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Effect of fever on pharmacokinetics and dosage regimen of intramuscularly administered amikacin in goats

机译:发烧对肌肉注射阿米卡星对山羊的药代动力学和剂量方案的影响

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A comparative pharmacokinetic study of amikacin (10 mg/kg intramuscular) by microbiological assay method in normal and experimentally induced febrile goats revealed that the plasma drug concentrations were significantly higher in febrile condition at most of the time intervals. Various pharmacokinetic parameters like t(1/2), AUC, AUMC, MRT and Vd(area) were significantly higher whereas total body clearance (Cl(B)) was significantly lower in febrile goats as compared to normal goats. Absorption half-life (t(1/2) ka) value differed non-significantly. For maintaining mean therapeutic level of 2 mg/ml, a priming dose (D*) of 14.732.28 mg/kg, followed by maintenance dose (D(o)) of 13.952.28 mg/kg at shorter dosage interval (t) of 8 hr may be useful in case of normal goats whereas lower doses (D* of 13.581.61 mg/kg followed by D(o) of 12.651.60 mg/kg) at longer tau of 12 hr may be advised in case of febrile goats.
机译:通过微生物测定方法对正常和实验诱导的高热山羊进行丁胺卡那霉素(10 mg / kg肌内)的比较药代动力学研究表明,在大多数时间间隔内,高热条件下血浆药物浓度显着较高。与正常山羊相比,高热山羊的各种药代动力学参数,如t(1/2),AUC,AUMC,MRT和Vd(面积)显着较高,而总体清除率(Cl(B))则显着降低。吸收半衰期(t(1/2)ka)值无显着差异。为了维持2 mg / ml的平均治疗水平,在较短的剂量间隔(t)时,初始剂量(D *)为14.732.28 mg / kg,随后为13.952.28 mg / kg的维持剂量(D(o))。对于正常的山羊,最好在8小时内使用,但建议在更长的12小时内使用较低的剂量(D *为13.581.61 mg / kg,然后D(o)为12.651.60 mg / kg)。高热山羊。

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