Tags

Type your tag names separated by a space and hit enter

Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of urapidil and aripiprazole in human plasma and its application to human pharmacokinetic study.
Biomed Chromatogr. 2013 Jul; 27(7):916-23.BC

Abstract

A sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for simultaneous determination of urapidil and aripiprazole in human plasma. A simple liquid-liquid extraction with ethyl acetate was used for the sample preparation. Chromatographic separation was achieved on a Phenomenex C18 (4.6 × 50 mm, 5 µm) column with 0.1% formic acid-acetonitrile (10:90, v/v) as the mobile phase with flow rate of 0.6 mL/min. The quantitation of the target compounds was determined in a positive ion multiple reaction monitoring mode. Calibration plots were linear over the range of 2.0-2503.95 ng/mL for urapidil and 1.0-500.19 ng/mL for aripiprazole. The lower limit of quantitation for urapidil and aripiprazole was 2.0 and 1.0 ng/mL, respectively. Mean recovery was in the range of 69.94-75.62% for both analytes and internal standards. Intra-day and inter-day precisions of the assay at three concentrations were 2.56-5.89% with accuracy of 92.31-97.83% for urapidil, and 3.14-6.84% with accuracy of 91.38-94.42% for aripiprazole. The method was successfully applied to human pharmacokinetic study of urapidil and aripiprazole in healthy human male volunteers.

Authors+Show Affiliations

Sri Venkateswara University, Department of Chemistry, Tirupati, A.P., 517502, India.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

23463771

Citation

Ambavaram, Vijaya Bhaskar Reddy, et al. "Liquid Chromatography-tandem Mass Spectrometry Method for Simultaneous Quantification of Urapidil and Aripiprazole in Human Plasma and Its Application to Human Pharmacokinetic Study." Biomedical Chromatography : BMC, vol. 27, no. 7, 2013, pp. 916-23.
Ambavaram VB, Nandigam V, Vemula M, et al. Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of urapidil and aripiprazole in human plasma and its application to human pharmacokinetic study. Biomed Chromatogr. 2013;27(7):916-23.
Ambavaram, V. B., Nandigam, V., Vemula, M., Kalluru, G. R., & Gajulapalle, M. (2013). Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of urapidil and aripiprazole in human plasma and its application to human pharmacokinetic study. Biomedical Chromatography : BMC, 27(7), 916-23. https://doi.org/10.1002/bmc.2882
Ambavaram VB, et al. Liquid Chromatography-tandem Mass Spectrometry Method for Simultaneous Quantification of Urapidil and Aripiprazole in Human Plasma and Its Application to Human Pharmacokinetic Study. Biomed Chromatogr. 2013;27(7):916-23. PubMed PMID: 23463771.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of urapidil and aripiprazole in human plasma and its application to human pharmacokinetic study. AU - Ambavaram,Vijaya Bhaskar Reddy, AU - Nandigam,Venugopal, AU - Vemula,Madhavi, AU - Kalluru,Gangadhara Reddy, AU - Gajulapalle,Madhavi, Y1 - 2013/03/06/ PY - 2012/11/29/received PY - 2013/01/22/revised PY - 2013/01/23/accepted PY - 2013/3/7/entrez PY - 2013/3/7/pubmed PY - 2014/4/8/medline SP - 916 EP - 23 JF - Biomedical chromatography : BMC JO - Biomed Chromatogr VL - 27 IS - 7 N2 - A sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for simultaneous determination of urapidil and aripiprazole in human plasma. A simple liquid-liquid extraction with ethyl acetate was used for the sample preparation. Chromatographic separation was achieved on a Phenomenex C18 (4.6 × 50 mm, 5 µm) column with 0.1% formic acid-acetonitrile (10:90, v/v) as the mobile phase with flow rate of 0.6 mL/min. The quantitation of the target compounds was determined in a positive ion multiple reaction monitoring mode. Calibration plots were linear over the range of 2.0-2503.95 ng/mL for urapidil and 1.0-500.19 ng/mL for aripiprazole. The lower limit of quantitation for urapidil and aripiprazole was 2.0 and 1.0 ng/mL, respectively. Mean recovery was in the range of 69.94-75.62% for both analytes and internal standards. Intra-day and inter-day precisions of the assay at three concentrations were 2.56-5.89% with accuracy of 92.31-97.83% for urapidil, and 3.14-6.84% with accuracy of 91.38-94.42% for aripiprazole. The method was successfully applied to human pharmacokinetic study of urapidil and aripiprazole in healthy human male volunteers. SN - 1099-0801 UR - https://www.unboundmedicine.com/medline/citation/23463771/Liquid_chromatography_tandem_mass_spectrometry_method_for_simultaneous_quantification_of_urapidil_and_aripiprazole_in_human_plasma_and_its_application_to_human_pharmacokinetic_study_ L2 - https://doi.org/10.1002/bmc.2882 DB - PRIME DP - Unbound Medicine ER -