Optimization of an HPLC method for determination of gabapentin in dosage forms through derivatization with 1-fluoro-2,4-dinitrobenzene

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Abstract

A rapid, sensitive and accurate high performance liquid chromatography with UV detection method was developed and validated for the quantification of gabapentin in dosage forms. Gabapentin was quantified after pre-column derivatization with 1-fluoro-2,4-dinitrobenzene. Amlodipine was used as an internal standard. The chromatographic separation was carried out on a Nova-Pak C18 column using a mixture of acetonitrile-sodium dihydrogenphosphate (pH 2.5; 0.05 M) (70 : 30, v/v) as mobile phase with UV detection at 360 nm. The method was linear over the range of 10-500 μg/ml of gabapentin (r 2>0.999). The within-day and between-day precision values were in the range of 0.86-1.11%. The method was successfully used for quantitative determination and dissolution rate study of Neurontin capsules. © 2007 Pharmaceutical Society of Japan.

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Souri, E., Jalalizadeh, H., & Shafiee, A. (2007). Optimization of an HPLC method for determination of gabapentin in dosage forms through derivatization with 1-fluoro-2,4-dinitrobenzene. Chemical and Pharmaceutical Bulletin, 55(10), 1427–1430. https://doi.org/10.1248/cpb.55.1427

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