期刊
MACROMOLECULAR RAPID COMMUNICATIONS
卷 29, 期 16, 页码 1410-1414出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.200800137
关键词
drug delivery systems; micelles; nanoparticles; nanopump; self-assembly
资金
- National Natural Science Foundation of China [50625310, 20774051]
Complex micelles were obtained from PS-b-PNIPAM-b-PAA micelles and PEG-b-P4VP block copolymers via the strong electrostatic interaction and hydrogen bonding between PAA and P4VP blocks in water. The PS block formed the core and the PAA/P4VP complex shell functioned as a semi-permeable membrane which could control the permeation of small molecules. Between the core and shell, the large fluid-filled space that was formed with the thermoresponsive PNIPAM gel could retain the loaded drug for a long period of time. With increasing temperature, the shrinkage of the PNIPAM coils pumped the drug out of the complex micelles. The complex micelles functioned as a contractive nanopump, which could potentially be applied as a thermosensitive controlled release system.
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