Simultaneous determination of gabapentin, pregabalin, vigabatrin, and topiramate in plasma by HPLC with fluorescence detection

•Gabapentin, pregabalin, vigabatrin, and topiramate were determined in plasma.•Simple NBD-Cl derivatization method using HPLC and FLD was developed.•NBD-Cl derivatization products were identified using MS spectrometry.•The method meets validation criteria, good agreement was found with reference met...

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Veröffentlicht in:Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2014-07, Vol.962, p.82-88
Hauptverfasser: Martinc, Boštjan, Roškar, Robert, Grabnar, Iztok, Vovk, Tomaž
Format: Artikel
Sprache:eng
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Zusammenfassung:•Gabapentin, pregabalin, vigabatrin, and topiramate were determined in plasma.•Simple NBD-Cl derivatization method using HPLC and FLD was developed.•NBD-Cl derivatization products were identified using MS spectrometry.•The method meets validation criteria, good agreement was found with reference method.•The method is suitable for determination of plasma concentration of studied drugs. Therapeutic drug monitoring (TDM) of antiepileptic drugs (AEDs) has been recognized as a useful tool in management of epilepsy. We developed a simple analytical method for simultaneous determination of four second generation AEDs, including gabapentin (GBP), pregabalin (PGB), vigabatrin (VGB), and topiramate (TOP). Analytes were extracted from human plasma using universal solid phase extraction, derivatized with 4-chloro-7-nitrobenzofurazan (NBD-Cl) and analyzed by HPLC with fluorescence detection. Using mass spectrometry we confirmed that NBD-Cl reacts with sulfamate group of TOP similarly as with amine group of the other three analytes. The method is linear (r2>0.998) across investigated analytical ranges (0.375–30.0μg/mL for GBP, PGB, and VGB; 0.50–20.0μg/mL for TOP). Intraday and interday precision do not exceed 9.40%. The accuracy is from 95.6% to 106%. The recovery is higher than 80.6%, and the lower limit of quantification is at least 0.5μg/mL. The method is selective and robust. For TOP determination the method was compared to a previously published method and the results obtained by the two methods were in good agreement. The developed method is suitable for routine TDM.
ISSN:1570-0232
1873-376X
DOI:10.1016/j.jchromb.2014.05.030