Improved transdermal delivery of prostaglandin E1 through hairless mouse skin: combined use of carboxymethyl-ethyl-β-cyclodextrin and penetration enhancers
Author:
Affiliation:
1. Faculty of Pharmaceutical Sciences, Kumamoto University, 5–1 Oe-honmachi, Kumamoto 862, Japan
2. Research Laboratories, Hisamitsu Pharmaceutical Co. Inc., 408 Tashiro, Tosu, Saga 841, Japan
Abstract
Publisher
Oxford University Press (OUP)
Subject
Pharmaceutical Science,Pharmacology
Link
http://academic.oup.com/jpp/article-pdf/44/2/119/37243900/j.2042-7158.1992.tb03574.x.pdf
Reference14 articles.
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2. Lipid-protein-partitioning (LPP) theory of skin enhancer activity: finite dose technique;Goodman;Int. J. Pharm.,1989
3. An in vitro method for studying percutaneous absorption;Loveday;J. Soc. Cosm. Chem.,1961
4. Prostaglandin E1 is more effective, when incorporated in lipid microspheres, for treatment of peripheral vascular diseases in man;Mizushima;J. Pharm. Pharmacol.,1983
5. Kinetics of dehydration and isomerization of prostaglandins E1 and E2;Monkhouse;J. Pharm. Sci.,1973
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