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Simultaneous analysis of mitotane and its main metabolites in human blood and urine samples by SPE-HPLC technique
Authors:Mornar Ana  Sertić Miranda  Turk Nikša  Nigović Biljana  Koršić Mirko
Institution:1. University of Zagreb, Faculty of Pharmacy and Biochemistry, , 10 000 Zagreb, Croatia;2. School of Medicine, University of Zagreb, , 10 000 Zagreb, Croatia;3. Department of Gastroenterology, University Department of Medicine, Zagreb University Hospital Center, , 10 000 Zagreb, Croatia;4. Department of Endocrinology, University Department of Medicine, Zagreb University Hospital Center, , 10 000 Zagreb, Croatia
Abstract:Adrenocortical carcinoma (ACC) is a rare malignancy with an incompletely understood pathogenesis and a poor prognosis. The adrenalytic activity of mitotane has made it the most important single drug in the treatment of ACC. Unfortunately, the exact mechanism of mitotane action is still unknown. It is believed that mitotane belongs to the class of drugs that require metabolic transformation by cytochrome P450 for therapeutic action; therefore determination of plasma levels of not only mitotane but also its metabolites would help in carrying out the treatment. The objective of this work was to develop and validate an SPE‐HPLC method for simultaneous determination of mitotane and its metabolites in different biological fluids. The sample preparation consisted of a solid‐phase extraction on a Discovery DSC18 cartridge, while analysis of extracts was performed on a Symmetry C18 column. The usefulness of the proposed method was confirmed by analysis of plasma, red cell and urine samples from patient chronically treated with 1.5 g of mitotane. The patient involved in this study had a high plasma concentration of mitotane and none of the investigated metabolites were found. In order to investigate whether the polymorphism of CYP2C9 and CYP2C19 enzymes could be related to the metabolism of mitotane, RT‐PCR analysis was performed. Copyright © 2012 John Wiley & Sons, Ltd.
Keywords:mitotane  metabolites  SPE‐HPLC  RT‐PCR  CYP450
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