Chitosan/Alginate Nanoparticles Stabilized by Poloxamer for the Controlled Release of 5-Fluorouracil

被引:27
作者
Xing, Jinfeng [1 ]
Deng, Liandong [1 ]
Dong, Anjie [1 ]
机构
[1] Tianjin Univ, Dept Polymer Sci & Engn, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
chitosan; biocompatibility; drug delivery systems; ORAL DELIVERY; SWELLING BEHAVIOR; DRUG-RELEASE; IN-VITRO; ALGINATE; CHITOSAN; MICROCAPSULES; MICROSPHERES; BEADS; MICROPARTICLE;
D O I
10.1002/app.32083
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study, stable 5-fluorouracil (5-FU)-loaded chitosan (CS)/alginate (Alg) nanoparticles (NPs) were prepared with poloxamer as a surfactant. The effects of the Alg concentration, CS/Alg weight ratio, and poloxamer concentration on the properties of the 5-FU-loaded CS/Alg NPs were studied. The results of dynamic light scattering and transmission electron microscopy indicated that stable 5-FU-loaded CS/Alg NPs of around 200 nm with low-size polydispersities were achieved. Furthermore, the in vitro release of the 5-FU-loaded CS/Alg NPs was investigated in phosphate buffer solution at pH 7.4. The results show that the encapsulation efficiency of 5-FU depended on the drug feeding amount (DFA), poloxamer concentration, Alg concentration, and CS concentration. However, the in vitro release rate of the 5-FU-loaded CS/Alg NPs was only related to the DFA, Alg concentration, and CS concentration and was independent of the poloxamer concentration. The time of 5-FU release from the CS/Alg NPs could be-controlled to be sustained for more than 12 h. According to this study, CS/Alg NPs stabilized by poloxamer could serve as a suitable candidate for the controlled release of 5FU. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 117: 2354-2359, 2010
引用
收藏
页码:2354 / 2359
页数:6
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