含血小板裂解液的红麻纳米纤维素水凝胶用于全层伤口愈合的评价。

Payal Bhatnagar, Jia-Xian Law, Shiow-Fern Ng
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引用次数: 0

摘要

引言:愈合全层伤口通常具有挑战性和耗时,并伴有疤痕和感染等并发症。由于健康供体的可用性和免疫功能低下患者的适用性,标准治疗,劈开皮肤移植有局限性。方法:自体血小板裂解液(PL)由于其含有生长因子(GF),对于免疫系统较弱的卧床病人来说是一种更安全的选择,因此在组织再生潜力方面很受欢迎。然而,PL临床疗效不一致,成本高,半衰期短。为了解决这些问题,本研究通过制造壳聚糖/纳米晶纤维素(CS/NCC)水凝胶来探索一种新的递送系统,以可持续地将自体PL递送到伤口部位。值得注意的是,NCC是由红麻韧皮纤维经酸水解制备的,并通过物理包埋整合到CS基质中,而不需要任何化学交联剂。然后用自体PL富集复合水凝胶,进一步表征其物理化学性质、体外GF释放量以及与皮肤细胞的相容性。在分子水平上,利用qPCR促进了伤口愈合基因的基因表达,表明添加pl的水凝胶上调了细胞外基质基因的表达。一项使用全层创面模型的体内研究表明,与对照组相比,cs - nc - pl水凝胶敷料在14天内实现了81.8%的创面愈合。结果:组织学分析显示上皮再生、血管生成和胶原沉积增强。其中,cs - nc - pl水凝胶组在第14天羟脯氨酸含量显著高于对照组(60.62±11.46 μg/100 mg)。免疫组化结果显示,肌成纤维细胞存在和血管生成标志物α-SMA和CD31水平升高,在第7天达到峰值。结论:这些研究结果表明cs - nc - pl水凝胶是一种很有前途的个性化伤口敷料,可以改善住院患者的愈合效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of a Kenaf Nanocrystalline Cellulose-based Hydrogel Containing Platelet Lysate for Full-thickness Wound Healing.

Introduction: Healing full-thickness wounds is often challenging and time-consuming, with complications such as scarring and infections. The standard treatment, split skin grafting, has limitations due to the availability of healthy donors and suitability for immunocompromised patients.

Methods: Autologous platelet lysate (PL) has been popular for tissue regenerative potential because it contains growth factors (GF) and is a safer option for bedridden patients with weak immune systems. However, PL has inconsistent clinical efficacy, high costs, and a short half-life. To address these issues, this study explores a novel delivery system by fabricating a chitosan/nanocrystalline cellulose (CS/NCC) hydrogel to sustainably deliver autologous PL to the wound site. Notably, NCC was prepared from kenaf bast fibers using acid hydrolysis and integrated into the CS matrix through physical entrapment without any chemical crosslinkers. The composite hydrogel was then enriched with autologous PL and further characterized for its physicochemical properties, in vitro GF release, and compatibility with skin cells. At the molecular level, gene expression of wound healing genes was facilitated using qPCR, revealing that the PL-supplemented hydrogel upregulated the expression of extracellular matrix genes. An in vivo study using a full-thickness wound model demonstrated that the CS-NCC-PL hydrogel dressing achieved 81.8% wound closure within 14 days, compared to the control groups.

Results: Histological analysis indicated enhanced re-epithelialization, angiogenesis, and collagen deposition. Particularly, the CS-NCC-PL hydrogel group showed a significantly higher hydroxyproline content (60.62 ± 11.46 μg/100 mg) by day 14. Immunohistochemistry results revealed elevated levels of α-SMA and CD31, markers of myofibroblast presence and angiogenesis, peaking at day 7.

Conclusion: These findings suggest that the CS-NCC-PL hydrogel is a promising personalized wound dressing for bedridden patients, offering improved healing outcomes in hospital settings.

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