Folate-functionalized nanoparticles for controlled ergosta-4,6,8(14),22-tetraen-3-one delivery

被引:11
作者
Liang, Xuhua [1 ]
Sun, Yang [2 ]
Liu, Lusha [1 ]
Ma, Xuan [1 ]
Hu, Xiaoyun [3 ]
Fan, Jun [1 ]
Zhao, Yingyong [4 ]
机构
[1] NW Univ Xian, Sch Chem Engn, Xian 710069, Shaanxi, Peoples R China
[2] Xian Univ Arts & Sci, Dept Chem & Chem Engn, Xian 710059, Peoples R China
[3] NW Univ Xian, Dept Phys, Xian 710069, Shaanxi, Peoples R China
[4] NW Univ Xian, Biomed Key Lab Shaanxi Prov, Xian 710069, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Ergosta-4,6,8(14),22-tetraen-3-one (ergone); Nanoparticles; Folate receptor; Targeted therapeutics; Slow release capacity; Anticancer; BIOLOGICAL EVALUATION; CELLS;
D O I
10.1016/j.ijpharm.2012.12.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To improve the therapeutic effect of ergosta-4,6,8(14),22-tetraen-3-one (ergone), a folate-decorated ergone-bovine serum albumin nanoparticles (abbreviated FA-ergone-BSANPs) was prepared. The properties were extensively studied by Zetasizer Nano Particle Size Analyzer and TEM, which indicated the prepared nanoparticles were spherical in shape and uniform in size with a zeta potential of -23.8 mV. The drug-loading capacity also has been determined with drug loading content of 2.73% and encapsulation efficiency of 61.8%. In vitro release studies proved the much slow drug release from the nanoparticles during circulating in the blood stream and the increase of drug release at the target sites. The FA-ergone-BSANPs showed enhanced cellular uptake, increased targeting capacity, and increased cytotoxicity against KB cells over-expressing folate receptor (FR), which indicated that its potent cell-killing activity is specific for cells that express the FR. In vivo experiment also confirmed that FA-ergone-BSANPs represent a FR-targeted chemotherapeutic that can produce potent activity against FR-positive tumors. In conclusion, this report has a great significance in pharmacology and clinical medicine as well as methodology. Further detailed dose-optimization studies will be required for better understanding in vivo pharmacokinetic and bio-distribution behaviors. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
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