Development and validation of an LC-MS/MS method for pharmacokinetic study of lobetyolin in rats



Título del documento: Development and validation of an LC-MS/MS method for pharmacokinetic study of lobetyolin in rats
Revista: Brazilian Journal of Pharmaceutical Sciences
Base de datos: PERIÓDICA
Número de sistema: 000451810
ISSN: 1984-8250
Autores: 1
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2
Instituciones: 1Shandong University of Traditional Chinese Medicine, School of Pharmaceutical Sciences, Jinan, Shandong. China
2Jiaozhou People’s Hospital, Qingdao, Shandong. China
Año:
Volumen: 58
País: Brasil
Idioma: Inglés
Tipo de documento: Artículo
Enfoque: Experimental, aplicado
Resumen en inglés A simple and selective liquid chromatography tandem with mass spectrometry (LC-MS/ MS) method for quantification of lobetyolin in rat plasma was developed and validated. Chromatographic separation was achieved on a Thermo ODS C18 reversed-phase column using 0.1% aqueous formic acid-methanol (50:50, v/v) in an isocratic elution mode at a flow rate of 0.4 mL.min-1. LC/MS performance was done in a positive ion ESI mode and the MS/MS transitions were monitored at m/z 419.3 [M+Na]+ → m/z 203.1 for lobetyolin and m/z 394.9 [M+Na]+ → m/z 231.9 for IS, respectively. The assay exhibited a linear dynamic range over 1.0-500 ng.mL-1 for lobetyolin in plasma. Both the precision (%RSD) and accuracy (RE%) were within acceptable criteria (<15%). Recoveries ranged from 87.0% to 95.6%, and the matrix effects were from 91.0% to 101.3%. After oral administration, the peak plasma concentration of lobetyolin was obtained as 60.1 ng.mL-1 at 1.0 h. The proposed LC-MS/MS method could be applied to a pharmacokinetic study employing 66 samples from 6 Wistar rats
Disciplinas: Química
Palabras clave: Química farmacéutica,
Lobetiolina,
Farmacocinética
Keyword: Medicinal chemistry,
Lobetyolin,
Pharmacokinetics
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