British Journal of Clinical Pharmacology · 1994 · 43 citations · 25 references
PharmacyClinical PharmacokineticsPharmacologyDrug MetabolismHepatic PharmacokineticsPharmacokinetic ModelingDrug DispositionHepatic Drug MetabolismImmunoassay AnalysisPharmacokinetics In Liver DiseaseTransplant PharmacokineticsTransplant PharmacologyDrug Elimination Half-lifeFirst-order Absorption ModelsMetabolite PharmacokineticsPharmacokinetics In Liver TransplantationPharmacokinetics In TransplantationPharmacokinetics Of Immunosuppressive AgentsTacrolimus PharmacokineticsTerminal Half-life Estimation
1. Blood and urine concentrations of the macrolide immunosuppressant FK506 and its metabolites were measured in seven orthotopic liver transplant patients after the first oral dose of FK506 (0.04 +/- 0.02 mg kg-1) used as primary immunosuppressant. A specific h.p.l.c.-MS assay was used, allowing the measurement of parent drug and eight metabolites. Results were compared with those obtained using a microparticle enzyme immunoassay (MEIA). 2. Blood drug concentrations were described by an open two compartment model with first-order absorption giving the following mean data: tmax: 1.9 (h), Cmax: 17.4 (microgram l-1), AUC: 328.1 (microgram l-1 h), t1/2,1: 0.74 (h). The terminal elimination half-life was estimated at about 26 h using the h.p.l.c.-MS assay. 3. The metabolites found in blood were demethyl-FK506 and demethyl-hydroxy-FK506, while in urine FK506 and eight of its metabolites were detected.
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FK 506 FOR LIVER, KIDNEY, AND PANCREAS TRANSPLANTATION
ThomasE. Starzl, John J. Fung, Raman Venkataramman et al. · The Lancet · 1989 · 1.1K citations
Medicine, Pharmacokinetics, Surgery +12
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Medicine, Pharmacology, Toxicology +17
A highly sensitive method to assay FK-506 levels in plasma.
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Pharmacokinetics of FK 506 in transplant patients.
Raman Venkataramanan, Amita Jain, Vijay Warty et al. · PubMed · 1991 · 135 citations · Full text