Effect Of Amprolium and Toltrazuril On disposition kinetics Of Tylvalosin In Infected Broiler Chickens With Mycoplasma Gallisepticum

Ahmed R. E. Mahdy, Zinab Mohamed
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Abstract

A fter a single oral treatment, the pharmacokinetic characteristics of tylvalosin alone and in combination with either amprolium or toltrazuril in Mycoplasma gallisepticum-infected broiler chickens were evaluated. 18 chickens were divided into 3 equal groups, group one was given tylvalosin only, group two was given tylvalosin and amprolium and group three was given tylvalosin and toltrazuril. The best model for describing tylvalosin serum levels in our study was found to be a twocompartment open model. The maximum serum concentration of tylvalosin was 1.62±0.03, 1.2±0.02, and 1.41±0.01 μg/ml reached at 2.95±0.014, 2.8±0.01, and 2.83±0.02 h in group one, group two, and group three respectively. A significant (P<0.001)increasesin V/F and Cl/F10.19±0.11(mg)/(μg/ ml), 1.54±0.04(mg)/(μg/ml)/h and 8.56±0.07(mg)/(μg/ml), 1.31±0.03 (mg)/ (μg/ml)/h were found in group two and group three, respectively in comparison with group one 7.24 ± 0.06 (mg)/(μg/ml), 1.09±0.02 (mg)/(μg/ml)/h. The absorption and elimination half-lives of tylvalosin were 1.69 ± 0.016 h, 10.63± 0.330h and 1.56± 0.01h, 9.63± 0.41h and 1.58±0.02 h, 9.64±0.35 h in group one, group two, and group three respectively. The area under the curve was significantly (P < 0.001) decreased in group two and group three which were 13.6±0.06 and 15.98±0.14 μg/ml/h respectively, in comparison with group one which was 18.7±0.093 μg/ml/h. It was found that the serum concentration of tylvalosin in group one after twenty-four hours is higher than MIC for the used Mycoplasma gallisepticum (0.25 μg/ml) unlike the second and third group, so it is recommended to give tylvalosin every twenty-four hours if it is given alone while when it is given with amprolium and toltrazuril it should be given every twelve hours.
氨丙铵和托曲祖利对鸡链球菌支原体感染后泰洛菌素处置动力学的影响
在单次口服治疗后,评价了泰洛菌素单用及与氨丙铵或托曲祖利合用在鸡链球菌支原体感染的肉仔鸡体内的药动学特征。将18只鸡随机分为3组,第1组只给予泰洛菌素,第2组给予泰洛菌素和氨苯铵,第3组给予泰洛菌素和托曲祖利。在我们的研究中,描述泰瓦络素血清水平的最佳模型被发现是一个双室开放模型。第1组、第2组和第3组大鼠tylvalosin血清最高浓度分别为1.62±0.03、1.2±0.02和1.41±0.01 μg/ml,分别在2.95±0.014、2.8±0.01和2.83±0.02 h时达到。与对照组(7.24±0.06 (mg)/(μg/ml)、1.09±0.02 (mg)/(μg/ml)/h、对照组(1.54±0.04(mg)/(μg/ml)/h、对照组(8.56±0.07(mg)/(μg/ml))、对照组(1.31±0.03)(mg)/(μg/ml)/h相比,对照组(7.19±0.06)(mg)/(μg/ml)、对照组(1.09±0.02)(mg)/(μg/ml)/h)的V/F、Cl/F均显著升高(P<0.001)。第1组、第2组和第3组噻虫苷的吸收和消除半衰期分别为1.69±0.016 h、10.63±0.30 h和1.56±0.01h、9.63±0.41h和1.58±0.02 h、9.64±0.35 h。2组和3组的曲线下面积分别为13.6±0.06和15.98±0.14 μg/ml/h,较1组的18.7±0.093 μg/ml/h显著减小(P < 0.001)。结果发现,与第2、3组不同,第1组患者用药24小时后血清泰洛菌素浓度高于MIC (0.25 μg/ml),建议单独用药时每24小时给药一次,与氨苯氨铵、托曲zuril合用时每12小时给药一次。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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