Bronchopulmonary Disposition of the Ketolide Telithromycin (HMR 3647)
Open Access
- 1 November 2001
- journal article
- clinical trial
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 45 (11) , 3104-3108
- https://doi.org/10.1128/aac.45.11.3104-3108.2001
Abstract
Telithromycin (HMR 3647) is the first member of a new family of antimicrobials, the ketolides, developed specifically for the treatment of community-acquired respiratory tract infections. Telithromycin has proven in vitro activity against both common and atypical respiratory tract pathogens. The penetration of telithromycin into bronchopulmonary tissues and subsequent elimination from these sites were evaluated in four groups (groups A, B, C, and D) of six healthy male subjects who received telithromycin at 800 mg once daily for 5 days. Subjects in groups A, B, C, and D underwent fiberoptic bronchoscopy and bronchoalveolar lavage 2, 8, 24, and 48 h after receipt of the last dose, respectively. The concentration of telithromycin in the alveolar macrophages, epithelial lining fluid (ELF), and plasma was determined by the agar diffusion method with Bacillus subtilis ATCC 6633 as the test organism. The concentration of telithromycin in alveolar macrophages markedly exceeded that in plasma, reaching up to 146 times the concentration in plasma 8 h after dosing (median concentration, 81 mg/liter). Telithromycin was retained in alveolar macrophages 24 h after dosing (median concentration, 23 mg/liter), and it was still quantifiable 48 h after dosing (median concentration, 2.15 mg/liter). Telithromycin median concentrations in ELF also markedly exceeded concentrations in plasma (median concentration in ELF, 3.7 mg/liter 8 h after dosing). Telithromycin achieves high and sustained concentrations in ELF and in alveolar macrophages, while it maintains adequate levels in plasma, providing an ideal pharmacokinetic profile for effective treatment of community-acquired respiratory tract infections caused by either common or atypical, including intracellular, respiratory tract pathogens.Keywords
This publication has 21 references indexed in Scilit:
- Macrolide–ketolide inhibition of MLS‐resistant ribosomes is improved by alternative drug interaction with domain II of 23S rRNAMolecular Microbiology, 2000
- In Vitro Activity of the Ketolide HMR 3647 (RU 6647) for Legionella spp., Its Pharmacokinetics in Guinea Pigs, and Use of the Drug To Treat Guinea Pigs with Legionella pneumophila PneumoniaAntimicrobial Agents and Chemotherapy, 1999
- Interactions between HMR 3647, a New Ketolide, and Human Polymorphonuclear NeutrophilsAntimicrobial Agents and Chemotherapy, 1998
- Susceptibilities of Legionella spp. to Newer Antimicrobials In VitroAntimicrobial Agents and Chemotherapy, 1998
- Antibiotic penetration in the respiratory tract and implications for the selection of antimicrobial therapyCurrent Opinion in Pulmonary Medicine, 1997
- Prognosis and Outcomes of Patients With Community-Acquired PneumoniaJAMA, 1996
- Intrapulmonary pharmacokinetics of clarithromycin and of erythromycinAntimicrobial Agents and Chemotherapy, 1995
- Penetration of cefpodoxime proxetil in lung parenchyma and epithelial lining fluid of noninfected patientsAntimicrobial Agents and Chemotherapy, 1992
- The pharmacokinetics of azithromycin and their clinical significanceEuropean Journal of Clinical Microbiology & Infectious Diseases, 1991
- Relationship of high tissue concentrations of azithromycin to bactericidal activity and efficacy in vivoJournal of Antimicrobial Chemotherapy, 1990