期刊
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
卷 118, 期 -, 页码 1871-1879出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijbiomac.2018.07.036
关键词
Chitosan; Poly(methacrylic acid); pH-responsive; Graphene oxide; Drug delivery; Cancer chemotherapy
资金
- Tabriz Payame Noor University
- Tabriz University of Medical Sciences
The aim of this study was the design and development of a novel de novo drug delivery system for cancer chemotherapy. For this purpose, chitosan (CS) functionalized using phthalic anhydride followed by 4-cyano, 4-[(phenylcarbothioyl) sulfanyl] pentanoic acid as a chain transfer agent (CFA) to afford CS-CFA macroinitiator. The synthesized CS-CTA macroinitiator was then copolymerized with methacrylic acid (MAA) monomer using reversible addition-fragmentation chain transfer (RAFT) polymerization technique to produce chitosan-graftpoly(methacrylic acid) (CS-g-PMAA) graft copolymer. Afterward, graphene oxide (GO) nanosheets were incorporated into the synthesized copolymer through the physical interactions. The CS-g-PMAA/GO nanocomposite was loaded with doxorubicin hydrochloride (DOX) as a universal anticancer drug. The biocompatibility, DOXloading capacity, and pH dependent drug release behavior of the developed nanocomposite were also investigated. As the experimental results, as well as superior biological and physicochemical features of CS and GO, we envision that the developed CS-g-PMAA/GO nanocomposite may be applied as de novo drug delivery nanosystern for cancer chemotherapy. (C) 2018 Published by Elsevier B.V.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据