Nanostructured lipid carriers for oral delivery of baicalin: In vitro and in vivo evaluation

被引:66
作者
Luan, Jingjing [1 ]
Zheng, Fang [1 ]
Yang, Xiaoye [1 ]
Yu, Aihua [1 ]
Zhai, Guangxi [1 ]
机构
[1] Shandong Univ, Coll Pharm, Dept Pharmaceut, Jinan 250012, Peoples R China
关键词
Baicalin; Nanostructured lipid carriers; Uniform design; Bioavailability; Pharmacokinetics; NANOPARTICLES; BIOAVAILABILITY; FORMULATION;
D O I
10.1016/j.colsurfa.2014.11.015
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The present study aimed to develop a novel baicalin-loaded nanostructured lipid carrier (BA-NLC) system for oral delivery to enhance the bioavailability. BA-NLC were prepared by emulsion-evaporation and low temperature-solidification technique and optimized by a five-factor four-level uniform design. The characteristics of BA-NLC including morphology, particle size, zeta potential, entrapment efficiency and drug loading were investigated. The results showed that the optimized BA-NLC was nearly spherical in shape with a mean diameter of 244.7 nm. The entrapment efficiency and drug loading were 59.51 +/- 0.57% and 3.54 perpendicular to 0.11%, respectively. In vitro drug release revealed a pattern with burst release initially and sustained release afterwards for BA-NLC. Moreover, BA-NLC exhibited prolonged MRT and increased AUC compared to pure BA. All the detailed evidence indicated that BA-NLC could be a potential delivery system for the oral administration of BA. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:154 / 159
页数:6
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