Pharmacokinetics of Troglitazone in Patients with Renal Insufficiency

Authors: Knowlton P.W.1; Loi C-M.1; Vassos A.B.2; Blum R.A.3; Brodfuehrer J.I.1; Randinitis E.J.1; Sedman A.J.2; Koup J.R.1

Source: Clinical Drug Investigation, Volume 17, Number 2, 1 February 1999 , pp. 127-136(10)

Publisher: Adis International

Buy & download fulltext article:

OR

Price: $62.95 plus tax (Refund Policy)

Abstract:

Objective: The pharmacokinetic profiles of troglitazone and two metabolites were evaluated following a single 400mg oral dose of troglitazone in 20 patients with various degrees of renal function.

Methods: Plasma troglitazone and metabolite concentrations were determined by high performance liquid chromatography, and troglitazone free fraction was determined by ultracentrifugation.

Results: Mean maximum plasma concentration and area under the curve for total troglitazone appeared lower in patients with severe renal impairment (SRI) compared with those with normal renal function (NRF). Troglitazone free fraction was higher in patients with SRI (4.85%) than in subjects with NRF (1.66%), producing similar exposure values for unbound troglitazone, the moiety presumed to exert the pharmacological effect. Regression analysis revealed poor correlations of creatinine clearance value with total troglitazone, unbound troglitazone, and metabolite pharmacokinetic parameter values.

Conclusion: These data indicated that renal function does not predict troglitazone pharmacokinetics and systemic exposure to unbound troglitazone is unaltered with renal impairment. Thus, troglitazone dose adjustment based on pharmacokinetics is not required in patients with renal insufficiency.

Keywords: Troglitazone, pharmacokinetics; Oral; Kidney-disorders; Clinical-pharmacokinetics; Metabolites

Document Type: Original article

Affiliations: 1: Department of Pharmacokinetics and Drug Metabolism, Parke-Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USA 2: Department of Clinical Pharmacology, Parke-Davis Pharmaceutical Research Division, Ann Arbor, Michigan, USA 3: Clinical Pharmacokinetics Laboratory, Millard Fillmore Hospital, Buffalo, New York, USA

Publication date: 1999-02-01

Related content

Tools

Key

Free Content
Free content
New Content
New content
Open Access Content
Open access content
Subscribed Content
Subscribed content
Free Trial Content
Free trial content

Text size:

A | A | A | A
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages. print icon Print this page