Dual-drug delivery system based on hydrogel/micelle composites

被引:254
作者
Wei, Lan [1 ]
Cai, Chunhua [1 ]
Lin, Jiaping [1 ]
Chen, Tao [1 ]
机构
[1] E China Univ Sci & Technol, Key Lab Ultrafine Mat, Minist Educ, Sch Mat Sci & Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Drug release; Dual-drug delivery; Hydrogel; Micelle; Polypeptide; BLOCK-COPOLYMER MICELLES; ANGLE NEUTRON-SCATTERING; DIBLOCK COPOLYMERS; CONTROLLED-RELEASE; THERMOSENSITIVE HYDROGELS; INTRACELLULAR DELIVERY; STRUCTURAL-PROPERTIES; TRIBLOCK COPOLYMERS; AQUEOUS-SOLUTION; IN-VITRO;
D O I
10.1016/j.biomaterials.2009.01.006
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We present a dual-drug delivery system (DDDS) of hydrogel/polypeptide micelle composites in this work. The DDDS was constructed from aspirin (Asp) dispersed poly(vinyl alcohol) (PVA) or Chitosan (CS)/PVA hydrogel and doxorubicin (DOX) loaded poly(L-glutamic acid)-b-poly(propylene oxide)-b-poly (L-glutamic acid) (GPG) micelles. Independent release behaviors of the two drugs are observed. Asp has a short-term release while DOX has a long-term and sustained release behavior in all the DDDSs. The release of DOX from all the DDDSs is environmentally controlled due to the pH and temperature sensitivity of the GPG micelle. Asp shows the pH controlled release behavior in CS/PVA/micelle DDDS due to the pH sensitivity of CS hydrogel. The releasing profiles were analyzed using a power law equation proposed by Peppas. It reveals that the release of Asp is anomalous transport in all the hydrogel/micelle DDDSs. The release of DOX is Fickian type in PVA/micelle system, and changes to anomalous transport in CS/PVA/micelle system according to the release exponent n. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2606 / 2613
页数:8
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