Carpenter James W, Tully Thomas N, Gehring Ronette, Guzman David Sanchez-Migallon
J Avian Med Surg. 2017 Jun;31(2):95-101. doi: 10.1647/2015-131.
To determine the pharmacokinetics of piperacillin/tazobactam in Hispaniolan Amazon parrots ( Amazona ventralis ), 8 healthy adult parrots of both sexes were used in a 2-part study. In a pilot study, piperacillin (87 mg/kg) in combination with tazobactam (11 mg/kg) was administered intramuscularly (IM) to 2 birds, and blood samples were obtained at 0, 0.5, 1, 1.5, 2, 3, 4, 6, 8, and 10 hours after administration. Based on the results obtained, a main study was done in which piperacillin/tazobactam was administered at 2 different doses. In 3 birds, the initial dose of piperacillin (87 mg/kg)/tazobactam (11 mg/kg) IM was administered, and in 3 birds, the dose was doubled to piperacillin (174 mg/kg)/tazobactam (22 mg/kg) IM. In all 6 birds, blood samples were obtained at 0, 5, 15, and 30 minutes and at 1, 1.5, 2, 2.5, 3, and 4 hours after administration. Quantification of plasma piperacillin and tazobactam concentrations was determined by validated liquid chromatography-mass spectrometry assay. Pharmacokinetic parameters were determined by noncompartmental analysis. After intramuscular administration, the mean ± standard error values of T (h) was 0.52 ± 0.05 and 0.32 ± 0.07, T (h) was 0.28 ± 0.09 and 0.25 ± 0.10, C (μg/mL) was 86.34 ± 20.62 and 9.03 ± 2.88, and C/dose was 0.99 ± 0.24 and 0.83 ± 0.26 for piperacillin (87 mg/kg) and tazobactam (11 mg/kg), respectively. When the doses were doubled, the T (h) was 0.65 ± 0.08 and 0.34 ± 0.02, T (h) was 0.28 ± 0.12 and 0.14 ± 0.06, C (μg/mL) was 233.0 ± 6.08 and 22.13 ± 2.35, and C/dose was 1.34 ± 0.03 and 1.02 ± 0.11 for piperacillin and tazobactam, respectively. Results indicate that piperacillin is rapidly absorbed and reaches high initial concentrations; however, it is also rapidly eliminated in the Hispaniolan Amazon parrot, and tazobactam has similar pharmacokinetics as piperacillin. Administration of piperacillin at 87 mg/kg IM q3-4h is recommended for this species to control infections attributed to susceptible bacteria with a minimum inhibitory concentration of ≤4 μg/mL.
为了确定哌拉西林/他唑巴坦在伊斯帕尼奥拉亚马逊鹦鹉(Amazona ventralis)体内的药代动力学,在一项分为两部分的研究中使用了8只健康的成年雌雄鹦鹉。在一项预试验中,对2只鸟肌肉注射(IM)哌拉西林(87 mg/kg)与他唑巴坦(11 mg/kg)的组合,并在给药后0、0.5、1、1.5、2、3、4、6、8和10小时采集血样。根据所得结果,进行了一项主要研究,其中以2种不同剂量给予哌拉西林/他唑巴坦。对3只鸟肌肉注射初始剂量的哌拉西林(87 mg/kg)/他唑巴坦(11 mg/kg),对另外3只鸟,剂量加倍至哌拉西林(174 mg/kg)/他唑巴坦(22 mg/kg)肌肉注射。在所有6只鸟中,于给药后0、5、15和30分钟以及1、1.5、2、2.5、3和4小时采集血样。通过经过验证的液相色谱 - 质谱分析法测定血浆哌拉西林和他唑巴坦浓度。通过非房室分析确定药代动力学参数。肌肉注射后,对于哌拉西林(87 mg/kg)和他唑巴坦(11 mg/kg),T(h)的平均值±标准误分别为0.52±0.05和0.32±0.07,T(h)为0.28±0.09和0.25±0.10,C(μg/mL)为86.34±20.62和9.03±2.88,C/剂量为0.99±0.24和0.83±0.26。当剂量加倍时,哌拉西林和他唑巴坦的T(h)分别为0.65±0.08和0.34±0.02,T(h)为0.28±0.12和0.14±0.06,C(μg/mL)为233.0±6.08和22.13±2.35,C/剂量为1.34±0.03和1.02±0.11。结果表明,哌拉西林吸收迅速并达到较高的初始浓度;然而,它在伊斯帕尼奥拉亚马逊鹦鹉体内也迅速消除,并且他唑巴坦的药代动力学与哌拉西林相似。对于该物种,建议以87 mg/kg肌肉注射,每3 - 4小时给药一次,以控制由最低抑菌浓度≤4 μg/mL的敏感细菌引起的感染。