Control of adriamycin cytotoxic activity using thermally responsive polymeric micelles composed of poly(N-isopropylacrylamide-co-N,N-dimethylacrylamide)-b-poly(D,L-lactide)

被引:119
|
作者
Kohori, F
Sakai, K
Aoyagi, T
Yokoyama, M
Yamato, M
Sakurai, Y
Okano, T
机构
[1] Waseda Univ, Dept Appl Chem, Shinjuku Ku, Tokyo 1698555, Japan
[2] Tokyo Womens Med Univ, Inst Biomed Engn, Shinjuku Ku, Tokyo 1628666, Japan
关键词
poly(N-isopropylacrylamide); poly(D; L-lactide); thermal response; polymeric micelles; adriamycin; cytotoxicity;
D O I
10.1016/S0927-7765(99)00070-3
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Adriamycin (ADR)-loaded thermally responsive polymeric micelles composed of poly(N-isopropylacrylamide-co-N,N-dimethylacrylamide)-b-poly(D,L-lactide were prepared by dialysis from its dimethylacetamide solution against water. Microfiltration was successfully applied to removal of block copolymer associates, which were smaller than micellar structures. By this microfiltration polymeric micelles showing a lower critical solution temperature (LCST) at 40 degrees C in phosphate buffered saline was obtained with a monodispersed size distribution of 69.2 nm in cumulant average diameter. ADR-loaded micelles released more ADR at 42.5 degrees C (above the LCST) than at 37 degrees C (below the LCST). ADR-loaded micelles did not show much cytotoxic activity against bovine aorta endothelial cells at 37 degrees C, in contrast to high cytotoxicity at 42.5 degrees C. On the other hand, free ADR expressed high cytotoxicity at both the incubation temperatures. Thus, thermally responsive polymeric micelles showed distinct control of ADR cytotoxic activity by temperature, while free ADR did not. From these results, an effective target therapy against solid tumors is feasible for these polymeric micelles by a combination of selective delivery to tumor sites based on stable micellar structures at 37 degrees C and enhanced cytotoxic activity of these drug-loaded micelles at 42.5 degrees C by local heating at tumor sites. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:195 / 205
页数:11
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