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Simultaneous Determination of Parecoxib and Its Metabolite Valdecoxib Concentrations in Beagle Plasma by UPLC-MS/MS and Application for Pharmacokinetics Study

机译:UPLC-MS / MS同时测定比格犬血浆中帕瑞昔布及其代谢产物瓦尔地昔布的浓度及其在药代动力学研究中的应用

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摘要

A method for the simultaneous determination of parecoxib and its metabolite valdecoxib in beagle plasma by UPLC-MS/MS was developed and validated. After the plasma was extracted by acetonitrile precipitation, the analytes were separated on an Acquity UPLC BEH C18 column (2.1 mm × 50 mm, 1.7 μm) using acetonitrile-formic acid as the mobile phase in gradient mode. The analytes were monitored by multiple reaction monitoring (MRM) in electrospray negative ion mode. The mass transfer pairs were m/z 368.97→119.01 for parecoxib, m/z 312.89→118.02 for valdecoxib, and m/z 379.98→316.02 for celecoxib (internal standard, IS). The correlation coefficients of parecoxib and valdecoxib ranged from 5 to 4000 ng/mL were greater than 0.9998. The recovery of parecoxib and valdecoxib was greater than 82.54%. The inter- and intra-day precision RSD values were 1.36~3.65% and 2.28~5.91%, respectively. The accuracy of RE values were −1.38%~1.96%. Finally, the matrix effect (ME) and stability were also within acceptable criteria. This method had been successfully applied to the pharmacokinetics of parecoxib and valdecoxib in beagle plasma after injection of parecoxib (1.33 mg/kg, intramuscular injection).
机译:建立并验证了通过UPLC-MS / MS同时测定比格犬血浆中帕瑞考昔及其代谢产物瓦尔德考昔的方法。通过乙腈沉淀提取血浆后,使用乙腈-甲酸作为流动相,在梯度模式下,在Acquity UPLC BEH C18色谱柱(2.1 mm×50 mm,1.7μm)上分离分析物。通过多反应监测(MRM)以电喷雾负离子模式监测分析物。派瑞昔布的传质对为m / z 368.97→119.01,伐地昔布为m / z 312.89→118.02,塞来昔布为m / z 379.98→316.02(内标,IS)。 parecoxib和valdecoxib的相关系数在5到4000 ng / mL之间,大于0.9998。 parecoxib和valdecoxib的回收率大于82.54%。日间和日内精确RSD值分别为1.36〜3.65%和2.28〜5.91%。 RE值的准确性为-1.38%〜1.96%。最后,基质效应(ME)和稳定性也在可接受的标准之内。该方法已成功应用于帕瑞昔布注射(1.33 mg / kg,肌肉内注射)后帕瑞昔布和伐地昔布在比格犬血浆中的药代动力学。

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