Biopharmaceutics & Drug Disposition · 1994 · 47 citations · 4 references
PharmacyPharmacokineticsPharmacologyBioavailabilityClinical PharmacologyDrug DeliveryDrug AbsorptionDrug DispositionOral BioavailabilityBioavailability Of Topical DrugsBioavailability Of Topical FormulationsConcentration ProfilesCutaneous AbsorptionInterindividual VariationOral Absorption AssessmentPharmacokinetics Of Topical DrugsTopical Application
The percutaneous absorption of diclofenac was studied in ten healthy volunteers treated with Emulgel containing 1.16% diclofenac diethylammonium for 8 d as follows: a single application of 5 g Emulgel on days 1 and 8, and two applications d-1 on days 2-7. Plasma concentration profiles of unchanged diclofenac and urinary concentrations of total diclofenac and metabolites (sum of free and conjugated) were determined. High inter-individual variations in plasma and urine data were recorded, due probably to the permeability and the hydration of the skin. Steady state was reached after 2 d of twice-daily administration. Plasma concentrations were low but remained in the range 10-50 nmol L-1 over the full day for most of the subjects, indicating prolonged absorption from the application site.
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Pharmacokinetics and Metabolism of the Anti-Inflammatory Agent Voltaren
H. Stierlin, P.H. Degen, J. W. Faigle et al. · Scandinavian Journal of Rheumatology · 1978 · 182 citations
A. Sioufi, F. Pommier, J. Godbillon · Journal of Chromatography B Biomedical Sciences and Applications · 1991 · 34 citations