根尼平交联细菌纤维素/壳聚糖水凝胶的原位合成肿胀、药物释放行为及抗菌评价

Joachim E. Arikibe, R. Lata, D. Rohindra
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引用次数: 0

摘要

在木醋杆菌培养液中加入壳聚糖,原位合成了细菌纤维素/壳聚糖水凝胶。将合成的BC-Chs浸在genipin (Gp)中,得到交联膜BC-Chs-Gp。在BC- chs水凝胶的FTIR光谱中,由于N-H拉伸而出现了酰胺I和酰胺II带,证实了壳聚糖在BC网络中的存在。扫描电镜(SEM)研究表明,与BC- chs和BC相比,BC- chs - gp具有更紧密的纤维网络。BC-Chs和BC-Chs- gp的抗拉强度均低于杨氏模量。与BC-Chs相比,交联BC-Chs的水溶胀率和含水率最低。采用Korsmeyer-Peppas模型进行富马酸喹硫平24h体外释药研究。抑菌试验结果表明,BC-Chs和BC-Chs- gp对大肠杆菌和金黄色葡萄球菌均有抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In situ Synthesis of Bacterial Cellulose/Chitosan Hydrogels Crosslinked with Genipin; Swelling, Drug Release Behavior and Antibacterial Evaluation
Bacterial cellulose (BC)/chitosan (Chs) hydrogel was synthesised in situ by adding chitosan to the Acetobacter xylinum culture. The synthesized BC-Chs was immersed in genipin (Gp) to yield crosslinked membrane, BC-Chs-Gp. The emergence of the amide I and II bands due to N-H stretching in the FTIR spectra of BC-Chs hydrogels confirmed the incorporation of chitosan into the BC network. The internal morphology studied by Scanning Electron Microscopy (SEM) revealed BC-Chs-Gp had a more compact fibril network compared to BC-Chs and BC. The tensile strength of BC-Chs and BC-Chs-Gp were lower than their Young's modulus. Crosslinked BC-Chs showed the lowest swelling in water and moisture content compared to BC-Chs. In vitro drug release studies of quetiapine fumarate over 24 h followed the Korsmeyer-Peppas model. Antibacterial evaluation showed BC-Chs and BC-Chs-Gp were active against Escherichia coli and Staphylococcus aureus.
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