An Overview of Chitosan-Xanthan Gum Matrices as Controlled Release Drug Carriers

Suha M Dadou, M. Antonijević, B. Chowdhry, A. Badwan
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引用次数: 5

Abstract

Naturally occurring polysaccharides and/or their chemically modified derivatives have been widely investigated in relation to their use as components of controlled release sys tems for drug delivery. The aforementioned is due, in part, to their distinct properties such as abundant availability and biocompatibility as well as environmental and eco nomic advantages. Chitosan (CS) and xanthan gum (XG) based matrices have received growing scientific/pharmaceutical interest as oral controlled release drug carriers. Herein, recent advances spanning the last two decades in CS-XG based drug delivery systems are reviewed with the emphasis being on oral tablet formulations, due to their versatility as pharmaceutical dosage forms. The mechanism of interaction between CS and XG, by means of computational and experimental approaches, is scrutinized. Results obtained from the literature establish the possibility of fabricating a controlled release drug delivery system based on CS and XG matrices. This can be achieved by monitor ing and manipulating the physiochemical properties of the two polymers as well as the experimental variables affecting their drug retardation efficiency, without the need to employ special equipment or sophisticated experimental techniques/methodologies.
壳聚糖-黄原胶基质作为控释药物载体的研究进展
天然存在的多糖和/或其化学修饰衍生物已被广泛研究作为药物缓释系统的组成部分。上述部分是由于其独特的特性,如丰富的可利用性和生物相容性以及环境和经济优势。壳聚糖(CS)和黄原胶(XG)基基质作为口服控释药物载体受到越来越多的科学/药学关注。本文回顾了过去二十年来基于CS-XG的药物输送系统的最新进展,重点是口服片剂配方,因为它们作为药物剂型具有多功能性。通过计算和实验的方法,研究了CS和XG之间的相互作用机制。从文献中获得的结果建立了基于CS和XG基质制备控释给药系统的可能性。这可以通过监测和操纵两种聚合物的物理化学性质以及影响其药物阻滞效率的实验变量来实现,而无需使用特殊设备或复杂的实验技术/方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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