| Autor: |
Tu, Xiao‐Yan, Meng, Chao, Wang, Yun‐Fei, Ma, Li‐Wei, Wang, Bao‐Yan, He, Jin‐Lin, Ni, Pei‐Hong, Ji, Xiang‐Ling, Liu, Ming‐Zhu, Wei, Hua |
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| Zdroj: |
Macromolecular Rapid Communications; Mar2018, Vol. 39 Issue 5, p1-1, 8p |
| Abstrakt: |
Abstract: Adaptation of cyclic brush polymer for drug delivery applications remains largely unexplored. Herein, cyclic brush copolymer of poly(2‐hydroxyethyl methacrylate‐g‐poly(N‐isopropylacrylamide‐st‐N‐hydroxyethylacrylamide)) (cb‐P(HEMA‐g‐P(NIPAAm‐st‐HEAAm))), comprising a cyclic core of PHEMA and thermosensitive brushes of statistical copolymer of P(NIPAAm‐st‐HEAAm), is designed and synthesized successfully via a graft‐from approach using atom transfer free radical polymerization from a cyclic multimacroinitiator. The composition of the brush is optimized to endow the resulting cyclic brush copolymer with a lower critical solution temperature (LCST) slightly above the physiological temperature, but lower than the localized temperature of tumor tissue, which is suitable for the hyperthermia‐triggered anticancer drug delivery. Critical aggregation concentration determination reveals better stability for the unimolecular nanoparticle formed by the cyclic brush copolymer than that formed by the bottlebrush analogue. The dramatically increased size with elevated temperatures from below to above the LCST confirms hyperthermia‐induced aggregation for both formulations. Such structural destabilization promotes significantly the drug release at 40 °C. Most importantly, the drug‐loaded cyclic brush copolymer shows enhanced in vitro cytotoxicity against HeLa cells than the bottlebrush counterpart. The better stability and higher therapeutic efficacy demonstrates that the thermosensitive cyclic brush copolymer is a better formulation than bottle brush copolymer for controlled drug release applications. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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