Abstract
A column-switching liquid chromatography/electrospray ionization tandem mass spectrometry to determine paclitaxel and its metabolites, 6α-hydroxypaclitaxel and p-3′-hydroxypaclitaxel, in human plasma was developed. The analytical system had a Shim-Pack MAYI-ODS (10×4.6mm i.d.) trapping column with deproteinization ability that concentrates analytes and removes water-soluble components. This method covered a linearity range of 5-5000ng/mL of concentrations in plasma for paclitaxel, a range of 0.87-870ng/mL for 6α-hydroxypaclitaxel and a range of 0.87-435ng/mL for p-3′-hydroxypaclitaxel. The intra-day precision and inter-day precision of analysis were less than 11.1%, and the accuracy was within ±14.4% at concentrations of 5, 50, 500 and 5000ng/mL for paclitaxel, 0.87, 8.7, 87 and 870ng/mL for 6α-hydroxypaclitaxel, and 0.87, 8.7, 87 and 435ng/mL for p-3′-hydroxypaclitaxel. The total run time was 30min. Our method was successfully applied to clinical pharmacokinetic investigation.
Original language | English |
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Pages (from-to) | 539-544 |
Number of pages | 6 |
Journal | Biomedical Chromatography |
Volume | 27 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2013 Apr |
Keywords
- Column-switching
- Human plasma
- Metabolite
- Paclitaxel
ASJC Scopus subject areas
- Analytical Chemistry
- Biochemistry
- Molecular Biology
- Pharmacology
- Drug Discovery
- Clinical Biochemistry