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Lipid microspheres as novel drug carriers.

作者信息

Mizushima Y

机构信息

Department of Internal Medicine, St. Marianna University, Kawasaki, Japan.

出版信息

Drugs Exp Clin Res. 1985;11(9):595-600.

PMID:3880046
Abstract

Lipid microsphere preparations of corticosteroid, non-steroid anti-inflammatory drugs and prostaglandin E1 (PGE1) all showed more potent activity than the free drugs. Lipo-PGE1 in particular was significantly more active than free PGE1 at about one-tenth the dose of free PGE1. A large mass of data obtained in studies of liposomes suggest many applications for the lipid microsphere, which is considered to be a very promising carrier in drug delivery systems.

摘要

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