pH-sensitive controlled release of doxorubicin from polyelectrolyte multilayers

被引:28
|
作者
Wang, Lin [1 ]
Ren, Ke-feng [1 ]
Wang, Hai-bo [1 ]
Wang, Yin [1 ]
Ji, Jian [1 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金; 对外科技合作项目(国际科技项目); 高等学校博士学科点专项科研基金;
关键词
Controlled drug release; Doxorubicin; Hydrazone bond; Layer-by-layer assembly; pH-sensitive; DRUG-DELIVERY SYSTEM; BIOLOGICAL EVALUATION; FILMS; FABRICATION; NANOPARTICLES; MICELLES; PRODRUG; TUMORS;
D O I
10.1016/j.colsurfb.2014.11.017
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Controlled and stimulated release of small drug molecules from polyelectrolyte multilayers is still a challenge due to the limitations to incorporate and control the interactions between small molecules and multilayers. Herein we reported a facile method to fabricate polyelectrolyte multilayers with pH-sensitive controlled release of doxorubicin (DOX). A pH-responsive polyelectrolyte was prepared by conjugating DOX onto hyaluronan (HA) via pH-responsive hydrazone bond with an 8% grafting degree. The HA-DOX was then incorporated into the multilayers via the layer-by-layer assembly with poly-L-lysine (PLL). The growth of the multilayers was tracked by spectroscopic ellipsometry. The morphology and structure of the films were characterized by scanning electron microscopy and UV-vis spectroscopy, respectively. The in vitro drug release experiments indicated that the release of DOX was pH-dependent: there was almost no release at pH 7.4, while the releases were significantly promoted at pH 6.0 and 5.0. Furthermore, human hepatoma (HepG2) cells were remarkably inhibited under the conditions at pH 5.0 when they were cultured with the (HA-DOX/PLL) multilayers. The multilayers with the properties of pH-sensitive DOX release would be potentially applied to the biomedical devices for tumor treatments. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 133
页数:7
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