Determination of Talniflumate and Niflumic Acid in Human Plasma by Liquid Chromatography-Tandem Mass Spectrometry
A simple and rapid quantification method was developed for determining both talniflumate and niflumic acid in human plasma. After simple protein precipitation with acetonitrile, the analytes were chromatographed on a reversed-phase C18 column and detected by LC/MS/MS with electrospray ionization. Th...
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Published in | Analytical Sciences Vol. 25; no. 4; pp. 571 - 574 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Singapore
The Japan Society for Analytical Chemistry
01.04.2009
Springer Nature Singapore Nature Publishing Group |
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ISSN | 0910-6340 1348-2246 1348-2246 |
DOI | 10.2116/analsci.25.571 |
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Abstract | A simple and rapid quantification method was developed for determining both talniflumate and niflumic acid in human plasma. After simple protein precipitation with acetonitrile, the analytes were chromatographed on a reversed-phase C18 column and detected by LC/MS/MS with electrospray ionization. The assay accuracy and precision were within the FDA guidance for the analytical method validation. This method was used to measure the plasma concentrations of both compounds from healthy subjects after a single oral dose of talniflumate, 740 mg. |
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AbstractList | A simple and rapid quantification method was developed for determining both talniflumate and niflumic acid in human plasma. After simple protein precipitation with acetonitrile, the analytes were chromatographed on a reversed-phase C
18
column and detected by LC/MS/MS with electrospray ionization. The assay accuracy and precision were within the FDA guidance for the analytical method validation. This method was used to measure the plasma concentrations of both compounds from healthy subjects after a single oral dose of talniflumate, 740 mg. A simple and rapid quantification method was developed for determining both talniflumate and niflumic acid in human plasma. After simple protein precipitation with acetonitrile, the analytes were chromatographed on a reversed-phase C18 column and detected by LC/MS/MS with electrospray ionization. The assay accuracy and precision were within the FDA guidance for the analytical method validation. This method was used to measure the plasma concentrations of both compounds from healthy subjects after a single oral dose of talniflumate, 740 mg. A simple and rapid quantification method was developed for determining both talniflumate and niflumic acid in human plasma. After simple protein precipitation with acetonitrile, the analytes were chromatographed on a reversed-phase C(18) column and detected by LC/MS/MS with electrospray ionization. The assay accuracy and precision were within the FDA guidance for the analytical method validation. This method was used to measure the plasma concentrations of both compounds from healthy subjects after a single oral dose of talniflumate, 740 mg.A simple and rapid quantification method was developed for determining both talniflumate and niflumic acid in human plasma. After simple protein precipitation with acetonitrile, the analytes were chromatographed on a reversed-phase C(18) column and detected by LC/MS/MS with electrospray ionization. The assay accuracy and precision were within the FDA guidance for the analytical method validation. This method was used to measure the plasma concentrations of both compounds from healthy subjects after a single oral dose of talniflumate, 740 mg. A simple and rapid quantification method was developed for determining both talniflumate and niflumic acid in human plasma. After simple protein precipitation with acetonitrile, the analytes were chromatographed on a reversed-phase C(18) column and detected by LC/MS/MS with electrospray ionization. The assay accuracy and precision were within the FDA guidance for the analytical method validation. This method was used to measure the plasma concentrations of both compounds from healthy subjects after a single oral dose of talniflumate, 740 mg. |
Author | KIM, Kibum KANG, Wonku |
Author_xml | – sequence: 1 fullname: KANG, Wonku organization: College of Pharmacy, Catholic University of Daegu – sequence: 1 fullname: KIM, Kibum organization: College of Pharmacy, Catholic University of Daegu |
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Cites_doi | 10.1016/j.jpba.2007.04.028 10.1016/j.jchromb.2005.05.008 10.1016/S0378-4347(00)80107-3 10.2116/analsci.22.1597 10.1016/j.jchromb.2008.10.010 10.1016/S0021-9673(01)96107-2 10.1007/BF02976244 10.1002/bmc.412 |
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SubjectTerms | Analytical Chemistry Benzofurans - administration & dosage Benzofurans - blood Benzofurans - pharmacokinetics Chemical Precipitation Chemistry Chromatography, Liquid Humans Ionization Linear Models Liquid chromatography Mass spectrometry Niflumic Acid - administration & dosage Niflumic Acid - blood Niflumic Acid - pharmacokinetics Proteins - chemistry Pyridines - administration & dosage Pyridines - blood Pyridines - pharmacokinetics Sensitivity and Specificity Solvents - chemistry Tandem Mass Spectrometry Time Factors |
Title | Determination of Talniflumate and Niflumic Acid in Human Plasma by Liquid Chromatography-Tandem Mass Spectrometry |
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