Effect of intramuscular administration of oxytetracycline on serum kinetics of diminazene aceturate in healthy male Sahel goats

S. Gana, P. Onyeyili, B. Umaru, Hyellavala Joseph Fomnya, S. Ngulde, A. L. Karatu
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引用次数: 1

Abstract

Serum kinetics of diminazene aceturate following intramuscular (IM) administration of diminazene aceturate alone at 3.5 mg/kg and its combination with oxytetracycline at 20 mg/kg were evaluated in 6 healthy male Sahel goats to ascertain the effect of oxytetracycline on serum concentration and pharmacokinetic parameters of diminazene aceturate. Two groups (A and B) of three goats each were used, and oxytetracycline was administered 30 minutes prior to diminazene aceturate administration. Blood samples were collected at various intervals (0.17 h – 72 h) post-drug administration, and diminazene serum concentrations were measured using the method of Klatt and Hadju. Kinetic determinants were calculated employing a two-compartment open model. Mean serum concentrations of diminazene aceturate of 2.43 ± 0.95 μg/ml and 1.73 ± 0.44 μg/ml at 0.17 h were measured in groups A and B, respectively. These serum concentrations were found to increase until a peak concentration of 6.91 ± 0.59 μg/ml and 7.55 ± 1.20 μg/ml were reached at 2.0 h in groups A and B, respectively. The peak concentrations subsequently decreased at 72 h post diminazene aceturate administration with serum concentrations of 0.00 ± 0.00 and 0.32 ± 0.28 μg/ml in groups A and B, respectively. Pharmacokinetics parameters like the volume of distribution (Vd), elimination half-life (T½β), concentration maximum (Cmax), absorption rate constant (α), and area under the curve from 0 to 72 h (AUC0 – 72) were significantly higher in goats treated with diminazene aceturate and oxytetracycline combination while total body clearance (Cl), and elimination rate constant (β), were significantly higher in goats treated with diminazene aceturate alone. The mean residence time (MRT) of diminazene aceturate increased from 19.70 ± 2.53 h in diminazene aceturate treatment to 25.11 ± 1.81 h in diminazene aceturate and oxytetracycline treatment. Oxytetracycline was therefore found to alter the elimination pattern of diminazene aceturate in oxytetracycline pre-treated goats.
肌肉注射土霉素对健康雄性萨赫勒山羊醋酸迪纳苯血清动力学的影响
研究了6只健康雄性萨赫勒山羊肌注醋酸迪纳那3.5 mg/kg及联用土霉素20 mg/kg后的血清动力学,以确定土霉素对醋酸迪纳那血清浓度和药动学参数的影响。采用A组和B组,每组3只山羊,在给药前30分钟给药土霉素。在给药后不同时间间隔(0.17 h ~ 72 h)采集血样,采用Klatt和Hadju法测定血清中氨基苯的浓度。采用双室开放模型计算动力学决定因素。A组和B组大鼠0.17 h血清乙酸地咪那烯平均浓度分别为2.43±0.95 μg/ml和1.73±0.44 μg/ml。a组和B组血清浓度在2.0 h分别达到峰值6.91±0.59 μg/ml和7.55±1.20 μg/ml。在给药72 h后,A组和B组的血药浓度分别为0.00±0.00和0.32±0.28 μg/ml,峰值浓度下降。药代动力学参数分布体积(Vd)、消除半衰期(T½β)、最大浓度(Cmax)、吸收速率常数(α)和0 ~ 72 h曲线下面积(AUC0 - 72)显著高于醋酸迪纳齐和土霉素联合用药的山羊,而单独用药的山羊的总清除率(Cl)和消除速率常数(β)显著高于盐酸迪纳齐。醋酸迪纳特纳的平均停留时间(MRT)由盐酸迪纳特纳组的19.70±2.53 h增加到盐酸迪纳特纳和土环素组的25.11±1.81 h。因此,我们发现土霉素可以改变土霉素预处理山羊体内乙酰氨基苯乙酯的消除模式。
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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