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Doxorubicin-loaded PEG-PCL copolymer micelles enhance cytotoxicity and intracellular accumulation of doxorubicin in adriamycin-resistant tumor cells
Author(s) -
Min Han,
Diao,
Fu,
Yulan Hu,
Jiang Jiang,
Tsutsumi,
Wei Nie,
Chen,
Jian-Qing Gao
Publication year - 2011
Publication title -
international journal of nanomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.245
H-Index - 128
eISSN - 1178-2013
pISSN - 1176-9114
DOI - 10.2147/ijn.s23099
Subject(s) - doxorubicin , micelle , cytotoxicity , multiple drug resistance , chemistry , drug delivery , materials science , pharmacology , biophysics , chemotherapy , in vitro , biochemistry , medicine , biology , organic chemistry , surgery , aqueous solution , antibiotics
Multidrug resistance remains a major obstacle to successful cancer chemotherapy. Some chemical multidrug resistance inhibitors, such as ciclosporin and verapamil, have been reported to reverse resistance in tumor cells. However, the accompanying side effects have limited their clinical application. In this study, we have developed a novel drug delivery system, ie, a polyethyleneglycol-polycaprolactone (PEG-PCL) copolymer micelle encapsulating doxorubicin, in order to circumvent drug resistance in adriamycin-resistant K562 tumor cells.

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