羧甲基纤维素钠盐-药物在薄膜中的扩散过程研究

A. Shurshina, E. Kulish
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引用次数: 0

摘要

本文研究了羧甲基纤维素钠盐和抗生素硫酸阿米卡星为基材的药膜的传输特性。研究表明,这种薄膜对水蒸气的吸附和药物的释放过程是以一种异常的扩散模式进行的,这可以用玻璃状聚合物(包括羧甲基纤维素的钠盐)弛豫过程的减慢来解释。随着引入药物量的增加,薄膜中水蒸气的吸附和阿米卡星释放的扩散系数都有规律地减小。值得注意的是,羧基甲基纤维素-阿米卡星硫酸钠盐形成的薄膜在白天溶解于水中,并且不提供药物的长时间释放。为了降低聚合物膜在水中的溶解度,用氯化钙对聚合物膜进行了表面改性。结果表明,改性不会改变膜的扩散方式,但会引起膜的扩散系数有规律的变化——膜在氯化钙溶液中保存的时间越长,药膜对水蒸气的吸附扩散系数和药物阿米卡星从膜中释放的扩散系数越小。认为以羧甲基纤维素钠盐为基料对聚合物膜进行表面改性是使其具有药物缓释作用的有效途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of the diffusion process in films sodium salt of carboxymethyl cellulose – drug
The transport properties of medicinal films based on sodium salt of carboxymethylcellulose and the antibiotic amikacin sulfate have been studied in this work. It has been shown that the process of sorption of water vapor by such films and the release of a drug from them proceeds in an abnormal diffusion mode, which is explained by the slowdown of relaxation processes in glassy polymers, which include the sodium salt of carboxymethylcellulose. An increase of the amount of the introduced drug is accompanied by a regular decrease in the diffusion coefficients of both the process of sorption of water vapor and the release of amikacin from the films. It is noted that the formed films of sodium salt of carboxymethylcellulose-amikacin sulfate dissolve in water during the day and do not provide a prolonged release of the drug. To reduce the solubility of the films in water, the surface modification of the polymer film with calcium chloride has been carried out. It has been found that the modification does not lead to a change in the diffusion mode, but is accompanied by a regular change in the diffusion coefficients – the longer the formed films were kept in a calcium chloride solution, the lower the diffusion coefficients of the sorption of water vapor by medicinal films and the diffusion coefficients of the release of the drug amikacin from the film. It is argued that the surface modification of polymer films based on the sodium salt of carboxymethylcellulose is an effective way of imparting to them the effect of prolonging the release of a drug.
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