Chronopharmacokinetics of Cyclosporine A in the Wistar rat following oral administration
Autor: | S. Moussamih, K Kabbaj, I. Houti, A. Batalla, Jean Oustrin, Christian Labat, Malmary Mf |
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Rok vydání: | 1992 |
Předmět: |
Male
Pharmacology Time Factors Clinical chemistry Chemistry Radioimmunoassay Administration Oral Biological Availability Absorption (skin) Intestinal absorption Rats Intestinal Absorption Pharmacokinetics Oral administration Cyclosporine Animals Pharmacology (medical) Centrifugation Dosing Rats Wistar |
Zdroj: | European Journal of Drug Metabolism and Pharmacokinetics. 17:135-144 |
ISSN: | 2107-0180 0378-7966 |
DOI: | 10.1007/bf03188782 |
Popis: | The pharmacokinetics of Cyclosporine A (CsA) was studied in male Wistar rats weighting 300 +/- 50 g trained to a 12:12 light-dark cycle. Oral administration (40 mg/kg) was performed at 1 of 4 different temporal stages: 09.00 h, 15.00 h, 21.00 h or 03.00 h (local time) i.e. 0200, 0800, 1400 or 2000 HALO (hours after light on). Blood samples were collected over 72-96 h after dosing, plasma was separated by centrifugation at 37 degrees C and stored frozen until assay, using radioimmunoassay (RIA). Two experiments were performed: the first with 4 groups of 48 rats and a non-specific polyclonal antibody (P-RIA); and the second with only 2 groups of 48 rats and a more specific monoclonal antibody (M-RIA). Plasma concentration data were evaluated with model-based linear pharmacokinetic concepts, with apparent zero-order or first-order absorption and n-exponential disposition (n = 1, 2 or 3): models MN0 or MN1. A compartment-independent approach was also conducted and led to area under the plasma concentration-time curve (AUC) and mean residence time (MRT) determinations. A comparison of the pharmacokinetic profiles across time of administration indicates that absorption, first-pass metabolism and tissue distribution of CsA in the rat are circadian-dosing stage dependent. |
Databáze: | OpenAIRE |
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