LIPID MICROSPHERES FOR DRUG-DELIVERY FROM THE PHARMACEUTICAL VIEWPOINT

被引：1
|
作者：
YAMAGUCHI, T [1 ]
MIZUSHIMA, Y [1 ]
机构：
[1] ST MARIANNA UNIV,SCH MED,INST MED SCI,MIYAMAE KU,KAWASAKI,KANAGAWA 216,JAPAN
来源：
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS | 1994年 / 11卷 / 04期
关键词：
LIPID MICROSPHERE; DRUG DELIVERY; PROSTAGLANDIN E(1); LIPO-PGE(1); TARGETING;
D O I：
暂无
中图分类号：
R9 [药学];
学科分类号：
1007 ;
摘要：
Lipid microsphere (LM) preparations of corticosteroid, nonsteroid, anti-inflammatory drugs and prostaglandins all showed more potent activity than free drugs. The LM, with a diameter of 0.2 mu m, were drug carriers prepared from soybean oil and lecithin, with the drug being incorporated within the LM. This study suggests that the LM is a very promising carrier in a drug delivery system. Future trends in this field are outlined, followed by a discussion of physicochemical properties in the evaluation of novel emulsion delivery systems.
引用
收藏
页码：215 / 229
页数：15
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