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Ultra-performance liquid chromatography-tandem mass spectrometry for the determination of lacidipine in human plasma and its application in a pharmacokinetic study.
J Pharm Biomed Anal. 2008 Aug 05; 47(4-5):923-8.JP

Abstract

A selective, rapid and sensitive ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-ESI-MS/MS) method was developed and validated for the quantification of lacidipine in human plasma. With nifedipine as an internal standard, sample pretreatment involved a simple liquid-liquid extraction with tert-butyl methyl ether of 1 ml plasma. The analysis was carried out on an Acquity UPLC BEH C18 column (50 mm x 2.1 mm, 1.7 microm) with flow rate of 0.28 ml/min. The mobile phase was 30 mM ammonium acetate buffer-acetonitrile (18:82, v/v, pH 5.5). The detection was performed on a triple-quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) mode via electrospray ionization (ESI). Linear calibration curves were obtained in the concentration range of 0.025-10.000 ng/ml, with a lower limit of quantification of 0.025 ng/ml. The intra- and inter-day precision (R.S.D.) values were below 15% and accuracy (RE) was -12.7% to 11.9% at all QC levels. The method was successfully applied to a clinical pharmacokinetic study of lacidipine in healthy volunteers following oral administration.

Authors+Show Affiliations

Clinical Pharmacy & Pharmacology Institute, The Second Xiang Ya Hospital, Central South University, Changsha 410011, PR China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

18534803

Citation

Tang, Jing, et al. "Ultra-performance Liquid Chromatography-tandem Mass Spectrometry for the Determination of Lacidipine in Human Plasma and Its Application in a Pharmacokinetic Study." Journal of Pharmaceutical and Biomedical Analysis, vol. 47, no. 4-5, 2008, pp. 923-8.
Tang J, Zhu R, Zhao R, et al. Ultra-performance liquid chromatography-tandem mass spectrometry for the determination of lacidipine in human plasma and its application in a pharmacokinetic study. J Pharm Biomed Anal. 2008;47(4-5):923-8.
Tang, J., Zhu, R., Zhao, R., Cheng, G., & Peng, W. (2008). Ultra-performance liquid chromatography-tandem mass spectrometry for the determination of lacidipine in human plasma and its application in a pharmacokinetic study. Journal of Pharmaceutical and Biomedical Analysis, 47(4-5), 923-8. https://doi.org/10.1016/j.jpba.2008.04.018
Tang J, et al. Ultra-performance Liquid Chromatography-tandem Mass Spectrometry for the Determination of Lacidipine in Human Plasma and Its Application in a Pharmacokinetic Study. J Pharm Biomed Anal. 2008 Aug 5;47(4-5):923-8. PubMed PMID: 18534803.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Ultra-performance liquid chromatography-tandem mass spectrometry for the determination of lacidipine in human plasma and its application in a pharmacokinetic study. AU - Tang,Jing, AU - Zhu,Ronghua, AU - Zhao,Ruike, AU - Cheng,Gang, AU - Peng,Wenxing, Y1 - 2008/04/25/ PY - 2008/03/16/received PY - 2008/04/08/revised PY - 2008/04/10/accepted PY - 2008/6/7/pubmed PY - 2008/9/4/medline PY - 2008/6/7/entrez SP - 923 EP - 8 JF - Journal of pharmaceutical and biomedical analysis JO - J Pharm Biomed Anal VL - 47 IS - 4-5 N2 - A selective, rapid and sensitive ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-ESI-MS/MS) method was developed and validated for the quantification of lacidipine in human plasma. With nifedipine as an internal standard, sample pretreatment involved a simple liquid-liquid extraction with tert-butyl methyl ether of 1 ml plasma. The analysis was carried out on an Acquity UPLC BEH C18 column (50 mm x 2.1 mm, 1.7 microm) with flow rate of 0.28 ml/min. The mobile phase was 30 mM ammonium acetate buffer-acetonitrile (18:82, v/v, pH 5.5). The detection was performed on a triple-quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) mode via electrospray ionization (ESI). Linear calibration curves were obtained in the concentration range of 0.025-10.000 ng/ml, with a lower limit of quantification of 0.025 ng/ml. The intra- and inter-day precision (R.S.D.) values were below 15% and accuracy (RE) was -12.7% to 11.9% at all QC levels. The method was successfully applied to a clinical pharmacokinetic study of lacidipine in healthy volunteers following oral administration. SN - 0731-7085 UR - https://www.unboundmedicine.com/medline/citation/18534803/Ultra_performance_liquid_chromatography_tandem_mass_spectrometry_for_the_determination_of_lacidipine_in_human_plasma_and_its_application_in_a_pharmacokinetic_study_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0731-7085(08)00223-9 DB - PRIME DP - Unbound Medicine ER -