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Analysis of benzo[a]pyrene metabolites formed by rat hepatic microsomes using high pressure liquid chromatography: optimization of the method
M. Moserová, V. Kotrbová, D. Aimová, M. Sulc, E. Frei, M. Stiborová,
Jazyk angličtina Země Slovensko
Typ dokumentu časopisecké články
NLK
Free Medical Journals
od 2008
PubMed Central
od 2008 do 2019
Europe PubMed Central
od 2008 do 2018
ProQuest Central
od 2008-06-01 do 2019-01-31
Open Access Digital Library
od 2008-01-01
Open Access Digital Library
od 2008-01-01
Open Access Digital Library
od 2009-06-19
Nursing & Allied Health Database (ProQuest)
od 2008-06-01 do 2019-01-31
Health & Medicine (ProQuest)
od 2008-06-01 do 2019-01-31
Public Health Database (ProQuest)
od 2008-06-01 do 2019-01-31
Sciendo
od 2009-06-19
ROAD: Directory of Open Access Scholarly Resources
od 2008
- Publikační typ
- časopisecké články MeSH
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.
Citace poskytuje Crossref.org
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