Literature DB >> 8685537

Plasma disposition kinetics of albendazole metabolites in pigs fed different diets.

L I Alvarez1, C A Saumell, S F Sanchez, C E Lanusse.   

Abstract

The influence of diet on the disposition kinetics of albendazole (ABZ) and its metabolites in pigs was investigated. ABZ was administered orally at 10 mg kg-1 to pigs fed either a commercially produced 35 per cent protein/grain concentrate diet (concentrate group), a whey-based diet supplemented with corn grain (whey/grain group) or grazed on pasture (pasture group). Blood samples were taken serially for 96 hours and plasma was analysed by high performance liquid chromatography (HPLC) for ABZ, ABZ sulphoxide (ABZSO), ABZ sulphone (ABZSO2) and amino-ABZSO2 (NH2ABZSO2). ABZ was not detected in plasma at any time after the treatment, and ABZSO and ABZSO2 were the main metabolites detected between 0.5 and 30 to 48 hours after treatment in all the experimental animals. Low concentrations of the NH2ABZSO2 metabolite were found in plasma between 18 and 36 hours after the administration of ABZ to all the groups of pigs. The pharmacokinetic behaviour of the ABZ metabolites in pigs fed either the concentrate of the whey/concentrate diet was substantially different from that observed in pigs grazing on pasture. The peak concentration (C(max)) and areas under the concentration-time curves (AUC) for ABZSO and ABZSO2 were significantly higher (P < 0.01) in the pigs fed on pasture, and were correlated with significantly longer elimination half-lives and mean residence times for both metabolites.

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Year:  1996        PMID: 8685537     DOI: 10.1016/s0034-5288(96)90010-7

Source DB:  PubMed          Journal:  Res Vet Sci        ISSN: 0034-5288            Impact factor:   2.534


  8 in total

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Journal:  Antimicrob Agents Chemother       Date:  2011-09-19       Impact factor: 5.191

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3.  Pharmacokinetics, Safety, and Tolerability of Oxfendazole in Healthy Adults in an Open-Label Phase 1 Multiple Ascending Dose and Food Effect Study.

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4.  Population Pharmacokinetic-Pharmacodynamic Model of Oxfendazole in Healthy Adults in a Multiple Ascending Dose and Food Effect Study and Target Attainment Analysis.

Authors:  Thanh Bach; Gregory A Deye; Ellen E Codd; John Horton; Patricia Winokur; Guohua An
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5.  Improvement of Albendazole Bioavailability with Menbutone Administration in Sheep.

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Journal:  Animals (Basel)       Date:  2022-02-14       Impact factor: 2.752

6.  Assessment of Diet-Related Changes on Albendazole Absorption, Systemic Exposure, and Pattern of Urinary Excretion in Treated Human Volunteers.

Authors:  L Ceballos; E Nieves; M Juárez; R Aveldaño; M Travacio; J Martos; R Cimino; J L Walson; A Krolewiecki; C Lanusse; L Alvarez
Journal:  Antimicrob Agents Chemother       Date:  2021-08-17       Impact factor: 5.191

7.  Assessment of serum pharmacokinetics and urinary excretion of albendazole and its metabolites in human volunteers.

Authors:  Laura Ceballos; Alejandro Krolewiecki; Marisa Juárez; Laura Moreno; Fabian Schaer; Luis I Alvarez; Rubén Cimino; Judd Walson; Carlos E Lanusse
Journal:  PLoS Negl Trop Dis       Date:  2018-01-18

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Authors:  Tina V A Hansen; Andrew R Williams; Matthew Denwood; Peter Nejsum; Stig M Thamsborg; Christian Friis
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2017-11-09       Impact factor: 4.077

  8 in total

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