One-step synthesis of interpenetrating network hydrogels: Environment sensitivities and drug delivery properties

被引:16
作者
Lu, Jingqiong [1 ]
Li, Yinhui [1 ]
Hu, Deng [1 ]
Chen, Xiaoling [1 ]
Liu, Yongmei [1 ]
Wang, Liping [2 ]
Ashraf, Muhammmad Aqeel [3 ,4 ]
Zhao, Yansheng [1 ]
机构
[1] Taiyuan Univ Technol, Coll Chem & Chem Engn, Taiyuan 030024, Peoples R China
[2] Univ S Australia, Sch Pharm & Med Sci, Sansom Inst Hlth Res, Adelaide, SA 5001, Australia
[3] Univ Malaya, Fac Sci, Dept Geol, Kuala Lumpur 50603, Malaysia
[4] Univ Malaysia Sabah, Fac Sci & Nat Resources, Kota Kinabalu 88400, Sabah, Malaysia
关键词
Poly(aspartic acid); Carboxymethyl chitosan; IPN; Hydrogel; Drug release; IPN HYDROGEL; ATR-FTIR; CHITOSAN;
D O I
10.1016/j.sjbs.2015.06.012
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A novel interpenetrating network hydrogel for drug controlled release, composed of modified poly(aspartic acid) (KPAsp) and carboxymethyl chitosan (CMCTS), was prepared in aqueous system. The surface morphology and composition of hydrogels were characterized by SEM and FTIR. The swelling properties of KPAsp, KPAsp/CMCTS semi-IPN and KPAsp/CMCTS IPN hydrogels were investigated and the swelling dynamics of the hydrogels was analyzed based on the Fickian equation. The pH, temperature and salt sensitivities of hydrogels were further studied, and the prepared hydrogels showed extremely sensitive properties to pH, temperature, the ionic salts kinds and concentration. The results of controlled drug release behaviors of the hydrogels revealed that the introduction of IPN observably improved the drug release properties of hydrogels, the release rate of drug from hydrogels can be controlled by the structure of the hydrogels and pH value of the external environment, a relative large amount of drug released was preferred under simulated intestinal fluid. These results illustrated high potential of the KPAsp/CMCTS IPN hydrogels for application as drug carriers. (C) 2015 Production and hosting by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:S22 / S31
页数:10
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