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Development of an UPLC-MS/MS micromethod for quantitation of cinitapride in plasma and its application in a
Gabriel Marcelín-Jiménez1, Leticia Contreras2, Javier Esquivel2
1Global Bioanalytical Consulting, S.C., Heriberto Frías No. 1439, Int. 402, Col. Del Valle, Del. Benito Juárez, Mexico City 03100, Mexico.
Aim:
Cinitapride (CIN) is a benzamide-derived molecule used for the treatment of gastroesophageal reflux and dyspepsia. Its pharmacokinetics are controversial due to the use of supratherapeutic doses and the lack of sensitive methodology. Therefore, a sensitive and accurate micromethod was developed for its quantitation in human plasma.
Results:
CIN was extracted from 300 µl of heparinized plasma by liquid-liquid extraction using cisapride as internal standard, and analyzed with an ultra performance liquid chromatograph employing positive multiple-reaction monitoring-MS.
Conclusion:
The method proved to be rapid, accurate and stable within a range between 50 and 2000 pg/ml and was successfully validated and applied in a pharmacokinetic interaction trial, where it was demonstrated that oral co-administration of simethicone does not modify the bioavailability of CIN.
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