Use of chiral liquid chromatography-tandem mass spectrometry to investigate the metabolism of racemic cholecystokinin-B antagonists

Citation
Ap. Watt et al., Use of chiral liquid chromatography-tandem mass spectrometry to investigate the metabolism of racemic cholecystokinin-B antagonists, J CHROMAT A, 896(1-2), 2000, pp. 217-227
Citations number
12
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
Volume
896
Issue
1-2
Year of publication
2000
Pages
217 - 227
Database
ISI
SICI code
Abstract
In an attempt to establish the enantiomeric specificity of metabolism for a series of racemic cholecystokinin-B receptor antagonists, chiral LC-MS-MS conditions were established using a Pirkle DNBL chiral stationary phase ope rating in the reversed-phase mode. Rat liver microsomal incubations of the compounds were analysed using these conditions and it was demonstrated that resolution of oxygenated and demethylated metabolites could be achieved. A single model compound was investigated in detail by obtaining product-ion spectra on all mono-oxygenated species in an attempt to correlate these and identify enantiomeric pairs of metabolites. In this example a lack of diff erentiation in the product ion spectra did not allow correlation but the re sults suggest that such an approach may still be viable for the chiral meta bolic analysis of racemic material. (C) 2000 Elsevier Science B.V. All righ ts reserved.