Rat percutaneous transport of diclofenac and influence of hydrogenated soya phospholipids.
- 1 January 1987
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 35 (9), 3807-3812
- https://doi.org/10.1248/cpb.35.3807
Abstract
Poor penetration of diclofenac through in vitro rat dorsal skin including subcutaneous tissue was observed. The poor penetration of diclofenac seemed to be predominantly due to the poor permeability of the stratum corneum. Hydrogenated soya phospholipids (phospholipid) in aqueous gel form increased the penetration of diclofenac in the in vitro study, by increasing diclofenac transport through the stratum corneum. In the in vivo percutaneous absorption of diclofenac, the presence of phospholipid in aqueous gel form increased both plasma diclofenac concentration and diclofenac accumulation in the dorsal skin tissues, including subcutaneous tissue. Since a marked accumulation of diclofenac in the subcutaneous tissue after application of the aqueous gel was observed both in vivo and in vitro, percutaneous application of diclofenac in the aqueous gel form, prepared with phospholipid, may be available for topical treatment rather than for systemic treatment.This publication has 2 references indexed in Scilit:
- Sustained-release of sodium diclofenac from suppositoryInternational Journal of Pharmaceutics, 1985
- Rectal delivery of antiinflammatory drugs. I. The influence of antiinflammatory drugs on rectal absorption of .BETA.-lactam antibiotics.CHEMICAL & PHARMACEUTICAL BULLETIN, 1981