首页> 外文期刊>The Veterinary Journal >The pharmacokinetics and in vitro/ex vivo cyclooxygenase selectivity of parecoxib and its active metabolite valdecoxib in cats
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The pharmacokinetics and in vitro/ex vivo cyclooxygenase selectivity of parecoxib and its active metabolite valdecoxib in cats

机译:parecoxib及其活性代谢产物valdecoxib在猫体内的药代动力学和体内/体外环氧合酶选择性

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摘要

Parecoxib (PX) is an injectable prodrug of valdecoxib (VX, which is a selective cyclo-oxyganase-2 (COX-2)) inhibitor licensed for humans. The aim of the present study was to evaluate pharmacokinetics and in vitro/ex vivo cyclooxygenase selectivity of PX and VX in cats. In a whole blood in vitro study, PX did not affect either COX enzymes whereas VX revealed a COX-2 selective inhibitory effect in feline whole blood. The IC50 values of VX for COX-2 and COX-1 were 0.45 and 38.6 mu M, respectively.
机译:Parecoxib(PX)是伐地昔布(VX,是选择性环氧化酶2(COX-2))抑制剂的可注射前药,可用于人类。本研究的目的是评估猫体内PX和VX的药代动力学和体外/离体环氧合酶的选择性。在体外全血研究中,PX不影响任何一种COX酶,而VX显示出对猫全血的COX-2选择性抑制作用。 VX对COX-2和COX-1的IC50值分别为0.45和38.6μM。

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