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Enantioselective renal excretion of albendazole metabolites in patients with neurocysticercosis
Author(s) -
Lanchote V.L.,
Takayanagui O.M.,
Mateus F.H.
Publication year - 2004
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.20071
Subject(s) - albendazole , neurocysticercosis , chemistry , enantioselective synthesis , excretion , pharmacology , organic chemistry , biochemistry , pathology , surgery , catalysis , medicine
The present study investigates the urinary excretion of the enantiomers of (+)‐ and (–)‐albendazole sulfoxide (ASOX) and albendazole sulfone (ASON) in 12 patients with neurocysticercosis treated with albendazole for 8 days (7.5 mg/kg/12 h). Serial blood samples (0–12 h) and urine (three periods of 8 h) were collected after administration of the last dose of albendazole. Plasma and urine (+)‐ASOX, (–)‐ASOX, and ASON metabolites were determined by HPLC using a chiral phase column (Chiralpak AD) with fluorescence detection. The pharmacokinetic parameters ( P < 0.05) for (+)‐ASOX, (–)‐ASOX, and ASON metabolites are reported as means (95% CI); amount excreted (Ae) = 3.19 (1.53–4.85) vs. 0.72 (0.41–1.04) vs. 0.08 (0.03–0.13) mg; plasma concentration‐time area under the curve, AUC 0–24 = 3.56 (0.93–6.18) vs. 0.60 (0.12–1.08) vs. 0.38 (0.20–0.55) μg.h/ml, and renal clearance Cl R = 1.20 (0.66–1.73) vs. 2.72 (0.39–5.05) vs. 0.25 (0.13–0.37) l/h. Sulfone formation capacity, expressed as the Ae ratio ASON/ASOX + ASON, was 2.21 (1.43–2.99). These data point to enantioselectivity in the renal excretion of ASOX as a complementary mechanism to the metabolism responsible for the plasma accumulation of (+)‐ASOX. The results also suggest that the metabolite ASON is partially eliminated as a reaction product of the subsequent metabolism. Chirality 16:520–525, 2004 . © 2004 Wiley‐Liss, Inc.