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伐地米星在实验性气管内鸡毒支原体感染模型中的体内药代动力学/药效学特征

In vivo pharmacokinetic/pharmacodynamic profiles of valnemulin in an experimental intratracheal Mycoplasma gallisepticum infection model.

作者信息

Xiao Xia, Sun Jian, Yang Tao, Fang Xi, Wu Dong, Xiong Yan Q, Cheng Jie, Chen Yi, Shi Wei, Liu Ya-Hong

机构信息

College of Veterinary Medicine, National Reference Laboratory of Veterinary Drug Residues (SCAU), South China Agricultural University, Guangzhou, China.

Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, USA David Geffen School of Medicine at UCLA, Los Angeles, California, USA.

出版信息

Antimicrob Agents Chemother. 2015 Jul;59(7):3754-60. doi: 10.1128/AAC.00200-15. Epub 2015 Apr 6.

Abstract

Valnemulin, a semisynthetic pleuromutilin antibiotic derivative, is greatly active against Mycoplasma. The objective of our study was to evaluate the effectiveness of valnemulin against Mycoplasma gallisepticum in a neutropenic intratracheal model in chickens using a pharmacokinetic/pharmacodynamic (PK-PD) method. The PK of valnemulin after intramuscular (i.m.) administration at doses of 1, 10, and 20 mg/kg of body weight in M. gallisepticum-infected neutropenic chickens was evaluated by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Real-time PCR (RT-PCR) was used for quantitative detection of M. gallisepticum. The ratio of the 24-h area under the concentration-time curve divided by the MIC (AUC24/MIC) correlated well with the in vivo antibacterial effectiveness of valnemulin (R(2) = 0.9669). The AUC24/MIC ratios for mycoplasmastasis (a reduction of 0 log10 color-changing unit [CCU] equivalents/ml), a reduction of 1 log10 CCU equivalents/ml, and a reduction of 2.5 log10 CCU equivalents/ml are 28,820, 38,030, and 56,256, respectively. In addition, we demonstrated that valnemulin at a dose of 6.5 mg/kg resulted in a reduction of 2.5 log10 CCU equivalents/ml. These investigations provide a solid foundation for the usage of valnemulin in poultry with M. gallisepticum infections.

摘要

伐地米星是一种半合成截短侧耳素类抗生素衍生物,对支原体具有很强的活性。我们研究的目的是采用药代动力学/药效学(PK-PD)方法,在鸡的中性粒细胞减少气管内模型中评估伐地米星对鸡毒支原体的有效性。通过液相色谱-串联质谱法(LC-MS/MS)评估了在感染鸡毒支原体的中性粒细胞减少的鸡中,以1、10和20mg/kg体重的剂量肌肉注射(i.m.)后伐地米星的药代动力学。实时荧光定量聚合酶链反应(RT-PCR)用于鸡毒支原体的定量检测。浓度-时间曲线下24小时面积与最低抑菌浓度(MIC)的比值(AUC24/MIC)与伐地米星的体内抗菌效果相关性良好(R(2)=0.9669)。支原体清除(0 log10变色单位[CCU]当量/ml的降低)、1 log10 CCU当量/ml的降低和2.5 log10 CCU当量/ml的降低的AUC24/MIC比值分别为28820、38030和56256。此外,我们证明6.5mg/kg剂量的伐地米星可使CCU当量/ml降低2.5 log10。这些研究为伐地米星在感染鸡毒支原体的家禽中的应用提供了坚实的基础。

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