用于伤口敷料的乳清蛋白负载 3D 打印聚(乳酸)支架。

Hanne Meryem Kayadurmus, Azadeh Rezaei, Elif Ilhan, Sumeyye Cesur, Ali Sahin, Oguzhan Gunduz, Deepak M Kalaskar, Nazmi Ekren
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引用次数: 0

摘要

慢性皮肤伤口是一项全球性的临床挑战,需要采取有效的治疗策略。本研究探讨了三维打印聚乳酸(PLA)支架在伤口愈合应用中的潜力,该支架在不同浓度(25%、35% 和 50%)的浓缩乳清蛋白(WPC)的作用下得到增强。聚乳酸的生物相容性、生物可降解性和热稳定性使其成为医疗应用的理想材料。添加 WPC 的目的是模仿皮肤的细胞外基质,增强聚乳酸支架的生物活性。傅立叶变换红外光谱(FTIR)结果证实,在基于聚乳酸的三维打印支架中成功添加了 WPC。扫描电子显微镜(SEM)图像显示,聚乳酸/木塑支架与纯聚乳酸支架的孔隙大小无明显差异。机械强度测试表明,纯聚乳酸和含 50% WPC 的聚乳酸支架具有相似的拉伸强度。然而,WPC 浓度较低的支架显示出较低的拉伸强度。值得注意的是,与纯聚乳酸相比,所有聚乳酸/木塑支架的断裂应变都有所增加。含有 25% WPC 的聚乳酸的膨胀能力最高,比纯聚乳酸高出约 130%。WPC 浓度较高的支架也显示出较高的膨胀率和降解率。随着 WPC 浓度的增加,药物释放时间也会延长。培养七天后,与纯聚乳酸支架相比,含 50% WPC 的聚乳酸支架的细胞存活率明显提高。这种创新方法可为个性化伤口护理策略铺平道路,提供量身定制的治疗和靶向给药。不过,还需要进一步研究来优化这些支架的特性,并验证它们在临床环境中的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Whey protein-loaded 3D-printed poly (lactic) acid scaffolds for wound dressing applications.

Chronic skin wounds pose a global clinical challenge, necessitating effective treatment strategies. This study explores the potential of 3D printed Poly Lactic Acid (PLA) scaffolds, enhanced with Whey Protein Concentrate (WPC) at varying concentrations (25, 35, and 50% wt), for wound healing applications. PLA's biocompatibility, biodegradability, and thermal stability make it an ideal material for medical applications. The addition of WPC aims to mimic the skin's extracellular matrix and enhance the bioactivity of the PLA scaffolds. Fourier Transform Infrared Spectroscopy results confirmed the successful loading of WPC into the 3D printed PLA-based scaffolds. Scanning Electron Microscopy (SEM) images revealed no significant differences in pore size between PLA/WPC scaffolds and pure PLA scaffolds. Mechanical strength tests showed similar tensile strength between pure PLA and PLA with 50% WPC scaffolds. However, scaffolds with lower WPC concentrations displayed reduced tensile strength. Notably, all PLA/WPC scaffolds exhibited increased strain at break compared to pure PLA. Swelling capacity was highest in PLA with 25% WPC, approximately 130% higher than pure PLA. Scaffolds with higher WPC concentrations also showed increased swelling and degradation rates. Drug release was found to be prolonged with increasing WPC concentration. After seven days of incubation, cell viability significantly increased in PLA with 50% WPC scaffolds compared to pure PLA scaffolds. This innovative approach could pave the way for personalized wound care strategies, offering tailored treatments and targeted drug delivery. However, further studies are needed to optimize the properties of these scaffolds and validate their effectiveness in clinical settings.

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