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负载莫匹罗星的核壳型普朗尼克-果胶-角蛋白纳米纤维可改善人角质形成细胞行为、血管生成活性及伤口愈合情况。

Mupirocin loaded core-shell pluronic-pectin-keratin nanofibers improve human keratinocytes behavior, angiogenic activity and wound healing.

作者信息

Mirhaj Marjan, Varshosaz Jaleh, Labbaf Sheyda, Emadi Rahmatollah, Seifalian Alexander Marcus, Sharifianjazi Fariborz, Tavakoli Mohamadreza

机构信息

Department of Materials Engineering, Isfahan University of Technology, Isfahan 84156-83111, Iran.

Novel Drug Delivery Systems Research Centre, Department of Pharmaceutics, School of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Int J Biol Macromol. 2023 Dec 31;253(Pt 2):126700. doi: 10.1016/j.ijbiomac.2023.126700. Epub 2023 Sep 4.

Abstract

In the current study, a core-shell nanofibrous wound dressing based on Pluronic-F127 (F127) containing 2 wt% mupirocin (Mup) core and pectin (Pec)-keratin (Kr) shell was fabricated through coaxial electrospinning technique, and the blended nanofibers were also fabricated from the same materials. The fiber diameter and specific surface area of the blended nanofibers were about 101.56 nm and 20.16 m/g, while for core-shell nanofibers they were about 97.32 nm and 25.26 m/g, respectively. The resultant blended and core-shell nanofibers experienced a degradation of 27.65 % and 32.28 % during 7 days, respectively. The drug release profile of core-shell nanofibers revealed a sustained release of Mup over 7 days (87.66 %), while the blended F127-Pec-Kr-Mup nanofibers had a burst release within the first few hours (89.38 % up to 48 h) and a cumulative release of 91.36 % after 7 days. Due to the controlled release of Mup, the core-shell structure significantly improved the human keratinocytes behavior, angiogenic potential and wound healing in a rat model compared to the blended structure. In conclusion, the F127-Mup/Pec-Kr core-shell nanofibrous wound dressing appears to be a promising candidate for the prevention of infection, and can potentially accelerate the recovery and healing of chronic and ischemic wounds.

摘要

在本研究中,通过同轴静电纺丝技术制备了一种基于普朗尼克 - F127(F127)的核壳纳米纤维伤口敷料,其含有2 wt%的莫匹罗星(Mup)内核和果胶(Pec) - 角蛋白(Kr)外壳,并且还由相同材料制备了混合纳米纤维。混合纳米纤维的纤维直径和比表面积分别约为101.56 nm和20.16 m/g,而核壳纳米纤维的分别约为97.32 nm和25.26 m/g。在7天内,所得的混合纳米纤维和核壳纳米纤维分别降解了27.65%和32.28%。核壳纳米纤维的药物释放曲线显示莫匹罗星在7天内持续释放(87.66%),而混合的F127 - Pec - Kr - Mup纳米纤维在最初几小时内有突发释放(48小时内达89.38%),7天后累积释放为91.36%。由于莫匹罗星的控释,与混合结构相比,核壳结构在大鼠模型中显著改善了人角质形成细胞行为、血管生成潜力和伤口愈合。总之,F127 - Mup/Pec - Kr核壳纳米纤维伤口敷料似乎是预防感染的有前景的候选物,并且可能加速慢性和缺血性伤口的恢复和愈合。

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