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Anal Biochem ; 91(1): 138-45, 1978 Nov.
Article in English | MEDLINE | ID: mdl-9762092

ABSTRACT

The aglycone, 3-hydroxybenzo[a]pyrene, was metabolized to 3-benzo[a]pyrenyl-beta-D-glucopyranosiduronic acid in the presence of uridine 5'-diphosphoglucuronic acid and rabbit liver microsomes. The course of the biosynthetic reaction was followed by fluorimetry and reverse-phase, paired-ion high pressure liquid chromatography (HPLC). Also, the HPLC system was used to analyze for glucuronide and 3-hydroxybenzo[a]pyrene during the isolation procedure. The existence of a glucuronide of 3-hydroxybenzo[a]pyrene was determined by radiotracer and enzymic techniques, utilizing the HPLC system. Field desorption and direct inlet mass spectral techniques were used to characterize the 3-hydroxybenzo[a]pyrene glucuronide.


Subject(s)
Benzopyrenes/isolation & purification , Carcinogens/isolation & purification , Animals , Benzopyrenes/analysis , Benzopyrenes/metabolism , Carcinogens/analysis , Carcinogens/metabolism , Chromatography, High Pressure Liquid/methods , In Vitro Techniques , Mass Spectrometry , Microsomes, Liver/metabolism , Rabbits , Spectrometry, Fluorescence
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