NGR-modified pH-sensitive liposomes for controlled release and tumor target delivery of docetaxel

被引:22
|
作者
Gu, Zili [1 ]
Chang, Minglu [1 ]
Fan, Yang [1 ]
Shi, Yanbin [2 ]
Lin, Guimei [1 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, 44 West Wenhua Rd, Jinan 250012, Shandong, Peoples R China
[2] Qilu Univ Technol, Sch Mech & Automot Engn, Jinan 250353, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Docetaxel; Long circulation; NGR; pH-sensitive liposomes; Tumor targeting; PROTEIN DELIVERY; DRUG-DELIVERY; NANOPARTICLES; SYSTEM;
D O I
10.1016/j.colsurfb.2017.09.052
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
As current tumor chemotherapy faces many challenges, it is important to develop drug delivery systems with increased tumor-targeting ability, enhanced therapeutic effects and reduced side effects. In this study, a pH-sensitive liposome was constructed containing CHEMS-anchored PEG2000 for extended circulation and NGR peptide as the targeting moiety. The NGR-modified docetaxel-loaded pH-sensitive extended-circulation liposomes (DTX/NGR-PLL) prepared possess suitable physiochemical properties, including particle size of approximately 200 nm, drug encapsulation efficiency of approximately 70%, and pH-sensitive drug release properties. Experiments performed in vitro and in vivo on human fibrosarcoma cells (HT-1080) and human breast adenocarcinoma cells (MCF-7) verified the specific targeting ability and enhanced antitumor activity to HT-1080 cells. The results of intravenous administration demonstrated that NGR-modified liposomes can significantly and safely accumulate in tumor tissue in xenografted nude mice. In conclusion, the liposomes constructed hold promise as a safe and efficient drug delivery system for specific tumor treatment. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:395 / 405
页数:11
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