Drugs-in-cyclodextrins-in liposomes: a novel concept in drug delivery
- 5 December 1994
- journal article
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 112 (3), 249-258
- https://doi.org/10.1016/0378-5173(94)90361-1
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Coupling of ligands to liposomes independently of solute entrapment: observations on the formed vesiclesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1993
- New Generation VaccinesPublished by Springer Nature ,1993
- Effect of the complexation of some nonsteroidal anti-inflammatory drugs with β-cyclodextrin on the interaction with phosphatidylcholine liposomesInternational Journal of Pharmaceutics, 1992
- Improvement of the in vitro dissolution characteristics of famotidine by inclusion in β-cyclodextrinInternational Journal of Pharmaceutics, 1990
- β-Cyclodextrin as an excipient in solid oral dosage forms: in vitro and in vivo evaluation of spray-dried diazepam-β-cyclodextrin productsInternational Journal of Pharmaceutics, 1989
- Dehydration-Rehydration Vesicles: A Simple Method for High Yield Drug Entrapment in LiposomesNature Biotechnology, 1984
- The effect of lipid composition of small unilamellar liposomes containing melphalan and vincristine on drug clearance after injection into miceBiochemical Pharmacology, 1983
- Cyclodextrin-induced hemolysis and shape changes of human erythrocytes in vitro.Journal of Pharmacobio-Dynamics, 1982
- Plasma-induced release of solutes from small unilamellar liposomes is associated with pore formation in the bilayersBiochemical Journal, 1981
- Inclusion CompoundsJournal of Pharmaceutical Sciences, 1975