Analysis of benzo[a]pyrene metabolites formed by rat hepatic microsomes using high pressure liquid chromatography: optimization of the method
A simple and sensitive method was developed to separate the carcinogenic polycyclic aromatic hydrocarbon (PAH), benzo[a]pyrene (BaP), and six of its oxidation metabolites generated by rat hepatic microsomes enriched with cytochrome P450 (CYP) 1A1, by high pressure liquid chromatography (HPLC). The H...
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Published in | Interdisciplinary toxicology Vol. 2; no. 4; pp. 239 - 244 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Slovakia
Versita
01.12.2009
De Gruyter Poland Slovak Toxicology Society SETOX |
Subjects | |
Online Access | Get full text |
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Summary: | A simple and sensitive method was developed to separate the carcinogenic polycyclic aromatic hydrocarbon (PAH), benzo[a]pyrene (BaP), and six of its oxidation metabolites generated by rat hepatic microsomes enriched with cytochrome P450 (CYP) 1A1, by high pressure liquid chromatography (HPLC). The HPLC method, using an acetonitrile/water gradient as mobile phase and UV detection, provided appropriate separation and detection of both mono- and di-hydroxylated metabolites of BaP as well as BaP diones formed by rat hepatic microsomes and the parental BaP. In this enzymatic system, 3-hydroxy BaP, 9-hydroxy BaP, BaP-4,5-dihydrodiol, BaP-7,8-dihydrodiol, BaP-9,10-dihydrodiol and BaP-dione were generated. Among them the mono-hydroxylated BaP metabolite, 3-hydroxy BaP followed by di-hydroxylated BaP products, BaP-7,8-dihydrodiol and BaP-9,10-dihydrodiol, predominated, while BaP-dione was a minor metabolite. This HPLC method will be useful for further defining the roles of the CYP1A1 enzyme with both in vitro and in vivo models in understanding its real role in activation and detoxification of BaP. |
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Bibliography: | ark:/67375/QT4-4B6D4RSZ-H v10102-009-0024-0.pdf istex:D33DE91848F18A37C9F3DA057633C68C177B84D0 ArticleID:v10102-009-0024-0 |
ISSN: | 1337-6853 1337-9569 |
DOI: | 10.2478/v10102-009-0024-0 |