访问量:   最后更新时间:--

郝海红

博士生导师
硕士生导师
教师姓名:郝海红
教师英文名称:High
教师拼音名称:haohaihong
电子邮箱:
所在单位:动物科学技术学院、动物医学院
学历:博士研究生毕业
办公地点:华中农业大学国家兽药残留基准实验室118
学位:博士
职称:教授
在职信息:在职
毕业院校:华中农业大学
所属院系:动物科学技术学院、动物医学院
学科:兽医学其他专业    基础兽医学    
其他联系方式

邮编:

通讯/办公地址:

论文成果
Exploration of Clinical Breakpoint of Danofloxacin for Glaesserella parasuis in Plasma and in PELF
发布时间:2022-03-03    点击次数:

影响因子:4.639

DOI码:10.3390/antibiotics10070808

发表刊物:Antibiotics-Basel

项目来源:This work was funded by grants from National key research and development program (2016YFD0501302/20

关键字:Glaesserella parasuis; PK-PD cutoff values; clinical breakpoint; clinical cutoff values; danofloxacin; epidemiological cutoff values.

摘要:Background: In order to establish the clinical breakpoint (CBP) of danofloxacin against G. parasuis, three cutoff values, including epidemiological cutoff value (ECV), pharmacokinetic-pharmacodynamic (PK-PD) cutoff value (COPD) and clinical cutoff value (COCL), were obtained in the present study. Methods: The ECV was calculated using ECOFFinder base on the MIC distribution of danfloxacin against 347 G. parasuis collected from disease pigs. The COPD was established based on in vivo and ex vivo PK-PD modeling of danofloxacin both in plasma and pulmonary epithelial lining fluid (PELF) using Hill formula and Monte Carlo analysis. The COCL was established based on the relationship between the possibility of cure (POC) and MIC in the clinical trials using the "WindoW" approach, nonlinear regression and CART analysis. Results: The MIC50 and MIC90 of danofloxacin against 347 G. parasuis were 2 μg/mL and 8 μg/mL, respectively. The ECV value was set to 8 μg/mL using ECOFFinder. Concentration-time curves of danofloxacin were fitted with a two-compartment PK model. The PK parameters of the maximum concentration (Cmax) and area under concentration-time curves (AUC) in PELF were 3.67 ± 0.25 μg/mL and 24.28 ± 2.70 h·μg/mL, higher than those in plasma (0.67 ± 0.01 μg/mL and 4.47 ± 0.51 h·μg/mL). The peak time (Tmax) in plasma was 0.23 ± 0.07 h, shorter than that in PELF (1.61 ± 0.15 h). The COPD in plasma and PELF were 0.125 μg/mL and 0.5 μg/mL, respectively. The COCL calculated by WindoW approach, nonlinear regression and CART analysis were 0.125-4 μg/mL, 0.428 μg/mL and 0.56 μg/mL, respectively. The 0.5 μg/mL was selected as eligible COCL. The ECV is much higher than the COPD and COCL, and the clinical breakpoint based on data in plasma was largely different from that of PELF. Conclusions: Our study firstly established three cutoff values of danofloxacin against G. parasuis. It suggested that non-wild-type danofloxacin-resistant G. parasuis may lead to ineffective treatment by danofloxacin.

合写作者:Zonghui Yuan,Jun Li,Xiao Huang,Shiwei Fang,Kun Mi,Xu Wang,Lingli Huang,Peng Zhang,Xun Luo

第一作者:Anxiong Huang,Zihui Xu

论文类型:期刊论文

通讯作者:Haihong Hao*

卷号:10

期号:7

页面范围:808

字数:5000

是否译文:

发表时间:2021-06-01

收录刊物:SCI

发布期刊链接:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8300709/