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含环丙沙星和吲哚美辛药物的同轴电纺纳米纤维的细胞相容性和抗菌性能

Cytocompatibility and Antibacterial Properties of Coaxial Electrospun Nanofibers Containing Ciprofloxacin and Indomethacin Drugs.

作者信息

Khalili Shahla, Ghane Nazanin, Nouri Khorasani Saied, Heydari Fariba, Atwal Arjan, Davoodi Pooya

机构信息

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

Torabinejad Dental Sciences Research Center, School of Dentistry, Isfahan University of Medical Sciences, Isfahan 81746-73461, Iran.

出版信息

Polymers (Basel). 2022 Jun 24;14(13):2565. doi: 10.3390/polym14132565.

Abstract

A coaxial nanofibrous scaffold of poly (ε-caprolactone) and gelatin/cellulose acetate encapsulating anti-inflammatory and antibacterial drugs was co-electrospun for skin tissue regeneration. Indomethacin and ciprofloxacin as model drugs were added to the core and the shell solutions, respectively. The effect of the drugs’ presence and crosslinking on the scaffold properties was investigated. TEM images confirmed the core−shell structure of the scaffold. The fiber diameter and the pore size of the scaffold increased after crosslinking. The tensile properties of the scaffold improved after crosslinking. The crosslinked scaffold illustrated a higher rate of swelling, and a lower rate of degradation and drug release compared to the uncrosslinked one. Fitting the release data into the Peppas equation showed that Fickian diffusion was the dominant mechanism of drug release from the scaffolds. The results of biocompatibility evaluations showed no cytotoxicity and suitable adhesion and cell growth on the prepared core−shell structure. The antibacterial activity of the scaffolds was studied against one of the most common pathogens in skin wounds, where the existence of ciprofloxacin could prevent the growth of the Staphylococcus aureus bacteria around the scaffold. The obtained results suggested a new coaxial nanofibrous scaffold as a promising candidate for simultaneous tissue regeneration and controlled drug release.

摘要

为了实现皮肤组织再生,制备了一种同轴纳米纤维支架,该支架由聚(ε-己内酯)与包裹有抗炎和抗菌药物的明胶/醋酸纤维素共同电纺而成。分别将吲哚美辛和环丙沙星作为模型药物添加到核溶液和壳溶液中。研究了药物的存在和交联对支架性能的影响。透射电镜图像证实了支架的核壳结构。交联后支架的纤维直径和孔径增大。交联后支架的拉伸性能得到改善。与未交联的支架相比,交联后的支架显示出更高的溶胀率、更低的降解率和药物释放率。将释放数据拟合到Peppas方程表明,菲克扩散是药物从支架中释放的主要机制。生物相容性评估结果表明,所制备的核壳结构无细胞毒性,具有良好的细胞黏附性和细胞生长性能。研究了支架对皮肤伤口最常见病原体之一的抗菌活性,环丙沙星的存在可以抑制支架周围金黄色葡萄球菌的生长。所得结果表明,一种新型同轴纳米纤维支架有望成为同时进行组织再生和控制药物释放的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fc/9269477/dac7164c0141/polymers-14-02565-g001.jpg

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