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首页> 外文期刊>The Veterinary Journal >Disposition kinetics of moxifloxacin in lactating ewes
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Disposition kinetics of moxifloxacin in lactating ewes

机译:莫西沙星在泌乳母羊中的处置动力学

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The present study was planned to investigate the plasma disposition kinetics and the pattern of moxifloxacin elimination in the milk of lactating ewes (n=6) following a single intravenous (IV) bolus or intramuscular (IM) injections at a dosage of 5 mg/kg in all animals. A crossover study was carried out in two phases separated by 21 days. Plasma and milk samples were collected serially for 72 h and moxifloxacin concentrations were assayed using high performance liquid chromatography with fluorescence detection. A two-compartment open model best described the decrease of moxifloxacin concentration in the plasma after IV injection. The disposition after IM administration moxifloxacin was best described by a one-compartment model. Following IV administration, the distribution half-life (t(1/2alpha)) was 0.22+/-0.02 h. The elimination half-life was 1.77+/-0.23 h. The volume of distribution at steady state (V(dss)) was 0.84+/-0.12L/kg, the total body clearance (Cl(tot)) was 0.34+/-0.04 L/h/kg and the area under the curve (AUC) was 14.74+/-2.16 microg h/mL. Following IM administration, the mean T(max), C(max), t(1/2el) and AUC values for plasma data were 1.45+/-0.02 h, 2.21+/-0.27 microg/mL, 2.68+/-0.19 h and 14.21+/-2.35 microg h/mL. The IM bioavailability was 96.35+/-17.23% and the in vitro protein binding of moxifloxacin ranged from 32-37%. Penetration of moxifloxacin from the blood into milk was rapid and extensive, and the moxifloxacin concentrations in milk exceeded those in plasma from 1h after administration. The kinetic values AUC(milk)/AUC(plasma) and C(maxmilk)/C(maxplasma) ratios indicated a wide penetration of moxifloxacin from the bloodstream to the mammary gland. The in vitro minimum inhibitory concentration (MIC) of moxifloxacin for Mannheimia haemolytica was found to be 0.035 microg/mL.
机译:本研究计划调查以5 mg / kg剂量单次静脉内(IV)推注或肌内(IM)注射后的泌乳母羊(n = 6)的血浆处置动力学和莫西沙星乳汁消除模式在所有动物中。交叉研究分两个阶段进行,相隔21天。连续收集血浆和牛奶样品72小时,并使用带有荧光检测功能的高效液相色谱法测定莫西沙星的浓度。两室开放模型最能描述静脉注射后血浆中莫西沙星浓度的降低。一室模型最好地描述了IM给药莫西沙星后的处置情况。静脉内给药后,分布半衰期(t(1 / 2alpha))为0.22 +/- 0.02 h。消除半衰期为1.77 +/- 0.23小时。稳态时的分布体积(V(dss))为0.84 +/- 0.12L / kg,总身体清除率(Cl(tot))为0.34 +/- 0.04 L / h / kg,曲线下面积(AUC)为14.74 +/- 2.16微克h / mL。 IM给药后,血浆数据的平均T(max),C(max),t(1 / 2el)和AUC值分别为1.45 +/- 0.02 h,2.21 +/- 0.27 microg / mL,2.68 +/- 0.19 h和14.21 +/- 2.35 microg h / mL。 IM的生物利用度为96.35 +/- 17.23%,莫西沙星的体外蛋白结合率为32-37%。给药后1h,莫西沙星从血液中渗透到牛奶中的速度迅速而广泛,牛奶中的莫西沙星浓度超过血浆中的浓度。动力学值AUC(牛奶)/ AUC(血浆)和C(最大牛奶)/ C(最大血浆)之比表明莫西沙星从血流到乳腺的广泛渗透。莫西沙星对溶血曼海姆氏菌的体外最低抑菌浓度(MIC)为0.035 microg / mL。

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