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Delivery of anticancer drug using pH-sensitive micelles from triblock copolymer MPEG-b-PBAE-b-PLA.
Yang, Chufen; Xue, Zhaolin; Liu, Yinglin; Xiao, Jiayu; Chen, Jingrui; Zhang, Lijuan; Guo, Jianwei; Lin, Wenjing.
Afiliação
  • Yang C; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, PR China.
  • Xue Z; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, PR China.
  • Liu Y; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, PR China.
  • Xiao J; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, PR China.
  • Chen J; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, PR China.
  • Zhang L; School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640, PR China.
  • Guo J; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, PR China.
  • Lin W; School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, PR China. Electronic address: jingjingfable@126.com.cn.
Mater Sci Eng C Mater Biol Appl ; 84: 254-262, 2018 Mar 01.
Article em En | MEDLINE | ID: mdl-29519437
To improve the drug release rate in well-controlled manner, a new pH-sensitive triblock amphiphilic copolymer methyl poly(ethylene glycol) ether-b-poly(ß-amino esters)-b-poly lactic acid (MPEG-b-PBAE-b-PLA) and its self-assembled micelles were developed for anticancer drug delivery. The average molecular weight and molecular structure of MPEG-b-PBAE-b-PLA were confirmed by gel permeation chromatography (GPC) and 1H NMR. The formation of self-assembled micelles, the microstructures at different pH values, and the distribution of doxorubicin (DOX) were investigated by dissipative particle dynamics (DPD) simulation combined with experimental techniques. The copolymers formed stable core-shell-type micelles in water. The critical micelle concentration (CMC) values, particle sizes and zeta potentials of the blank micelles increased along with globule-extended conformational transitions when the pH values decreased from 7.4 to 5.0, due to the protonation of amine groups of PBAE. Obvious increases in the particle sizes and the drug loading content of micelles were observed with increasing DOX. The in vitro release behavior of DOX from the micelles was pH-dependent. The DOX release rate was improved obviously as pH decreased from pH7.4 to pH5.0, with over 96% of DOX was released within 48h. The drug release mechanism under different conditions was also analyzed using theoretical formulas. All the results suggest that the pH-sensitive MPEG-b-PBAE-b-PLA micelles might be a prospective candidate as anticancer drug delivery carrier with well-controlled release behavior.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poliésteres / Polietilenoglicóis / Polímeros / Portadores de Fármacos / Micelas / Antineoplásicos Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mater Sci Eng C Mater Biol Appl Ano de publicação: 2018 Tipo de documento: Article País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poliésteres / Polietilenoglicóis / Polímeros / Portadores de Fármacos / Micelas / Antineoplásicos Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mater Sci Eng C Mater Biol Appl Ano de publicação: 2018 Tipo de documento: Article País de publicação: Holanda