Preparation of acetylsalicylic acid-acylated chitosan as a novel polymeric drug for drug controlled release

被引:29
作者
Liu, Changkun [1 ]
Wu, Yiguang [1 ]
Zhao, Liyan [1 ]
Huang, Xinzheng [1 ]
机构
[1] Shenzhen Univ, Sch Chem & Chem Engn, Shenzhen 518060, Guangdong, Peoples R China
关键词
Acetylsalicylic acid; Chitosan; Controlled release; DISSOLUTION PROFILES; SALICYLIC-ACID; ASPIRIN; FIBERS;
D O I
10.1016/j.ijbiomac.2015.03.063
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The acetylsalicylic acid-acylated chitosan (ASACTS) with high degree of substitution (DS) was successfully synthesized, and characterized with FTIR, H-1 NMR and elemental analysis methods. The optimum synthesis conditions were obtained which gave the highest DS (about 60%) for ASACTS. Its drug release experiments were carried out in simulated gastric and intestine fluids. The results show that the drugs in the form of acetylsalicylic acid (ASA) and salicylic acid (SA) were released in a controlled manner from ASACTS only in simulated gastric fluid. The release profile can be best fitted with logistic and Weibull model. The research results reveal that ASACTS can be a potential polymeric drug for the controlled release of ASA and SA in the targeted gastric environment. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:189 / 194
页数:6
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