Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9745526 | Chemometrics and Intelligent Laboratory Systems | 2005 | 9 Pages |
Abstract
The use of this new steady state kinetic constraint embedded into MCR-ALS makes it possible to fit three-way LC-MS enzyme incubation data to extract enzyme kinetic parameters such as the Michaelis constant (KM), the maximum velocity (vmax), and inhibition constants (KI). Specifically, we show that the use of this MCR-ALS algorithm allows for the analysis of data that can be difficult to handle using other means, including the occurrence of isobaric metabolites, chromatographic peak overlap, variable background contributions, and chromatographic peak distortions caused by chromatographic column overloading and by matrix effects. We have applied this approach to the study of the simultaneous incubation of two cytochrome P450 isoenzymes, CYP2D6 and CYP3A4, with dextromethorphan, an over-the-counter cough suppressant.
Related Topics
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Authors
Raymundo Sánchez-Ponce, Sarah C. Rutan,