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pH-Responsive Micelles Assembled by Three-Armed Degradable Block Copolymers with a Cholic Acid Core for Drug Controlled-Release.
Feng, Jingjie; Wen, Weiqiu; Jia, Yong-Guang; Liu, Sa; Guo, Jianwei.
Afiliación
  • Feng J; School of Chemical Engineering & Light Industry, Guangdong University of Technology, Guangzhou 510006, China. fjj121036@163.com.
  • Wen W; School of Chemical Engineering & Light Industry, Guangdong University of Technology, Guangzhou 510006, China. 15024028760@163.com.
  • Jia YG; School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, China. ygjia@scut.edu.cn.
  • Liu S; School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, China. sliu@scut.edu.cn.
  • Guo J; School of Chemical Engineering & Light Industry, Guangdong University of Technology, Guangzhou 510006, China. guojw@gdut.edu.cn.
Polymers (Basel) ; 11(3)2019 Mar 18.
Article en En | MEDLINE | ID: mdl-30960495
ABSTRACT
One of the most famous anticancer drugs, paclitaxel (PTX), has often been used in drug controlled-release studies. The polymers derived from bio-compound bile acids and degradable poly(ε-caprolactone) (PCL) form a reservoir and have been used as a drug delivery system with great advantages. Herein, we grafted poly(N,N-diethylaminoethyl methacrylate) and poly(poly(ethylene glycol) methyl ether methacrylate) into the bile acid-derived three-armed macroinitiator CA-(PCL)3, resulting in the amphiphilic block copolymers CA-(PCL-b-PDEAEMA-b-PPEGMA)3. These pH-responsive three-armed block copolymers self-assembled into micelles in aqueous solution and PTX was encapsulated into the micellar core to form PTX-loaded micelles with a drug loading of 29.92 wt %. The micelles were stable in PBS at pH 7.4 and showed a pH-triggered release behavior of PTX under acidic environments, in which 55% of PTX was released at pH 5.0 in 80 h. These cholic acid-based functionalized three-armed block polymers present good biocompatibility, showing great potential for drug controlled-release.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Polymers (Basel) Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Polymers (Basel) Año: 2019 Tipo del documento: Article País de afiliación: China