Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10554105 | Journal of Pharmaceutical and Biomedical Analysis | 2005 | 8 Pages |
Abstract
All analytes and the internal standard were separated from acidified plasma by solid phase extraction. Afterwards the extracted samples were analyzed by HPLC/MS in the positive electrospray ionization mode (ESI) and selected ion monitoring (SIM). The total run time was 7 min between injections. The assay had a lower limit of quantification of 50.0 ng/mL for each analyte using 1 mL of plasma. The calibration curves were linear in the measured range between 50.0 and 750 ng/mL plasma. The overall precision and accuracy for all concentrations of quality controls and standards was better than 15%. No indications were found for possible instabilities of niacin, niacinamide and nicotinuric acid in plasma at â20 °C, in the extraction solvent or after repeated thawing/freezing cycles. In stabilities were observed in whole blood and in plasma at room temperature. The recovery of the extraction method ranged from 86 to 89% for the three analytes.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
P. Pfuhl, U. Kärcher, N. Häring, A. Baumeister, Mona Abdel Tawab, M. Schubert-Zsilavecz,