Validated LC-MS/MS method for quantification of gabapentin in human plasma: application to pharmacokinetic and bioequivalence studies in Korean volunteers

• Published in: Biomedical chromatography 2007-08, Vol.21 (8), p.829-835
• Main Authors: Park, Jin-Hee, Jhee, Ok-Hwa, Park, Song-Hee, Lee, Jung-Sik, Lee, Min-Ho, Shaw, Leslie M., Kim, Kwang-Hyun, Lee, Jong-Ho, Kim, Yong-Seok, Kang, Ju-Seop
• Format: Article
• Language: English
• Subjects: Administration, Oral; Amines - blood; Amines - pharmacokinetics; Anticonvulsants - blood; Anticonvulsants - pharmacokinetics; Atmospheric Pressure; bioequivalence study; Cross-Over Studies; Cyclohexanecarboxylic Acids - blood; Cyclohexanecarboxylic Acids - pharmacokinetics; gabapentin; gamma-Aminobutyric Acid - blood; gamma-Aminobutyric Acid - pharmacokinetics; Humans; LC-MS/MS; pharmacokinetics; Reference Standards; Sensitivity and Specificity; Tandem Mass Spectrometry - methods; Therapeutic Equivalency
• ISSN: 0269-3879; 1099-0801
• DOI: 10.1002/bmc.826

A sensitive validated liquid chromatography–tandem mass spectrometric method (LC‐MS/MS) for gabapentin (GB) in human plasma has been developed and applied to pharmacokinetic (PK) and bioequivalence (BE) studies in human. In a randomized crossover design with a 1‐week period, each subject received a 300 mg GB capsule. The procedure involves a simple protein precipitation with acetonitrile and separated by LC with a Gemini C18 column using acetonitrile–10 mm ammonium acetate (20:80, v/v, pH 3.2) as mobile phase. The GB and internal standard [(S)‐(+)‐α‐aminocyclohexanepropionic acid hydrate] were analyzed using an LC‐API 2000 MS/MS in multiple reaction monitoring mode. The ionization was optimized using ESI(+) and selectivity was achieved using MS/MS analysis, m/z 172.0 → 154.0 and m/z 172.0 → 126.0 for GB and IS, respectively. The assay exhibited good linearity over a working range of 20–5000 ng/mL for GB in human plasma with a lower limit of quantitation of 20 ng/mL. No endogenous compounds were found to interfere with the analysis. The accuracy and precision were shown for concentrations over the standard ranges. This method was successfully applied for the PK and BE studies by analysis of blood samples taken up to 36 h after an oral dose of 300 mg of GB in 24 healthy volunteers. Copyright © 2007 John Wiley & Sons, Ltd.