Ex vivo diffusion of albendazole and its sulfoxide metabolite into Ascaris suum and Fasciola hepatica

• Published in: Parasitology research (1987) Vol. 87; no. 11; pp. 929 - 934
• Main Authors: ALVAREZ, L. I, MOTTIER, M. L, SANCHEZ, S. F, LANUSSE, C. E
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01.11.2001
• Subjects: Albendazole - analogs & derivatives; Albendazole - pharmacokinetics; Animals; Anthelmintics - pharmacokinetics; Antibiotics. Antiinfectious agents. Antiparasitic agents; Antiparasitic agents; Area Under Curve; Ascaris suum - metabolism; Biological and medical sciences; Chromatography, High Pressure Liquid; Fasciola hepatica - metabolism; Medical sciences; Pharmacology. Drug treatments; Sheep; Swine; Anthelmintic; Metabolite; Interspecific comparison; Plathelmintha; Parasite; Trematoda; Uptake; Fasciola hepatica; Albendazole; Ex vivo; Benzimidazole derivatives; Parasiticid; Helmintha; Ascaris suum; Sulfoxide; Nemathelminthia; Invertebrata; Diffusion; Nematoda
• ISSN: 0932-0113; 1432-1955
• DOI: 10.1007/s004360100471

The current experiments compare the pattern of ex vivo uptake (diffusion) of albendazole (ABZ) and albendazole sulfoxide (ABZSO) by Ascaris suum and Fasciola hepatica. Specimens of A. suum and F. hepatica were collected from untreated animals (pigs and sheep, respectively) and incubated with either ABZ or ABZSO for different time periods (5-180 min). After incubation. the parasite material was analysed by HPLC to quantify the amount of ABZ and/or ABZSO. The parent drug and its active ABZSO metabolite were recovered from the parasites after ex vivo incubation for different time periods throughout the assay. Total drug availability in A. suum, expressed as area under the concentration versus time curve (AUC) over 180 min of incubation, was significantly greater (P<0.05) for ABZ parent drug (AUC = 4.19 +/- 0.59 microg x h xg(-1)) compared with the more polar ABZSO metabolite (AUC = 0.25 +/- 0.01 micro x h x g(-1)). Similar results were observed after the incubation of both molecules with F. hepatica, where the AUC values obtained were 10.6 +/- 0.28 microg x h x g(-1) and 2.04 +/- 0.33 microg x h x g(-1) for ABZ and ABZSO, respectively. The greater diffusion and availability of ABZ in both helminths correlate with the higher lipophilicity of the parent drug, compared with its sulfoxide metabolite. The amount of both molecules measured in A. suum was significantly lower (P<0.05) than that recovered in F. hepatica. The complexity of the histological structure of the nematode cuticle compared with the external tegument of the trematode may account for such a difference in drug diffusion between the species. These findings complement previous observations on the patterns of in vivo uptake of ABZ by different helminth parasites, contributing to the understanding of the pharmacological anthelmintic action of these moieties.