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Gatifloxacin and ethionamide as the foundation for therapy of tuberculosis.

Abstract
The use of gatifloxacin (GAT) in combination with ethionamide (ETA) with or without pyrazinamide (PZA) for a 12-week treatment period followed by an 8-week observation period was evaluated in a model of tuberculosis in mice. Mice treated with GAT at 300 mg/kg of body weight in combination with ETA (25 mg/kg) for 5 days per week had sterile lungs, whereas mice treated with GAT (100 mg/kg) and ETA (25 mg/kg) had about 10 CFU/lung; however, there was regrowth of the organisms in both groups at the end of the observation period. When PZA (450 mg/kg 5 days per week) was added to the high-dose GAT-ETA regimen, no viable mycobacteria were present after the 8-week observation period. GAT in combination with ETA and PZA has great promise for the treatment of tuberculosis.
AuthorsMichael H Cynamon, Mary Sklaney
JournalAntimicrobial agents and chemotherapy (Antimicrob Agents Chemother) Vol. 47 Issue 8 Pg. 2442-4 (Aug 2003) ISSN: 0066-4804 [Print] United States
PMID12878502 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Anti-Infective Agents
  • Antitubercular Agents
  • Fluoroquinolones
  • Gatifloxacin
  • Ethionamide
Topics
  • Administration, Intranasal
  • Animals
  • Anti-Infective Agents (therapeutic use)
  • Antitubercular Agents (therapeutic use)
  • Colony-Forming Units Assay
  • Dose-Response Relationship, Drug
  • Drug Resistance, Multiple, Bacterial
  • Ethionamide (therapeutic use)
  • Female
  • Fluoroquinolones
  • Gatifloxacin
  • Lung (microbiology)
  • Mice
  • Mice, Inbred C57BL
  • Mycobacterium tuberculosis (drug effects)
  • Tuberculosis (drug therapy, microbiology)

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