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载葡聚糖的聚环氧乙烷/明胶-聚乙烯醇/壳聚糖电纺核壳纳米纤维敷料用于治疗皮肤利什曼病。

Glucantime-loaded electrospun core-shell nanofibers composed of poly(ethylene oxide)/gelatin-poly(vinyl alcohol)/chitosan as dressing for cutaneous leishmaniasis.

机构信息

School of Chemical and Petroleum Engineering, Shiraz University, Shiraz, Iran.

School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Int J Biol Macromol. 2020 Nov 15;163:288-297. doi: 10.1016/j.ijbiomac.2020.06.240. Epub 2020 Jun 28.

Abstract

Leishmaniasis, one of the main concerns of the World Health Organization, is a parasitic disease caused by Leishmania species. The main objective of this study was to prepare a topical drug delivery system that can deliver glucantime to the site of cutaneous Leishmania wounds. Using the electrospinning method, a core-shell nanofibrous mat composed of macromolecules including polyethylene oxide, gelatin, poly (vinyl alcohol) and chitosan was prepared. The prepared nanofibers were characterized by scanning electron microscopy (SEM), transmission electron microscopy, Fourier transform infrared spectroscopy (FT-IR), tensile test and in vitro drug release test. The anti-Leishmania activities of drug-loaded nanofibers against Leishmania promastigotes and its cytotoxicity on fibroblasts were determined respectively by flow-cytometry and indirect MTT methods. Results of morphological studies showed that uniform nanofibers were prepared without any bead with average diameter of 404 nm. The TEM investigation confirmed the core-shell structure of the fibers. The in-vitro drug release assay was executed using Franz diffusion cell, which indicted 84% of glucantime was released during the first 9 h. The results indicated that 4 and 6 cm of nanofibers mat were significantly killed promatigotes up to 78%. Moreover, the MTT assay also showed that the fabricated nanofibers do not possess any cytotoxicity towards fibroblast cells.

摘要

利什曼病是世界卫生组织关注的主要疾病之一,是一种由利什曼原虫引起的寄生虫病。本研究的主要目的是制备一种局部药物传递系统,将葡萄糖酸锑钠递送至皮肤利什曼病伤口部位。本研究采用静电纺丝法,制备了一种由聚氧化乙烯、明胶、聚乙烯醇和壳聚糖等大分子组成的核壳纳米纤维垫。通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)、傅里叶变换红外光谱(FT-IR)、拉伸试验和体外药物释放试验对所制备的纳米纤维进行了表征。通过流式细胞术和间接 MTT 法分别测定了载药纳米纤维对利什曼原虫前鞭毛体的抗利什曼活性及其对成纤维细胞的细胞毒性。形态学研究结果表明,制备出了无珠状、平均直径为 404nm 的均匀纳米纤维。TEM 研究证实了纤维的核壳结构。采用 Franz 扩散池进行体外药物释放试验,结果表明在最初的 9h 内释放了 84%的葡萄糖酸锑钠。结果表明,4cm 和 6cm 的纳米纤维垫可显著杀死多达 78%的前鞭毛体。此外,MTT 试验还表明,所制备的纳米纤维对成纤维细胞没有任何细胞毒性。

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