Stepwise optimization approach for improving LC-MS/MS analysis of zwitterionic antiepileptic drugs with implementation of experimental design
Autor: | Darko Ivanović, Biljana Jančić Stojanović, Nađa Kostić, Tijana Rakić, Yannis Dotsikas, Mirjana Medenica, Anđelija Malenović |
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Rok vydání: | 2013 |
Předmět: |
Detection limit
Analyte Chromatography Chemistry Capillary action 010401 analytical chemistry Analytical chemistry Linearity 010501 environmental sciences Tandem mass spectrometry 01 natural sciences 0104 chemical sciences chemistry.chemical_compound Sensitivity (control systems) Response surface methodology Derivatization Spectroscopy 0105 earth and related environmental sciences |
Zdroj: | Journal of Mass Spectrometry. 48:875-884 |
ISSN: | 1076-5174 |
DOI: | 10.1002/jms.3236 |
Popis: | In this article, a step-by-step optimization procedure for improving analyte response with implementation of experimental design is described. Zwitterionic antiepileptics, namely vigabatrin, pregabalin and gabapentin, were chosen as model compounds to undergo chloroformate-mediated derivatization followed by liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) analysis. Application of a planned stepwise optimization procedure allowed responses of analytes, expressed as areas and signal-to-noise ratios, to be improved, enabling achievement of lower limit of detection values. Results from the current study demonstrate that optimization of parameters such as scan time, geometry of ion source, sheath and auxiliary gas pressure, capillary temperature, collision pressure and mobile phase composition can have a positive impact on sensitivity of LC-MS/MS methods. Optimization of LC and MS parameters led to a total increment of 53.9%, 83.3% and 95.7% in areas of derivatized vigabatrin, pregabalin and gabapentin, respectively, while for signal-to-noise values, an improvement of 140.0%, 93.6% and 124.0% was achieved, compared to autotune settings. After defining the final optimal conditions, a time-segmented method was validated for the determination of mentioned drugs in plasma. The method proved to be accurate and precise with excellent linearity for the tested concentration range (40.0 ng ml−1–10.0 × 103 ng ml−1). Copyright © 2013 John Wiley & Sons, Ltd. |
Databáze: | OpenAIRE |
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