Wilson R C, Green N K
Am J Vet Res. 1986 Mar;47(3):650-2.
Eight adult sheep were given 2.2 mg of minocycline hydrochloride/kg of body weight IV before and after blood was collected to induce hypoproteinemia. The blood collection produced a significant (P less than 0.01) reduction in PCV, hemoglobin, and total serum protein values. Pharmacokinetic evaluation of the serum drug concentration vs time data was performed, using a noncompartmental model based on statistical moment theory. Pharmacokinetic values obtained from the sheep with normal serum protein were 5.94 +/- 1.78 ml/kg/min for clearance, 1.32 +/- 0.16 L/kg for the steady-state volume of distribution, and 3.89 +/- 0.80 hours for mean residence time. Significant differences were not found in these values obtained from the sheep when they were hypoproteinemic. The effective half-life, reported as the harmonic mean, increased from 2.57 hours in sheep before blood collection to 2.91 hours in sheep when they were hypoproteinemic. The 2.2 mg of minocycline/kg administered once or twice daily would not be expected to produce adequate serum concentrations for most susceptible microorganisms. Some evidence that minocycline disposition may follow zero-order kinetics is presented.
对八只成年绵羊在采血前后静脉注射2.2毫克盐酸米诺环素/千克体重,以诱导低蛋白血症。采血导致红细胞压积、血红蛋白和血清总蛋白值显著降低(P<0.01)。基于统计矩理论,使用非房室模型对血清药物浓度与时间数据进行药代动力学评估。血清蛋白正常的绵羊的药代动力学值为清除率5.94±1.78毫升/千克/分钟,稳态分布容积1.32±0.16升/千克,平均驻留时间3.89±0.80小时。从低蛋白血症绵羊获得的这些值未发现显著差异。以调和平均数表示的有效半衰期从采血前绵羊的2.57小时增加到低蛋白血症绵羊的2.91小时。每天给药一次或两次的2.2毫克米诺环素/千克预计不会对大多数易感微生物产生足够的血清浓度。文中给出了一些米诺环素处置可能遵循零级动力学的证据。