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Diffusion of Oral and Intravenous 400 mg Once-Daily Moxifloxacin into Lung Tissue at Pharmacokinetic Steady-State
- Source :
- Journal of Chemotherapy. 15:558-562
- Publication Year :
- 2003
- Publisher :
- Informa UK Limited, 2003.
-
Abstract
- The degree of penetration of an antibiotic into the infection site is an important factor for its therapeutic efficacy, particularly in respiratory tract infections. In the present study, we examined the lung tissue diffusion of moxifloxacin at a dose of 400 mg administered intravenously or orally once-daily, and the results were correlated to microbiological data to estimate the clinical efficacy of moxifloxacin in lower community-acquired respiratory infections. This was a prospective, randomized, parallel-group trial, open-label, single-center study. Patients undergoing lung surgery for bronchial cancer which necessitates the removal of an anatomical piece of lung tissue were randomized into twelve treatment groups, dependent upon the time of surgery and the moxifloxacin formulation, i.v. or oral, administered. During surgery, one blood sample was taken at the time of tissue collection to determine moxifloxacin plasma concentration. At the same time, tissue samples were taken by pulmonary exeresis. A validated new high performance liquid chromatography assay was used to determine moxifloxacin concentrations in plasma and lung tissue. A total of 49 patients (25 for i.v. administration, 24 for oral administration, 44 men and 5 women, mean age, 61 years, mean body weight, 72 kg, mean creatinine clearance was 84 ml/min/1.73 m2) were enrolled. The mean +/- SD steady-state moxifloxacin ratios between lung and plasma concentrations were respectively: 3.53 +/- 1.89 and 4.36 +/- 1.48 for i.v. and oral administration. The mean steady-state moxifloxacin maximal lung concentrations (Cmax) were respectively 12.37 microg/g and 16.21 microg/g for i.v. and oral administration. Moxifloxacin both intravenously and orally exhibits high penetration in lung tissue, with tissue concentrations far above the MIC90s for most of the susceptible pathogens commonly involved, thus underlining its suitability for the treatment of community-acquired, lower respiratory tract infections.
- Subjects :
- Adult
Male
medicine.medical_specialty
Lung Neoplasms
Moxifloxacin
Cmax
Administration, Oral
Biological Availability
Gastroenterology
Drug Administration Schedule
Postoperative Complications
Pharmacokinetics
Reference Values
Risk Factors
Oral administration
Internal medicine
Pneumonia, Bacterial
Humans
Medicine
Tissue Distribution
Pharmacology (medical)
Prospective Studies
Respiratory system
Infusions, Intravenous
Lung
Antibacterial agent
Pharmacology
Aza Compounds
Dose-Response Relationship, Drug
Respiratory tract infections
business.industry
Antibiotic Prophylaxis
Middle Aged
Surgery
Treatment Outcome
Infectious Diseases
medicine.anatomical_structure
Oncology
Quinolines
Female
business
Fluoroquinolones
Follow-Up Studies
medicine.drug
Subjects
Details
- ISSN :
- 19739478 and 1120009X
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Journal of Chemotherapy
- Accession number :
- edsair.doi.dedup.....fee37f27490bf4c5376821d16f3dd1fb
- Full Text :
- https://doi.org/10.1179/joc.2003.15.6.558