Liposomal retention of a modified anti-inflammatory steroid
- 15 August 1976
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 158 (2) , 473-476
- https://doi.org/10.1042/bj1580473
Abstract
In studies with synthetic lecithins, dipalmitoylphosphatidylcholine was found to be the preferred form for liposomal retention of cortisol esters at 37 degrees C. Cortisol palmitate was retained longer than cortisol octanoate, whereas unesterified cortisol escaped readily from liposomes. Such a liposome composition may allow the controlled release of modified anti-inflammatory agents, particularly when used for intra-articular administration.This publication has 8 references indexed in Scilit:
- Tilted hydrocarbon chains of dipalmitoyl lecithin become perpendicular to the bilayer before meltingBiophysical Journal, 1975
- Liposomes as Vehicles for the Local Release of DrugsClinical Science, 1975
- DRUG-CARRIER POTENTIAL OF LIPOSOMES IN CANCER CHEMOTHERAPYThe Lancet, 1974
- Preparation and prolonged tissue retention of liposome-encapsulated chelating agents.1974
- Effects of intra-articular corticosteroids in vivo on synovial fluid variables in rheumatoid synovitis.Annals of the Rheumatic Diseases, 1974
- Lateral phase separation in phospholipid membranesBiochemistry, 1973
- Enzyme entrapment in liposomesFEBS Letters, 1971
- High-efficiency liquid-scintillation counting of 14C-labelled material in aqueous solution and determination of specific activity of labelled proteinsBiochemical Journal, 1965