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https://hdl.handle.net/2440/60695
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Type: | Journal article |
Title: | Elucidation of the pharmacokinetic/pharmacodynamic determinant of colistin activity against Pseudomonas aeruginosa in murine thigh and lung infection models |
Author: | Dudhani, R. Turnidge, J. Coulthard, K. Milne, R. Rayner, C. Li, J. Nation, R. |
Citation: | Antimicrobial Agents and Chemotherapy, 2010; 54(3):1117-1124 |
Publisher: | Amer Soc Microbiology |
Issue Date: | 2010 |
ISSN: | 0066-4804 1098-6596 |
Statement of Responsibility: | Rajesh V. Dudhani, John D. Turnidge, Kingsley Coulthard, Robert W. Milne, Craig R. Rayner, Jian Li, and Roger L. Nation |
Abstract: | Colistin is increasingly used as last-line therapy against Gram-negative pathogens. The pharmacokinetic (PK)/pharmacodynamic (PD) index that best correlates with the efficacy of colistin remains undefined. The activity of colistin against three strains of Pseudomonas aeruginosa was studied in neutropenic mouse thigh and lung infection models. The PKs of unbound colistin were determined from single-dose PK studies together with extensive plasma protein binding analyses. Dose-fractionation studies were conducted over 24 h with a dose range of 5 to 160 mg/kg of body weight/day. The bacterial burden in the thigh or lung was measured at 24 h after the initiation of treatment. Relationships between antibacterial effect and measures of exposure to unbound (f) colistin (area under the concentration-time curve [fAUC/MIC], maximum concentration of drug in plasma [fCmax]/MIC, and the time that the concentration in plasma is greater than the MIC [fT > MIC]) were examined by using an inhibitory sigmoid maximum-effect model. Nonlinearity in the PKs of colistin, including its plasma protein binding, was observed. The PK/PD index that correlated best with its efficacy was fAUC/MIC in both the thigh infection model (R² = 87%) and the lung infection model (R² = 89%). The fAUC/MIC targets required to achieve 1-log and 2-log kill against the three strains were 15.6 to 22.8 and 27.6 to 36.1, respectively, in the thigh infection model, while the corresponding values were 12.2 to 16.7 and 36.9 to 45.9 in the lung infection model. The findings of this in vivo study indicate the importance of achieving adequate time-averaged exposure to colistin. The results will facilitate efforts to define the more rational design of dosage regimens for humans. |
Keywords: | Thigh Lung Animals Humans Mice Pseudomonas aeruginosa Pseudomonas Infections Lung Diseases Neutropenia Disease Models, Animal Colistin Anti-Bacterial Agents Microbial Sensitivity Tests Area Under Curve Specific Pathogen-Free Organisms Female |
Rights: | Copyright © 2010, American Society for Microbiology. All Rights Reserved. |
DOI: | 10.1128/AAC.01114-09 |
Published version: | http://dx.doi.org/10.1128/aac.01114-09 |
Appears in Collections: | Aurora harvest 5 Molecular and Biomedical Science publications |
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