壳聚糖
生物相容性
戊二醛
化学
黏膜黏附
微球
毒品携带者
药物输送
纳米技术
化学工程
色谱法
材料科学
有机化学
工程类
作者
Vivek Ranjan Sinha,Anil Kumar Singla,Shweta Wadhawan,R.D. Kaushik,Rachna Kumria,Kavita Bansal,Shikha Dhawan
标识
DOI:10.1016/j.ijpharm.2003.12.026
摘要
Chitosan is a biodegradable natural polymer with great potential for pharmaceutical applications due to its biocompatibility, high charge density, non-toxicity and mucoadhesion. It has been shown that it not only improves the dissolution of poorly soluble drugs but also exerts a significant effect on fat metabolism in the body. Gel formation can be obtained by interactions of chitosans with low molecular counterions such as polyphosphates, sulphates and crosslinking with glutaraldehyde. This gelling property of chitosan allows a wide range of applications such as coating of pharmaceuticals and food products, gel entrapment of biochemicals, plant embryo, whole cells, microorganism and algae. This review is an insight into the exploitation of the various properties of chitosan to microencapsulate drugs. Various techniques used for preparing chitosan microspheres and evaluation of these microspheres have also been reviewed. This review also includes the factors that affect the entrapment efficiency and release kinetics of drugs from chitosan microspheres.
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