Previous Article | Next Article ![]()
Antimicrobial Agents and Chemotherapy, Mar 1995, 750-753, Vol 39, No. 3
PS Skinner, SK Furney, DA Kleinert and IM Orme
In this study the compounds levofloxacin and sparfloxacin, as well as three
experimental compounds (AMQ2, AMQ4, and AMQ5), were compared with isoniazid
and rifabutin in terms of their capacity to inhibit the intracellular
growth of the drug-susceptible Mycobacterium tuberculosis strain Erdman and
the isoniazid-resistant katG gene-negative strain 24 within monolayers of
mouse bone marrow-derived macrophages. Both levofloxacin and sparfloxacin,
as well as compound AMQ4, had substantial activity in this physiologically
relevant model, further confirming the potential usefulness of this class
of compounds in the therapy of tuberculosis.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Comparison of activities of fluoroquinolones in murine macrophages infected with Mycobacterium tuberculosis
Department of Microbiology, Colorado State University, Fort Collins 80523, USA.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»