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Analysis of Amisulpride in Human Plasma by SPE and LC with Fluorescence Detection

A rapid, precise, accurate, and selective high-performance liquid chromatographic method with fluorescence detection has been validated and used for analysis of amisulpride in human plasma after a simple solid-phase extraction procedure. Compounds were separated on a CN column with 0.03 M potassium...

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Detalles Bibliográficos
Autores principales: Kudris, Illia V., Skakun, Nona N., Orlova, Irina N., Libina, Victoria V., Kulikov, Artem U.
Formato: Texto
Lenguaje:English
Publicado: Vieweg Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3030746/
https://www.ncbi.nlm.nih.gov/pubmed/21423321
http://dx.doi.org/10.1007/s10337-010-1832-2
Descripción
Sumario:A rapid, precise, accurate, and selective high-performance liquid chromatographic method with fluorescence detection has been validated and used for analysis of amisulpride in human plasma after a simple solid-phase extraction procedure. Compounds were separated on a CN column with 0.03 M potassium dihydrogen phosphate (pH 6.5)–acetonitrile 65:35 (v/v) as mobile phase. Fluorescence detection was performed at excitation and emission wavelengths of 274 and 370 nm, respectively. Calibration plots were linear over the concentration range 10–1,000 ng mL(−1) in human plasma, and the lower limit of quantification was 10 ng mL(−1). Accuracy was between 0.4 and 6.4% and precision was between 3.1 and 7.5%. Amisulpride was sufficiently stable through three freeze–thaw cycles, during storage for 6 h at room temperature, and for 2 months at −22 °C. The method is suitable for the analysis of clinical samples from pharmacokinetic studies.