抗坏血酸棕榈酸酯/羟丙基-β-环糊精包合物负载纳米纤维膜,用于加速糖尿病伤口愈合

IF 24.5 Q1 CHEMISTRY, PHYSICAL
Dan Zhao, Jingchong Liu, Guotao Liu, Liangxuan Hou, Liping Zhou, Changtao Wang, Yongqiang Wen
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引用次数: 0

摘要

慢性皮肤伤口中积累的活性氧(ROS)会阻碍伤口的愈合,因此有必要及时消除伤口附近的 ROS。抗坏血酸棕榈酸酯(AP)是一种有效的抗氧化剂,但其溶解性受到限制,这在很大程度上限制了它的应用。本研究旨在通过将抗坏血酸棕榈酸酯封装在 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) 内,获得 AP/CD 包合物 (IC),从而提高其溶解性。这一进展有助于利用聚乙烯醇(PVA)和季铵壳聚糖(QCS),通过电纺丝技术开发抗氧化和抗菌纳米纤维膜。所开发的 PVA/QCS 与 AP/CD-IC 结合的纳米纤维(PVA/QCS-IC)可增加 AP 的释放,并具有良好的抗氧化性。与未在 HP-β-CD 中封装 AP 的 PVA/QCS 结合 AP 纳米纤维(PVA/QCS-AP)相比,PVA/QCS-IC 纳米纤维可显著保护人类皮肤成纤维细胞免受氧化应激,并提高 Col-I 的表达水平。此外,PVA/QCS-IC 纳米纤维还能抑制大肠杆菌、金黄色葡萄球菌和绿脓杆菌的生长。此外,将 PVA/QCS-IC 纳米纤维用作糖尿病小鼠的伤口敷料时,可有效促进糖尿病伤口愈合、促进胶原蛋白沉积并减轻皮肤炎症反应。研究结果表明,PVA/QCS-IC 纳米纤维是一种既能提高 AP 溶解度又能提高其治疗潜力的有前途的解决方案,可作为糖尿病伤口护理应用的潜在候选材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ascorbyl palmitate/hydroxypropyl-β-cyclodextrin inclusion complex loaded nanofibrous membrane for accelerated diabetic wound healing

Ascorbyl palmitate/hydroxypropyl-β-cyclodextrin inclusion complex loaded nanofibrous membrane for accelerated diabetic wound healing

Ascorbyl palmitate/hydroxypropyl-β-cyclodextrin inclusion complex loaded nanofibrous membrane for accelerated diabetic wound healing

Reactive oxygen species (ROS) accumulation in chronic skin wounds impedes the healing process, thus it is necessary to eliminate the ROS from the vicinity of the wound in time. Ascorbyl palmitate (AP) is a potent antioxidant that suffers from solubility constraints, which largely limits its application. This study aims to improve AP's solubility by encapsulating it within 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) to acquire AP/CD inclusion complex (IC). This advancement facilitates the development of antioxidant and antibacterial nanofibrous membranes via electrospinning, utilizing polyvinyl alcohol (PVA) and quaternary ammonium chitosan (QCS). The developed PVA/QCS combined with AP/CD-IC (PVA/QCS-IC) nanofibers increase the release of AP, boasting good antioxidant property. In comparison to the PVA/QCS combined with AP counterparts (PVA/QCS-AP), where AP is not encapsulated in HP-β-CD, the PVA/QCS-IC nanofibers provide notable protection against oxidative stress in human skin fibroblasts and increased Col-I expression levels. Additionally, the PVA/QCS-IC nanofibers are able to suppress the growth of E. coli, S. aureus, and P. aeruginosa. Furthermore, the PVA/QCS-IC nanofibers could effectively promote diabetic wound healing, facilitate collagen deposition, and reduce skin inflammation response when applied as a wound dressing in diabetic mice. The results suggest that the PVA/QCS-IC nanofibers represent a promising solution for both enhancing AP solubility and its therapeutic potential, positioning them as potential candidates for diabetic wound care applications.

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