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Org Biomol Chem ; 17(22): 5570-5577, 2019 06 05.
Artigo em Inglês | MEDLINE | ID: mdl-31114827

RESUMO

Nano drug delivery is a promising domain in biomedical theranostics and has aroused more and more attention in recent years. We report here an amphiphilic polymer TPG1, bearing a H2O2-sensitive benzil and an AIE fluorophore tetraphenylethene (TPE) unit, which is able to self-assemble into spherical nanosized micelles in aqueous solution. Doxorubicin (DOX) can be encapsulated into TPG1 micelles efficiently with the loading capability of up to 59% by weight. The benzil moiety could be cleaved via the Baeyer-Villiger type reaction in the presence of H2O2, leading to the decomposition of TPG1 micelles and release of DOX. In vitro studies indicated that DOX-loaded TPG1 micelles can be internalized by cancer cells, followed by unloading encapsulated DOX under the stimulation of H2O2. The drug release process can be monitored by the AIE fluorescence from the degradation products containing a TPE moiety. MTT assays against HeLa and HepG2 cancer cells demonstrated that DOX-loaded micelles showed good anticancer efficacy. The polymer TPG1 and the corresponding decomposed products showed great biocompatibility. Our data suggest that TPG1 has the potential to be employed for the controlled drug delivery system.


Assuntos
Doxorrubicina/farmacologia , Sistemas de Liberação de Medicamentos , Corantes Fluorescentes/química , Peróxido de Hidrogênio/farmacologia , Fenilglioxal/análogos & derivados , Polímeros/farmacologia , Estilbenos/química , Sobrevivência Celular/efeitos dos fármacos , Doxorrubicina/química , Portadores de Fármacos/química , Portadores de Fármacos/farmacologia , Células HeLa , Células Hep G2 , Humanos , Peróxido de Hidrogênio/química , Micelas , Estrutura Molecular , Imagem Óptica , Fenilglioxal/química , Fenilglioxal/farmacologia , Polímeros/química
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