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Gabapentin, Pregabalin and Vigabatrin Quantification in Human Serum by GC-MS After Hexyl Chloroformate Derivatization
T. Hložek, M. Bursová, P. Coufal, R. Čabala,
Language English Country England, Great Britain
Document type Journal Article
NLK
Open Access Digital Library
from 1996-01-01
Medline Complete (EBSCOhost)
from 2011-11-01 to 1 year ago
PubMed
27590034
DOI
10.1093/jat/bkw070
Knihovny.cz E-resources
- MeSH
- Amines analysis blood MeSH
- Anticonvulsants analysis blood MeSH
- Computer-Aided Design MeSH
- Formates chemistry MeSH
- gamma-Aminobutyric Acid analogs & derivatives analysis blood MeSH
- Calibration MeSH
- Cyclohexanecarboxylic Acids analysis blood MeSH
- Humans MeSH
- Gas Chromatography-Mass Spectrometry MeSH
- Pregabalin analysis blood MeSH
- Vigabatrin analysis blood MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
A simple, sensitive and robust method for simultaneous determination of antiepileptic drugs (gabapentin, pregabalin and vigabatrin) in human serum using GC-MS was developed and validated for clinical toxicology purposes. This method employs an emerging class of derivatization agents - alkyl chloroformates allowing the efficient and rapid derivatization of both the amino and carboxylic groups of the tested antiepileptic drugs within seconds. The derivatization protocol was optimized using the Design of Experiment statistical methodology, and the entire sample preparation requires less than 5 min. Linear calibration curves were obtained in the concentration range from 0.5 to 50.0 mg/L, with adequate accuracy (97.9-109.3%) and precision (<12.1%). The method was successfully applied to quantification of selected γ-aminobutyric acid analogs in the serum of patients in both therapeutic and toxic concentration ranges.
References provided by Crossref.org
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- $a A simple, sensitive and robust method for simultaneous determination of antiepileptic drugs (gabapentin, pregabalin and vigabatrin) in human serum using GC-MS was developed and validated for clinical toxicology purposes. This method employs an emerging class of derivatization agents - alkyl chloroformates allowing the efficient and rapid derivatization of both the amino and carboxylic groups of the tested antiepileptic drugs within seconds. The derivatization protocol was optimized using the Design of Experiment statistical methodology, and the entire sample preparation requires less than 5 min. Linear calibration curves were obtained in the concentration range from 0.5 to 50.0 mg/L, with adequate accuracy (97.9-109.3%) and precision (<12.1%). The method was successfully applied to quantification of selected γ-aminobutyric acid analogs in the serum of patients in both therapeutic and toxic concentration ranges.
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