#B25-jfb-15-00084" class="html-bibr">25</a>,<a href="#B60-jfb-15-00084" class="html-bibr">60</a>,<a href="#B63-jfb-15-00084" class="html-bibr">63</a>].</p>
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<p>(<b>A</b>) Scheme of the hierarchical structure of MC with biomimicry to bone matrix nanostructure [<a href="#B76-jfb-15-00084" class="html-bibr">76</a>]; (<b>B</b>) scheme, transmitted electron microscopic image and selected area diffraction pattern of MC. Black arrow: collagen fibril; white arrow: mineral crystals in parallel direction. Insert picture shows the selected area diffraction pattern of domain A [<a href="#B76-jfb-15-00084" class="html-bibr">76</a>]; (<b>C</b>) photographs of an implanted MC fixed by PEEK plates (between yellow arrows) and 10/0 threads (in black) [<a href="#B85-jfb-15-00084" class="html-bibr">85</a>]; (<b>D</b>,<b>E</b>) CT images show an enlarged gap between MC and remnant cranium at POY 1, and a fragmented MC at POY 2, and yellow arrows highlightes the border of resorbed implant [<a href="#B85-jfb-15-00084" class="html-bibr">85</a>]. (<b>F</b>) Pre-operative CT images of a 4-month-old patient with a cranial defect (I, II) and post-operative CT images taken at POY 3 after reconstruction using ReFit<sup>®</sup> MC (III, IV) [<a href="#B88-jfb-15-00084" class="html-bibr">88</a>]. (<b>G</b>) Cranium of baby sheep after cranioplasty with compact MC/PCL (left, uneventful) and titanium mesh (right, with cranial protrusion marked by red arrows) [<a href="#B91-jfb-15-00084" class="html-bibr">91</a>]. (<b>H</b>,<b>I</b>) Photographs and micro-CT images of hybrid MC/PCL composites [<a href="#B90-jfb-15-00084" class="html-bibr">90</a>]; (<b>J</b>) Post-operative CT reconstruction of the cranium of baby sheep at POM 3, treated with blank (I, minimal regeneration), hybrid MC/PCL (II, complete regeneration), porous MC/PCL (III, partial regeneration with remaining voids highlighted with red circle), and compact MC/PCL (IV, minimal degradation without bone-implant bonding at the interface, marked by blue arrow) [<a href="#B90-jfb-15-00084" class="html-bibr">90</a>]. Reprinted from Refs. [<a href="#B85-jfb-15-00084" class="html-bibr">85</a>,<a href="#B90-jfb-15-00084" class="html-bibr">90</a>]; Reprinted with permission from Refs. [<a href="#B76-jfb-15-00084" class="html-bibr">76</a>,<a href="#B88-jfb-15-00084" class="html-bibr">88</a>]. Copyright 2024, Elsevier; Ref. [<a href="#B91-jfb-15-00084" class="html-bibr">91</a>]. Copyright 2017, American Chemical Society.</p>
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<p>(<b>A</b>,<b>B</b>) Photographs and microscopic images of Osteoplug<sup>®</sup> burr hole plug [<a href="#B104-jfb-15-00084" class="html-bibr">104</a>]; (<b>C</b>) CT images taken post-operatively (I) and at POM 15 (II), showing increased bone volume at the burr hole after implantation with a 3D-printed PCL plug. Red circles highlight the defected areas [<a href="#B103-jfb-15-00084" class="html-bibr">103</a>]; (<b>D</b>,<b>E</b>) a 3 × 3 cm<sup>2</sup> cranial defect and the corresponding customised 3D-printed PCL cranioplasty implant [<a href="#B27-jfb-15-00084" class="html-bibr">27</a>]; (<b>F</b>) CT images of the defect shown in (<b>D</b>), taken post-operatively (I) and at POM 6 (II), showing bone regeneration [<a href="#B27-jfb-15-00084" class="html-bibr">27</a>]; (<b>G</b>) Photograph of a 3D-printed, customised PCL cranioplasty implant taken intraoperatively [<a href="#B106-jfb-15-00084" class="html-bibr">106</a>]; (<b>H</b>) CT images of a cranial defect (9.7 × 8.9 cm<sup>2</sup>) taken post-operatively (I) and at POM 20 (II), showing significant restoration of the cranium structure after reconstruction with a 3D-printed PCL implant [<a href="#B105-jfb-15-00084" class="html-bibr">105</a>]; (<b>I</b>) three-dimensional reconstruction of a band-shaped cranial defect at POM 12 after frontal-orbital advancement and cranioplasty using 3D-printed PCL mesh, showing a significant void surrounding the cranium (in green) and occupied by partly degraded PCL (in blue) [<a href="#B107-jfb-15-00084" class="html-bibr">107</a>]. Reprinted from Refs. [<a href="#B104-jfb-15-00084" class="html-bibr">104</a>,<a href="#B105-jfb-15-00084" class="html-bibr">105</a>,<a href="#B106-jfb-15-00084" class="html-bibr">106</a>]; Reprinted with permission from Ref. [<a href="#B103-jfb-15-00084" class="html-bibr">103</a>]. Copyright 2017, Future Medicine Ltd.; Ref. [<a href="#B27-jfb-15-00084" class="html-bibr">27</a>]. Copyright 2024, Georg Thieme Verlag KG; Ref. [<a href="#B107-jfb-15-00084" class="html-bibr">107</a>]. Copyright 2024, Wolters Kluwer Health, Inc., Philadelphia, PA, USA.</p>
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<p>Schemes of cell recruitment are mediated by a regenerative cranioplasty implant via different mechanisms, including direct chemotaxis, application of physical stimuli, and immunomodulation. MSC = mesenchymal stem cells. Image created with BioRender (<a href="http://www.biorender.com" target="_blank">www.biorender.com</a>, accessed on 31 January 2024) with permission to publish.</p>
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<p>(<b>A</b>) Schematic view of anatomy in calvarial and temporal regions showing the multiple layers of soft tissues [<a href="#B165-jfb-15-00084" class="html-bibr">165</a>]; (<b>B</b>) illustration of craniectomy, during which the scalp (▲), temporalis (★), and dura mater (◆) are dissected from the cranium [<a href="#B174-jfb-15-00084" class="html-bibr">174</a>,<a href="#B175-jfb-15-00084" class="html-bibr">175</a>]; (<b>C</b>) schematic view and key results of a study demonstrating the contribution of dura mater and pericranium to the bony regeneration in sub-critical cranial defects of rats. * denotes statistical significance (<span class="html-italic">p</span> &lt; 0.05) [<a href="#B118-jfb-15-00084" class="html-bibr">118</a>]. (<b>D</b>) Pre-implantation photographs, post-surgical Stevenel’s blue and Van Gieson’s picro fuchsin differential tissue staining (SVG staining, blue = soft tissue, red = mineralised bone, black = scaffold), and CT reconstructions (yellow = new bone) at POW 8 for porous β-TCP scaffold with (I) porous cap and (II) solid cap [<a href="#B173-jfb-15-00084" class="html-bibr">173</a>]. Both materials were implanted into cranial defects of rabbits, where the top of the scaffold directly interacts with Galea aponeurotica. Reprinted from Ref. [<a href="#B174-jfb-15-00084" class="html-bibr">174</a>]; Reprinted with permission from Ref. [<a href="#B165-jfb-15-00084" class="html-bibr">165</a>]. Copyright 2024, Thieme; Refs. [<a href="#B118-jfb-15-00084" class="html-bibr">118</a>,<a href="#B173-jfb-15-00084" class="html-bibr">173</a>]. Copyright 2024, Wolters Kluwer Health, Inc.</p>
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<p>(<b>A</b>) Diagram showing the origin and mode of ossification for different regions of craniofacial bones [<a href="#B184-jfb-15-00084" class="html-bibr">184</a>]; (<b>B</b>) hematoxylin and eosin staining section of a collagen–calcium phosphate scaffold seeded with bone marrow-derived mesenchymal stem cells and implanted into the cranium of Wistar rats for 8 weeks. The blue arrow highlights mineralised new bone, the red arrow highlights dense bone at the periphery of the scaffold, and the loosely packed tissue highlighted by the black arrow is a necrotic region in the scaffold centre [<a href="#B185-jfb-15-00084" class="html-bibr">185</a>]. (<b>C</b>) Histological sections (Masson trichrome and hematoxylin and eosin) of cranial defects regenerated by polycaprolactone microfibrous scaffold seeded with mesenchymal stem cells and primed for endochondral ossification (left) and intramembranous ossification (right). Red arrows highlight bone vessels. OB = original bones; NB = new bones [<a href="#B186-jfb-15-00084" class="html-bibr">186</a>]. Reprinted with permission from Refs. [<a href="#B184-jfb-15-00084" class="html-bibr">184</a>,<a href="#B185-jfb-15-00084" class="html-bibr">185</a>]. Copyright 2024, Elsevier; Reprinted from Ref. [<a href="#B186-jfb-15-00084" class="html-bibr">186</a>].</p>
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17 pages, 4509 KiB  
Review
Animal Models for Investigating Osseointegration: An Overview of Implant Research over the Last Three Decades
by Antonio Scarano, Ahmad G. A. Khater, Sergio Alexandre Gehrke, Francesco Inchingolo and Sergio Rexhep Tari
J. Funct. Biomater. 2024, 15(4), 83; https://doi.org/10.3390/jfb15040083 - 27 Mar 2024
Cited by 8 | Viewed by 2984
Abstract
Dental implants and bone augmentation are among dentistry’s most prevalent surgical treatments; hence, many dental implant surfaces and bone grafts have been researched to improve bone response. Such new materials were radiologically, histologically, and histomorphometrically evaluated on animals before being used on humans. [...] Read more.
Dental implants and bone augmentation are among dentistry’s most prevalent surgical treatments; hence, many dental implant surfaces and bone grafts have been researched to improve bone response. Such new materials were radiologically, histologically, and histomorphometrically evaluated on animals before being used on humans. As a result, several studies used animals to evaluate novel implant technologies, biocompatibility, surgical techniques, and osseointegration strategies, as preclinical research on animal models is essential to evaluate bioactive principles (on cells, compounds, and implants) that can act through multiple mechanisms and to predict animal behavior, which is difficult to predict from in vitro studies alone. In this study, we critically reviewed all research on different animal models investigating the osseointegration degree of new implant surfaces, reporting different species used in the osseointegration research over the last 30 years. Moreover, this is the first study to summarize reviews on the main animal models used in the translational research of osseointegration, including the advantages and limitations of each model and determining the ideal location for investigating osseointegration in small and large animal models. Overall, each model has advantages and disadvantages; hence, animal selection should be based on the cost of acquisition, animal care, acceptability to society, availability, tolerance to captivity, and housing convenience. Among small animal models, rabbits are an ideal model for biological observations around implants, and it is worth noting that osseointegration was discovered in the rabbit model and successfully applied to humans. Full article
(This article belongs to the Section Dental Biomaterials)
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<p>Schematic illustration of the anatomical sites used on rats to evaluate biomaterials during bone healing. (<b>A</b>) Bone defect in the tibia and calvaria. (<b>B</b>) Different biomaterials used for histological evaluation. (<b>C</b>) Edentulous space, incisor, and premolar that can be used to insert mini-implants or post-extractive implant. This figure was created using <a href="http://Biorender.com" target="_blank">Biorender.com</a>.</p>
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<p>(<b>A</b>,<b>B</b>) Mini-implants positioned in tibia. (<b>C</b>) Histological aspect of mini-implant after bone healing [<a href="#B24-jfb-15-00083" class="html-bibr">24</a>].</p>
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<p>Schematic illustration of the anatomical sites used on rabbits to evaluate biomaterials during bone healing. Bone defect to simulate post-extraction sites. This figure was created using <a href="http://Biorender.com" target="_blank">Biorender.com</a>.</p>
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<p>(<b>A</b>) Bone defect in the tibia. (<b>B</b>) Histological specimen of dental implant positioned in the tibia and observed under a fluorescence microscope [<a href="#B43-jfb-15-00083" class="html-bibr">43</a>].</p>
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<p>(<b>A</b>) Dental implant with standard dimension (4 × 13 mm) during placement in the knee joint. (<b>B</b>) Radiographic assessment of two dental implants placed in the knee joint. (<b>C</b>) Block section of knee joint before histological analysis [<a href="#B44-jfb-15-00083" class="html-bibr">44</a>].</p>
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<p>Schematic illustration of the anatomical sites used on sheep to evaluate biomaterials during bone healing. (<b>A</b>) Bone defects in tibia, femur, and sinus lifting. (<b>B</b>) Different biomaterials used for bone defect treatments. (<b>C</b>) Biomaterials in particles, blocks, or membranes that can be used to treat bone defects. This figure was created using <a href="http://Biorender.com" target="_blank">Biorender.com</a>.</p>
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<p>(<b>A</b>) Osteotomy for sinus lifting. (<b>B</b>) Sinus membrane lifting. (<b>C</b>) Extra-oral skin suture [<a href="#B59-jfb-15-00083" class="html-bibr">59</a>].</p>
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<p>Bone defects in the tibia are used to evaluate different bone grafts [<a href="#B60-jfb-15-00083" class="html-bibr">60</a>].</p>
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<p>Schematic illustration of anatomical sites used in minipigs to evaluate biomaterials. Different biomaterials used for bone defect treatments. Anatomy of teeth shows their complexity; it is challenging to perform extractions without fracturing the roots. This figure was created using <a href="http://Biorender.com" target="_blank">Biorender.com</a>.</p>
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<p>(<b>A</b>) Dental implants placed in the maxilla. (<b>B</b>) Plaster model after impressions for denture construction. (<b>C</b>) Metal prosthesis placement [<a href="#B73-jfb-15-00083" class="html-bibr">73</a>].</p>
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<p>(<b>A</b>) Implants placed in mandible. (<b>B</b>) and (<b>C</b>) Prosthesis placement [<a href="#B81-jfb-15-00083" class="html-bibr">81</a>].</p>
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