Rapid Quantification of Gabapentin, Pregabalin, and Vigabatrin in Human Serum by Ultraperformance Liquid Chromatography With Mass-Spectrometric Detection

• Published in: Therapeutic drug monitoring Vol. 35; no. 1; pp. 48 - 53
• Main Authors: CHAHBOUNI, Abdel, SINJEWEL, Arno, DEN BURGER, Jeroen C. G, VOS, René M, WILHELM, Abraham J, VELDKAMP, Agnes I, SWART, Eleanora L
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins 01-02-2013; Lippincott Williams & Wilkins Ovid Technologies
• Subjects: Amines - blood; Anticonvulsants - blood; Biological and medical sciences; Blood Chemical Analysis - methods; Chromatography; Chromatography, High Pressure Liquid - methods; Convulsions & seizures; Cyclohexanecarboxylic Acids - blood; Drug Stability; Drug use; Epilepsy; gamma-Aminobutyric Acid - analogs & derivatives; gamma-Aminobutyric Acid - blood; Humans; Mass spectrometry; Medical sciences; Pharmacology; Pharmacology. Drug treatments; Pregabalin; Tandem Mass Spectrometry - methods; Vigabatrin - blood; Human; Biological fluid; LC―MS; 4-Aminobutyrate transaminase; Gabapentin; Enzyme; Transferases; Enzyme inhibitor; HPLC chromatography; Exploration; Anticonvulsant; Liquid chromatography; Pregabalin; Analgesic; Vigabatrin; Transaminases; Serum; Diagnosis; Detection; Mass spectrometry
• DOI: 10.1097/FTD.0b013e31827788c0
• EISSN: 1536-3694
• ISSN: 0163-4356

Gabapentin (GBP), pregabalin (PRG), and vigabatrin (VIG) are used for the prevention and treatment of epileptic seizures. The developed method was applied to samples from subjects participating in a pharmacokinetic study of GBP.
Sample pretreatment consisted of adding 20 μL of trichloroacetic acid (30%; vol/vol) and 200 μL of GBP-d4 in acetonitrile as an internal standard to 20 μL of serum. Chromatographic separation was performed on an Acquity separation module using a Kinetex RP18 column. The aqueous and organic mobile phases were 2 mM ammonium acetate supplemented with 0.1% formic acid in water and acetonitrile, respectively. The detection by a tandem quadrupole mass spectrometer, operating in the positive mode using multiple reaction monitoring, was completed within 2 minutes.
The method was linear over the range of 0.03-25 mg/L for GBP, 0.03-25 mg/L for PRG, and 0.06-50 mg/L for VIG. The between- and within-run accuracies ranged from 90% to 107%. The between- and within-run imprecisions of the method were <10%. Stability data show no significant decrease of the analytes. A relative matrix effect of -1%, 0.2%, and -5% was determined for GBP, PRG, and VIG, respectively.
A simple and sensitive ultraperformance liquid chromatography-tandem mass spectrometry method was developed and validated for the simultaneous quantification of GBP, PRG, and VIG in human serum. The reported method provided the necessary linearity, precision, and accuracy to allow the determination of GBP, PRG, and VIG for therapeutic drug monitoring and clinical research purposes.