基于接枝罗望子核多糖的 Al3+ 交联水凝胶基质,用于在胃肠道环境中持续释放药物

Arpita Saha , Kaushik Mukherjee , Bijaya Ghosh , Tapan Kumar Giri
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引用次数: 0

摘要

离子交联水凝胶是持续给药的绝佳基质材料。以罗望子核多糖(TKP)为唯一基质材料制备的片剂无法实现药物的持续释放。这项工作的目的是对 TKP 进行改性,并开发出离子交联水凝胶基质片剂,用于持续给药。采用自由基聚合技术,用甲基丙烯酸(MAA)接枝 TKP。采用直接压缩法制备了使用 Al3+ 离子交联接枝 TKP 的水凝胶基质片剂。研究发现,Al3+ 离子对基质片剂的侵蚀、溶胀和扑热息痛的释放有很大影响。随着 Al3+ 离子浓度的增加,侵蚀、溶胀和扑热息痛的释放都会减慢。水凝胶基质片剂在酸性介质中的药物释放速度较慢,而在碱性介质中的药物释放速度相对较快。共聚物/氢氧化铝(Al(OH)3)比例为 1:1 的优化配方可持续释放药物超过 10 小时,且凝胶基质的溶胀和侵蚀程度较低。我们的结论是,Al3+ 离子交联接枝 TKP 是一种在胃肠道环境中持续给药的优良基质材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Grafted tamarind kernel polysaccharide based Al3+ cross-linked hydrogel matrices for sustained release of drug in the gastrointestinal milieu

Ionically cross-linked hydrogel serves as an excellent matrix material for the sustained delivery of drugs. Tablets prepared with tamarind kernel polysaccharide (TKP) as the sole matrix material could not provide sustained release of the incorporated drugs. The purpose of the work was to modify TKP and development of ionically cross-linked hydrogel matrix tablets for sustained drug delivery. Grafting of TKP was performed with methacrylic acid (MAA) following the free radical polymerization technique. Hydrogel matrix tablets using Al3+ ion cross-linked grafted TKP were prepared by direct compression method. Al3+ ions were found to considerably influence the erosion, swelling, and paracetamol release from the matrix tablet. Retardation of the erosion, swelling, and paracetamol release was observed with increasing the concentration of Al3+ ions. The hydrogel matrix tablets showed a slow release of drugs in an acidic medium and a relatively faster drug release in an alkaline medium. The optimized formulation having a co-polymer/aluminium hydroxide (Al(OH)3) ratio of 1:1, exhibited sustained drug release action for more than 10 h with lower swelling and erosion of the gel matrix. We conclude that Al3+ ion cross-linked grafted TKP is an excellent matrix material for sustained delivery of drugs in the gastrointestinal milieu.

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