the bactericidal activity of moxifloxacin, alone and in combination with isoniazid and rifampin, was studied on exponential and stationary phase cultures of Mycobacterium tuberculosis H37 Rv strain, the standard strain which is a wild type of M. tuberculosis strain, not exposed to any environment, susceptible to all anti-tuberculosis drugs. moxifloxacin alone was highly bactericidal, being intermediate in activity between isoniazid and rifampin on both types of culture. the speed of activity was slow with the stationary phase culture, causing a reduction from 6.41 log10 cfu/ml to 2.70 log10 cfu/ml on day 6 with the higher moxifloxacin concentration of 4 μg/ml and to 4.08 log10 cfu/ml with the lower concentration of 0.25 μg/ml. when ...
Moxifloxacin is an attractive drug for the treatment of isoniazid-resistant rifampicin-susceptible t...
International audienceWhile isoniazid and rifampin have been the cornerstone of tuberculosis therapy...
textabstractA number of antimycobacterial agents were evaluated with respect to their bacteriostatic...
Patients in whom acid-fast bacilli smear-positive pulmonary tuberculosis was newly diagnosed were ra...
Patients in whom acid-fast bacilli smear-positive pulmonary tuberculosis was newly diagnosed were ra...
Background: In vitro and animal studies have shown that moxifloxacin-containing combinations may imp...
Coadministration of moxifloxacin and rifampin was evaluated in a murine model ofMycobacterium tuberc...
The activity of moxifloxacin was enhanced by the addition of ethionamide but not by that of cycloser...
Moxifloxacin is the most active fluoroquinolone against Mycobacterium tuberculosis in vitro. However...
Patients in whom acid-fast bacilli smear-positive pulmonary tuberculosis was newly diagnosed were ra...
The bactericidal actions of ofloxacin and sulbactam-ampicillin, alone and in combination with rifamp...
BACKGROUND: The long duration of the current tuberculosis (TB) treatment is demanding and warrants t...
Aim: To investigate the in vitro activity of linezolid and ofloxacin in combination with first-line ...
Moxifloxacin is an 8-methoxyquinolone compound with activity against a wide range of bacteria. We te...
WOS: 000294274700020Aim: To investigate the in vitro activity of linezolid and ofloxacin in combinat...
Moxifloxacin is an attractive drug for the treatment of isoniazid-resistant rifampicin-susceptible t...
International audienceWhile isoniazid and rifampin have been the cornerstone of tuberculosis therapy...
textabstractA number of antimycobacterial agents were evaluated with respect to their bacteriostatic...
Patients in whom acid-fast bacilli smear-positive pulmonary tuberculosis was newly diagnosed were ra...
Patients in whom acid-fast bacilli smear-positive pulmonary tuberculosis was newly diagnosed were ra...
Background: In vitro and animal studies have shown that moxifloxacin-containing combinations may imp...
Coadministration of moxifloxacin and rifampin was evaluated in a murine model ofMycobacterium tuberc...
The activity of moxifloxacin was enhanced by the addition of ethionamide but not by that of cycloser...
Moxifloxacin is the most active fluoroquinolone against Mycobacterium tuberculosis in vitro. However...
Patients in whom acid-fast bacilli smear-positive pulmonary tuberculosis was newly diagnosed were ra...
The bactericidal actions of ofloxacin and sulbactam-ampicillin, alone and in combination with rifamp...
BACKGROUND: The long duration of the current tuberculosis (TB) treatment is demanding and warrants t...
Aim: To investigate the in vitro activity of linezolid and ofloxacin in combination with first-line ...
Moxifloxacin is an 8-methoxyquinolone compound with activity against a wide range of bacteria. We te...
WOS: 000294274700020Aim: To investigate the in vitro activity of linezolid and ofloxacin in combinat...
Moxifloxacin is an attractive drug for the treatment of isoniazid-resistant rifampicin-susceptible t...
International audienceWhile isoniazid and rifampin have been the cornerstone of tuberculosis therapy...
textabstractA number of antimycobacterial agents were evaluated with respect to their bacteriostatic...