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Search Results (1,397)

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Keywords = gold(I) complexes

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6 pages, 220 KiB  
Editorial
Special Issue: “Enzymes and Enzyme Inhibitors—Applications in Medicine and Diagnosis 2.0”
by Athina Geronikaki
Int. J. Mol. Sci. 2024, 25(24), 13422; https://doi.org/10.3390/ijms252413422 - 14 Dec 2024
Viewed by 290
Abstract
The first paper in this Special Issue explores the synthesis, characterization, biological, and catalytic activities of new gold(I) and silver(I) complexes that are stabilized by caffeine derivatives and used as NHC ligands [...] Full article
29 pages, 474 KiB  
Review
DNA-Based Technology for Herpesvirus Detection
by Gloria Maini, Giorgia Cianci, Matteo Ferraresi, Valentina Gentili and Daria Bortolotti
DNA 2024, 4(4), 553-581; https://doi.org/10.3390/dna4040037 - 13 Dec 2024
Viewed by 457
Abstract
The detection of viral DNA is considered crucial in both diagnosis and prognosis. Nowadays, molecular diagnostic approaches represent the most promising tools for the clinical detection of viral infections. This review aims to investigate the most used and promising DNA-based technologies for viral [...] Read more.
The detection of viral DNA is considered crucial in both diagnosis and prognosis. Nowadays, molecular diagnostic approaches represent the most promising tools for the clinical detection of viral infections. This review aims to investigate the most used and promising DNA-based technologies for viral detection, focusing on herpesviruses because of their ability to undergo latent and reactivation cycles, persisting lifelong in the host in association with several diseases. Molecular technologies, such as PCR-based assays, enhance sensitivity and specificity in identifying viral DNA from clinical samples such as blood, cerebrospinal fluid and saliva, indicating PCR and its derivatives as the gold standard methods for herpesvirus detection. In conclusion, this review underscores the need for continuous innovation in diagnostic methodologies to address the complexities of herpesvirus identification in different clinical samples. Full article
13 pages, 1541 KiB  
Article
Antibacterial and Anti-Influenza Activities of N-Heterocyclic Carbene–Gold Complexes
by Michele Pellegrino, Paola Checconi, Jessica Ceramella, Carla Prezioso, Dolores Limongi, Maria Marra, Annaluisa Mariconda, Alessia Catalano, Marta De Angelis, Lucia Nencioni, Maria Stefania Sinicropi, Pasquale Longo and Stefano Aquaro
Pharmaceuticals 2024, 17(12), 1680; https://doi.org/10.3390/ph17121680 - 12 Dec 2024
Viewed by 528
Abstract
Background/Objectives: Infectious diseases represent a serious threat due to rising antimicrobial resistance, particularly among multidrug-resistant bacteria and influenza viruses. Metal-based complexes, such as N-heterocyclic carbene–gold (NHC–gold) complexes, show promising therapeutic potential due to their ability to inhibit various pathogens. Methods: Eight NHC–gold [...] Read more.
Background/Objectives: Infectious diseases represent a serious threat due to rising antimicrobial resistance, particularly among multidrug-resistant bacteria and influenza viruses. Metal-based complexes, such as N-heterocyclic carbene–gold (NHC–gold) complexes, show promising therapeutic potential due to their ability to inhibit various pathogens. Methods: Eight NHC–gold complexes were synthesized and tested for antibacterial activity against Escherichia coli, Enterococcus faecalis, Staphylococcus aureus, and for anti-influenza activity in lung and bronchial epithelial cells infected with influenza virus A/H1N1. Antibacterial activity was assessed through the determination of the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC), while the viral load was quantified using qRT-PCR. Results: Complexes 3, 4, and 6 showed significant antibacterial activity at concentrations of 10–20 µg/mL. Additionally, these complexes significantly reduced viral load, with complexes 3 and 4 markedly inhibiting replication. Conclusions: These findings support the potential use of NHC–gold complexes in combined antimicrobial and antiviral therapies, representing an attractive option for fighting resistant infections. Full article
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Figure 1
<p><span class="html-italic">N</span>-heterocyclic carbene–gold complexes (1–8).</p>
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<p>Cell viability (ratio to control) of A549 cells treated with different concentrations of complexes 1–8 (5, 10, 20, 40, and 50 μM, blue dots) for 24 h evaluated by MTT assay. The red dotted line indicates a ratio of 0.9.</p>
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<p>Viral load quantified in supernatants from PR8-infected A549 cells, treated with complexes 1–8 (20 μM) for 24 h, by qRT-PCR. * <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Western blot analysis, with anti-influenza antibody, of influenza virus proteins in cell lysates (<b>a</b>) and the viral load measured in supernatants by qRT-PCR (<b>b</b>) from A549 cells infected with supernatants from the previous experiments, * <span class="html-italic">p</span> &lt; 0.01. In (<b>a</b>), actin was used as the loading control, and densitometric analysis was shown in the graph on the right of the Western blot image, expressed as the ratio of each viral protein (HA, NP, M1) to actin.</p>
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<p>Viral load quantified by qRT-PCR in supernatants from PR8-infected BEAS-2B cells treated with complexes 1–8 (20 μM) 1h before infection (b.i.), after infection (a.i.), and both 1h before and after infection, for 24 h. * <span class="html-italic">p</span> &lt; 0.05.</p>
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16 pages, 2217 KiB  
Review
Bromelain in Burn Care: Advancements in Enzymatic Debridement and Patient Outcomes
by Eliza-Maria Bordeanu-Diaconescu, Sabina Grama, Andreea Grosu-Bularda, Adrian Frunza, Mihaela-Cristina Andrei, Tiberiu-Paul Neagu and Ioan Lascar
Eur. Burn J. 2024, 5(4), 438-453; https://doi.org/10.3390/ebj5040039 - 12 Dec 2024
Viewed by 427
Abstract
The management of severe burns is a complex process that requires a multidimensional approach to ensure optimal healing of burn wounds, minimize complications, and improve the prognosis of patients. Surgical debridement is considered the gold standard for removing necrotic tissue; however, this approach [...] Read more.
The management of severe burns is a complex process that requires a multidimensional approach to ensure optimal healing of burn wounds, minimize complications, and improve the prognosis of patients. Surgical debridement is considered the gold standard for removing necrotic tissue; however, this approach involves risks such as bleeding, the potential removal of viable tissue during excision, and technical challenges in complex anatomical areas. Recent advancements highlight the role of enzymatic debridement using NexoBrid®, which offers a less invasive alternative to surgical excision while having the ability to selectively debride necrotic tissue and preserve viable tissue. NexoBrid® has shown efficacy in reducing debridement time, minimizing the need for additional surgeries, and improving overall wound healing outcomes. This review discusses the clinical indications, advantages, and considerations for choosing between surgical and enzymatic debridement. Emerging studies suggest the potential for enzymatic debridement to be safe and effective even for larger burn areas, making it a promising option in modern burn care. However, ongoing evaluation and integration into clinical protocols will be essential to fully realize its benefits in specialized burn treatment and to establish protocols. Full article
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Figure 1
<p>(<b>A</b>) Burn on arrival. (<b>B</b>) Wound bed after 4h of debridement using Bromelain. (<b>C</b>) Complete epithelization at 21 days after burn injury. Images are from our Burn Center and patient consent was obtained for the use of his case for scientific purposes.</p>
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<p>(<b>A</b>) Burn on arrival. (<b>B</b>) Wound bed after 4 h of debridement using Bromelain. (<b>C</b>) Day 7 after skin grafting. (<b>D</b>) Esthetic and functional outcome at 3 weeks after burn injury. Images are from our Burn Center and patient consent was obtained for the use of her case for scientific purposes.</p>
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<p>(<b>A</b>) Burn wound aspect on the second day after injury. (<b>B</b>) NexoBrid<sup>®</sup> application at the bedside the second day after burn injury. (<b>C</b>) Wound bed after 4 h of debridement. (<b>D</b>) Day 1 after skin grafting. (<b>E</b>) Esthetic and functional outcome 1 month after skin grafting. Images are from our Burn Center and patient consent was obtained for the use of his case for scientific purposes.</p>
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14 pages, 1522 KiB  
Article
Urinary Immune Complexes Reflect Renal Pathology in Lupus Nephritis
by Chenling Tang, Aygun Teymur and Tianfu Wu
Diagnostics 2024, 14(24), 2787; https://doi.org/10.3390/diagnostics14242787 - 12 Dec 2024
Viewed by 278
Abstract
Background/Objectives: Lupus nephritis (LN) is a serious complication of systemic lupus erythematosus (SLE), involving immune complex deposition in the kidneys. While renal biopsy is the diagnostic gold standard, its invasiveness limits frequent use, driving the need for non-invasive urinary biomarkers to monitor disease [...] Read more.
Background/Objectives: Lupus nephritis (LN) is a serious complication of systemic lupus erythematosus (SLE), involving immune complex deposition in the kidneys. While renal biopsy is the diagnostic gold standard, its invasiveness limits frequent use, driving the need for non-invasive urinary biomarkers to monitor disease progression and response to treatment. This study aimed to identify and validate urinary biomarkers for LN. Methods: Data from 10 LN-related omics databases, including urine, PBMCs, and kidney tissue, were analyzed. Differentially expressed proteins (DEPs) and genes (DEGs) were identified, and candidate biomarkers were validated via ELISA in an independent cohort of 87 urine samples. Results: We identified 78 biomarkers, with 14 overlapping across transcriptomic categories. Novel urinary biomarkers, including SERPING1, SLPI, and CD48, were validated. Urinary CD163, VCAM1, and ALCAM levels showed significant differences between LN and healthy controls, while urinary immune complexes (ICx) demonstrated superior diagnostic performance, with urinary ALCAM-ICx and CCL21-ICx achieving the highest AUC values. Conclusions: Our findings highlight the potential of urinary immune complexes and antigens as non-invasive biomarkers for LN. ALCAM, CD163, and SERPING1-ICx, in particular, were found as promising candidates for a urinary biomarker panel to aid in the diagnosis and monitoring of LN. Full article
(This article belongs to the Section Clinical Laboratory Medicine)
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<p>Omics Identification of LN concurrence biomarkers. (<b>A</b>) Venn diagram showing overlap of differentially expressed proteins (DEPs) and genes (DEGs) from urine protein array, kidney scRNA, kidney RNA-array, PBMC scRNA, and PBMC RNA-array datasets. (<b>B</b>) Heatmap displaying the expression levels (log2 fold change) of selected biomarkers, colored based on their frequency of occurrence across the databases. (<b>C</b>) Bar graph depicting the number of biomarkers with co-occurrence in 1 to 4 datasets. (<b>D</b>) Protein–protein interaction network of top DEPs/DEGs identified, visualized using STRING analysis.</p>
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<p>ELISA screening of potential urine biomarker candidates of LN. Box plots showing the results of ELISA validation for selected urinary antigens (top row) and their corresponding immune complexes (ICx, middle and bottom rows) across lupus nephritis (LN), chronic kidney disease (CKD), and healthy control (HC) groups. Biomarkers analyzed include CD163, SPP1, NGAL, ALCAM, VCAM1, SERPING1, BAFF, CCL21, TFPI, VSIG4, SLPI, and uCreatinine. All urinary biomarker levels (shown in Y-axis) were normalized by urinary creatinine. Statistical significance between groups is indicated by asterisks (* <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; **** <span class="html-italic">p</span> &lt; 0.00001).</p>
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<p>Diagnostic potential of urinary antigens and ICx. (<b>A</b>) Bar graphs displaying the area under the curve (AUC) values for individual biomarkers and immune complexes (ICx) in distinguishing LN from healthy controls (HC), LN flare from remission, LN from CKD, and CKD from HC. (<b>B</b>) Comparison of six machine-learning models for classifying LN versus HC, showing the average AUC values from 3-fold, 10-repeats. Models include random forest, support vector machine, K-nearest neighbors, decision tree, linear discriminant analysis, and logistic regression. (<b>C</b>) Heatmap illustrating the Spearman correlation between urinary biomarkers and clinical/pathological indices, including SLEDAI, AI (activity index), CI (chronicity index), age, WBC, uPCR, serum creatinine, and uRBC. Statistical significance is denoted by asterisks (* <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; **** <span class="html-italic">p</span> &lt; 0.00001).</p>
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14 pages, 17261 KiB  
Article
Yingde–Guangning Granitic Plutons Record Complex Tectonic Evolution During Paleozoic-Mesozoic: Implications for Gold Exploration in Western Guangdong, South China
by Buqing Wang, Huan Li, Zhihao Sun, Wei Quan, Yuxuan Huang and Mohamed Faisal
Minerals 2024, 14(12), 1259; https://doi.org/10.3390/min14121259 - 11 Dec 2024
Viewed by 294
Abstract
Western Guangdong, a part of the South China Block, has a complex geological history characterized by significant magmatic, metamorphic, and tectonic activities. This dynamic geological past, particularly during the Mesozoic era, created favorable conditions for the formation of various mineral deposits, including Au, [...] Read more.
Western Guangdong, a part of the South China Block, has a complex geological history characterized by significant magmatic, metamorphic, and tectonic activities. This dynamic geological past, particularly during the Mesozoic era, created favorable conditions for the formation of various mineral deposits, including Au, Ag, Cu, and Pb. This makes the region a key area for precious metal resources in China. Despite extensive metallogenic studies, detailed structural information for western Guangdong remains insufficient, highlighting the need for further investigation. Thus, effective delineation of deformation periods is crucial for revealing geodynamic history and understanding regional tectonic activities, which are extremely important for guiding mineral exploration. This work focuses on the outcrops of granitic plutons in the Yingde–Guangning area of western Guangdong to establish the structure–tectonic setting. The tectonic events likely shaped the widespread Paleozoic–Mesozoic granitic bodies, which record extensive information on regional tectonic evolution. To achieve the primary objective, systematic identification and kinematic analysis of the various stages of structural traces, such as foliations and joints, have been conducted. This research proposes, for the first time, that the western Guangdong area underwent four distinct tectonic stages: (1) Early Paleozoic NW-SE compression phase; (2) Triassic NE-SW compressional stress; (3) Jurassic NW-SE compressional force; and (4) Cretaceous NW-SE extension stage. In metallogenic terms, the NW-SE trending auriferous veins of the Yingde–Guangning region were mostly formed during the Triassic NE-SW compression stage, whereas the NE-SW trending vein-type gold mineralization developed during the tectonic regime transformation from Jurassic NW-SE compression to Cretaceous NW-SE extension. This research emphasizes that systematic tectonic geological studies of regional granites can effectively guide mineral prospecting. Full article
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<p>Regional geological map of the western part of the Guangdong region.</p>
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<p>Study area geological map, geologic sites, and regional mechanical property analysis. (<b>a</b>) Early Paleozoic NW-SE extrusion; (<b>b</b>) Triassic NE-SW extrusion; (<b>c</b>) NW-SE compression during the Jurassic; (<b>d</b>) NW-SE stretching in Cretaceous. Arrows indicate the direction of compressional/extensional principal stress.</p>
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<p>Strong compressive foliation in granite on the southeast flank of anticline. (<b>a</b>) Ordovician. (<b>b</b>) Silurian granites.</p>
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<p>(<b>Left</b>): quartz vein on northwest wing of anticline. (<b>Right</b>): mechanical property analysis.</p>
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<p>(<b>a</b>) Projection of Early Paleozoic granite foliations in the research area (strike, dip). (<b>b</b>) Rose diagram of Early Paleozoic granite foliation in the research area. (<b>c</b>) Stress analysis of the Early Paleozoic in the research area. Arrows indicate the direction of compressional/extensional principal stress.</p>
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<p>Triassic NE-SW extrusion tectonic activity and its mechanical properties. (<b>a</b>) Ordovician granite. (<b>b</b>) Triassic granite. (<b>c</b>) Early Paleozoic strata.</p>
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<p>(<b>a</b>) Projection of Triassic granite foliations in the research area (strike, dip). (<b>b</b>) Rose diagram of Triassic granite foliation in the research area. (<b>c</b>) Stress analysis of the Triassic in the research area. Arrows indicate the direction of compressional/extensional principal stress.</p>
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<p>NW-SE extrusion and tectonic superposition activities and their mechanical properties in the Jurassic period. (<b>a</b>) Jurassic granite. (<b>b</b>) Ordovician granite.</p>
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<p>(<b>a</b>) Projection of the Jurassic granite foliations in the research area (strike, dip). (<b>b</b>) Rose diagram of the Jurassic granite foliation in the research area. (<b>c</b>) Stress analysis of the Jurassic in the research area. Arrows indicate the direction of compressional/extensional principal stress.</p>
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<p>NW-SE stretching activities and their mechanical properties in the Cretaceous. (<b>a</b>) Triassic granite. (<b>b</b>) Jurassic granite. (<b>c</b>) Cambrian stratum.</p>
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<p>(<b>a</b>) Projection of the Cretaceous granite foliations in the research area (strike, dip). (<b>b</b>) Rose diagram of the Cretaceous granite foliation in the research area. (<b>c</b>) Stress analysis of the Cretaceous in the research area. Arrows indicate the direction of compressional/extensional principal stress.</p>
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<p>Geological map of the gold mining region.</p>
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<p>The outcrop of the Dakengtou mining area shows the attitude of main gold ore bodies: (<b>a</b>) Show outcrop I; (<b>b</b>) Show outcrop II.</p>
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15 pages, 3894 KiB  
Article
Acoustic Wave Sensor Detection of an Ovarian Cancer Biomarker with Antifouling Surface Chemistry
by Katharina Davoudian, Sandro Spagnolo, Edmund Chan, Tibor Hianik and Michael Thompson
Sensors 2024, 24(24), 7884; https://doi.org/10.3390/s24247884 - 10 Dec 2024
Viewed by 307
Abstract
Ovarian cancer (OC) must be detected in its early stages when the mortality rate is the lowest to provide patients with the best chance of survival. Lysophosphatidic acid (LPA) is a critical OC biomarker since its levels are elevated across all stages and [...] Read more.
Ovarian cancer (OC) must be detected in its early stages when the mortality rate is the lowest to provide patients with the best chance of survival. Lysophosphatidic acid (LPA) is a critical OC biomarker since its levels are elevated across all stages and increase with disease progression. This paper presents an LPA assay based on a thickness shear mode acoustic sensor with dissipation monitoring that involves a new thiol molecule 3-(2-mercaptoethanoxy)propanoic acid (HS-MEG-COOH). HS-MEG-COOH is an antifouling linker that provides (a) antifouling properties for gold substrates and (b) linking ability via its terminal carboxylic acid functional group. The antifouling ability of HS-MEG-COOH was tested in whole human serum. The new molecule was applied to the LPA assay in conjunction with a spacer molecule, 2-(2-mercaptoethoxy)ethan-1-ol (HS-MEG-OH), in a 1:1 v/v ratio. HS-MEG-COOH was covalently linked to gelsolin–actin, a protein complex probe that dissociates due to LPA-binding. LPA was detected in phosphate-buffered saline and undiluted human serum and achieved a low limit of detection (1.0 and 0.7 μM, respectively) which was below the concentration of LPA in healthy individuals. The antifouling properties of HS-MEG-COOH and the detection of LPA demonstrate the ability of the sensor to successfully identify the early-stage OC biomarker in undiluted human serum. Full article
(This article belongs to the Special Issue Integrated Sensor Systems for Medical Applications)
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<p>A representation of the biosensor surface and the detection of LPA through the removal of actin protein.</p>
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<p>(<b>A</b>) The antifouling thiol linker 3-(2-mercaptoethanoxy)propanoic acid (HS-MEG-COOH) and (<b>B</b>) the antifouling thiol spacer 2-(2-mercaptoethoxy)-ethanol (HS-MEG-OH).</p>
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<p>Contact angles and histogram values of SAMs on TSM-D crystals.</p>
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<p>The shifts in (<b>A</b>,<b>C</b>) frequency and (<b>B</b>,<b>D</b>) dissipation upon exposing human serum to various SAM surfaces on the TSM-D crystal. The arrows in (<b>A</b>,<b>B</b>) indicate the start of the flow of undiluted human serum. The results in parts (<b>C</b>,<b>D</b>) are the mean ± SD obtained from three independent experiments in each series.</p>
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<p>Comparing the serum fouling between the results of the present work (in colour) and the results of a previous study (grey) [<a href="#B21-sensors-24-07884" class="html-bibr">21</a>], by means of the frequency (<b>A</b>) and dissipation (<b>B</b>) changes. The G-A sensor involves the 1:1 <span class="html-italic">v</span>/<span class="html-italic">v</span> thiol mix, HS-MEG-COOH and HS-MEG-OH, in which HS-MEG-COOH was linked to the gelsolin(1-3)–actin protein complex. In the case of the aptasensor, DTT<sub>COOH</sub> was linked to an aptamer. The results are the mean ± SD obtained from three independent experiments.</p>
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<p>Frequency variations following the addition of (<b>A</b>) LPA-spiked PBS and (<b>B</b>) LPA-spiked human serum samples. The start of the flow of the corresponding compounds is indicated by arrows.</p>
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<p>Linear calibration curves shown as dotted lines for (<b>A</b>,<b>C</b>) LPA-spiked PBS and (<b>B</b>,<b>D</b>) LPA-spiked serum measurements. (<b>A</b>,<b>B</b>) show the linear correlation between frequency shifts and higher LPA concentrations 10–50 μM, while (<b>C</b>,<b>D</b>) show the linear correlation between frequency shifts and the logarithm of LPA concentrations 0.5–10 μM. The error bars indicate the standard deviation of the measurements, which were conducted in triplicate.</p>
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<p>Oxidation of 2-mercaptoethanol.</p>
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<p>Conversion of oxidized 2-mercaptoethanol to DS-2EtOEtCOTBu.</p>
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<p>The deprotection reaction step for producing DS-2EtOEtCOOH.</p>
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<p>The reduction reaction step for producing HS-MEG-COOH.</p>
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12 pages, 6688 KiB  
Case Report
Challenging Management of a Rare Complex Cerebral Arteriovenous Malformation in the Corpus Callosum and Post-Central Gyrus: A Case Study of a 41-Year-Old Female
by Corneliu Toader, Felix Mircea Brehar, Mugurel Petrinel Radoi, Razvan Adrian Covache-Busuioc, Matei Serban, Alexandru Vladimir Ciurea and Nicolaie Dobrin
J. Clin. Med. 2024, 13(24), 7494; https://doi.org/10.3390/jcm13247494 - 10 Dec 2024
Viewed by 349
Abstract
Background/Objectives: Cerebral arteriovenous malformations (AVMs) are rare but complex vascular anomalies, particularly challenging when located in eloquent regions such as the corpus callosum and post-central gyrus. This report aims to highlight the management and outcomes of a 41-year-old female patient with a hemorrhagic [...] Read more.
Background/Objectives: Cerebral arteriovenous malformations (AVMs) are rare but complex vascular anomalies, particularly challenging when located in eloquent regions such as the corpus callosum and post-central gyrus. This report aims to highlight the management and outcomes of a 41-year-old female patient with a hemorrhagic AVM in these critical areas, emphasizing the importance of early surgical intervention and advanced imaging techniques. Methods: The patient presented with a right-sided tonic–clonic seizure and expressive aphasia, prompting imaging that revealed a complex AVM with deep venous drainage and arterial supply from the anterior cerebral artery. A multidisciplinary team performed microsurgical resection via a left parasagittal fronto-parietal craniotomy. The surgical approach prioritized hematoma evacuation followed by a stepwise dissection of the AVM nidus under intraoperative monitoring. Results: Complete resection of the AVM was confirmed through postoperative angiographic and CT imaging. The patient showed stable recovery over 15 months, with no recurrence or new neurological deficits. This case demonstrates the critical role of advanced imaging, intraoperative strategies, and a multidisciplinary approach in achieving successful outcomes. Conclusions: Microsurgical resection remains the gold standard for AVMs in eloquent and deep-seated brain regions. Early diagnosis and tailored surgical interventions are crucial for managing these high-risk cases. This case underscores the importance of integrating advanced imaging, strategic surgical planning, and intraoperative monitoring to minimize complications and optimize long-term recovery. Full article
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<p>Four different MRI images from a preoperative scan provide a detailed view of a left fronto-parietal lesion. (<b>A</b>) is an axial T2-weighted view, which presents a horizontal cross-section of the brain, offering a detailed look at the lesion’s involvement in the left fronto-parietal region. (<b>B</b>) is a sagittal T2-weighted view, providing a vertical cross-section of the brain from the side, which highlights the vertical extent of the lesion and its relationship with the ventricular system. (<b>C</b>) is a coronal T2-weighted view, showing a frontal cross-section of the brain, demonstrating the lesion’s depth and impact on the surrounding cortical and subcortical structures. (<b>D</b>) is an axial diffusion-weighted imaging (DWI) view, presenting a horizontal cross-section that emphasizes the diffusion characteristics of the tissue around the lesion, revealing restricted diffusion related to the hemorrhagic event.</p>
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<p>Provides two lateral angiographic views that highlight the vascular structure of the left fronto-parietal AVM. (<b>A</b>) Arterial phase highlights the intricate network of abnormal vessels, with direct arteriovenous shunting. Feeding arteries arise predominantly from branches of the anterior cerebral artery (ACA), with abnormal venous drainage into dilated structures converging on the superior sagittal sinus. (<b>B</b>) Late arterial/early venous phase shows reduced vascular filling, indicating flow dynamics associated with the AVM. These findings correlate with the hemorrhagic event observed on preoperative MRI, providing critical insights for surgical planning.</p>
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<p>This figure presents a preoperative lateral angiographic image that illustrates the arterial phase of a left fronto-parietal AVM. The image reveals an intricate tangle of abnormal vessels typical of an AVM, with feeding arteries originating from branches of the ACA. The absence of a normal capillary bed is evident, and there is prominent arteriovenous shunting. The draining veins are directed toward the superior sagittal sinus, corresponding to the hemorrhagic lesion observed on the preoperative MRI. This angiographic view is crucial in characterizing the AVM and its hemodynamic properties prior to surgical intervention.</p>
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<p>(<b>A</b>) highlights the arterial phase, showing the absence of abnormal arterial feeders from the anterior cerebral artery, which previously supplied the AVM. (<b>B</b>) displays the venous phase, where the normalization of the venous drainage into the superior sagittal sinus is evident, with no abnormal venous structures visible. (<b>C</b>) demonstrates the delayed phase, confirming that no residual AVM or abnormal vascular connections remain postoperatively. This angiographic follow-up provides definitive evidence of successful AVM resection, with no complications or residual vascular abnormalities noted.</p>
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<p>This figure presents three axial CT images taken at the 3-month follow-up, evaluating the patient’s postoperative condition following the excision of a left fronto-parietal AVM. (<b>A</b>): Axial CT image demonstrating normal postoperative parenchymal appearance in the left fronto-parietal region, with no evidence of residual AVM, hemorrhage, or ischemic changes. (<b>B</b>): Axial CT image focusing on the soft tissue and adjacent brain structures, confirming the absence of edema or any abnormal enhancement around the surgical site. (<b>C</b>): Bone window CT image evaluating the integrity of the bone flap, showing proper placement and no signs of hardware failure, infection, or other complications.</p>
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<p>This figure presents a series of axial, coronal, and sagittal CT images, alongside a bone window, from the 12-month follow-up evaluation post-excision of a left fronto-parietal AVM. (<b>A</b>) Axial view showing the absence of residual AVM or hemorrhagic changes in the left fronto-parietal region, confirming the stability of the surgical site. (<b>B</b>) Coronal view illustrating the preserved brain structures with no signs of edema, recurrence, or new vascular anomalies. (<b>C</b>) Sagittal view highlighting the absence of mass effect or midline shift, with normal postoperative anatomy. (<b>D</b>) Bone window axial view verifying the integrity of the craniotomy site, with no complications such as bone resorption or infection.</p>
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<p>These images together confirm a favorable outcome, with no significant complications observed at the 15-month mark, supporting a good recovery trajectory for the patient. (<b>A</b>) Axial view reveals a stable postoperative site in the left fronto-parietal region, with no signs of residual AVM or recurrent hemorrhage. (<b>B</b>) Coronal view illustrates symmetrical ventricular structures and preserved parenchyma, with no evidence of new lesions or complications. (<b>C</b>) Sagittal view confirms the absence of pathological developments, with normal postoperative anatomy and no mass effect or midline shift.</p>
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16 pages, 5079 KiB  
Article
Thermodynamic Modeling and Research for Processing Complex Concentrate Blends in Custom Copper Smelters for Maximum Revenue
by Denis Shishin, Nagendra Tripathi, Svetlana Sineva and Evgueni Jak
Processes 2024, 12(12), 2820; https://doi.org/10.3390/pr12122820 - 9 Dec 2024
Viewed by 495
Abstract
Custom copper smelters, which are dependent on purchased concentrates, are facing increasing economic pressures amid falling treatment and refining fees. With the declining availability of high-grade, low-impurity concentrates, copper demand is expected to surge to support the transition to renewable energy. This study, [...] Read more.
Custom copper smelters, which are dependent on purchased concentrates, are facing increasing economic pressures amid falling treatment and refining fees. With the declining availability of high-grade, low-impurity concentrates, copper demand is expected to surge to support the transition to renewable energy. This study, which is based on recent observations of Chinese custom smelters, examines their strategies to address the challenge of purchasing concentrates at record-low treatment and refining charges. By investing in slag flotation technology, smelters can enhance copper, gold, and silver recovery. By blending high-grade and low-grade concentrates, they can capitalize on the gap between the recoverable and payable metals, which are often referred to as “free metals”, while also benefiting from byproducts, mainly sulfuric acid. While this approach offers economic opportunities, it introduces operational complexities. To mitigate these, laboratory testing, combined with advanced digital predictive tools based on thermodynamics, is crucial. This study demonstrates the use of thermodynamic models supported by experimental work for analyzing furnace operations. FactSage® software and a custom database are employed to define the operating window of two common flowsheets: (1) flash smelting + flash converting and (2) bottom-blown smelting + bottom-blowing converting. Full article
(This article belongs to the Special Issue Recent Trends in Extractive Metallurgy)
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<p>Global treatment charges and refining charges for custom smelters based on 25% Cu in concentrate. Compiled using data sources from FastMarkets and Wood Mackenzie [<a href="#B1-processes-12-02820" class="html-bibr">1</a>]. Metric tonnes are used in this study, i.e., 1 tonne = 1000 kg = 2204.6 lbs.</p>
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<p>Examples of payables and recovery functions for copper and gold used analysis of metal. Circles are typical values for the copper industry, wide lines show recovery functions based on discussions during smelter surveys, and diamond symbols are calculated using the thermodynamic model of this study (see <a href="#sec3dot2-processes-12-02820" class="html-sec">Section 3.2</a> below).</p>
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<p>A portion of Excel macro code initiating the calculation using FactSage 8.3<sup>®</sup>.</p>
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<p>Furnace setup used for equilibration [<a href="#B29-processes-12-02820" class="html-bibr">29</a>] and sample location for open-system equilibration. Photo on the right shows the sample location inside alumina tube.</p>
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<p>Typical microstructures of samples targeting conditions in a copper smelting furnace.</p>
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<p>Thermodynamic calculations of mass and energy balance for Case 1. Full-size high-resolution image is provided in the <a href="#app1-processes-12-02820" class="html-app">Supplementary Materials</a>.</p>
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<p>Thermodynamic calculations of mass and energy balance for Case 2. Full-size high-resolution image is provided in the <a href="#app1-processes-12-02820" class="html-app">Supplementary Materials</a>.</p>
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<p>Summary of conditions of a series of 25 equilibrium experiments.</p>
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<p>Comparison of observed and predicted values: Fe/SiO<sub>2</sub> in slag, wt.% Cu, and ppm of Au and Ag in slag.</p>
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<p>Analysis of accuracy of predicted values: Fe/SiO<sub>2</sub> in slag, wt.% Cu in slag.</p>
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16 pages, 6319 KiB  
Article
Application of a Screen-Printed Ion-Selective Electrode Based on Hydrophobic Ti3C2/AuNPs for K+ Determination Across Variable Temperatures
by Zhixue Yu, Hui Wang, Yue He, Dongfei Chen, Ruipeng Chen, Xiangfang Tang, Mengting Zhou, Junhu Yao and Benhai Xiong
Int. J. Mol. Sci. 2024, 25(23), 13204; https://doi.org/10.3390/ijms252313204 - 8 Dec 2024
Viewed by 672
Abstract
Monitoring potassium ion (K+) concentration is essential in veterinary medicine, particularly for preventing hypokalemia in dairy cows, which can severely impact their health and productivity. While traditional laboratory methods like atomic absorption spectrometry are accurate, they are also time-consuming and require [...] Read more.
Monitoring potassium ion (K+) concentration is essential in veterinary medicine, particularly for preventing hypokalemia in dairy cows, which can severely impact their health and productivity. While traditional laboratory methods like atomic absorption spectrometry are accurate, they are also time-consuming and require complex sample preparation. Ion-selective electrodes (ISEs) provide an alternative that is faster and more suitable for field measurements, but their performance is often compromised under variable temperature conditions, leading to inaccuracies. To address this, we developed a novel screen-printed ion-selective electrode (SPE) with hydrophobic Ti3C2 Mxene and gold nanoparticles (AuNPs), integrated with a temperature sensor. This design improves stability and accuracy across fluctuating temperatures by preventing water layer formation and enhancing conductivity. The sensor was validated across temperatures from 5 °C to 45 °C, achieving a linear detection range of 10⁵ to 10−1 M and a response time of approximately 15 s. It also demonstrated excellent repeatability, selectivity, and stability, making it a robust tool for K+ monitoring in complex environments. This advancement could lead to broader applications in other temperature-sensitive analytical fields. Full article
(This article belongs to the Special Issue Advances in Electrochemistry of Metal Nanomaterials)
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Graphical abstract

Graphical abstract
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<p>SEM images of bare SPE (<b>A</b>), SPE/Ti<sub>3</sub>C<sub>2</sub> (<b>B</b>), SPE/Ti<sub>3</sub>C<sub>2</sub>/AuNPs (<b>C</b>,<b>D</b>), SPE/OTS-Ti<sub>3</sub>C<sub>2</sub>/AuNPs (<b>E</b>), SPE/OTS-Ti<sub>3</sub>C<sub>2</sub>/AuNPs/K-ISM (<b>F</b>), and EDS mapping analysis (<b>G</b>).</p>
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<p>CV (<b>A</b>) and EIS (<b>B</b>) of different modification processes at 5.0 mM [Fe(CN)<sub>6</sub>]<sup>3−/4−</sup> solutions.</p>
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<p>Raman spectra of different modification processes.</p>
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<p>Contact angle measurements of bare SPE (<b>A</b>), SPE/Ti<sub>3</sub>C<sub>2</sub> (<b>B</b>), SPE/Ti<sub>3</sub>C<sub>2</sub>/AuNPs (<b>C</b>), and SPE/OTS- Ti<sub>3</sub>C<sub>2</sub>/AuNPs (<b>D</b>).</p>
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<p>Different modification processes were tested in water layer in 10<sup>−2</sup> M KCl and 10<sup>−2</sup> M CaCl<sub>2</sub>.</p>
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<p>Chronopotentigrams of different modified electrodes at 10<sup>−2</sup> M KCl.</p>
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<p>(<b>A</b>) Potential response of SPE/OTS-Ti<sub>3</sub>C<sub>2</sub>/AuNPs/K-ISM with increasing concentration of K<sup>+</sup> and (<b>B</b>) calibration curve.</p>
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<p>(<b>A</b>) LSV and (<b>B</b>) resistance change rate of temperature sensor at 5–45 °C.</p>
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<p>Potential of SPE/OTS-Ti<sub>3</sub>C<sub>2</sub>/AuNPs/K-ISM at different temperatures and K<sup>+</sup> concentrations.</p>
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<p>(<b>A</b>) The structure of the artificial neural network and (<b>B</b>) the calculated real and predicted values.</p>
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<p>(<b>A</b>) Stability and (<b>B</b>) selectivity of the SPE/OTS-Ti<sub>3</sub>C<sub>2</sub>/AuNPs/K-ISM.</p>
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<p>The preparation of SPE/OTS-Ti<sub>3</sub>C<sub>2</sub>/AuNPs/K-ISM.</p>
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<p>The preparation process of the temperature sensor.</p>
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18 pages, 5336 KiB  
Article
Quercetin Reduced and Stabilized Gold Nanoparticle/Al3+: A Rapid, Sensitive Optical Detection Nanoplatform for Fluoride Ion
by Titilope John Jayeoye, Roselina Panghiyangani, Sudarshan Singh and Nongnuj Muangsin
Nanomaterials 2024, 14(23), 1967; https://doi.org/10.3390/nano14231967 - 7 Dec 2024
Viewed by 475
Abstract
In this contribution, facile synthesis of gold nanoparticles (AuNPs) at ambient conditions is reported based on the use of the polyphenolic compound quercetin (QT) as the reducing and stabilizing agent at room temperature (RT). Under alkali-induced pH adjustment of QT solution and stirring [...] Read more.
In this contribution, facile synthesis of gold nanoparticles (AuNPs) at ambient conditions is reported based on the use of the polyphenolic compound quercetin (QT) as the reducing and stabilizing agent at room temperature (RT). Under alkali-induced pH adjustment of QT solution and stirring conditions at RT, QT could quickly reduce gold salt (Au3+) into its nanoparticle form (Au0), resulting in the formation of a sparkling red color colloidal solution (AuNPs) with an absorption maximum at 520 nm. Further, Fourier transform infrared spectroscopy (FTIR) was employed to showcase the role of QT in the nanomaterial’s synthesis process. The formed QT-AuNPs responded swiftly to Al3+ charging with color perturbation from red to grayish-purple, coupled with an absorption spectra red shift, owing to Al3+-induced aggregation of QT-AuNPs. However, when fluoride ion (F) was pre-mixed with an optimized Al3+ concentration, reversed color changes from grayish-purple to red were observed with a blue shift in the absorption spectra. Simply put, F formed a complex with Al3+, thus preventing Al3+-induced aggregation of QT-AuNPs. The analytical response A520/A650 was linear with F concentration ranging from 25.0 to 250.0 µM and 250.0–600.0 µM, with a detection limit of 7.5 µM. The developed QT-AuNPs/Al3+ detection probe was selective to only F charging, in comparison with other possible interfering anions. Real sample potentiality of the developed sensor was demonstrated on tap water samples, toothpaste, and fluoride-rich mouthwash, with reliable accuracy. Full article
(This article belongs to the Section Nanoelectronics, Nanosensors and Devices)
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<p>(<b>a</b>) UV–Vis absorption spectra of QT-AuNPs realized under different gold salt concentrations; the inset shows the phot images. (<b>b</b>) Plot of A<sub>520</sub>/A<sub>650</sub> against gold salt concentrations. (<b>c</b>) FTIR of the QT-green line and QT-AuNPs-red line and (<b>d</b>) TEM image of QT-AuNPs produced under 0.523 mM gold salt concentration as the optimum condition.</p>
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<p>(<b>a</b>) UV–Vis absorption spectra of a—QT-AuNPs, b—Al<sup>3+</sup> charging on QT-AuNPs, and c—Al<sup>3+</sup>/F<sup>−</sup> pre-mixed before QT-AuNPs addition; Al<sup>3+</sup> = 150 µM and F<sup>−</sup> = 600 µM. (<b>b</b>) Photo images of varying concentrations of Al<sup>3+</sup> (0–400 µM) on QT-AuNPs.</p>
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<p>(<b>a</b>) Photo images of the QT-AuNPs/Al<sup>3+</sup> colorimetric probe under F<sup>−</sup> ion charging from 0 to 600 µM. (<b>b</b>) UV–Vis absorption spectra of QT-AuNPs/Al<sup>3+</sup> detection probe corresponding to the photo images obtained in F<sup>−</sup> detection from 0 to 600 µM. (<b>c</b>) Plot of (A<sub>520</sub>/A<sub>650</sub>) against F<sup>−</sup> concentration from 0 to 600 µM. Plot of (A<sub>520</sub>/A<sub>650</sub>) against F<sup>−</sup> concentration from (<b>d</b>) 25–250 µM, and (<b>e</b>) 250–600 µM. The concentration of Al<sup>3+</sup> = 150 µM.</p>
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<p>(<b>a</b><span class="html-italic">–</span><b>c</b>) TEM images of the QT-AuNPs/Al<sup>3+</sup> colorimetric probe under F<sup>−</sup> ion charging at 0, 150, and 500 µM. (<b>d</b><span class="html-italic">–</span><b>f</b>) Hydrodynamic diameter from DLS corresponding to (<b>a</b><span class="html-italic">–</span><b>c</b>) of TEM and (<b>g</b>) zeta potential under F<sup>−</sup> concentration charging at a = 0, b = 150, and c = 500 μM. The concentration of Al<sup>3+</sup> = 150 µM.</p>
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<p>UV–Vis absorption spectra of QT-AuNPs/Al<sup>3+</sup> for repeated F<sup>−</sup> detection at (<b>a</b>) 150 and (<b>b</b>) 500 µM; the inset shows the photo images of the blank and the tested F<sup>−</sup>, for n = 8. (<b>c</b>) Photo images of F<sup>−</sup> and other possible interfering anions, where 1 = Br<sup>−</sup>, 2 = Cl<sup>−</sup>, 3 = I<sup>−</sup>, 4 = NO<sub>2</sub><sup>−</sup>, 5 = NO<sub>3</sub><sup>−</sup>, 6 = SO<sub>4</sub><span class="html-italic"><sup>2−</sup></span>, 7 = S<sub>2</sub>O<sub>3</sub><sup>−</sup>, 8 = SO<sub>3</sub><span class="html-italic"><sup>2−</sup></span>, 9 = HCO<sub>3</sub><sup>−</sup>, 10 = CO<sub>3</sub><span class="html-italic"><sup>2−</sup></span>, 11 = SCN<sup>−</sup>, 12 = H<sub>2</sub>PO<sub>4</sub><sup>−</sup>, 13 = HPO<sub>4</sub><span class="html-italic"><sup>2−</sup></span>, 14 = F, 15 = ALL, F<sup>−</sup> = 300 µM, and the others were 3000 µM. The concentration of Al<sup>3+</sup> = 150 µM, (<b>d</b>) UV–Vis absorption spectra corresponding to the shown images in (<b>c</b>,<b>e</b>). Plot of (A<sub>520</sub>/A<sub>650</sub>) against tested anions and F<sup>−</sup>.</p>
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<p>UV–Vis absorption spectra of QT-AuNPs/Al<sup>3+</sup> for repeated F<sup>−</sup> detection at (<b>a</b>) 150 and (<b>b</b>) 500 µM; the inset shows the photo images of the blank and the tested F<sup>−</sup>, for n = 8. (<b>c</b>) Photo images of F<sup>−</sup> and other possible interfering anions, where 1 = Br<sup>−</sup>, 2 = Cl<sup>−</sup>, 3 = I<sup>−</sup>, 4 = NO<sub>2</sub><sup>−</sup>, 5 = NO<sub>3</sub><sup>−</sup>, 6 = SO<sub>4</sub><span class="html-italic"><sup>2−</sup></span>, 7 = S<sub>2</sub>O<sub>3</sub><sup>−</sup>, 8 = SO<sub>3</sub><span class="html-italic"><sup>2−</sup></span>, 9 = HCO<sub>3</sub><sup>−</sup>, 10 = CO<sub>3</sub><span class="html-italic"><sup>2−</sup></span>, 11 = SCN<sup>−</sup>, 12 = H<sub>2</sub>PO<sub>4</sub><sup>−</sup>, 13 = HPO<sub>4</sub><span class="html-italic"><sup>2−</sup></span>, 14 = F, 15 = ALL, F<sup>−</sup> = 300 µM, and the others were 3000 µM. The concentration of Al<sup>3+</sup> = 150 µM, (<b>d</b>) UV–Vis absorption spectra corresponding to the shown images in (<b>c</b>,<b>e</b>). Plot of (A<sub>520</sub>/A<sub>650</sub>) against tested anions and F<sup>−</sup>.</p>
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<p>UV–Vis absorption spectra of QT-AuNPs/Al<sup>3+</sup> for real samples F<sup>−</sup> detection, including (<b>a</b>) tap water, (<b>b</b>) toothpaste, and (<b>c</b>) fluoride-rich mouthwash; the insets show the photo images corresponding to the blank sample, unpiked sample, and standard F<sup>−</sup>-spiked real samples at two concentrations, c and d. Al<sup>3+</sup> concentration was at 150 µM.</p>
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<p>Synthesis strategy for QT-AuNPs at RT.</p>
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<p>Mechanism of the QT-AuNPs/Al<sup>3+</sup>-based detection system for F<sup>−</sup>.</p>
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20 pages, 3992 KiB  
Article
Liposomal Formulation of an Organogold Complex Enhancing Its Activity as Antimelanoma Agent—In Vitro and In Vivo Studies
by Jacinta O. Pinho, Mariana Coelho, Catarina Pimpão, Jahnobi Konwar, Ana Godinho-Santos, Rute M. Noiva, Sophie R. Thomas, Angela Casini, Graça Soveral and Maria Manuela Gaspar
Pharmaceutics 2024, 16(12), 1566; https://doi.org/10.3390/pharmaceutics16121566 - 6 Dec 2024
Viewed by 555
Abstract
Background/Objectives: The therapeutic management of melanoma, the most aggressive form of skin cancer, remains challenging. In the search for more effective therapeutic options, metal-based complexes are being investigated for their anticancer properties. Cisplatin was the first clinically approved platinum-based drug and, based on [...] Read more.
Background/Objectives: The therapeutic management of melanoma, the most aggressive form of skin cancer, remains challenging. In the search for more effective therapeutic options, metal-based complexes are being investigated for their anticancer properties. Cisplatin was the first clinically approved platinum-based drug and, based on its success, other metals (e.g., gold) are being used to design novel compounds. Methods: the antimelanoma potential of a new organometallic cyclometalated Au(III) complex [[Au(CNOxN)Cl2] (CNOxN = 2-(phenyl-(2-pyridinylmethylene)aminoxy acetic acid))] (ST004) was evaluated in vitro and in vivo. Furthermore, the gold-based complex was incorporated in liposomes to overcome solubility and stability problems, to promote accumulation at melanoma sites and to maximize the therapeutic effect while controlling its reactivity. The antiproliferative activity of ST004 formulations was assessed in murine (B16F10) and human (A375 and MNT-1) melanoma cell lines after 24 and 48 h incubation periods. The proof-of-concept of the antimelanoma properties of ST004 formulations was carried out in subcutaneous and metastatic murine melanoma models. Results: the developed liposomal formulations showed a low mean size (around 100 nm), high homogeneity (with a low polydispersity index) and high incorporation efficiency (51 ± 15%). ST004 formulations exhibited antiproliferative activity with EC50 values in the μmolar range being cell-line- and incubation-period-dependent. On the opposite side, the benchmark antimelanoma compound, dacarbazine (DTIC), presented an EC50 > 100 μM. Cell cycle analysis revealed an arrest in G0/G1 phase for Free-ST004 in all cell lines. In turn, LIP-ST004 led to a G0/G1 halt in B16F10, and to an arrest in S phase in A375 and MNT-1 cells. Preliminary mechanistic studies in human red blood cells suggest that gold-based inhibition of glycerol permeation acts through aquaglyceroporin 3 (AQP3). In a metastatic murine melanoma, a significant reduction in lung metastases in animals receiving LIP-ST004, compared to free gold complex and DTIC, was observed. Conclusion: This study highlights the antimelanoma potential of a new gold-based complex. Additional studies, namely in vivo biodistribution profile and therapeutic validation of this organogold complex in other melanoma models, are expected to be performed in further investigations. Full article
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<p>(<b>a</b>) Proposed scheme of the reaction of C^N-cyclometalated Au(III) compounds with thiols and selenols of proteins. Different bridging groups (E) modulate the propensity of the compound toward cysteine arylation. Moreover, the reactivity of the compound can also be modulated by the ancillary ligands. The binding to selenol/thiolate groups of proteins proceeds via two steps: (i) the formation of a coordination adduct in which the gold(III) center binds directly to the S-/Se-nucleophiles, and (ii) C-S/Se cross-coupling reaction via reductive elimination and liberation of Au(0/I). (<b>b</b>) Structure of the tested organogold compound, [[Au(CNOxN)Cl2] (CNOxN = 2-(phenyl-(2-pyridinylmethylene)aminoxy acetic acid))], ST004.</p>
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<p>Antiproliferative activity of Free-ST004 and DTIC against melanoma cell lines B16F10, MNT-1 and A375. (<b>a</b>) Cell viability after 24 and 48 h incubation with ST004 in the free form at concentrations ranging from 10 to 100 μM. (<b>b</b>) Cell viability after 24 h incubation with DTIC at concentrations ranging from 20 to 100 μM. (<b>c</b>,<b>d</b>) Concentration–response curves of melanoma cell lines after 24 h (<b>c</b>) and 48 h (<b>d</b>) incubation with tested formulations. Results are expressed as mean ± SD (n = 2–3). DTIC: dacarbazine.</p>
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<p>Antiproliferative activity of LIP-ST004 against melanoma cell lines B16F10, MNT-1 and A375. Data correspond to cell viability after 24 and 48 h incubation with (<b>a</b>) LIP-ST004 at concentrations ranging from 10 to 100 μM; (<b>b</b>) unloaded liposomes were tested at the same lipid concentrations as ST004-loaded liposomes. Results are expressed as mean ± SD (n = 2). LIP-ST004: DMPC:DOPE:DSPE-PEG (50:45:5).</p>
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<p>Quantitative analysis of gated B16F10, A375 and MNT-1 melanoma cell lines cells in the G0/G1, S, and G2/M cell cycle phases in the absence (Control) or presence of DTIC at 70 μM (DTIC 70) or ST004 in free (Free-ST004) and liposomal (LIP-ST004) forms at 50, 30 and 40 μM for B16F10, A375 and MNT-1, respectively. LIP-ST004: DMPC:DOPE:DSPE-PEG(50:45:5). Results are expressed as mean ± SD (n = 3). Statistical analysis was performed using two-way ANOVA with Tukey’s test. * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001 and **** <span class="html-italic">p</span> &lt; 0.0001 vs. Control.</p>
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<p>Effect of ST004 on AQP3 activity in human red blood cells (RBCs). (<b>a</b>) Representative stopped-flow signal showing changes in scattering light intensity when cells are confronted with a hyperosmotic glycerol solution. After a first shrinkage due to water efflux, cells reswell due to glycerol entrance via aquaporin 3 (AQP3) (control). Cell treatment with ST004 impairs glycerol influx. (<b>b</b>) Glycerol permeability of RBCs incubated with ST004 (100 µM for 30 min). (<b>c</b>) Dose-response curves of AQP3 glycerol permeability inhibition by ST004 (0–100 µM). Data are shown as means ± SD of three independent experiments. *** <span class="html-italic">p</span> &lt; 0.001 vs control.</p>
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<p>Therapeutic effect of tested formulations in a metastatic murine melanoma model. Tumor induction was performed by an i.v. inoculation of 4.0 × 10<sup>6</sup> B16F10 cells/mouse. Mice received i.v. injections of ST004 and DTIC formulations at a dose of 3.5 mg/kg and 10 mg/kg, respectively. Treatments were given five consecutive times, once per day. Four experimental groups were established: Control, (that received PBS); Free –ST004; LIP –ST004 (DMPC:DOPE:DSPE-PEG); DTIC (positive control). (<b>a</b>) Experimental design, (<b>b</b>) Average animal body weight, (<b>c</b>) Representative images of lungs with melanoma metastases (black dots), (<b>d</b>) Metastasis score established from 1 to 4 according to the number of metastases in the lungs, (<b>e</b>) Average metastasis score for each experimental group. Statistical analysis was performed by unpaired t-test with Welch’s correction. * <span class="html-italic">p</span> &lt; 0.05 vs. Control. Results are expressed as mean ± SEM (n = 4–5).</p>
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<p>Representative histological images of lung samples stained with H&amp;E for the different groups under study: Control. Neoplastic cells vary from a round to a polygonal profile, with barely evident borders, occasionally containing small amounts of melanic pigment (arrowheads). Long arrows denote a mitotic figure; DTIC. Neoplastic cells maintain typical morphology and occasional melanic pigment (arrowheads). Apoptotic cells are interspersed with viable cells (circles); Free-ST004. Apoptotic cells are interspersed with viable cells (circles); Lip-ST004. Neoplastic cells are intermingled with small infiltrating lymphocytes (short arrows) and apoptotic neoplastic cells (circles). Scale bar in black 20 μm for all the images.</p>
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11 pages, 3743 KiB  
Article
Au Ordered Array Substrate for Rapid Detection and Precise Identification of Etomidate in E-Liquid Through Surface-Enhanced Raman Spectroscopy
by Yan Mo, Xiaoping Zhang, Ke Zou, Wen Xing, Xiayang Hou, Yu Zeng, Yugang Cai, Ruixiang Xu, Hongwen Zhang and Weiping Cai
Nanomaterials 2024, 14(23), 1958; https://doi.org/10.3390/nano14231958 - 6 Dec 2024
Viewed by 400
Abstract
Etomidate (ET), a medical anesthetic, is increasingly being incorporated into e-liquids for consumption and abuse as a new psychoactive substance (NPS), leading to significant social issues. In this work, large-area Au micro- and nano-structured ordered arrays were engineered as surface-enhanced Raman spectroscopy (SERS) [...] Read more.
Etomidate (ET), a medical anesthetic, is increasingly being incorporated into e-liquids for consumption and abuse as a new psychoactive substance (NPS), leading to significant social issues. In this work, large-area Au micro- and nano-structured ordered arrays were engineered as surface-enhanced Raman spectroscopy (SERS) substrates for fast detection and precise identification of ET and its metabolites. This ordered array, characterized by abundant electromagnetic enhancement hotspots and structural uniformity, imparts unique properties to the SERS substrate, including ultra-sensitivity, spectral signal reproducibility, and precise quantitative capabilities. Furthermore, it effectively mitigates interference from the complex matrix of e-liquids, facilitating the rapid detection of trace amounts of ET molecules. This SERS rapid detection technology can act as a preliminary screening method for gold-standard spectroscopic analysis, facilitating the on-site rapid screening of suspicious samples and thereby enabling efficient detection and precise verification. Full article
(This article belongs to the Special Issue Functional Nanomaterials for Sensing and Detection (2nd Edition))
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<p>Schematic diagram of template-based fabrication of Au micro- and nano-structured ordered arrays as sensitive SERS substrate for fast E-liquid detection and drug identification.</p>
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<p>(<b>A</b>) SEM image of the SERS substrate composed of Au ordered array. (<b>B</b>,<b>C</b>) The EDS analysis of the Au and Si elemental distribution in the SERS substrate. (<b>D</b>) The SEM cross-sectional observation of the substrate, along with the elemental distribution. (<b>E</b>) The theoretical simulation of the spatial electric field distribution of the structural unit of the array (sphere size 100 nm, gap distance 15 nm). (<b>F</b>) SERS spectra of 10<sup>−7</sup> M 4-MBA probe molecule and its spectral reproducibility. Each color curve corresponds to a spectrum acquisition point.</p>
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<p>(<b>A</b>) SERS spectrum of ET at a concentration of 10 ppm acquired from the Au nano-structured ordered array substrate. The comparison sample is Au nanoparticle (NP) film obtained by sputter deposition with identical parameters. (<b>B</b>) Theoretically simulated Raman spectrum of ET molecules, used to assign the characteristic vibrational peaks in the SERS spectrum.</p>
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<p>(<b>A</b>) Reproducibility of SERS spectra for 10 ppm ET molecules acquired from one substrate. (<b>B</b>) The intensity and relative standard deviation (RSD) of the vibrational peak at 1003 cm<sup>−1</sup> within and between SERS substrates. (<b>C</b>) SERS spectra of ET molecules with concentrations ranging from 1 to 50 ppm. (<b>D</b>) The linear relationship between the peak intensities at 618, 1003, and 1351 cm<sup>−1</sup> and the concentration.</p>
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<p>(<b>A</b>) SERS spectra of e-liquid oil and ET-containing sample with a concentration of 10 ppm. The dotted circle marks the most significant characteristic vibrational peaks that are exclusive to the ET molecule. (<b>B</b>) Spectral comparison of the SERS spectra of ET and its metabolite etomidate acid (ETA). The dotted cycles highlight the differences in the characteristic vibrational peaks of the two molecules.</p>
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11 pages, 1857 KiB  
Article
Enhanced Biomechanical Risk Assessment in Manual Lifting: Comparing Inertial Measurement Units with Optoelectronic Systems for Composite Lifting Index Calculation
by Tiwana Varrecchia, Filippo Motta, Giorgia Chini, Manuela Galli and Alberto Ranavolo
Appl. Sci. 2024, 14(23), 11292; https://doi.org/10.3390/app142311292 - 4 Dec 2024
Viewed by 527
Abstract
This study aims to improve the assessment of biomechanical risk in manual lifting tasks by introducing a method for calculating composite lifting index (CLI) using wearable inertial measurement units (IMUs). While the revised NIOSH lifting equation (RNLE) is widely used to evaluate the [...] Read more.
This study aims to improve the assessment of biomechanical risk in manual lifting tasks by introducing a method for calculating composite lifting index (CLI) using wearable inertial measurement units (IMUs). While the revised NIOSH lifting equation (RNLE) is widely used to evaluate the risk associated with lifting tasks, traditional methods often struggle with accuracy, especially in complex tasks. To address this, we compared the CLI values obtained using IMUs with those derived from a gold standard optoelectronic system during laboratory tests involving three levels of lifting risk. Ten participants performed standardized lifting tasks under controlled conditions, and the results showed that the IMU-based method provided comparable accuracy to the optoelectronic system, with negligible differences. Despite some variability in horizontal multiplier (HM) values, the IMU system demonstrated potential for real-world applications due to its ease of use and automatic calculation capabilities. Future improvements may include refining distance measurements and expanding the method for more complex lifting scenarios. This novel approach offers a practical and precise tool for ergonomic risk assessments, particularly in dynamic work environments. Full article
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<p>A representative subject who performed the lifting task (<b>A</b>) and a graphical representation of the task and experimental setup (<b>B</b>).</p>
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<p>Start and stop events are identified using the vertical position of the hand.</p>
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<p>Boxplots of the values of the DM, HM, and VM multipliers of the three tasks for the two methods (optoelectronic and IMU systems). The line in the box is the median value, the upper and lower limits of the box are the 25th and 75th percentiles, and the circles are outliers.</p>
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<p>Boxplots of the absolute error (E<sub>a</sub> in (<b>A</b>)) and the relative percentage error (E<sub>r</sub> in (<b>B</b>)) multipliers’ values by the two systems (optoelectronic and IMU systems) in the three tasks. The line in the box is the median value, the upper and lower limits of the box are the 25th and 75th percentiles, and the circles are outliers.</p>
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<p>Boxplots of the CLI values of the ten subjects on the three tasks from the two systems; the dotted lines refer to the theoretical values of the tasks. The line in the box is the median value, the upper and lower limits of the box are the 25th and 75th percentiles and the circles are outliers.</p>
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13 pages, 2989 KiB  
Article
Self-Assembled Lubricin (PRG-4)-Based Biomimetic Surface-Enhanced Raman Scattering Sensor for Direct Droplet Detection of Melamine in Undiluted Milk
by Mingyu Han, Mya Myintzu. Hlaing, Paul R. Stoddart and George W. Greene
Biosensors 2024, 14(12), 591; https://doi.org/10.3390/bios14120591 - 3 Dec 2024
Viewed by 513
Abstract
Surface-enhanced Raman scattering (SERS) is a powerful optical sensing platform that amplifies the target signals by Raman scattering. Despite SERS enabling a meager detection limit, even at the single-molecule level, SERS also tends to equally enhance unwanted molecules due to the non-specific binding [...] Read more.
Surface-enhanced Raman scattering (SERS) is a powerful optical sensing platform that amplifies the target signals by Raman scattering. Despite SERS enabling a meager detection limit, even at the single-molecule level, SERS also tends to equally enhance unwanted molecules due to the non-specific binding of noise molecules in clinical samples, which complicates its use in complex samples such as bodily fluids, environmental water, or food matrices. To address this, we developed a novel non-fouling biomimetic SERS sensor by self-assembling an anti-adhesive, anti-fouling, and size-selective Lubricin (LUB) coating on gold nanoparticle (AuNP) functionalized glass slide surfaces via a simple drop-casting method. Compared to a conventional AuNPs-SERS substrate, the biomimetic SERS meets the requirements of simple preparation and enables direct droplet detection without any sample pre-treatment. Atomic force microscopy was used to confirm the self-assembled Lubricin coating on the AuNP surface, acting as an anti-fouling and size-selective protection layer. A series of Raman spectra were collected using melamine as the target analyte, which was spiked into 150 mM NaCl solution or undiluted milk. It was demonstrated that the LUB coating effectively prevents the detrimental fouling generated by the proteins and fats in milk, ensuring the clear detection of melamine. Our sensor showed high selectivity and could detect melamine in milk at concentrations as low as 1 ppm. Given that the EU/US legal limit for melamine in food is 2.5 ppm, this sensor offers a promising, cost-effective solution for routine screening and has potential applications for detecting food adulteration in the food safety, environmental monitoring, aquaculture, and biomedical fields. Full article
(This article belongs to the Special Issue SERS-Based Biosensors: Design and Biomedical Applications)
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<p>(<b>A</b>) Representative AFM images of bare SERS. (<b>B</b>) Corresponding 3D image of <a href="#biosensors-14-00591-f001" class="html-fig">Figure 1</a>A. (<b>C</b>) Representative AFM images of biomimetic SERS. (<b>D</b>) Corresponding 3D image of <a href="#biosensors-14-00591-f001" class="html-fig">Figure 1</a>C. The AFM images were collected using contact mode and the Ra values listed on the images are averages of the RMS data for each. The average roughness shown was calculated from ten total traces of an individual image.</p>
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<p>Representative AFM normal–force distance curves of (<b>A</b>) bare SERS and (<b>B</b>) biomimetic DNA sensor.</p>
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<p>(<b>A</b>) SERS measurement of melamine in buffer made with bare SERS. (<b>B</b>) SERS measurements of pure milk and melamine–spiked undiluted milk made with the bare SERS sensor or biomimetic SERS, respectively.</p>
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<p>(<b>A</b>) SERS spectra of melamine–spiked buffer collected with biomimetic SERS and bare SERS. (<b>B</b>) SERS spectra of melamine–spiked undiluted milk or buffer with the same biomimetic SERS sensors and background spectra of bare SERS and biomimetic SERS without melamine.</p>
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<p>(<b>A</b>) SERS spectra under different concentrations of melamine in undiluted milk, ranging from 1 ppm to 500 ppm, were collected with biomimetic SERS. (<b>B</b>) Calibration curve of melamine peak intensity at 680 cm<sup>–1</sup> as a function of melamine concentration in undiluted milk.</p>
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<p>(<b>A</b>–<b>D</b>) Schematic illustration of the fabrication of the biomimetic SERS sensor. (<b>E</b>,<b>F</b>) SERS measurements of melamine-spiked undiluted milk with the bare SERS sensor and the biomimetic sensor, respectively.</p>
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