Antitumor activity of adriamycin-incorporated polymeric micelles of poly(γ-benzyl L-glutamate)/poly(ethylene oxide)

被引:28
作者
Jeong, Young-Il [2 ]
Na, Hee-Sam [1 ]
Cho, Kyoung-Oh [3 ]
Lee, Hyun-Chul [1 ]
Nah, Jae-Woon [2 ]
Cho, Chong-Su [4 ]
机构
[1] Chonnam Natl Univ, Sch Med, Dept Microbiol, Kwangju 501746, South Korea
[2] Sunchon Natl Univ, Dept Polymer Sci & Engn, Jeonnam 540742, South Korea
[3] Chonnam Natl Univ, Coll Vet Med, Biotherapy Human Resources Ctr, Kwangju 500757, South Korea
[4] Seoul Natl Univ, Dept Agr Biotechnol, Seoul 151921, South Korea
关键词
Polymeric micelle; Adriamycin; Multiblock copolymer; CT 26 colon carcinoma; Antitumor activity; BLOCK-COPOLYMER MICELLES; POLY(ETHYLENE OXIDE); TUMOR ACCUMULATION; TRIBLOCK COPOLYMER; ANTICANCER DRUG; RELEASE; PHASE; ACID); NANOPARTICLES; L-ASPARTATE);
D O I
10.1016/j.ijpharm.2008.08.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The multiblock copolymer composed of poly(gamma-benzyl L-glutamate) (PBLG) and poly(ethylene oxide) (PEO) was synthesized to prepare polymeric micelles as an anticancer drug carrier. Adriamycin (ADR) used as an anticancer drug was incorporated into the polymeric micelles prepared by the multiblock copolymer. The higher the drug feeding ratio, the higher the drug loading contents and the lower the drug loading efficiency. The increased drug feeding ratio resulted in increased particle sizes. At all of the formulations, particle sizes were less than 150 nm. The particles were observed as spherical shapes. ADR release from ADR-loaded polymeric micelles in vitro was decreased with an increased drug loading contents. In in vitro antitumor activity test using CT 26 tumor cells, polymeric micelles showed almost similar cytotoxicity when compared to ADR itself while polymeric micelles themselves did not affect cytotoxicity. In in vivo antitumor activity test using mice tumor xenograft model, the polymeric micelles showed improved survivability of mice with minimized weight changes and excellent tumor growth suppression efficacy. Polymeric micelles of the multiblock copolymer suggested to be a good candidate for anticancer drug delivery carrier. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:150 / 156
页数:7
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