Investigation of the hepatotoxicity profile of chemical entities using Liverbeads® and WIF-B9 in vitro models

The cytotoxicity profile of various chemical entities was evaluated using two in vitro hepatocyte models. Liverbeads((R)) is a cryopreserved model consisting of primary hepatocytes entrapped in alginate beads. WIF-139 is a hybrid cell line obtained by fusion of rat hepatoma (Fao) and human fibroblasts (WI38). Various reference hepatotoxicants were tested and ranked according to their equivalent concentration 50 (EC50) for various biochemical endpoints (lactate dehydrogenase (LDH) release, 3-(4,5 dimethylthiazol 2yl)-2,5-diphenyl-2H tetrazolium bromure (MTT) activity, adenosine triphosphate (ATP) and glutathione (GSH) levels). The ranking obtained was comparable in both models and consistent with previously published results on hepatocyte monolayers. Ketoconazole, erythromycin estolate, retinoic acid, telithromycin and alpha-naphthyl-isothiocyanate were among the most toxic chemicals in both models, with an EC50 < 200 mu M. Troleandomycin, spiramycin, erythromycin, diclofenac, taurodeoxycholate, warfarin, galactosamine, valproic acid and isoniazid were found to be less toxic. Few marked differences, potentially linked to metabolism pathways, were observed between EC50s in the two models for compounds such as cyclosporine A (10 and > 831 AM) and warfarin (5904 and 1489 mu M) in WIF-B9 and Liverbeads((R)), respectively. The results obtained indicate that Liverbeads((R)) and WIF-B9 cells are reliable in vitro models to evaluate the hepatotoxic potential of a wide range of chemicals, irrespective of structure and pharmaceutical class. (c) 2006 Elsevier Ltd. All rights reserved.