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Study on Preparation of Silymarin Solid Lipid Nanoparicles and in vitro Release(PDF)

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2012年19期
Page:
175-178
Research Field:
Publishing date:

Info

Title:
Study on Preparation of Silymarin Solid Lipid Nanoparicles and in vitro Release
Author(s):
YU LianLIU Si-jiaDU YanPING YangHU Yan-qiuMA Li-na
Heilongjiang Key Lab of University,College of Pharmaceutical,Jiamusi University,Jiamusi,Heilongjiang 154007
Keywords:
silymarinsolid lipid nanoparticlesemulsification ultrasonic dispersion method
PACS:
S 567.9
DOI:
-
Abstract:
Taking monostearin lipid as material,soybean lecithin and poloxamer 188 as emulsifier,silymarin as a model drug,SM-SLN were prepared by the emulsification ultrasonic dispersion method.The particle size,morphology,encapsulation efficiency,drug loading,in vitro release and stability were studied.The results showed that morphology of SM-SLN was round and smooth,and the average particle size was 150.6 nm and encapsulation efficiency 85.3%.Emulsification ultrasonic dispersion method was suitable for SM-SLN preparation,with high encapsulation efficiency,uniform particle size distribution and better stability.

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Last Update: 2014-09-09