Zhang Liping, Wang Jie, Ni Caihua, Zhang Yanan, Shi Gang
The Key Laboratory of Food Colloids and Biotechnology, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, China.
The Key Laboratory of Food Colloids and Biotechnology, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, China.
Mater Sci Eng C Mater Biol Appl. 2016 Jan 1;58:724-9. doi: 10.1016/j.msec.2015.09.044. Epub 2015 Sep 13.
A new kind of polyelectrolyte complex (PEC) based on cationic chitosan (CS) and anionic poly(2-acry1amido-2-methylpropanesulfonic 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.
利用聚合物 - 单体对反应体系制备了一种基于阳离子壳聚糖(CS)和阴离子聚(2 - 丙烯酰胺 - 2 - 甲基丙磺酸)(PAMPS)的新型聚电解质复合物(PEC)。壳聚糖与2 - 丙烯酰胺 - 2 - 甲基丙磺酸(AMPS)在水溶液中混合,随后进行AMPS的聚合反应。该复合物通过CS的NH3(+)基团与AMPS的SO3(-)基团之间的静电相互作用形成,从而形成CS - PAMPS复合纳米粒子。通过改变CS与AMPS的重量比获得了一系列纳米粒子,并对纳米粒子的结构和性能进行了研究。观察到纳米粒子具有球形形态,平均直径在255 nm至390 nm之间,随纳米粒子的组成而变化。这些纳米粒子用作阿霉素的药物载体,显示出相对较高的载药率和包封率。体外释放曲线表明,药物释放可通过调节释放介质的pH值来控制。纳米粒子具有制备过程简单、无有机溶剂、尺寸可控、良好的生物降解性和生物相容性等明显优点,有望在药物控释领域得到应用。