Abstract
Background: Due to the emergency of multidrug-resistant strains of Mycobacterium tuberculosis, is necessary the evaluation of new compounds.Findings: Tedizolid, a novel oxazolidinone, and ACH-702, a new isothiazoloquinolone, were tested against M. tuberculosis infected THP-1 macrophages. These two compounds significantly decreased the number of intracellular mycobacteria at 0.25X, 1X, 4X and 16X the MIC value. The drugs were tested either in nanoparticules or in free solution.Conclusion: Tedizolid and ACH-702 have a good intracellular killing activity comparable to that of rifampin or moxifloxacin. © 2014 Molina-Torres et al.; licensee BioMed Central Ltd.
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Molina-Torres, C. A., Barba-Marines, A., Valles-Guerra, O., Ocampo-Candiani, J., Cavazos-Rocha, N., Pucci, M. J., … Vera-Cabrera, L. (2014). Intracellular activity of tedizolid phosphate and ACH-702 versus Mycobacterium tuberculosis infected macrophages. Annals of Clinical Microbiology and Antimicrobials, 13(1). https://doi.org/10.1186/1476-0711-13-13
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