Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, Wroclaw University of Environmental and Life Sciences, Wroclaw 50-375, Poland.
Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, Wroclaw University of Environmental and Life Sciences, Wroclaw 50-375, Poland..
Poult Sci. 2022 Jan;101(1):101536. doi: 10.1016/j.psj.2021.101536. Epub 2021 Oct 13.
Florfenicol is a broad-spectrum antibacterial drug used in the treatment of farm animals, including poultry. This drug is poorly soluble in water, therefore, administration in drinking water may lead to high variability of concentrations in treated individuals. The use of injection preparations, however, requires individual administration and may have a negative effect on the quality of the carcass. In addition, the renal portal system in birds may reduce the bioavailability of the drug administered in the caudofemoral region of the body. The aim of this study was to compare the pharmacokinetics of florfenicol in turkeys after a single intravenous, intramuscular, and subcutaneous administration at a dose of 15 mg/kg body weight. Additionally, to evaluate the effect of renal portal system on drug kinetics, the intramuscular administration was divided into pectoral and caudofemoral administration. The study showed that the area under the concentration-time curve (AUC) was similar regardless of the route of administration. The mean values for clearance and volume of distribution were 0.33 L/kg/h and 0.92 L/kg, respectively. The mean residence time (MRT) was 2.87 h for an intravenous bolus, while for the extravascular administrations it was approx. 5.5 h. The elimination half-life was approx. 4 h regardless of the route of administration. The maximum plasma concentration did not differ statistically between intramuscular (approx. 6.8 mg/L) and subcutaneous (8.2 mg/L) administrations, while the time to appear for this concentration was the longest for caudofemoral administration (1.5 h). The bioavailability was 88.64% for subcutaneous administration, 77.95% for pectoral administration and 85.30% for caudofemoral administration. Overall, all 3 routes of extravascular administration allowed for efficient drug absorption. There was no evidence of an influence of the renal portal system on the kinetic parameters of the drug administered to the lower extremities of the body.
氟苯尼考是一种广谱抗菌药物,用于治疗包括家禽在内的农场动物。该药物在水中的溶解度低,因此,在饮用水中给药可能导致治疗个体中的浓度变化很大。然而,使用注射制剂需要进行个体给药,并且可能对胴体质量产生负面影响。此外,禽类的肾门静脉系统可能会降低在身体的股后区域给药的药物的生物利用度。本研究的目的是比较单次静脉、肌肉和皮下注射 15mg/kg 体重的氟苯尼考在火鸡中的药代动力学。此外,为了评估肾门静脉系统对药物动力学的影响,将肌肉内给药分为胸肌和股后给药。研究表明,无论给药途径如何,浓度-时间曲线下面积(AUC)相似。清除率和分布容积的平均值分别为 0.33 L/kg/h 和 0.92 L/kg。静脉推注的平均停留时间(MRT)为 2.87 小时,而血管外给药的 MRT 约为 5.5 小时。消除半衰期无论给药途径如何均约为 4 小时。最大血浆浓度在肌肉内(约 6.8mg/L)和皮下(8.2mg/L)给药之间没有统计学差异,而达到该浓度的时间对于股后给药最长(1.5 小时)。皮下给药的生物利用度为 88.64%,胸肌给药为 77.95%,股后给药为 85.30%。总体而言,所有 3 种血管外给药途径都能有效地吸收药物。没有证据表明肾门静脉系统对下肢给药的药物动力学参数有影响。