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- Open Access
Microdialysis study of imipenem distribution in muscle and lung extracellular fluids of infected rats
- Published: 21 March 2006
Keywords
- Imipenem
- Internal Jugular Vein
- Extracellular Fluid
- Isoflurane Anaesthesia
- Microdialysis Probe
Background
Imipenem is frequently used in ICUs to treat nosocomial infections. As infections mainly occur in tissue extra-cellular fluid, unbound antibiotic concentrations in this compartment are responsible for the antimicrobial effect. Micro-dialysis allows the measurement of unbound antibiotic concentrations. The aim of this study was to investigate the imipenem distribution in the blood, muscle and lung by micro-dialysis in a rat model of A. baumannii pneumonia, by comparing unbound concentrations between tissues and blood.
Method
Three days before the pharmacokinetic experiment, seven rats were rendered neutropenic by cyclophosphamide intra-peritoneal administration (150 mg/kg body weight). The day before the experiment, under isoflurane anaesthesia, rats were equipped with a femoral vein catheter, an internal jugular vein and a muscle microdialysis probe. At the end of this surgery, animals were infected intratracheally with an A. baumannii suspension (107CFU/ml). The day of the experiment, after tracheotomy and thoracotomy under isoflurane anaesthesia, the lung microdialysis probe was inserted. The study was conducted under inhaled anaesthesia and mechanical ventilation. Imipenem recoveries in the three media were determined in each rat by retrodialysis by drug before imipenem administration (30 mg/kg over 30 min intravenously), then microdialysis samples were collected during 150 min. At the end of experiment, after euthanasia, the lungs were removed and a quantitative bacteriological study was performed to confirm pneumonia.
Results
Unbound imipenem concentrations: (a) mean concentrations in blood, muscle and lung; mean ± SD concentrations in (b) lung, (c) blood and (d) muscle.
Conclusion
In this rat model of A. baumannii pneumonia, the imipenem distribution in the lung and muscle could be predicted from unbound blood concentrations since unbound blood, muscle and lung concentrations were superimposed.
Authors’ Affiliations
References
- Marchand S, et al.: Antimicrob Agents Chemother. 2005, 49: 2356-2361. 10.1128/AAC.49.6.2356-2361.2005PubMed CentralView ArticlePubMedGoogle Scholar