4.6 Article

Simultaneous determination of NTB-3119, a novel anti-tuberculosis agent, and its major metabolites in mouse plasma by LC-MS/MS and its application in preclinical pharmacokinetics study

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DOI: 10.1016/j.jpba.2022.115172

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NTB-3119; Quantification analysis; Anti-tuberculosis; LC-MS; MS; Pharmacokinetics

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In this study, three major metabolites of NTB-3119 were identified in vitro and in vivo. A sensitive and specific LC-MS/MS method was established for the quantitative analysis of NTB-3119 and its major metabolites in mouse plasma.
NTB-3119, a novel benzothiopyranone derivative, has been developed as a potential anti-tuberculosis(TB) drug with strong activity. In this study, three major metabolites of NTB-3119 were firstly identified in vitro and in vivo. A sensitive and specific liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was established for the quantitative analysis of NTB-3119 and its major metabolites NTB-3190, NTB-3202 and NTB-3204 in mouse plasma. The plasma samples were processed by protein precipitation with organic solvent. NTB-3119, NTB-3190, NTB-3202, NTB-3204 and NTB-4A (Internal Standard, IS) were separated by a Zorbax-SB C18 col-umn (100 mm x 2.1 mm, 3.5 mu m) with a gradient mobile phase of acetonitrile/water at a flow rate of 0.25 mL/ min. The analytes were detected by electrospray positive ion mode in Parallel Reaction Monitoring (PRM) mode on a high resolution mass spectrum (HRMS, Thermo Q Executive). The monitored transitions were m/z 456.15632 -> 360.06137 for NTB-3119, m/z 426.18214 -> 246.01891 for NTB-3190, m/z 472.15124 -> 360.06143 for NTB-3202, m/z 442.17706 -> 246.01903 for NTB-3204 and m/z 337.13691 -> 163.02081 for NTB-4A, respectively. Good linearity was conducted in the range of 5-2000 ng/mL for NTB-3119, NTB-3202 and NTB-3204 as well as 2.5-1000 ng/mL for NTB-3190. The inter-and intra-batch precision (RSD%) were both lower than 13.3 %, with the accuracy ranged from 88.0 % to 108.1 %. The analytes were proved to be stable during all samples storage, preparation and analytic procedures. The validated method was successfully applied to study the pharmacokinetics and bioavailability of NTB-3119 after oral treatment in Balb/c mouse.

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