期刊
MACROMOLECULES
卷 52, 期 5, 页码 1965-1975出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.9b00144
关键词
-
资金
- National Natural Science Foundation of China [21704095, 21525420, 21774113]
Stimuli-responsive polymeric vesicles have attracted great attention in drug delivery due to their intrinsic hollow structures and on demand release of drugs upon environmental stimuli. The drug-release kinetics from polymeric vesicles, which is usually dependent on the stimuli-responsive behaviors of the polymeric vesicle, has great impacts on the therapeutic efficacy. Over the past decade, polymerization-induced self-assembly (PISA) has been demonstrated to be a powerful strategy to prepare the polymeric vesicles. However, fabrication of stimuli-responsive vesicles with adjustable drug release kinetics via PISA has been rarely reported, which may be due to the poor selectivity of functional membrane-forming polymers in the PISA system. Herein, a series of vesicles with different pH-responsive behaviors were fabricated via RAFT dispersion copolymerization of (diisopropylamino)ethyl methacrylate (DIPEMA) and benzyl methacrylate (BzMA). Both the content of DIPEMA units in hydrophobic P(DIPEMA-co-BzMA) blocks and the DP of P(DIPEMA-co-BzMA) have great influence on the pH-responsive behaviors of the vesicles, which can be used to adjust the responsive release rate of RhB from the vesicles upon the same pH switch.
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