首页> 外文期刊>Journal of Veterinary Pharmacology and Therapeutics >Comparative pharmacokinetics and tissue distribution of quinocetone in crucian carp (Carassius auratus), common carp (Cyprinus carpio L.), and grass carp (Ctenopharyngodon idella) following the same experimental conditions
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Comparative pharmacokinetics and tissue distribution of quinocetone in crucian carp (Carassius auratus), common carp (Cyprinus carpio L.), and grass carp (Ctenopharyngodon idella) following the same experimental conditions

机译:在相同实验条件下,喹ce酮在cru鱼(Carassius auratus),鲤鱼(Cyprinus carpio L.)和草鱼(Ctenopharyngodon idella)中的药代动力学和组织分布的比较

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摘要

The pharmacokinetics and tissue distribution of quinocetone (QCT) in crucian carp (Carassius auratus), common carp (Cyprinus carpio L.), and grass carp (Ctenopharyngodon idella) were compared after oral administration of QCT (50mg/kg body weight) at water temperature of 24 +/- 1 degrees C. Similar QCT plasma concentration-time profiles were found in the three species of cyprinid fish at the same dosage regimen and water temperature, which were all fitted two-compartment open pharmacokinetic model. However, different pharmacokinetic parameters were observed in crucian carp, common carp, and grass carp. The absorption rate constants (K-a) of QCT were 1.65, 1.40 and 1.74/h, respectively and absorption half-lives (t(1/2k)) were 0.42, 0.49, and 0.40/h, respectively. The distribution half-life (t(1/2)) was 2.83, 0.67, and 0.88h, respectively, and elimination half-lives (t(1/2)) of QCT were 133.97, 63.55, and 40.76h, respectively. The maximum concentrations (C-max) of QCT in plasma were 0.315, 0.182, and 0.139g/mL and the time to peak concentrations (T-p) were 1.45, 0.96, and 1.08h, respectively. The area under the plasma concentration-time curves (AUC) were 12.35, 5.99, and 4.52gbold>h/bold>/mL, respectively. The distribution volumes (V-d/F) of QCT were calculated as 117.81, 128.71, and 220.10L/kg, respectively. The tissue analysis showed that a similar regularity was obtained in the three species of cyprinids with a single dose of 50mg/kg body weight after oral administration at the same water temperature. The tissue concentration of QCT in each fish was in order of liver>kidney>muscle, while the residues of QCT in the three species of cyprinid fish were in order of crucian carp>common carp>grass carp.
机译:比较了口服QCT(50mg / kg体重)时after鱼(Carassius auratus),鲤鱼(Cyprinus carpio L.)和草鱼(Ctenopharyngodon idella)中喹烯酮(QCT)的药代动力学和组织分布。温度为24 +/- 1摄氏度。在相同剂量和水温下,在三种塞浦路斯鱼类中发现了相似的QCT血浆浓度-时间曲线,它们均符合两室开放药代动力学模型。但是,在cru鱼,鲤鱼和草鱼中观察到不同的药代动力学参数。 QCT的吸收速率常数(K-a)分别为1.65、1.40和1.74 / h,吸收半衰期(t(1 / 2k))分别为0.42、0.49和0.40 / h。 QCT的分布半衰期(t(1/2))分别为2.83、0.67和0.88h,QCT的消除半衰期(t(1/2))分别为133.97、63.55和40.76h。血浆中QCT的最大浓度(C-max)为0.315、0.182和0.139g / mL,达到峰值浓度的时间(T-p)分别为1.45、0.96和1.08h。血浆浓度-时间曲线(AUC)下的面积分别为12.35、5.99和4.52g h / mL。 QCT的分配体积(V-d / F)分别计算为117.81、128.71和220.10L / kg。组织分析表明,在相同的水温下口服后,单剂量为50mg / kg体重的这三种鲤科鱼类中获得了相似的规律性。每条鱼的QCT组织浓度依次为肝脏>肾脏>肌肉,而3种塞浦路斯鱼的QCT残留依次为c鱼>鲤鱼>草鱼。

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