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Simultaneous Determination of Isoline and Its Two Major Metabolites Using High-Performance Liquid Chromatography
Author(s) -
Jun Tang,
Mian Zhang,
Zhengtao Wang,
Teruaki Akao,
Norio Nakamura,
Masao Hattori
Publication year - 2004
Publication title -
journal of analytical toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.161
H-Index - 76
eISSN - 1945-2403
pISSN - 0146-4760
DOI - 10.1093/jat/28.1.11
Subject(s) - chromatography , chemistry , pyrrolizidine , high performance liquid chromatography , microsome , analyte , potassium phosphate , methanol , extraction (chemistry) , alkaloid , elution , quantitative analysis (chemistry) , enzyme , biochemistry , organic chemistry , stereochemistry
A simple and reliable high-performance liquid chromatographic (HPLC) assay was developed for a simultaneous determination of isoline, a potent hepatotoxic pyrrolizidine alkaloid, and its two major metabolites, namely M1 (bisline) and M2 (bisline lactone, a new pyrrolizidine alkaloid). The latter two metabolites were produced during in vitro metabolism of isoline by rat and mouse microsomal enzyme systems. The analysis was conducted by a direct injection of aliquots of supernatant of the microsomal reaction mixture treated with the equal volume of ice-cold methanol onto a conventional reversed-phase analytical column (150 x 4.6 mm). The analytes were separated by a gradient elution with mobile phases A (0.01 M dihydro-potassium phosphate, pH 4.8) and B (acetonitrile). The assay has shown excellent precision and accuracy with less than 10% of overall intra- and interday variations and higher than 94% of overall accuracy. The developed HPLC method was successfully applied for the determination of the intact isoline and its two pH- and thermally labile metabolites produced in rat and mouse liver microsomal incubations.

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