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Self‐assembled UCST‐Type Micelles as Potential Drug Carriers for Cancer Therapeutics
Author(s) -
Huang Gang,
Li Hao,
Feng ShiTing,
Li Xiaoqiong,
Tong Guoquan,
Liu Jie,
Quan Changyun,
Jiang Qing,
Zhang Chao,
Li Ziping
Publication year - 2015
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201400546
Subject(s) - micelle , upper critical solution temperature , copolymer , polymer chemistry , amphiphile , chemistry , ethylene glycol , drug delivery , drug carrier , polymer , hydrophobic effect , chemical engineering , materials science , aqueous solution , organic chemistry , lower critical solution temperature , engineering
A methoxy‐poly(ethylene glycol)‐ block ‐poly(acrylamide‐ co ‐acrylonitrile) (mPEG‐ b ‐P(AAm‐ co ‐AN)) amphiphilic copolymer exhibiting upper critical solution temperature (UCST) behavior is synthesized, and micelles from this copolymer are fabricated. It is found that the thermal responses of these micelles are tunable through balancing the hydrophobic/hydrophilic blocks in the copolymer. The size of the doxorubicin (DOX)‐loaded micelles is dependent on the hydrophobic interaction as well as hydrogen bonding between polymer and drug molecules. As a proof of concept, the drug release behavior is studied in vitro, and the cumulative release of DOX increases at temperature above the UCST of blank micelles. 3‐(4,5‐dimethyl‐thiazol‐2‐yl)‐2,5‐diphenyl tetrazolium bromide (MTT) assays indicate that these polymers are non‐toxic towards human hepatic carcinoma cells (Bel 7402 cells) as well as human embryonic hepatocytes (L02 cells). DOX‐loaded micelles could effectively enter Bel 7402 cells in 2 h, and display much lower half inhibitory concentration compared with free DOX. These micelles may be exploited as a promising drug carrier for cancer therapeutics.