Determination of ximelagatran, melagatran and two intermediary metabolites in plasma by mixed-mode solid phase extraction and LC-MS/MS
| Autor: | Ulrika Logren, Henrik Svennberg, Martin Ahnoff, Kristina Dunér, Jonas Bäckström, Niklas Magnell |
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| Rok vydání: | 2006 |
| Předmět: |
Benzylamines
Formic acid Electrospray ionization Clinical Biochemistry Biochemistry Sensitivity and Specificity Antithrombins Analytical Chemistry chemistry.chemical_compound Liquid chromatography–mass spectrometry Tandem Mass Spectrometry Humans Solid phase extraction Chromatography Elution Extraction (chemistry) Anticoagulants Reproducibility of Results Cell Biology General Medicine chemistry Calibration Azetidines Ammonium acetate Quantitative analysis (chemistry) Chromatography Liquid |
| Zdroj: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 852(1-2) |
| ISSN: | 1570-0232 |
| Popis: | An analytical method was developed for the determination of ximelagatran, an oral direct thrombin inhibitor, its active metabolite melagatran, and the two intermediate metabolites, OH-melagatran and ethyl-melagatran in human plasma. Extraction of plasma was carried out on a mixed mode bonded sorbent material (C8/SO 3 − ). All four analytes, including their isotope-labelled internal standards, were eluted at high ionic strength with a mixture of 50% methanol and 50% buffer (0.25 M ammonium acetate and 0.05 M formic acid, pH 5.3) with an extraction recovery above 80%. The extracts were demonstrated to be clean in terms of a low concentration of albumin and lysoPC. The sample extraction was fully automated and performed in 96-well plates using a Tecan Genesis pipetting robot. Analysis of the extracts were performed with liquid chromatography followed by positive electrospray ionization mass spectrometry. The low organic content and the low pH of the extracts allowed for, after dilution 1:3 with buffer, direct injection onto the LC-column. The four analytes were separated on a C18 analytical LC-column using gradient elution with the acetonitrile concentration varying from 10 to 30% (v/v) and the ammonium acetate and acetic acid concentration kept constant at 10 and 5 mmol/L, respectively, at a flow rate of 0.75 mL/min. Linearity was achieved over the calibrated range 0.010–4.0 μmol/L with accuracy and relative standard deviation in the range 96.9–101.2% and 6.6–17.1%, respectively at LLOQ, and in the range 94.7–102.6% and 2.7–6.8%, respectively at concentrations above 3 × LLOQ. The method replaces a manual method, and displays the advantages of having a fully automated sample clean-up, no evaporation/reconstitution step, high recovery, and complete LC-separation of all four analytes. |
| Databáze: | OpenAIRE |
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