Introduction of cisplatin into polymeric micelle

被引:182
作者
Yokoyama, M [1 ]
Okano, T [1 ]
Sakurai, Y [1 ]
Suwa, S [1 ]
Kataoka, K [1 ]
机构
[1] SCI UNIV TOKYO,FAC IND SCI & TECHNOL,DEPT MAT SCI & TECHNOL,NODA,CHIBA 278,JAPAN
关键词
polymeric micelle; cisplatin; block copolymer; anticancer drug; drug delivery;
D O I
10.1016/0168-3659(95)00165-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cisplatin, an anticancer drug, was bound to aspartic acid residues of poly(ethylene glycol)-poly(aspartic acid) block copolymer (PEG-P(Asp)) by ligand substitution reaction at platinum atoms of cisplatin. At a molar ratio of cisplatin and the aspartic acid residue of 1:1, polymeric micelles were formed with an average diameter of 16 nm. A polymeric micelle fraction was easily purified by ultrafiltration, and a micellar structure of this fraction was stable in distilled water and NaCl solution at 37 degrees C for 24 h. The polymeric micelle showed 1/8 to 1/5 cytotoxicity of intact cisplatin against murine B 16 melanoma cells during 24-72 h incubation. This suggests release of platinum complexes from the micelle.
引用
收藏
页码:351 / 356
页数:6
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