Liquid chromatography tandem mass spectrometry determination method of bencycloquidium bromide: application to drug interaction study in human.]

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AuteurASSANHOU, ASSOGBA GABIN
Date d'ajout2026-06-02T16:06:57Z
Date de disponibilite2026-06-02T16:06:57Z
Date de publication2021
ResumeObjective: This study was conducted to develop a sensitive and effective LC-MS/MS method for the determination of bencycloquidium bromide (BCQB) and its application in pharmacokinetic drug interaction study between BCQB and paroxetine. Methods: The chromatographic separation was performed on Hedera ODS-2 C18 column with a mobile phase consisted of acetonitrile-10 mmol/l ammonium acetate containing 0.2% acetic acid (33:67, v/v) at 550 μl/min, and the plasma samples were processed using solid-phase extraction. The MS/MS transitions were m/z 330.2 → 142.0 for BCQB and m/z 344.2 → 156.1 for the I. S in positive ESI mode. Results: The validated method was linear over the concentration range of 2-1200 pg/ml with the correlation coefficient r2>0.998. The intra-and inter-batch precisions of the assay were lower than 8.2% and 9.1%, respectively. The lower limit of quantification (LLOQ) was 2 pg/ml. The stability data at different storage conditions of BCQB were within±5% RE. The mean AUC0-36 of BCQB was increased by approximately 33%, after the administration of BCQB alone and upon co-administration with paroxetine during the drug interaction study. Conclusion: The LC-MS/MS method validated in this study was robust, reproducible, accurate, precise and reliable and was successfully applied in the pharmacokinetic drug interaction studies.
DOI10.22159/ijpps.2021v13i10.5791
Autre identifiantBECDB-13484
URIhttps://dspace.uac.bj/handle/123456789/11547
Languefr
Fait partie deInternational Journal of Pharmacy and Pharmaceutical Sciences (Int J Pharm Pharm Sci)
SujetBencycloquidium bromide
SujetLC-MS/MS
SujetPharmacokinetic drug interaction
SujetParoxetine
TitreLiquid chromatography tandem mass spectrometry determination method of bencycloquidium bromide: application to drug interaction study in human.]
TypeArticle

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