Rapid and sensitive UPLC-MS/MS method for the determination of domperidone in human plasma and its application to pharmacokinetic study
In this study, a simple, rapid and sensitive ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method is described for determination of domperidone in human plasma samples using oxcarbazepine as the internal standard (IS). Sample preparation was accomplished through prote...
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Published in | Drug research Vol. 64; no. 6; p. 330 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
01.06.2014
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Abstract | In this study, a simple, rapid and sensitive ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method is described for determination of domperidone in human plasma samples using oxcarbazepine as the internal standard (IS). Sample preparation was accomplished through protein precipitation with methanol, and chromatographic separation was performed on an Acquity BEH C18 column (2.1 mm×50 mm, 1.7 μm) with gradient profile at a flow of 0.45 mL/min. Mass spectrometric analysis was performed using a QTrap5500 mass spectrometer coupled with an electro-spray ionization (ESI) source in the positive ion mode. The MRM transition of m/z 426.3→175.2 was used to quantify for domperidone. The linearity of this method was found to be within the concentration range of 0.25-100.0 ng/mL for domperidone in human plasma. Only 1.5 min was needed for an analytical run. The method herein described was superior to previous methods and was successfully applied to the pharmacokinetic study of domperidone in healthy Chinese volunteers after oral administration. |
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AbstractList | In this study, a simple, rapid and sensitive ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method is described for determination of domperidone in human plasma samples using oxcarbazepine as the internal standard (IS). Sample preparation was accomplished through protein precipitation with methanol, and chromatographic separation was performed on an Acquity BEH C18 column (2.1 mm×50 mm, 1.7 μm) with gradient profile at a flow of 0.45 mL/min. Mass spectrometric analysis was performed using a QTrap5500 mass spectrometer coupled with an electro-spray ionization (ESI) source in the positive ion mode. The MRM transition of m/z 426.3→175.2 was used to quantify for domperidone. The linearity of this method was found to be within the concentration range of 0.25-100.0 ng/mL for domperidone in human plasma. Only 1.5 min was needed for an analytical run. The method herein described was superior to previous methods and was successfully applied to the pharmacokinetic study of domperidone in healthy Chinese volunteers after oral administration. |
Author | Ye, L Wang, R Wang, Y-F Qiu, X-J Zheng, S-L |
Author_xml | – sequence: 1 givenname: X-J surname: Qiu fullname: Qiu, X-J organization: Department of Pharmacology, Medical College of Henan University of Science and Technology, Luoyang, China – sequence: 2 givenname: S-L surname: Zheng fullname: Zheng, S-L organization: The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China – sequence: 3 givenname: Y-F surname: Wang fullname: Wang, Y-F organization: Department of Pharmacology, Medical College of Henan University of Science and Technology, Luoyang, China – sequence: 4 givenname: R surname: Wang fullname: Wang, R organization: Department of Pharmacology, Medical College of Henan University of Science and Technology, Luoyang, China – sequence: 5 givenname: L surname: Ye fullname: Ye, L organization: The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24549964$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Calibration Chromatography, High Pressure Liquid - methods Domperidone - blood Domperidone - pharmacokinetics Drug Stability Humans Tandem Mass Spectrometry - methods |
Title | Rapid and sensitive UPLC-MS/MS method for the determination of domperidone in human plasma and its application to pharmacokinetic study |
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