4.4 Article

Formulation of pH-sensitive aminated chitosan-gelatin crosslinked hydrogel for oral drug delivery

期刊

JOURNAL OF SAUDI CHEMICAL SOCIETY
卷 25, 期 12, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jscs.2021.101384

关键词

Aminated chitosan; Gelatin; Drug release; pH-sensitive hydrogel

向作者/读者索取更多资源

This study aimed to develop efficient pH-sensitive hydrogel based on aminated chitosan (AmCs) and gelatin (Gel) biopolymers for oral drug delivery. The developed AmCs-Gel crosslinked hydrogel displayed variable pH-sensitive swelling profiles and showed acceptable biodegradability with no cellular toxicity, suggesting their applicability as pH-sensitive oral drug carriers. Adjusting the ratios of AmCs and Gel can achieve variable drug release and loading efficiency.
The objective of this study is to develop efficient pH-sensitive hydrogel based on aminated chitosan (AmCs) and gelatin (Gel) biopolymers for oral drug delivery. Herein, AmCs was chemically crosslinked with gelatin (Gel) biopolymer with different ratios, while their structures, thermal profiles and morphological properties were investigated by FTIR, TGA and SEM characterization tools, respectively. Moreover, gel-content, crosslinking density and rheological analysis were also performed. The results clarified that the developed AmCs-Gel crosslinked hydrogel displayed variable pH-sensitive swelling profiles. By increasing AmCs ratio, the swelling ratio was boosted at pH 1.2 and declined at pH 7.4. Besides, by increasing gelatin ratio in the hydrogel matrix, the loading efficiency of Oseltamivir phosphate (as a model of drug) was augmented and reached maximum value of 79.0% by AmCs-Gel (2:3) crosslinked hydrogel. The in vitro drug release profiles were investigated for 6 h in simulated gastric fluid [SGF; pH 1.2] and simulated colon fluid [SCF; pH 7.4]. Variable release profiles were realized depending on variation of AmCs and Gel ratios in the crosslinked hydrogel matrix. Finally, the formulated smart crosslinked AmCs-Gel hydrogels demonstrated acceptable biodegradability with no cellular toxicity, suggesting their applicability as pH-sensitive oral drug carriers. (C) 2021 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据