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Search Results (293)

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14 pages, 881 KiB  
Article
Clinical and Molecular Impact of Advanced Platelet-Rich Fibrin on Pain, Swelling, and Distal Periodontal Status of Mandibular Second Molars After Mandibular Third-Molar Extraction
by Ada Stefanescu, Irina-Georgeta Sufaru, Iulia Chiscop, Fabian Cezar Lupu, Cristian Martu, Bogdan Oprisan and Kamel Earar
Medicina 2024, 60(12), 2062; https://doi.org/10.3390/medicina60122062 - 14 Dec 2024
Viewed by 598
Abstract
Background and Objectives: This study aimed to evaluate the role of A-PRF (advanced platelet-rich fibrin) in the enhancement of wound healing and protecting the periodontal health of mandibular second molars after the extraction of mandibular third molars. Additionally, the study assessed the [...] Read more.
Background and Objectives: This study aimed to evaluate the role of A-PRF (advanced platelet-rich fibrin) in the enhancement of wound healing and protecting the periodontal health of mandibular second molars after the extraction of mandibular third molars. Additionally, the study assessed the levels of pro-inflammatory cytokines in the gingival crevicular fluid (GCF) of mandibular second molars as markers of inflammation. Materials and Methods: Twenty-five systemically healthy adult patients with bilateral removal of impacted mandibular third molars were included. Each patient received A-PRF in one extraction site, while the contralateral site served as a control. Periodontal parameters of the adjacent second molar, including probing depth (PD) and clinical attachment level (CAL), were measured in distal–vestibular (DV) and distal–lingual (DL) sites. Pain, swelling, and overall healing were subjectively evaluated. Levels of tumor necrosis factor-alpha (TNF-α), interleukin 1 beta (IL-1β), and interleukin 6 (IL-6) in the GCF were analyzed. Evaluations occurred at baseline and three months post-surgery. Results: A-PRF significantly improved PD (from 4.69 ± 0.61 mm to 3.85 ± 0.34 mm in DV, and from 4.71 ± 0.65 mm to 3.79 ± 0.27 mm in DL, respectively) and CAL (from 2.41 ± 0.25 mm to 1.82 ± 0.21 mm in DV, and from 2.40 ± 0.36 mm to 1.75 ± 0.19 mm in DL, respectively) of the adjacent second molar, compared to control sites, three months post-surgery. Pain and swelling scores were notably lower on the 7th postoperative day in the A-PRF group. A-PRF also reduced pro-inflammatory cytokines in GCF, significantly more than in control sites, at three months post-surgery. Conclusions: A-PRF enhances the periodontal and inflammatory status of adjacent teeth and wound healing after the extraction of mandibular third molars. Full article
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<p>Study’s flowchart.</p>
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<p>Percentage distribution of healing index 1 postoperatively at 7 and 14 days.</p>
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25 pages, 2439 KiB  
Systematic Review
Application of Advanced Platelet-Rich Fibrin in Oral and Maxillo-Facial Surgery: A Systematic Review
by Marek Chmielewski, Andrea Pilloni and Paulina Adamska
J. Funct. Biomater. 2024, 15(12), 377; https://doi.org/10.3390/jfb15120377 - 14 Dec 2024
Viewed by 567
Abstract
Background: Advanced platelet-rich fibrin (A-PRF) is produced by centrifuging the patient’s blood in vacuum tubes for 14 min at 1500 rpm. The most important component of A-PRF is the platelets, which release growth factors from their ⍺-granules during the clotting process. This process [...] Read more.
Background: Advanced platelet-rich fibrin (A-PRF) is produced by centrifuging the patient’s blood in vacuum tubes for 14 min at 1500 rpm. The most important component of A-PRF is the platelets, which release growth factors from their ⍺-granules during the clotting process. This process is believed to be the main source of growth factors. The aim of this paper was to systematically review the literature and to summarize the role of A-PRF in oral and maxillo-facial surgery. Materials and Methods: A systematic review was carried out, following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (PROSPERO: CRD42024584161). Results: Thirty-eight articles published before 11 November 2024 were included in the systematic review. The largest study group consisted of 102 patients, and the smallest study group consisted of 10 patients. A-PRF was most often analyzed compared to leukocyte-PRF (L-PRF) or blood cloth. A-PRF was correlated with lower postoperative pain. Also, A-PRF was highlighted to have a positive effect on grafting material integration. A-PRF protected areas after free gingival graft very well, promoted more efficient epithelialization of donor sites and enhanced wound healing. Conclusions: Due to its biological properties, A-PRF could be considered a reliable addition to the surgical protocols, both alone and as an additive to bio-materials, with the advantages of healing improvement, pain relief, soft tissue management and bone preservation, as well as graft integration. However, to determine the long-term clinical implications and recommendations for clinical practice, more well-designed randomized clinical trials are needed in each application, especially those with larger patient cohorts, as well as additional blinding of personnel and long follow-up periods. Full article
(This article belongs to the Special Issue Functional Biomaterials for Regenerative Dentistry)
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<p>A-PRF clot in glass-coated plastic tubes.</p>
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<p>PRISMA workflow.</p>
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<p>The risk of bias assessment using RoS 2 [<a href="#B2-jfb-15-00377" class="html-bibr">2</a>,<a href="#B19-jfb-15-00377" class="html-bibr">19</a>,<a href="#B20-jfb-15-00377" class="html-bibr">20</a>,<a href="#B21-jfb-15-00377" class="html-bibr">21</a>,<a href="#B24-jfb-15-00377" class="html-bibr">24</a>,<a href="#B25-jfb-15-00377" class="html-bibr">25</a>,<a href="#B26-jfb-15-00377" class="html-bibr">26</a>,<a href="#B27-jfb-15-00377" class="html-bibr">27</a>,<a href="#B28-jfb-15-00377" class="html-bibr">28</a>,<a href="#B29-jfb-15-00377" class="html-bibr">29</a>,<a href="#B30-jfb-15-00377" class="html-bibr">30</a>,<a href="#B31-jfb-15-00377" class="html-bibr">31</a>,<a href="#B32-jfb-15-00377" class="html-bibr">32</a>,<a href="#B33-jfb-15-00377" class="html-bibr">33</a>,<a href="#B34-jfb-15-00377" class="html-bibr">34</a>,<a href="#B35-jfb-15-00377" class="html-bibr">35</a>,<a href="#B36-jfb-15-00377" class="html-bibr">36</a>,<a href="#B37-jfb-15-00377" class="html-bibr">37</a>,<a href="#B38-jfb-15-00377" class="html-bibr">38</a>,<a href="#B39-jfb-15-00377" class="html-bibr">39</a>,<a href="#B40-jfb-15-00377" class="html-bibr">40</a>,<a href="#B44-jfb-15-00377" class="html-bibr">44</a>,<a href="#B45-jfb-15-00377" class="html-bibr">45</a>,<a href="#B46-jfb-15-00377" class="html-bibr">46</a>,<a href="#B47-jfb-15-00377" class="html-bibr">47</a>,<a href="#B48-jfb-15-00377" class="html-bibr">48</a>,<a href="#B49-jfb-15-00377" class="html-bibr">49</a>,<a href="#B50-jfb-15-00377" class="html-bibr">50</a>,<a href="#B51-jfb-15-00377" class="html-bibr">51</a>,<a href="#B52-jfb-15-00377" class="html-bibr">52</a>,<a href="#B53-jfb-15-00377" class="html-bibr">53</a>,<a href="#B54-jfb-15-00377" class="html-bibr">54</a>,<a href="#B55-jfb-15-00377" class="html-bibr">55</a>,<a href="#B56-jfb-15-00377" class="html-bibr">56</a>,<a href="#B57-jfb-15-00377" class="html-bibr">57</a>,<a href="#B58-jfb-15-00377" class="html-bibr">58</a>,<a href="#B59-jfb-15-00377" class="html-bibr">59</a>,<a href="#B60-jfb-15-00377" class="html-bibr">60</a>].</p>
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12 pages, 5389 KiB  
Article
Effects of Platelet-Rich Fibrin on Bone Healing Around Implants Placed in Maxillary Sinuses: A Histomorphometric Assessment in Rabbits
by Gustavo Augusto Grossi-Oliveira, Eduardo Dallazen, Thabet Asbi, João Matheus Fonseca-Santos, Paulo Domingos Ribeiro-Júnior, Jamil A. Shibli, Cinthya Massari Grecco, Osvaldo Magro-Filho, Carlos Fernando Mourão, Doron Haim, Yaniv Mayer and Leonardo P. Faverani
J. Funct. Biomater. 2024, 15(12), 375; https://doi.org/10.3390/jfb15120375 - 12 Dec 2024
Viewed by 623
Abstract
This study investigated the effect of platelet-rich fibrin (PRF) on bone healing around implants placed in elevated sinus cavities. Forty New Zealand albino rabbits were divided into eight groups, based on the time of sacrifice (14 or 40 days) and the material used: [...] Read more.
This study investigated the effect of platelet-rich fibrin (PRF) on bone healing around implants placed in elevated sinus cavities. Forty New Zealand albino rabbits were divided into eight groups, based on the time of sacrifice (14 or 40 days) and the material used: blood clot (control), hydroxyapatite (HA) from bovine bone, HA combined with PRF, and PRF alone. Each group consisted of five animals (n = 5). A histological analysis measured bone-to-implant contact (BIC) and bone area fraction occupancy (BAFO). The results showed significant increases in the BIC and BAFO values at 40 days compared to 14 days in most groups. At day 14, the HA+PRF group had higher BIC than the clot and the PRF alone groups. At 40 days, HA+PRF maintained the highest BIC across all groups (p < 0.05), though it did not show an advantage for BAFO. These findings indicate that combining HA with PRF promotes better osseointegration around implants placed immediately in maxillary sinus augmentation. Given the limited research on PRF’s biological impact, these results underscore the importance of evaluating PRF’s role in peri-implant healing and its potential benefits for clinical use in sinus augmentation. Full article
(This article belongs to the Special Issue New Biomaterials in Periodontology and Implantology)
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<p>Three-dimensional schematic overview of the step-by-step surgical procedure for sinus augmentation and implant placement in rabbits.</p>
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<p>Healing of the clot group at 14 and 40 days at 20× and 100× magnification stained with Stevenel’s blue and alizarin red.</p>
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<p>Healing of the HA group at 14 and 40 days at 20× and 100× magnification stained with Stevenel’s blue and alizarin red. * Residual HA particles.</p>
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<p>Healing of the HA+PRF group at 14 and 40 days at 20× and 100× magnification stained with Stevenel’s blue and alizarin red.</p>
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<p>Healing of the PRF group at 14 and 40 days at 20× and 100× magnification stained with Stevenel’s blue and alizarin red.</p>
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<p>Column graph showing bone-to-implant contact quantity in the experimental groups at 14 and 40 days. Ө δ ζ—statistical difference comparing groups at 14 days of healing. ε φ ω ψ χ—statistical difference comparing groups at 40 days of healing. Only HA (group 2) did not show a statistical difference from 14 to 40 days of healing.</p>
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<p>Column graph showing bone area fraction occupancy quantity in the experimental groups at 14 and 40 days. δ ζ—statistical difference comparing groups at 14 days of healing. Only HA (group 2) did not show a statistical difference from 14 to 40 days of healing.</p>
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16 pages, 3113 KiB  
Article
Effect of Liquid Blood Concentrates on Cell Proliferation and Cell Cycle- and Apoptosis-Related Gene Expressions in Nonmelanoma Skin Cancer Cells: A Comparative In Vitro Study
by Eva Dohle, Lianna Zhu, Robert Sader and Shahram Ghanaati
Int. J. Mol. Sci. 2024, 25(23), 12983; https://doi.org/10.3390/ijms252312983 - 3 Dec 2024
Viewed by 462
Abstract
Nonmelanoma skin cancer (NMSC) presents a significant challenge to global healthcare due to its rising incidence, prompting the search for innovative treatments to overcome the limitations of current therapies. Our study aims to explore the potential effects of the liquid blood concentrate platelet-rich [...] Read more.
Nonmelanoma skin cancer (NMSC) presents a significant challenge to global healthcare due to its rising incidence, prompting the search for innovative treatments to overcome the limitations of current therapies. Our study aims to explore the potential effects of the liquid blood concentrate platelet-rich fibrin (PRF) on basal cell carcinoma cells (BCCs) and squamous cell carcinoma cells (SCCs) in order to obtain results that may lead to new possible adjunctive therapies for managing localized skin cancers, particularly NMSC. Basal cell carcinoma (BCC) cells and squamous cell carcinoma (SCC) cells were indirectly treated with PRF generated via different relative centrifugation forces, namely high and low RCF PRF, for 7 days. PRF-treated cells were comparatively analyzed for cell viability, proliferation and cell cycle- and apoptosis-related gene expression. Analysis of MTS assay results revealed a significant decrease in cell viability in both BCC and SCC cells following PRF treatment for 7 days. Ki-67 staining showed a decreased percentage of Ki-67-positive cells in both BCC and SCC cells after 2 days of treatment compared to the control group. The downregulation of CCND1 gene expression in both cell types at 2 days along with the upregulation of p21 and p53 gene expression in SCC cells demonstrated the effect of PRF in inhibiting cell proliferation and inducing cell cycle arrest, especially during the initial phases of treatment. Increased expression of caspase-8 and caspase-9 was observed, indicating the activation of both extrinsic and intrinsic apoptotic pathways by PRF treatment. Although the exact immunomodulatory properties of PRF require further investigation, the results of our basic in vitro studies are promising and might provide a basis for future investigations of PRF as an adjunctive therapy for managing localized skin cancers, particularly NMSC. Full article
(This article belongs to the Section Molecular Immunology)
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<p>Cell viability of PRF-treated BCC and SCC compared to untreated cells. The cell viability of BCC and SCC treated with high and low RCF PRF or without PRF treatment as a control was assessed by the MTS assay at 2 days (<b>A</b>), 4 days (<b>B</b>), and 7 days (<b>C</b>). The line graphs (<b>D</b>,<b>E</b>) show the trend of the PRF effect on BCC and SCC cells over time. The relative cell viability percentage was calculated by comparing the cell viability of PRF-treated cells with that of untreated cells in the control group (=100%; n = 9). The bars represent the mean values and the corresponding standard deviations (SDs). Significance: ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Analysis of immunofluorescence staining images of Ki67. Representative merged images of immunofluorescence staining of Ki67 from BCC (<b>A</b>) and from SCC (<b>B</b>) on day 2, treated with high and low RCF PRF, and without PRF treatment (control). Scale bars: upper row = 50 μm; lower row = 25 μm. The relative percentage of Ki67-positive cells in BCC (<b>C</b>) and SCC (<b>D</b>) was calculated by comparing the percentage of Ki67-positive cells of PRF-treated cells to that of untreated cells in the control group (n = 9). The bars represent the mean values and the corresponding standard deviations (SDs). Significance: * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Relative gene expression of caspase 8. The relative gene expression of caspase 8 was assessed using quantitative real-time PCR. The expression levels of the caspase 8 gene in BCC (<b>A</b>–<b>C</b>) and SCC (<b>D</b>–<b>F</b>) in response to PRF treatment for 2, 4, and 7 days were compared with untreated cells in the control group (n = 9). None of the differences could be evaluated as statistically significant different. The results are presented as fold changes in gene expression relative to RPL37A.</p>
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<p>Relative gene expression of caspase 9. The relative gene expression of caspase 9 was assessed using quantitative real-time PCR. Caspase 9 gene expression levels in BCC (<b>A</b>–<b>C</b>) and SCC (<b>D</b>–<b>F</b>) treated with PRF for 2, 4, and 7 days were compared with untreated control cells (n = 9). The results are presented as fold changes in gene expression relative to RPL37A. Significance: * <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, and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Relative gene expression of CCND1. The relative gene expression of CCND1 was assessed by quantitative real-time PCR. CCND1 gene expression levels in BCC (<b>A</b>–<b>C</b>) and SCC (<b>D</b>–<b>F</b>) treated with PRF for 2, 4, and 7 days were compared with untreated control cells (n = 9). The results are presented as fold changes in gene expression relative to RPL37A. Significance: * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Relative gene expression of p21. Relative gene expression was assessed by quantitative real-time PCR. p21 gene expression levels in BCC (<b>A</b>–<b>C</b>) and SCC (<b>D</b>–<b>F</b>) treated with PRF for 2, 4, and 7 days were compared with untreated control cells (n = 9). The results are presented as fold changes in gene expression relative to RPL37A. Significance: * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Relative gene expression of p53. Relative gene expression was assessed by quantitative real-time PCR. P53 gene expression levels in BCC (<b>A</b>–<b>C</b>) and SCC (<b>D</b>–<b>F</b>) treated with PRF for 2, 4, and 7 days were compared with untreated control cells (n = 9). The results are presented as fold changes in gene expression relative to RPL37A. * <span class="html-italic">p</span> &lt; 0.05, **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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11 pages, 2911 KiB  
Article
Arthrocentesis of Temporomandibular Joints—A Clinical Comparative Study
by Marta Siewert, Rafał Pokrowiecki, Paweł J. Zawadzki and Zygmunt Stopa
Life 2024, 14(12), 1594; https://doi.org/10.3390/life14121594 - 3 Dec 2024
Viewed by 425
Abstract
The objective of this study was to compare single-needle arthrocentesis with the conventional two-needle arthrocentesis, as well as the additional intracapsular injection of hyaluronic acid or platelet-rich fibrin. A total of 96 patients with established osteoarthritis (OA) (n = 48) or with [...] Read more.
The objective of this study was to compare single-needle arthrocentesis with the conventional two-needle arthrocentesis, as well as the additional intracapsular injection of hyaluronic acid or platelet-rich fibrin. A total of 96 patients with established osteoarthritis (OA) (n = 48) or with internal de-arrangement (DD) (n = 48) were assigned single-needle arthrocentesis with distension of the joint or conventional two-needle arthrocentesis with or without intracapsular injection of the medication (hyaluronic acid (HA) or platelet-rich plasma (PRP)) performed every month over a period of 6 months. The maximum mouth opening and pain, as measured by the visual analog scale (VAS), were compared. Each group exhibited significant improvement, i.e., a decrease in pain and an increase in mouth opening. The single-puncture technique provided similar pain reduction as the two-needle approach but provided significantly better results in terms of maximum mouth opening. The reduction in pain was similar when comparing the OA and DD cohorts; however, patients with disc displacement achieved significantly better mouth opening than OA. Intracapsular application of medication contributed to a significant decrease in pain in both HA and PRP groups, with platelet-rich fibrin being significantly superior to HA in terms of mouth opening improvement. Full article
(This article belongs to the Section Medical Research)
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<p>Intraoperative photographs showing two arthrocentesis techniques: (<b>A</b>) a two-needle approach where fluid is introduced into the TMJ through a posterior entry point and evacuated simultaneously through an anterior exit point, which provides passive joint lavage; (<b>B</b>,<b>C</b>) a single puncture technique where fluid is pumped into the TMJ through a posterior point and then evacuated through the same needle after removal of the syringe, which provides a pressured lavage through joint capsule hydro-dissection and stretching; (<b>D</b>) intracapsular application of medication after arthrocentesis (HA or PRF).</p>
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<p>Change in mean VAS and MMO scores (N = 96)<b>.</b> A one-way analysis of variance (ANOVA) with repeated measures showed a significant difference between the variables: F = 205.36, <span class="html-italic">p</span>-value ≤ 0.001 for the VAS decrease and F = 91.54, <span class="html-italic">p</span>-value ≤ 0.001 for increase in MMO before and after the treatment.</p>
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<p>Graph showing gradual decrease in pain between each treatment in the OA and DD cohorts.</p>
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<p>Graph showing gradual increase in maximal mouth opening between each treatment in the OA and DD cohorts.</p>
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<p>Graph showing gradual decrease in pain between each treatment in the HA and PRP cohorts.</p>
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<p>Graph showing gradual increase in maximal mouth opening between each treatment in the HA and PRP cohorts.</p>
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14 pages, 3787 KiB  
Article
Distinct Hemostasis and Blood Composition in Spiny Mouse Acomys cahirinus
by Nikita S. Filatov, Rafael R. Khismatullin, Airat I. Bilyalov, Alina I. Khabirova, Shakhnoza M. Salyakhutdinova, Roman V. Ursan, Roza N. Kasimova, Alina D. Peshkova, Insaf I. Gazizov, Elena I. Shagimardanova, Mary V. Woroncow, Andrey P. Kiyasov, Rustem I. Litvinov and Oleg A. Gusev
Int. J. Mol. Sci. 2024, 25(23), 12867; https://doi.org/10.3390/ijms252312867 - 29 Nov 2024
Viewed by 445
Abstract
The spiny mouse (Acomys species) is capable of scarless wound regeneration through largely yet unknown mechanisms. To investigate whether this capacity is related to peculiarities of the hemostatic system, we studied the blood of Acomys cahirinus in comparison to Mus musculus (Balb/c) [...] Read more.
The spiny mouse (Acomys species) is capable of scarless wound regeneration through largely yet unknown mechanisms. To investigate whether this capacity is related to peculiarities of the hemostatic system, we studied the blood of Acomys cahirinus in comparison to Mus musculus (Balb/c) to reveal differences in blood composition and clotting in both males and females. In response to surgical manipulations, blood clots formed in wounds of Acomys comprised a stronger hemostatic seal with reduced surgical bleeding in comparison with Balb/c. Acomys demonstrated notably shorter tail bleeding times and elevated clottable fibrinogen levels. Histological analysis revealed that clots from Acomys blood had densely packed fibrin-rich clots with pronounced fibrin segregation from erythrocytes. Acomys exhibited superior plasma clot stiffness as revealed with thromboelastography. The latter two characteristics are likely due to hyperfibrinogenemia. Light transmission platelet aggregometry demonstrated that ADP-induced platelet aggregates in Acomys males are stable, unlike the aggregates formed in the plasma of Balb/c undergoing progressive disaggregation over time. There were no apparent distinctions in platelet contractility and baseline expression of phosphatidylserine. Hematological profiling revealed a reduced erythrocytes count but increased mean corpuscular volume and hemoglobin content in Acomys. These results demonstrate the distinctive hemostatic potential of Acomys cahirinus, which may contribute to their remarkable regenerative capacity. Full article
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<p>Results of the tail bleeding assay (<b>A</b>) and levels of clottable fibrinogen in blood plasma (<b>B</b>) of male and female <span class="html-italic">Acomys cahirinus</span> mice versus Balb/c. The results are presented as mean ± SD (n = 5 for each species and gender group). * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Representative histological images of blood clots from <span class="html-italic">Acomys cahirinus</span> (<b>A</b>,<b>C</b>) and Balb/c (<b>B</b>,<b>D</b>) (n = 3 for each). Arrows indicate <span class="html-italic">red</span> fibrin in the clot. Erythrocytes are <span class="html-italic">yellow</span>. (<b>E</b>) Characteristic dense <span class="html-italic">red</span> fibrin accumulations within the <span class="html-italic">Acomys cahirinus</span> blood clot. Multiple giant densely packed clusters and fibrous structures of fibrin are visualized (within dashed ovals), mostly separated from <span class="html-italic">yellow</span> erythrocytes. (<b>F</b>) Typical loose distribution of fibrin within the Balb/c blood clot. A significant predominance of loosely arranged fibrin (<span class="html-italic">red</span>), colocalized with erythrocytes (stained <span class="html-italic">pink</span>, not <span class="html-italic">yellow</span> as in the <span class="html-italic">Acomys</span> clot). Single islets of fibrin aggregates (marked by dashed ovals) were observed. Picro–Mallory stain. Magnification 25× (<b>A</b>–<b>D</b>) and 200× (<b>E</b>,<b>F</b>).</p>
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<p>TEG parameters of whole blood (<b>A</b>–<b>C</b>) and PFP (<b>D</b>–<b>F</b>) in male and female <span class="html-italic">Acomys cahirinus</span> and Balb/c: <span class="html-italic">R</span> (reaction time), α-angle (fibrin polymerization rate), and <span class="html-italic">G</span> (shear elastic modulus). n = 6 for paired whole blood samples and n = 9 for PFP samples from males; n = 5 for paired blood and PFP samples in females. The results are presented as mean ± SD. * <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, **** <span class="html-italic">p</span> &lt; 0.0001. ns—not significant.</p>
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<p>Parameters of clot contraction in whole blood (<b>A</b>,<b>B</b>) and in PRP (<b>C</b>,<b>D</b>) from <span class="html-italic">Acomys cahirinus</span> and Balb/c males and females. n = 6 for paired whole blood samples and n = 5 for PRP samples from males; n = 5 for paired blood and PRP samples from females. The results are presented as mean ± SD. * <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. ns—not significant.</p>
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<p>Averaged light transmission aggregograms recorded after ADP-induced platelet aggregation in PRP from male (<b>A</b>) and female (<b>B</b>) <span class="html-italic">Acomys cahirinus</span> and Balb/c (n = 5 for each species and gender group). Two-way ANOVA test in (<b>A</b>): <span class="html-italic">p</span> &lt; 0.05 at 12 min, <span class="html-italic">p</span> &lt; 0.01 at 15 min, <span class="html-italic">p</span> &lt; 0.001 at 20–30 min.</p>
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<p>A characteristic thromboelastogram and the key parameters of clot formation: <span class="html-italic">R</span>—reaction time, α—alpha angle, <span class="html-italic">MA</span>—maximum amplitude.</p>
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10 pages, 8101 KiB  
Article
Long-Term Success of Dental Implants in Atrophic Maxillae: A 3-Year Case Series Using Hydroxyapatite and L-PRF
by Marco Andre Lomba Alves, Jakson Both, Carlos Fernando Mourão, Bruna Ghiraldini, Fabio Bezerra, Jose Mauro Granjeiro, Suelen Cristina Sartoretto and Monica Diuana Calasans-Maia
Bioengineering 2024, 11(12), 1207; https://doi.org/10.3390/bioengineering11121207 - 28 Nov 2024
Viewed by 535
Abstract
Dental implants are essential for the prosthetic rehabilitation of edentulous patients, requiring adequate bone volume and density for osseointegration and load support. The posterior region of the maxilla, commonly deficient in bone quality and quantity, represents a clinical challenge. This case series reports [...] Read more.
Dental implants are essential for the prosthetic rehabilitation of edentulous patients, requiring adequate bone volume and density for osseointegration and load support. The posterior region of the maxilla, commonly deficient in bone quality and quantity, represents a clinical challenge. This case series reports an analysis involving 69 dental implants in the atrophic maxilla of nine patients. The procedures adopted combined alloplastic hydroxyapatite grafting and leukocyte platelet-rich fibrin (L-PRF) applied to the alveolar ridge and maxillary sinus lift. With an average follow up of three years after the installation of the prostheses, an implant success rate of 98.5% was observed, showing integration and functional stability. The strategy of combining hydroxyapatite with L-PRF proved to be effective in increasing bone volume and promoting osseointegration. These findings indicate that the technique and biomaterials are viable for rehabilitating atrophic maxillae in the posterior region, offering long-lasting clinical results and a high success rate. Full article
(This article belongs to the Special Issue Biomaterials for Bone Repair and Regeneration)
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<p>(<b>A</b>) Biomaterial for grafting: L-PRF combined with porous synthetic hydroxyapatite granules. (<b>B</b>) Lateral wall of the maxillary sinus exposed for grafting with the biomaterial. (<b>C</b>) Implant placement: eight implants installed five months post-graft surgery. (<b>D</b>) Rehabilitation: fixed prostheses placed four months after implant installation. (<b>E</b>,<b>F</b>) Panoramic radiographs showing maxillary atrophy (<b>E</b>) and bone restoration with implant placement following grafting (<b>F</b>).</p>
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<p>Scanning electron microscopy of Alobone<sup>®</sup> Poros. (<b>A</b>) 50×; (<b>B</b>) 250×; (<b>C</b>) 500×; (<b>D</b>) 1500×; (<b>E</b>,<b>F</b>) 5000×. The size of the micrometer bar is indicated in each image. The micrographs show a highly porous architecture. The surface of the granules appears rough and irregular with small particles aggregated together to form larger, rough structures. This surface roughness can enhance osteoconductive, helping in the attachment of osteoblasts (bone-forming cells).</p>
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<p>(<b>A</b>) X-ray diffractogram of Alobone Poros indicating hydroxyapatite (HA, *) and β-tricalcium phosphate (β-TCP, o) phases. (<b>B</b>) Fourier-transform infrared spectrum highlighting hydroxyl (OH<sup>−</sup>) and phosphate (PO<sub>4</sub><sup>−3</sup>) groups.</p>
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<p>Panoramic radiographs of two clinical cases, (<b>A</b>,<b>C</b>) initial radiographs and (<b>B</b>,<b>D</b>) radiographs with the implants installed in the grafted areas 5 months after surgery.</p>
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29 pages, 1949 KiB  
Systematic Review
Patient Experience and Wound Healing Outcomes Using Different Palatal Protection Methods After Free Gingival Grafts: A Systematic Review
by Tomasz Jankowski, Agnieszka Jankowska, Mirona Palczewska-Komsa, Maciej Jedliński, Wojciech Kazimierczak and Joanna Janiszewska-Olszowska
J. Funct. Biomater. 2024, 15(12), 360; https://doi.org/10.3390/jfb15120360 - 27 Nov 2024
Viewed by 1114
Abstract
(1) Background: A free gingival graft (FGG) is a common technique used to reconstruct or enhance the area of keratinized mucosa, while a connective tissue graft (CTG) is utilized to boost soft tissue thickness, thereby promoting stability in interproximal marginal bone levels. Most [...] Read more.
(1) Background: A free gingival graft (FGG) is a common technique used to reconstruct or enhance the area of keratinized mucosa, while a connective tissue graft (CTG) is utilized to boost soft tissue thickness, thereby promoting stability in interproximal marginal bone levels. Most reported complications following FGG procedure are associated with the donor site. In addition to a painful, open wound in the palate, the most frequent complications linked to FGG harvesting include excessive bleeding, postoperative bone exposure, and recurrent herpes lesions. Numerous methods for securing the donor site after a free gingival graft surgery have been documented in research publications. The main objective of this systematic review was to assess various techniques for protecting the palate after graft harvesting and their impact on patient experience, with a focus on pain management. The secondary objective was to evaluate these techniques in relation to donor site wound healing. (2) Methods: The search was performed across four databases: Medline (PubMed Central), Scopus, Web of Science, and Embase, in accordance with PRISMA guidelines and the recommendations set forth in the Cochrane Handbook for Systematic Reviews of Interventions. The initial search took place on 9 October 2023, followed by an update on 28 June 2024. The search utilized the following keywords: (“wound” OR “injury”) AND (“graft” OR “free gingival graft” OR “graft harvesting”) AND (“healing” OR “recovery”) AND “palate”. (3) Results: After conducting the follow-up search, a total of 958 papers were identified: 193 from PubMed, 314 from Scopus, 101 from Web of Science, and 350 from Embase. Ultimately, of the 49 papers that remained, 11 were excluded due to not fulfilling the inclusion criteria, leaving 38 full-text papers on free gingival grafts (FGG) for qualitative analysis. (4) Conclusions: Various methods for palatal protection after free gingival grafts (FGG) are described in the literature, stemming from biological, physical, or chemical sources. Most studies in this review examined platelet-rich fibrin and suggested that it provides no benefits for patients’ subjective experiences or wound healing outcomes. While photobiomodulation appears to support wound epithelialization, it does not influence pain perception. Alternatives such as propolis, hyaluronic acid, and medicinal plant extracts show potential for palatal protection; however, further research is needed to thoroughly evaluate their effectiveness. Full article
(This article belongs to the Special Issue New Biomaterials in Periodontology and Implantology)
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<p>Photograph of a palatal wound created immediately after harvesting a free graft from the palate.</p>
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<p>Prisma 2020 flow diagram.</p>
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<p>The qualitative analysis for randomized clinical trials [<a href="#B17-jfb-15-00360" class="html-bibr">17</a>,<a href="#B18-jfb-15-00360" class="html-bibr">18</a>,<a href="#B19-jfb-15-00360" class="html-bibr">19</a>,<a href="#B20-jfb-15-00360" class="html-bibr">20</a>,<a href="#B21-jfb-15-00360" class="html-bibr">21</a>,<a href="#B22-jfb-15-00360" class="html-bibr">22</a>,<a href="#B23-jfb-15-00360" class="html-bibr">23</a>,<a href="#B24-jfb-15-00360" class="html-bibr">24</a>,<a href="#B25-jfb-15-00360" class="html-bibr">25</a>,<a href="#B26-jfb-15-00360" class="html-bibr">26</a>,<a href="#B27-jfb-15-00360" class="html-bibr">27</a>,<a href="#B28-jfb-15-00360" class="html-bibr">28</a>,<a href="#B29-jfb-15-00360" class="html-bibr">29</a>,<a href="#B30-jfb-15-00360" class="html-bibr">30</a>,<a href="#B31-jfb-15-00360" class="html-bibr">31</a>,<a href="#B32-jfb-15-00360" class="html-bibr">32</a>,<a href="#B33-jfb-15-00360" class="html-bibr">33</a>,<a href="#B34-jfb-15-00360" class="html-bibr">34</a>,<a href="#B35-jfb-15-00360" class="html-bibr">35</a>,<a href="#B36-jfb-15-00360" class="html-bibr">36</a>,<a href="#B37-jfb-15-00360" class="html-bibr">37</a>,<a href="#B38-jfb-15-00360" class="html-bibr">38</a>,<a href="#B39-jfb-15-00360" class="html-bibr">39</a>,<a href="#B40-jfb-15-00360" class="html-bibr">40</a>,<a href="#B41-jfb-15-00360" class="html-bibr">41</a>,<a href="#B42-jfb-15-00360" class="html-bibr">42</a>,<a href="#B43-jfb-15-00360" class="html-bibr">43</a>,<a href="#B44-jfb-15-00360" class="html-bibr">44</a>,<a href="#B45-jfb-15-00360" class="html-bibr">45</a>,<a href="#B46-jfb-15-00360" class="html-bibr">46</a>,<a href="#B47-jfb-15-00360" class="html-bibr">47</a>,<a href="#B48-jfb-15-00360" class="html-bibr">48</a>,<a href="#B49-jfb-15-00360" class="html-bibr">49</a>,<a href="#B50-jfb-15-00360" class="html-bibr">50</a>,<a href="#B51-jfb-15-00360" class="html-bibr">51</a>,<a href="#B52-jfb-15-00360" class="html-bibr">52</a>,<a href="#B53-jfb-15-00360" class="html-bibr">53</a>,<a href="#B54-jfb-15-00360" class="html-bibr">54</a>].</p>
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19 pages, 6477 KiB  
Article
First- vs. Second-Generation Autologous Platelet Concentrates and Their Implications for Wound Healing: Differences in Proteome and Secretome
by Hanna L. Stiller, Natarajan Perumal, Caroline Manicam, Emily R. Trzeciak, Julia Todt, Kerstin Jurk, Andrea Tuettenberg, Sven Schumann, Eik Schiegnitz and Sebastian Blatt
Bioengineering 2024, 11(11), 1171; https://doi.org/10.3390/bioengineering11111171 - 20 Nov 2024
Viewed by 712
Abstract
Differences in cell count and growth factor expression between first- and second-generation autologous platelet concentrates (APCs) have been well described. The debate over which formula best supports wound healing in various surgical procedures is still ongoing. This study aims to assess the whole [...] Read more.
Differences in cell count and growth factor expression between first- and second-generation autologous platelet concentrates (APCs) have been well described. The debate over which formula best supports wound healing in various surgical procedures is still ongoing. This study aims to assess the whole proteome assembly, cell content, immunological potential and pro-angiogenic potential of second-generation APC, Platelet-Rich Fibrin (PRF) vs. first-generation APC, Platelet-Rich Plasma (PRP). The global proteome of the APCs was analyzed using nano-liquid chromatography mass spectrometry. Blood cell concentrations were determined by an automated cell counter. The effect of APCs on macrophage polarization was analyzed by flow cytometry. A yolk sac membrane (YSM) assay was used to monitor the neo-vessel formation and capillary branching in vivo. Cell count analysis revealed a higher number/concentration of leukocytes in PRF vs. PRP. Incubation of macrophages with PRP or platelet-free plasma (PFP) did not induce a significant pro-inflammatory state but led to a shift to the M0/M2 phenotype as seen in wound healing for all tested formulas. Label-free proteomics analysis identified a total of 387 proteins from three biological replicates of the respective designated groups. PRF induced increased formation of neo-vessels and branching points in vivo in comparison to PRP and PFP (each p < 0.001), indicating the enhanced pro-angiogenic potential of PRF. Overall, PRF seems superior to PRP, an important representative of first-generation formulas. Inclusion of leucocytes in PRF compared to PRP suggested rather an anti-inflammatory effect on macrophages. These results are important to support the versatile clinical applications in regenerative medicine for second-generation autologous platelet concentrates to optimize wound healing. Full article
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<p>Yolk sac membrane (YSM) assay. (<b>A</b>): In ovo analysis of PRF (2) and PFP (*) in safe distance from the embryo (1). (<b>B</b>): Microscopical analysis of the induced vessels (3) in direct contact with the PRF (2) and in safe distance from the embryo (1). (<b>C</b>): Vessel analysis after grayscale conversion and background extraction with FIJI software (Version 2.9.0). Arrow: vessel.</p>
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<p>(<b>a</b>) Cytological analysis of PRF, PRP, and PFP compared to EDTA-blood in platelets, erythrocytes, and leukocytes (ns: <span class="html-italic">p</span> &gt; 0.05; *: <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; ****: <span class="html-italic">p</span> &lt; 0.0001). (<b>b</b>) Cytological analysis of PRF, PRP, and PFP compared to EDTA-blood in neutrophilic granulocytes, lymphocytes, and monocytes (ns: <span class="html-italic">p</span> &gt; 0.05; *: <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>Platelet-rich plasma (PRP) and platelet-free plasma (PFP) polarize human monocyte derived macrophages to a “M0/M2-like” phenotype. Macrophages were polarized or treated with PRP or PFP. Following 2 days of incubation, surface marker expression was evaluated with flow cytometry. The bar diagram indicates the mean fluorescence intensity (MFI) of each marker, normalized to the matching donor “M0” control. The histograms show one representative result (<span class="html-italic">n</span> = 4 donors, means ± SD, * <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, and **** <span class="html-italic">p</span> &lt; 0.0001 analyzed by two-way ANOVA, corrected for multiple comparisons using Tukey tests).</p>
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<p>Representative protein profiles of the designated groups comprising the soluble proteins from sPRF, sPRP, and sPFP, and cell-derived proteins from pPRF, pPRP, and pPFP resolved in 1DE-PAGE after colloidal blue staining.</p>
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<p>Label-free quantitative proteomics analysis of the supernatant and pellet fragments of the APC. (<b>a</b>) Heat map depicts the hierarchical clustering of 387 total proteins based on the log<sub>2</sub> protein intensity corresponding to the designated groups. (<b>b</b>) Bar charts show the degree of mean percentage of top abundant proteins in the designated groups. (<b>c</b>,<b>d</b>) Venn diagrams illustrate the total number of proteins identified in all samples.</p>
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<p>Heat map depicts the hierarchical clustering of the total of 268 significantly differentially abundant proteins in the designated comparison groups. Significance threshold is at <span class="html-italic">p</span> &lt; 0.05. The up-regulated proteins are shown in red and the down-regulated proteins are in green.</p>
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<p>Volcano plots illustrate the significantly differentially abundant proteins identified based on the log<sub>2</sub> difference in the (<b>a</b>) pPRF vs. sPRF, (<b>b</b>) pPRP vs. sPRP (<b>c</b>) pPFP vs. sPFP, (<b>d</b>) sPRF vs. sPFP, (<b>e</b>) sPRP vs. sPFP, (<b>f</b>) sPRF vs. sPRP, (<b>g</b>) pPRF vs. pPFP, (<b>h</b>) pPRP vs. pPFP, and (<b>i</b>) pPRF vs. pPRP. The significance threshold is at <span class="html-italic">p</span> &lt; 0.05. The up-regulated proteins are shown in red and the down-regulated proteins are in green.</p>
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<p>Heat map depicts the top significant enriched biological functions and canonical pathways of the differentially abundant proteins in the designated comparison groups. The significance of enrichment (−log<sub>10</sub> (B-H <span class="html-italic">p</span>-value) is scaled by color intensity; <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Microscopic analysis of vessel formation in the yolk sac membrane (YSM) assay for PRF (<b>A</b>) and PFP (<b>B</b>). The red arrow in (<b>A</b>) highlights the enhanced vessel formation in the PRF group compared to PFP. Panel (<b>C</b>) quantifies vessel formation, and (<b>D</b>) depicts the number of branching points, demonstrating a statistically significant increase in pro-angiogenic activity in the PRF group (**** <span class="html-italic">p</span> &lt; 0.0001).</p>
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11 pages, 647 KiB  
Article
Assessing the Effectiveness of A-PRF+ for Treating Periodontal Defects: A Prospective Interventional Pilot Study Involving Smokers
by Ada Stefanescu, Dorin Ioan Cocoș, Gabi Topor, Fabian Cezar Lupu, Doriana Forna-Agop and Kamel Earar
Medicina 2024, 60(11), 1897; https://doi.org/10.3390/medicina60111897 - 19 Nov 2024
Viewed by 691
Abstract
Background and Objectives: This study aimed to evaluate the effects of advanced platelet-rich fibrin (A-PRF+) tissue regeneration therapy on clinical periodontal parameters in non-smokers and smoker patients. The anticipated biological mechanisms of A-PRF+ include stimulating angiogenesis, thereby promoting the formation of new blood [...] Read more.
Background and Objectives: This study aimed to evaluate the effects of advanced platelet-rich fibrin (A-PRF+) tissue regeneration therapy on clinical periodontal parameters in non-smokers and smoker patients. The anticipated biological mechanisms of A-PRF+ include stimulating angiogenesis, thereby promoting the formation of new blood vessels, which is essential for tissue healing. Additionally, A-PRF+ harnesses the regenerative properties of platelet-rich fibrin, contributing to the repair and regeneration of periodontal tissues. Materials and Methods: The study was conducted on 55 patients, divided into two groups: non-smoker patients (n = 29) and smoker patients (n = 26). A single operator conducted the surgical procedure. Following the administration of local anesthesia with articaine 4% with adrenaline 1:100,000 precise intracrevicular incisions were made, extending towards the adjacent teeth, until the interproximal spaces, with meticulous attention to conserving the interdental gingival tissue to the greatest extent possible. Extended, full-thickness vestibular and oral flaps were carefully lifted, and all granulation tissue was meticulously removed from the defect without altering the bone contour. After debridement of the defects, A-PRF+ was applied. BOP (bleeding on probing), PI (plaque index), CAL (clinical attachment loss), and probing depth (PD) were determined at baseline and six months post-surgery. Results: Significant reductions were observed in PD and CAL after six months. In the non-smokers group, PD decreased from 7.0 ± 1.0 mm to 3.1 ± 0.1 mm (p < 0.001), while in the smokers group, PD decreased from 6.9 ± 1.1 mm to 3.9 ± 0.3 mm (p < 0.001). CAL decreased in the non-smokers group from 5.8 ± 0.7 mm to 2.6 ± 0.2 mm and from 5.7 ± 0.9 mm to 3.2 ± 0.2 mm (p < 0.001) in smokers. Notably, the reductions in CAL and PD were statistically more significant in the non-smokers group. Conclusions: Even though the clinical periodontal improvements were considerable in smoker patients, they did not reach the level observed in non-smoker patients. Full article
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<p>Processing and application of A-PRF+. (<b>A</b>) The A-PRF+ clots are prepared to be inserted intraoperatively. (<b>B</b>) Placement of A-PRF+ clots at the level of intra-osseous defects (distal at 2.1 and mesial at 2.3).</p>
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11 pages, 1831 KiB  
Article
The Effect of Advanced Platelet-Rich Fibrin Plus (A-PRF+) on Graft Stability in Dental Implants and Alveolar Ridge Augmentation Procedures: A New Low-Speed Standardized Centrifugation Protocol
by Benjamin Walch, Andreas Kolk, Dominik Scheibl, Maria Guarda, Sarah Christine Maier and Lena Denk
Dent. J. 2024, 12(11), 349; https://doi.org/10.3390/dj12110349 - 31 Oct 2024
Viewed by 1481
Abstract
Background: Platelet-rich fibrin (PRF) is a concentrate derived from autologous blood, containing platelets, fibrin, and growth factors (GF) obtained through centrifugation. PRF can be mixed with bone replacement material to form sticky bone, which is then introduced into the desired area for [...] Read more.
Background: Platelet-rich fibrin (PRF) is a concentrate derived from autologous blood, containing platelets, fibrin, and growth factors (GF) obtained through centrifugation. PRF can be mixed with bone replacement material to form sticky bone, which is then introduced into the desired area for stabilizing and graft-covering. Depending on the centrifugation protocol, the effectiveness of the end products can vary. This controlled clinical study examines the impact of our established PRF protocol in alveolar augmentation and dental implant placement on vertical bone loss. Materials and Methods: A total of 362 implants were performed in 170 patients at the Department of Oral and Maxillofacial Surgery at the University Hospital Innsbruck between 2018 and 2021. After accounting for lost implants, we retrospectively evaluated a radiological vertical bone loss exceeding 1 mm in the first year as the primary endpoint. Results: The use of PRF was significantly associated with vertical bone loss > 1 mm (OR = 0.32, 95% CI (0.13–0.81), p = 0.016). There were no significant associations between PRF and the number of implants lost, the type of augmentation, or bone loss. Discussion: A-PRF+ sticky bone grafts, when combined with bone graft materials, show reduced resorption rates, indicating their potential to enhance graft stability in oral implantology. Our data indicate that the Medifuge MF 100 (Silfradent srl, Forlì, Italy) is effective in producing A-PRF+. Full article
(This article belongs to the Section Oral and Maxillofacial Surgery)
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<p>Patient collection flowchart.</p>
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<p>A-PRF+ sticky bone.</p>
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<p>3.7 mm vertical bone loss of buccal augmentation.</p>
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<p>Bar chart of PRF and Bone loss, <span class="html-italic">n</span> = 277 implants.</p>
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16 pages, 1371 KiB  
Article
Impact of Infrabony Defects Treatment on Periodontal Markers and Glycated Hemoglobin Using Platelet-Rich Fibrin, Guided Tissue Regeneration, and Access-Flap Surgery
by Ada Stefanescu, Irina-Georgeta Sufaru, Cristian Martu, Diana-Maria Anton, Gabriel Rotundu and Kamel Earar
Medicina 2024, 60(11), 1769; https://doi.org/10.3390/medicina60111769 - 29 Oct 2024
Viewed by 843
Abstract
Background and Objectives: This study evaluated the outcomes of single open-flap debridement, open-flap debridement (OFD) plus resorbable membrane placement, and OFD with resorbable membrane placement plus platelet-rich fibrin (PRF) in terms of periodontal clinical parameters and glycated hemoglobin (HbA1c) levels in 24 [...] Read more.
Background and Objectives: This study evaluated the outcomes of single open-flap debridement, open-flap debridement (OFD) plus resorbable membrane placement, and OFD with resorbable membrane placement plus platelet-rich fibrin (PRF) in terms of periodontal clinical parameters and glycated hemoglobin (HbA1c) levels in 24 adult patients with stage 3 grade C periodontitis and type II diabetes mellitus. Materials and Methods: The primary outcome measure for this study was the clinical attachment level (CAL); secondary outcomes included additional periodontal parameters, such as the plaque index (PI), bleeding on probing (BOP), probing depth (PD), as well as glycated hemoglobin (HbA1c) levels to evaluate the systemic impact of the treatments on glycemic control. The parameters were assessed before and at three and six months post-surgery. In Group A, the flap was sutured closed; in Group B, an absorbable collagen membrane was placed over the defect; and in Group C, PRF was utilized in the defect, with two additional PRF membranes used to cover the defect. The wound healing index (WHI) was recorded at 7 and 14 days after the surgery. Results: The initial findings indicated no significant differences in the periodontal parameters among the three groups. However, improvements in the PD and CAL were most notable in Group C, followed by Group B, with Group A showing the slightest improvement. At six months, there was a highly significant difference in the CAL (p < 0.001). Group C (4.92 ± 0.35) and Group B (4.99 ± 0.31) demonstrated the most significant improvements in the CAL compared to Group A (5.89 ± 0.57). At seven days post-surgery, Group C demonstrated significant healing, with 85% of the sites showing complete healing. By the 14-day mark, all sites in Group C indicated complete healing. Although the HbA1c values did not exhibit statistically significant differences among the groups at baseline, at the 6-month evaluation, all groups showed significantly lower values than baseline. However, the comparison between groups revealed significantly improved values for Group C. Conclusions: The study’s results suggest that PRF is an exceptional material for infrabony defects treatment and notably improves HbA1c levels. Full article
(This article belongs to the Special Issue Advances in Clinical Medicine and Dentistry)
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<p>Study’s flowchart.</p>
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<p>Percentage distribution of healing index with a score of 1 at 7 and 14 days postoperatively.</p>
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18 pages, 3160 KiB  
Article
Investigating the Biological Efficacy of Albumin-Enriched Platelet-Rich Fibrin (Alb-PRF): A Study on Cytokine Dynamics and Osteoblast Behavior
by Emanuelle Stellet Lourenço, Neilane Rodrigues Santiago Rocha, Renata de Lima Barbosa, Rafael Coutinho Mello-Machado, Victor Hugo de Souza Lima, Paulo Emilio Correa Leite, Mariana Rodrigues Pereira, Priscila Ladeira Casado, Tomoyuki Kawase, Carlos Fernando Mourão and Gutemberg Gomes Alves
Int. J. Mol. Sci. 2024, 25(21), 11531; https://doi.org/10.3390/ijms252111531 - 27 Oct 2024
Viewed by 1146
Abstract
The development of effective biomaterials for tissue regeneration has led to the exploration of blood derivatives such as leucocyte- and platelet-rich fibrin (L-PRF). A novel variant, Albumin-Enriched Platelet-Rich Fibrin (Alb-PRF), has been introduced to improve structural stability and bioactivity, making it a promising [...] Read more.
The development of effective biomaterials for tissue regeneration has led to the exploration of blood derivatives such as leucocyte- and platelet-rich fibrin (L-PRF). A novel variant, Albumin-Enriched Platelet-Rich Fibrin (Alb-PRF), has been introduced to improve structural stability and bioactivity, making it a promising candidate for bone regeneration. This study aimed to evaluate Alb-PRF’s capacity for cytokine and growth factor release, along with its effects on the proliferation, differentiation, and mineralization of human osteoblasts in vitro. Alb-PRF membranes were analyzed using histological, scanning electron microscopy, and fluorescence microscopy techniques. Cytokine and growth factor release was quantified over seven days, and osteoinductive potential was evaluated with MG-63 osteoblast-like cells. Structural analysis showed Alb-PRF as a biphasic, highly cellularized material that releases lower levels of inflammatory cytokines and higher concentrations of platelet-derived growth factor (PDGF) and vascular endothelial growth factor (VEGF) compared to L-PRF. Alb-PRF exhibited higher early alkaline phosphatase activity and in vitro mineralization (p < 0.05) and significantly increased the OPG/RANKL mRNA ratio (p < 0.05). These results indicate that Alb-PRF has promising potential as a scaffold for bone repair, warranting further in vivo and clinical assessments to confirm its suitability for clinical applications. Full article
(This article belongs to the Special Issue Research and Application of Platelet-Rich Plasma (PRP))
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<p>Images of histological sections of the membranes. (<b>A</b>) L-PRF membrane at its extremity, where both a dense fibrin network (*) and the buffy coat (BC) can be identified with a high density of cells; Alb-PRF forms a biphasic material with a fibrin network phase shown in (<b>B</b>), connected to a dense albumin barrier (Alb) shown in (<b>C</b>). This albumin portion is also cellularized (arrow), as it can be seen at a higher magnification (<b>D</b>).</p>
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<p>Scanning electron micrographs of the Alb-PRF (<b>above</b>) and L-PRF (<b>below</b>) membranes after elution in culture medium at times of 1, 14, and 28 days. Images were obtained at 15 kV, at different magnifications (JEOL JSM 7100F, JEOL, Japan). The scale bar in each figure indicates 1 μm.</p>
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<p>Qualitative panel of cellular distribution in the structure of L-PRF and Alb-PRF membranes (<b>A</b>). Images were taken from three different portions of the membranes, as shown for an Alb-PRF membrane with approximately 3 cm of length (<b>B</b>). Cell nuclei were evidenced by fluorescence microscopy after staining with DAPI in the upper, middle, and lower regions of the L-PRF membrane and visualization of three random fields of the Alb-PRF membrane (images obtained with a ×20 objective). The scale bar in (<b>A</b>) represents 100 μm, while in (<b>B</b>) it represents 3 mm.</p>
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<p>Quantification of total proteins released into the culture medium after exposure to L-PRF and Alb-PRF membranes for 1, 7, 14, 21 and 28 days. Points indicate mean and standard deviation (<span class="html-italic">n</span> = 5). The lines present linear regressions with R<sup>2</sup> values of 0.8293 and 0.8639 for L-PRF and Alb-PRF, respectively.</p>
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<p>Heatmap of the variation in concentrations of 27 analytes measured in culture media after incubation of L-PRF and Alb-PRF membranes, at times of 1 and 7 days. (*) Significantly different values between these experimental groups (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Cell viability of MG-63 exposed to 24 h extracts from L-PRF and Alb-PRF membranes, diluted at different concentrations with culture media, where the percentage dilution indicates the proportion added of the original extraction media (100% dilution). Results are represented as mean and standard deviation (SD) (<span class="html-italic">n</span> = 5) of cell viability as a percentage of the unexposed experimental control (EC), as measured by the XTT test. High-density, non-cytotoxic polystyrene beads were employed as negative control (C−), and latex fragments were used as a positive control of cytotoxicity (C+). (*) Significantly different values from all other experimental groups and EC (<span class="html-italic">p</span> &lt; 0.05). A dashed line indicates 100% viability (as a percentage of the control group).</p>
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<p>Cellular proliferation of MG-63 osteoblasts exposed to 25% of the 24 h extracts of L-PRF and Alb-PRF at 1, 3, and 7 days, with unexposed cells as a control. Results presented as a mean and SD (<span class="html-italic">n</span> = 5) of the staining of DNA by the CVDE assay, which is directly relative to cell density. (*) Significantly different from the other experimental groups, at the same time (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Measurement of alkaline phosphatase concentrations obtained after exposure of MG-63 osteoblasts to 25% conditioned media of each membrane, at 1, 3, 7, 14, and 21 days. Bars indicate mean and standard deviation (<span class="html-italic">n</span> = 5). (*) Significantly different values between groups in the same experimental time (<span class="html-italic">p</span> &lt; 0.05). Mineralization medium was employed as a positive control (C+).</p>
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<p>The quantification of mineralization was determined by alizarin red after exposure of MG-63 osteoblasts to 25% dilution of the extracts at 1, 3, and 7 days. The bars indicate the mean and standard deviation (<span class="html-italic">n</span> = 3). (*) Significantly different from all other groups at the same experimental time (<span class="html-italic">p</span> &lt; 0.05). Mineralization medium was employed as a positive control (C+).</p>
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<p>Quantification of mRNA expression of different inflammatory and bone metabolism-related markers, after exposure of MG-63 osteoblasts to 25% conditioned media for 1 day. (<b>A</b>) IL-6; (<b>B</b>) IL-8; (<b>C</b>) IFN-y; (<b>D</b>) IL-10; (<b>E</b>) FGF2; (<b>F</b>) OPG; (<b>G</b>) RANKL; the (<b>H</b>) OPG/RANKL ratio. Bars indicate the mean and standard deviation (<span class="html-italic">n</span> = 3). (*) Significantly different from all other groups (<span class="html-italic">p</span> &lt; 0.05). Results were calculated as a proportion of Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) expression.</p>
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14 pages, 555 KiB  
Review
Treatment of Oroantral Communication and Fistulas with the Use of Blood-Derived Platelet-Rich Preparations Rich in Growth Factors: A Systematic Review
by Paulina Adamska, Magdalena Kaczoruk-Wieremczuk, Dorota Pylińska-Dąbrowska, Marcin Stasiak, Michał Bartmański, Adam Zedler and Michał Studniarek
Int. J. Mol. Sci. 2024, 25(21), 11507; https://doi.org/10.3390/ijms252111507 - 26 Oct 2024
Viewed by 922
Abstract
The formation of an oroantral communication (OAC) or fistula (OAF) is a rare complication resulting from the presence of processes in the lateral parts of the maxilla or for iatrogenic reasons. The most common causes of OAC or OAF are tooth extraction with [...] Read more.
The formation of an oroantral communication (OAC) or fistula (OAF) is a rare complication resulting from the presence of processes in the lateral parts of the maxilla or for iatrogenic reasons. The most common causes of OAC or OAF are tooth extraction with periapical lesions. The aims of this systematic review were to assess the use of platelet-derived preparations rich in growth factors in the treatment of OAC or OAF, to determine the success of treating the communication or fistula, as well as impact on postoperative complications and the course of healing. The study was performed following PRISMA guidelines (PROSPERO: CRD42024570758). The inclusion criteria were as follows: at least ten patients, the presence of oroantral communication or oroantral fistula, treatment with platelet-derived preparations rich in growth factors, and information regarding the response to treatment. In order to find relevant studies, international databases, including PubMed, Google Scholar, Web of Science Core Collection, MDPI, Wiley, and Cochrane Library were searched. The last search was performed on 31 August 2024. Seven articles were included in the systematic review. In total, platelet-derived preparations rich in growth factors were used in 164 patients. Only studies in which OAC was treated and with platelet-rich fibrin (PRF) met the inclusion criteria. Only PRF was used as the sole treatment method in three studies. When OAC is greater than 5 mm, platelet-derived preparations rich in growth factors should be considered adjuncts to treatment, not the sole treatment method. The success rate of OAC treatment was 90–100%. The use of blood products to close OAC may be an effective therapeutic alternative. Proper patient qualification and the use of an appropriate protocol are crucial. There is a need for future well-designed case-control or cohort studies as well as randomized controlled trials to provide the required level of evidence. Full article
(This article belongs to the Special Issue Precision Medicine for Oral Diseases and Cancers)
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<p>PRISMA flow diagram depicting the process followed for the selection of the studies.</p>
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10 pages, 4551 KiB  
Article
Effect of Ethyl-Cyanoacrylate and Platelet-Rich Fibrin on Fresh Sockets of Rabbits Subjected to Anticoagulant Therapy
by Eduardo Rosas, Fernando José Dias, Dimitrius Pitol, Sergio Olate, João Paulo Mardegan Issa and Eduardo Borie
J. Clin. Med. 2024, 13(21), 6389; https://doi.org/10.3390/jcm13216389 - 25 Oct 2024
Viewed by 543
Abstract
Objectives: There are no studies related to the use of PRF associated with cyanoacrylates in fresh post-extraction sockets. Thus, the aim of this study was to assess the effect of ethyl-cyanoacrylate combined with PRF in fresh sockets of rabbits subjected to anticoagulant [...] Read more.
Objectives: There are no studies related to the use of PRF associated with cyanoacrylates in fresh post-extraction sockets. Thus, the aim of this study was to assess the effect of ethyl-cyanoacrylate combined with PRF in fresh sockets of rabbits subjected to anticoagulant therapy. Methods: Twelve adults rabbits were selected and premedicated with heparin 1 week before surgery to induce and simulate anticoagulant therapy. Upper and lower first premolars on the right side were extracted and then were divided into four groups of three animals each, with the groups distributed according to the type of intervention in the sockets (n = 6): (1) clot and suture (control); (2) PRF and suture; (3) clot and ethyl-cyanoacrylate; (4) PRF and ethyl-cyanoacrylate. At 12 weeks, the animals were sacrificed and the sockets were analyzed histologically and quantitatively. Total bone area, inflammation infiltrate, and adhesive remnants were assessed. Results: No remnants of adhesive were found in the samples. Groups 1 and 2 showed the highest bone area (G1 = 37.87% ± 17.86; G2 = 30.31 ± 9.36) with significant differences to those treated with ethyl-cyanoacrylate adhesive (G3 = 26.6% ± 11.82; G4 = 24.29% ± 6.25). Conclusions: The groups that used ethyl-cyanoacrylate as a closure method in sockets exhibited less bone area than the groups that used sutures. Both groups that used PRF as therapy did not show a significant improvement in bone healing at 12 weeks compared with the clot groups. Full article
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<p>(<b>A</b>,<b>B</b>). Histological analysis of the sockets at 12 weeks. G1—suture and clot—robust bone formation (bf), presence of blood vessels (arrows), osteoblasts (arrowheads), and the alveolar nerve (an) were observed. Mag.: ×10.</p>
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<p>(<b>A</b>,<b>B</b>). Histological analysis of the sockets at 12 weeks. G2—PRF and suture—robust bone formation (bf), presence of blood capillaries (arrows), lax tissue similar to adipose cells (ac), the alveolar nerve (an), and structures suggestive of a blood clot (cl) were noted. Mag.: ×10.</p>
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<p>(<b>A</b>,<b>B</b>). Histological analysis of the sockets at 12 weeks. G3—ethyl-cyanoacrylate and clot—It is possible to observe bone formation (bf), bone islets (arrowhead), structures similar to adipose cells (ac), structures similar to blood clots (cl), and the alveolar nerve (an). Mag.: ×10.</p>
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<p>(<b>A</b>,<b>B</b>). Histological analysis of the sockets at 12 weeks. G4—ethyl-cyanoacrylate and PRF—bone formation (bf), bone islets (arrowhead), blood capillaries (arrow), structures similar to fat cells (ac), and structures similar to blood clots (cl) can be observed. Mag.: ×10.</p>
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<p>Percentage of bone area quantification. Note the differences between groups: a (<span class="html-italic">p</span> = 0.018); b (<span class="html-italic">p</span> = 0.01); c (<span class="html-italic">p</span> =0.037).</p>
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