Gabapentin, Pregabalin and Vigabatrin Quantification in Human Serum by GC-MS After Hexyl Chloroformate Derivatization
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27590034
DOI
10.1093/jat/bkw070
PII: bkw070
Knihovny.cz E-zdroje
- MeSH
- aminy analýza krev MeSH
- antikonvulziva analýza krev MeSH
- design s pomocí počítače MeSH
- formiáty chemie MeSH
- GABA analogy a deriváty analýza krev MeSH
- gabapentin MeSH
- kalibrace MeSH
- kyseliny cyklohexankarboxylové analýza krev MeSH
- lidé MeSH
- plynová chromatografie s hmotnostně spektrometrickou detekcí MeSH
- pregabalin analýza krev MeSH
- vigabatrin analýza krev MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- aminy MeSH
- antikonvulziva MeSH
- formiáty MeSH
- GABA MeSH
- gabapentin MeSH
- hexylchloroformate MeSH Prohlížeč
- kyseliny cyklohexankarboxylové MeSH
- pregabalin MeSH
- vigabatrin 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.
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