Pharmacokinetic disposition of 14C-glyburide in patients with varying renal function
The pharmacokinetics of 14C-labeled glyburide were studied in 13 men with varying degrees of renal impairment. Patients received a single, 5 mg oral dose of glyburide as a solution (10 microCi/ml/mg) after a high-carbohydrate breakfast. Serial plasma and breath samples were collected for 48 hours and urine and feces were collected for 5 to 7 days. Patients with normal to moderately impaired renal function (creatinine clearance (CLCR) of 29 to 131 ml/min/1.7 m2) had glyburide plasma t1/2 values of 2.0 to 5.0 hours, with no relationship between CLCR and glyburide clearance. One subject with severe renal impairment (CLCR = 5 ml/min/1.7 m2) had decreased glyburide clearance that resulted in a t1/2 of 11 hours. The elimination of metabolites was more dependent on renal status but was only significantly affected in the patient with severe renal impairment.
- Research Organization:
- Ferris State College, Big Rapids, MI
- OSTI ID:
- 5677130
- Journal Information:
- Clin. Pharmacol. Ther.; (United States), Vol. 3
- Country of Publication:
- United States
- Language:
- English
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DRUGS
EXCRETION
ADSORPTION
BIOCHEMICAL REACTION KINETICS
CARBON 14 COMPOUNDS
CREATININE
FECES
METABOLISM
PATIENTS
RENAL CLEARANCE
TRACER TECHNIQUES
UROGENITAL SYSTEM DISEASES
AZOLES
BIOLOGICAL MATERIALS
BIOLOGICAL WASTES
CLEARANCE
DISEASES
HETEROCYCLIC COMPOUNDS
IMIDAZOLES
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ISOTOPE APPLICATIONS
KINETICS
LABELLED COMPOUNDS
MATERIALS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
REACTION KINETICS
SORPTION
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551001* - Physiological Systems- Tracer Techniques