Stereoselective analysis of carvedilol in human plasma using HPLC/MS/MS after chiral derivatization
A relatively high-throughput high-performance liquid chromatography/tandem mass spectrometry (HPLC–MS/MS) method using a chiral derivatization reagent was developed for the quantitative determination of carvedilol enantiomers in human plasma. S-carvedilol and R-carvedilol are extracted from human pl...
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Veröffentlicht in: | Journal of pharmaceutical and biomedical analysis 2004-11, Vol.36 (3), p.609-615 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A relatively high-throughput high-performance liquid chromatography/tandem mass spectrometry (HPLC–MS/MS) method using a chiral derivatization reagent was developed for the quantitative determination of carvedilol enantiomers in human plasma.
S-carvedilol and
R-carvedilol are extracted from human plasma by protein precipitation using acetonitrile containing racemic [
2H
5]-carvedilol as an internal standard. Extracts are then derivatized with 2,3,4,6-tetra-
O-acetyl-beta-glucopyranosyl isothiocyanate (GITC) and analysed using HPLC–MS/MS with a TurboIonspray (TIS) interface and selected reaction monitoring. Using 150
μL of plasma, the method was validated over a concentration range of 0.2–200
ng/mL. The maximum within-run precision observed in a three run quality control was 8.2% for
S-carvedilol and 6.7% for
R-carvedilol, respectively. The maximum percentage bias observed at all quality control sample concentrations was 9.4% for
S-carvedilol and 11.6% for
R-carvedilol, respectively. The HPLC–MS/MS method was also compared with a previously developed high-performance LC/fluorescence method by analysing 25 samples containing racemic carvedilol. Based on results obtained, these two methods were found to be equivalent. However, compared with LC/fluorescence method, HPLC–MS/MS method is more sensitive, uses less plasma, and also employs a less time-consuming sample preparation process. |
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ISSN: | 0731-7085 1873-264X |
DOI: | 10.1016/j.jpba.2004.07.008 |