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   <subfield code="a">Pharmacokinetics of quinine in patients with chronic renal failure</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[P. Rimchala, J. Karbwang, K. Sukontason, V. Banmairuroi, P. Molunto, K. Na-Bangchang]</subfield>
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   <subfield code="a">Methods: We investigated the pharmacokinetics of quinine (Qn) following administration of a single oral dose of 600 mg Qn sulphate in six male Thai patients with a moderate degree of chronic renal failure (CRF), and six male Thai subjects with normal renal function. Results: The drug was well tolerated in both groups of subjects; no major adverse reactions were observed. A marked alteration in the pharmacokinetics of Qn was found in patients with CRF compared to healthy subjects; there were six signifiicant changes in the pharmacokinetic parameters. Absorption was delayed, but increased in CRF (tmax 4.5 vs 1.6 h, Cmax 6.17 vs 3.45 μg·ml−1). Total clearance was significantly reduced 0.94 vs 2.84 ml·min−1·kg−1, whereas Vz/f remained unchanged (1.82 vs 2.78 1·kg−1). This resulted in the increased values of AUC and prolongation of the t1/2z and MRT in the patients (AUC 181.5 vs 61.8 μg·min−1·ml−1, t1/2z 26 vs 9.7 h, MRT 36.4 vs 11.3 h). Median concentrations of plasma unbound fraction of Qn collected at 4 h after drug administration in patients and healthy subjects were 7.3 vs 9.8%, respectively.</subfield>
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   <subfield code="a">Quinine</subfield>
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   <subfield code="a">chronic renal failure</subfield>
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   <subfield code="a">Rimchala</subfield>
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   <subfield code="D">J.</subfield>
   <subfield code="u">Clinical Parmacology Unit, Department of Clinical Tropical Medicine, Faculty of Medicine, Mahidol University, 420/6 Rajvithi Road, 10400, Pyathai, Bangkol, Thailand</subfield>
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   <subfield code="a">Sukontason</subfield>
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   <subfield code="t">European Journal of Clinical Pharmacology</subfield>
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