Complexation study and anticellular activity enhancement by doxorubicin-cyclodextrin complexes on a multidrug-resistant adenocarcinoma cell line

被引:37
作者
Al-Omar, A
Abdou, S
De Robertis, L
Marsura, A
Finance, C
机构
[1] Univ Nancy 1, Fac Sci Pharmaceut & Biol, CNRS, UMR, F-54001 Nancy, France
[2] Ctr Etud & Rech Macromol Vegetales, CNRS, UPR 5301, F-38041 Grenoble 9, France
关键词
D O I
10.1016/S0960-894X(99)00150-X
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Ability of molecular complexes of [Doxorubicin (DX)-cyclodextrin (Cd)] to enhance the anticellular activity of antineoplasic drug Doxorubicin and to reverse its multidrug resistance has been investigated. A spectroscopic study of the alpha,beta, and gamma-[DX-Cds] complexes has been investigated in relation to their biological effects on a multidrug resistant (MDR) human rectal adenocarcinoma cell line (HRT-18). A ten fold enhancement of DX anticellular activity in presence of beta-cyclodextrin alone was detected, (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1115 / 1120
页数:6
相关论文
共 14 条
[11]  
PEREZSOLER R, 1990, CANCER RES, V50, P4260
[12]   ADRIAMYCIN STIMULATES LOW-AFFINITY CA-2+ BINDING AND LIPID-PEROXIDATION BUT DEPRESSES MYOCARDIAL-FUNCTION [J].
SINGAL, PK ;
PIERCE, GN .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 250 (03) :H419-H425
[13]   CURE OF XENOGRAFTED HUMAN CARCINOMAS BY BR96-DOXORUBICIN IMMUNOCONJUGATES [J].
TRAIL, PA ;
WILLNER, D ;
LASCH, SJ ;
HENDERSON, AJ ;
HOFSTEAD, S ;
CASAZZA, AM ;
FIRESTONE, RA ;
HELLSTROM, I ;
HELLSTROM, KE .
SCIENCE, 1993, 261 (5118) :212-215
[14]  
WARREN L, 1992, CANCER RES, V52, P3241