Moxifloxacin target site concentrations in patients with pulmonary TB utilizing microdialysis: a clinical pharmacokinetic study
Author(s) -
M. Tobias Heinrichs,
Sergo Vashakidze,
Ketino Nikolaishvili,
Irina Sabulua,
Nestani Tukvadze,
Nino Bablishvili,
Shota Gogishvili,
Brent P. Little,
Adam Bernheim,
Jeannette Guarner,
Charles A. Peloquin,
Henry M. Blumberg,
Hartmut Derendorf,
Russell R. Kempker
Publication year - 2017
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkx421
Subject(s) - moxifloxacin , pharmacokinetics , medicine , cmax , microdialysis , lung , dosing , drug , in vivo , pharmacodynamics , antibiotics , surgery , pharmacology , gastroenterology , urology , chemistry , biology , microbiology and biotechnology , central nervous system , biochemistry
Moxifloxacin is a second-line anti-TB drug that is useful in the treatment of drug-resistant TB. However, little is known about its target site pharmacokinetics. Lower drug concentrations at the infection site (i.e. in severe lung lesions including cavitary lesions) may lead to development and amplification of drug resistance. Improved knowledge regarding tissue penetration of anti-TB drugs will help guide drug development and optimize drug dosing.
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