In Vivo Pharmacodynamic Evaluation of Omadacycline against Staphylococcus aureus in the Neutropenic Mouse Pneumonia Model

被引:11
|
作者
Lepak, Alexander J. [1 ]
Zhao, Miao [1 ,3 ]
Marchillo, Karen [3 ]
VanHecker, Jamie [3 ]
Andes, David R. [1 ,2 ,3 ]
机构
[1] Univ Wisconsin, Dept Med, Sch Med & Publ Hlth, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Med Microbiol & Immunol, Madison, WI 53706 USA
[3] William S Middleton Mem VA Hosp, Madison, WI 53705 USA
关键词
Staphylococcus aureus; omadacycline; pharmacodynamics; pneumonia; MURINE; PHARMACOKINETICS; TIGECYCLINE; PHOSPHATE; THIGH;
D O I
10.1128/AAC.02058-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Omadacycline is an effective therapy for community-acquired bacterial pneumonia (CABP). Given its potent activity against methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant S. aureus (MRSA), we sought to determine the pharmacodynamic activity and target pharmacokinetic/pharmacodynamic (PK/PD) exposures associated with a therapeutic effect in the neutropenic mouse pneumonia model against 10 MSSA/MRSA strains. The area under the concentration- time curve (AUC)/MIC associated with 1-log kill was noted at 24-h epithelial lining fluid (ELF) and plasma AUC/MIC exposures of similar to 2 (ELF range, <0.93 to 19; plasma range, <1.06 to 17) and 2-log kill was noted at 24-h ELF and plasma AUC/MIC exposures of similar to 12 (ELF range, 2.5 to 130; plasma range, 3.5 to 151).
引用
收藏
页数:6
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