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首页> 外文期刊>Journal of the Indian Chemical Society >Effect of chitosan molecular weight of chitosan-citrate film on site specific in vitro release of Ofloxacin
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Effect of chitosan molecular weight of chitosan-citrate film on site specific in vitro release of Ofloxacin

机译:壳聚糖柠檬酸膜的壳聚糖分子量对氧氟沙星体外定点释放的影响

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摘要

Chitosan, a biodegradable and biocompatible polysaccharide, is a potentially useful material in various fields. Chitosan films with different molecular weights (MW) of chitosan were developed followed by incorporation of Ofloxacin as a model drug by a casting/solvent evaporation technique. And citrate cross-linked films were prepared simply by dipping film into sodium citrate solution. The swelling ratio of citrate/chitosan film was sensitive to pH and ionic strength studied here. These films were characterized by release and swelling studies, Differential sanning colorimetry (DSC), Opical microscope coupled with Raman spectroscopy, Scanning electron colorimetry (SEM), Drug release based on cross linking time. Concentration of cross linking agent significantly influenced the in vitro release of drug as well of swelling of the films. The higher the MW of chitosan lower release rate was observed. The present study showed that MW and cross linking time of films regulated the varying swelling and drug release at pH 3.5 and pH 6.2. In addition, it indicated that the citrate/chitosan films were useful in drug delivery i.e. site-specific controlled drug release in stomach.
机译:壳聚糖是一种可生物降解和生物相容的多糖,是在各个领域中潜在有用的材料。研制出具有不同分子量(MW)的壳聚糖的壳聚糖膜,然后通过流延/溶剂蒸发技术将氧氟沙星作为模型药物掺入。只需将膜浸入柠檬酸钠溶液中即可制备柠檬酸盐交联膜。柠檬酸盐/壳聚糖膜的溶胀率对此处研究的pH和离子强度敏感。这些膜的特征在于释放和溶胀研究,差示桑宁比色法(DSC),光学显微镜和拉曼光谱法,扫描电子比色法(SEM),基于交联时间的药物释放。交联剂的浓度显着影响药物的体外释放以及膜的溶胀。壳聚糖的MW越高,观察到的释放速率越低。本研究表明,膜的分子量和交联时间调节了pH 3.5和pH 6.2时溶胀和药物释放的变化。另外,它表明柠檬酸盐/壳聚糖膜可用于药物递送,即在胃中定点控制药物释放。

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