Chitosan-g-PEG nanoparticles ionically crosslinked with poly(glutamic acid) and tripolyphosphate as protein delivery systems

被引:88
|
作者
Papadimitriou, Sofia A. [1 ]
Achilias, Dimitris S. [1 ]
Bikiaris, Dimitrios N. [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Chem, Lab Polymer Chem & Technol, Thessaloniki 54124, Greece
关键词
Chitosan; Poly(ethylene glycol); Bovine serum albumin; Poly(glycolic acid); Tripolyphosphate; Nanoparticles; GAMMA-GLUTAMIC ACID; GRAFTED CHITOSAN; IN-VITRO; DRUG; RELEASE; INSULIN; COMPLEX; HYDROGEL;
D O I
10.1016/j.ijpharm.2012.04.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the present study chitosan grafted copolymers with poly(ethylene glycol) (CS-g-PEG) were prepared and studied using PEG with molecular weights 2000 and 5000 g/mol. The materials were characterized using H-1 NMR, FTIR and WAXD techniques. These polyelectrolytes were ionically crosslinked with tripolyphosphate (TPP) and poly(glutamic acid) (PGA) at different polymer/crosslinking agent ratios (1:1, 2:1, 3:1 and 4:1, w/w) for the nanoencapsulation of bovine serum albumin (BSA). Prepared nanoparticles are spherical in shape with a mean diameter ranging from 150 to 600 nm. The size depends mainly to the molecular weight of the PEG and the crosslinking agent used. The PEG molecular weight also seems to affect the release rate of BSA especially the first burst effect which appears to be high in copolymers containing PEG5000, compared with copolymer prepared with PEG2000, and it is also higher when PGA was used as crosslinking agent, instead of TPP. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:318 / 327
页数:10
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