Preparation of polyelectrolyte complex nanoparticles of chitosan and poly(2-acryl amido-2-methylpropanesulfonic acid) for doxorubicin release

被引:30
|
作者
Zhang, Liping [1 ]
Wang, Jie [1 ]
Ni, Caihua [1 ]
Zhang, Yanan [1 ]
Shi, Gang [1 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Key Lab Food Colloids & Biotechnol, Minist Educ, Wuxi 214122, Peoples R China
基金
中国国家自然科学基金;
关键词
Polyelectrolyte complex; Poly(2-acrylamido-2-methylpropanesulfonic acid); Nanoparticle; Biocompatible; Controlled release; CHARGED BLOCK-COPOLYMERS; GENE DELIVERY; CO-DELIVERY; MICELLES; CELLS; WATER; INTERPOLYELECTROLYTE; CYTOTOXICITY; MORPHOLOGY; PARTICLES;
D O I
10.1016/j.msec.2015.09.044
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A new kind of polyelectrolyte complex (PEC) based on cationic chitosan (CS) and anionic poly(2-acrylamido-2-methylpropanesulfcinic acid) (PAMPS) was prepared using a polymer-monomer pair reaction system. Chitosan was mixed with 2-acry1amido-2-methylpropanesulfonic acid) (AMPS) in an aqueous solution, followed by polymerization of AMPS. The complex was formed by electrostatic interaction of NH3+ groups of CS and SO3- groups of AMPS, leading to a formation of complex nanoparticles of CS-PAMPS. A series of nanoparticles were obtained by changing the weight ratio of CS to AMPS, the structure and properties of nanoparticles were investigated. It was observed that the nanoparticles possessed spherical morphologies with average diameters from 255 nm to 390 nm varied with compositions of the nanoparticles. The nanoparticles were used as drug vehicles for doxorubicin, displaying relative high drug loading rate and encapsulation rate. The vitro release profiles revealed that the drug release could be controlled by adjusting pH of the release media. The nanoparticles demonstrated apparent advantages such as simple preparation process, free of organic solvents, size controllable, good biodegradability and biocompatibility, and they could be potentially used in drug controlled release field. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:724 / 729
页数:6
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