Simultaneous assessment of the pharmacokinetics of a pleuromutilin, lefamulin, in plasma, soft tissues and pulmonary epithelial lining fluid

被引:64
作者
Zeitlinger, M. [1 ]
Schwameis, R. [1 ]
Burian, A. [1 ]
Burian, B. [1 ]
Matzneller, P. [1 ]
Mueller, M. [1 ]
Wicha, W. W. [2 ]
Strickmann, D. B. [2 ]
Prince, W. [2 ]
机构
[1] Med Univ Vienna, Dept Clin Pharmacol, Wahringer Gurtel 18-20, A-1090 Vienna, Austria
[2] Nabriva Therapeut AG, Leberstr 20, A-1110 Vienna, Austria
关键词
SKIN-STRUCTURE INFECTIONS; ACUTE BACTERIAL SKIN; ANTIMICROBIAL ACTIVITY; BC-3781; MICRODIALYSIS; CLARITHROMYCIN; AZITHROMYCIN; ANTIBIOTICS; RESISTANCE; LAVAGE;
D O I
10.1093/jac/dkv442
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Lefamulin is a pleuromutilin antibiotic under evaluation for the treatment of bacterial infections, including respiratory tract infections. Currently, there are no high-quality pharmacokinetic data on drug tissue concentrations of lefamulin available. A single dose of intravenous lefamulin (150 mg) was given to 12 healthy men. The registered EudraCT number for this study was 2010-021938-54. Lefamulin concentrations were simultaneously measured in plasma, skeletal muscle tissue, subcutaneous adipose tissue and epithelial lining fluid (ELF) over 24 h, and corresponding pharmacokinetic parameters were calculated. Microdialysis was used to measure unbound lefamulin concentrations in skeletal muscle tissue and subcutaneous adipose tissue, which were similar to unbound lefamulin concentrations in plasma. Bronchoalveolar lavage was performed 1, 2, 4 and 8 h post-dose to determine lefamulin concentrations in ELF. Unbound lefamulin levels showed a 5.7-fold higher exposure in ELF compared with that in plasma, demonstrating good penetration to the target site. Lefamulin may be an addition to the therapeutic armamentarium for the treatment of infections. Simultaneous measurements of unbound drug concentration can guide target attainment for future therapeutic trials.
引用
收藏
页码:1022 / 1026
页数:5
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