Construction of pH-sensitive lysozyme/pectin nanogel for tumor methotrexate delivery

被引:76
|
作者
Lin, Liufeng [1 ,2 ]
Xu, Wei [1 ,2 ]
Liang, Hongshan [1 ,2 ]
He, Lei [1 ,2 ]
Liu, Shilin [1 ,2 ]
Li, Yan [1 ,2 ]
Li, Bin [1 ,2 ]
Chen, Yijie [1 ,2 ]
机构
[1] Huazhong Agr Univ, Coll Food Sci & Technol, Wuhan 430070, Peoples R China
[2] Huazhong Agr Univ, Key Lab Environm Correlat Dietol, Minist Educ, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
Biopolymer; Nanogels; Methotrexate; pH-sensitivity; Cytotoxicity; MESOPOROUS SILICA NANOPARTICLES; HEPATOMA-TARGETING DELIVERY; DRUG-DELIVERY; HEPATOCELLULAR-CARCINOMA; COPOLYMER MICELLES; CONTROLLED-RELEASE; ANTITUMOR-ACTIVITY; THERMAL-TREATMENT; CELLULAR UPTAKE; RECENT PROGRESS;
D O I
10.1016/j.colsurfb.2014.12.051
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Novel nano-particles were developed from lysozyme-pectin through self-assembly, and the nanogels could be used as a carrier for the antitumor agent, methotrexate (MTX). The nanogels exhibited spherical with diameters about 109 +/- 2 nm and narrow particle size distribution, as well as negative surface charge. Furthermore, the particle size and morphology of the nanogels hardly changed with the incorporation of MTX. The loading capacity of MTX in nanogels could reach 17.58 +/- 0.85%. MTX-loaded nanogels were pH-dependent, accelerated release of MTX at a decreasing pH from 7.4 to 5.3. The MU assay indicated that encapsulated MTX exhibited higher anticancer activity than free MTX. Meanwhile, MTX-loaded nanogels could be effectively endocytosed by HepG2 cells, resulting in enhanced cancer-cell apoptosis comparing to free MTX. It indicated that the nanogels had good biocompatibility and low toxicity. The obtained nanogels had great potential in the development of a new nanocarrier for anti-cancer drug delivery. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:459 / 466
页数:8
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