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首页> 外文期刊>International Journal of Pharmacology and Toxicology >Pharmacokinetics of clarithromycin after single intravenous and intracrop bolus administrations to broiler chickens
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Pharmacokinetics of clarithromycin after single intravenous and intracrop bolus administrations to broiler chickens

机译:单次静脉内和作物内推注对肉鸡的克拉霉素的药代动力学

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The pharmacokinetics of clarithromycin at a dose of 7.5 mg/kg body weight was evaluated after single intravenous (i.v.) and intracrop (i.c.) bolus administrations in broilers. An HPLC assay using pure clarithromycin base as a standard was used to measure its concentrations in plasma. Following an i.v. bolus injection, the plasma concentration-time curves of clarithromycin were best represented by two-compartment open models. The drug was rapidly distributed and moderately eliminated with half-lives of distribution ( t 1/2α ) and elimination ( t 1/2β ) of 0.38 and 4.58 h, respectively. The volume of distribution was large with (V dss ) value of 6.89 L. The total body clearance ( Cl B ) was 1.2 L/h. After i.c. bolus administration of the same dose, clarithromycin was moderately absorbed in broilers with an intermediate absorption half-life ( T ?ab ) of 0.72 h with peak plasma concentration ( C max ) of 1.69 μg/ml attained at 1.7 h ( T max ) and systemic bioavailability of 66.54%. The elimination half-life following i.c. administration was 2.11 h. The extent of plasma protein binding percent was 52%. The study recommends the use of clarithromycin in broilers because of its good pharmacokinetic profile indicated by good absorption, bioavailability and plasma concentrations ≥ MICs of many sensitive microorganisms.
机译:在肉鸡中单次静脉内(i.v.)和作物内(i.c.)推注给药后,评估了7.5 mg / kg体重克拉霉素的药代动力学。使用纯克拉霉素碱作为标准品的HPLC测定法测量其在血浆中的浓度。继i.v.推注时,克拉霉素的血浆浓度-时间曲线最好用两室开放模型表示。该药物迅速分布并被适度消除,分布的半衰期(t 1 /2α)和消除(t 1 /2β)分别为0.38和4.58 h。分布体积很大,(V dss)值为6.89L。总身体清除率(Cl B)为1.2 L / h。在i.c.之后推注相同剂量的克拉霉素,在肉鸡中被中等吸收,中间吸收半衰期(T?ab)为0.72 h,在1.7 h(T max)达到的峰值血浆浓度(C max)为1.69μg/ ml。全身生物利用度为66.54%。 i.c.之后的消除半衰期管理为2.11小时。血浆蛋白结合百分比的程度为52%。该研究建议在肉鸡中使用克拉霉素,因为克拉霉素具有良好的药代动力学特征,其表现为许多敏感微生物的良好吸收,生物利用度和血浆浓度≥MIC。

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