Targeting delivery of tocopherol and doxorubicin grafted-chitosan polymeric micelles for cancer therapy: In vitro and in vivo evaluation

被引:45
|
作者
Nam, Joung-Pyo [1 ]
Lee, Kyeong-Jae [1 ]
Choi, Joung-Woo [2 ]
Yun, Chae-Ok [2 ]
Nah, Jae-Woon [1 ]
机构
[1] Sunchon Natl Univ, Dept Polymer Sci & Engn, Coll Engn, Sunchon, Jeollanam Do, South Korea
[2] Hanyang Univ, Dept Bioengn, Coll Engn, Seoul 133791, South Korea
基金
新加坡国家研究基金会;
关键词
Chitosan; Doxorubicin; pH-sensitive; Targeted delivery; VITAMIN-E; MULTIDRUG-RESISTANCE; COPOLYMER MICELLES; BLOCK-COPOLYMER; GENE DELIVERY; STEARIC ACID; NANOPARTICLES; SUCCINATE; CARRIERS;
D O I
10.1016/j.colsurfb.2015.06.018
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this study, we report the development of a novel, redox-sensitive chitosan-based targeted drug delivery system, containing two drugs. We determined whether the synthesized polymeric micelles (HPTOC-DOX) were suitable as a drug carrier. The formation of HPTOC-DOX micelles was confirmed by H-1 NMR. HPTOC-DOX formed micelles of approximately 151.9 similar to 311.2 nm in size in aqueous solution. Analysis of the drug release profile of HPTOC-DOX in different pH conditions (pH 5.2, 6.2, and 7.4) indicated that DOX was released from HPTOC-DOX micelles at acidic pH (5.2 or 6.2), while almost no DOX was released at pH 7.4. In vitro cell cytotoxicity and hemolysis assays indicated that HPTOC-DOX micelles safely deliver anti-cancer drugs and decrease the cytotoxicity of DOX. In vitro anti-cancer activity assays, confocal laser scanning microscopy analysis of SK-BR-3 cells, and in vivo anti-tumor activity in SK-BR-3-derived tumor-bearing mice were used to evaluate synergistic drug effects and the effect of the targeting peptide (anti-human epidermal growth factor receptor 2 [HER2] target peptide, epitope form; LTVSPWY) on receptor-mediated endocytosis. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:254 / 262
页数:9
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