Self-Assembled Nanoparticles Based on Amphiphilic Anticancer Drug-Phospholipid Complex for Targeted Drug Delivery and Intracellular Dual-Controlled Release

被引:66
作者
Li, Yang [1 ,2 ]
Lin, Jinyan [1 ,2 ]
Yang, Xiangrui [1 ]
Li, Yanxiu [1 ]
Wu, Shichao [1 ]
Huang, Yu [1 ]
Ye, Shefang [1 ]
Xie, Liya [3 ]
Dai, Lizong [1 ]
Hou, Zhenqing [1 ]
机构
[1] Xiamen Univ, Coll Mat, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Affiliated Hosp 1, Xiamen 361002, Peoples R China
基金
中国国家自然科学基金;
关键词
anticancer-phospholipid complex; self-assembly; nanoparticles; targeted drug delivery; sustained/controlled drug release; FUNCTIONALIZED NANOSCALE MICELLES; PLA HYBRID NANOPARTICLES; MITOMYCIN-C; TUMOR-CELLS; THERAPEUTICS; METHOTREXATE; INHIBITORS; EFFICACY; PRODRUG;
D O I
10.1021/acsami.5b05038
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Integrating advantages of mitomycin C (MMC)-phospholipid complex for increased drug encapsulation efficiency and reduced premature drug release, DSPE-PEG-folate (DSPE-PEG-FA) for specific tumor targeting, we reported a simple one-pot self-assembly route to prepare the MMC- phospholipid complex-loaded DSPE-PEG-based nanoparticles (MP-PEG-FA NPs). Both confocal imaging and flow cytometry demonstrated that MMC was distributed into nuclei after cellular uptake and intracellular drug delivery. More importantly, the systemically administered MP-PEG-FA NPs led to increased blood persistence and enhanced tumor accumulation in He La tumor-bearing nude mice. This study introduces a simple and effective strategy to design the anticancer drug phospholipid complex-based targeted drug delivery system for sustained/controlled drug release.
引用
收藏
页码:17573 / 17581
页数:9
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