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Development of an Adult Physiologically Based Pharmacokinetic Model of Solithromycin in Plasma and Epithelial Lining Fluid
Solithromycin is a fluoroketolide antibiotic under investigation for community‐acquired bacterial pneumonia (CABP). We developed a whole‐body physiologically based pharmacokinetic (PBPK) model for solithromycin in adults using PK‐Sim and MoBi version 6.2, which incorporated time‐dependent CYP3A4 aut...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744174/ https://www.ncbi.nlm.nih.gov/pubmed/29068158 http://dx.doi.org/10.1002/psp4.12252 |
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author | Salerno, Sara N. Edginton, Andrea Cohen‐Wolkowiez, Michael Hornik, Christoph P. Watt, Kevin M. Jamieson, Brian D. Gonzalez, Daniel |
author_facet | Salerno, Sara N. Edginton, Andrea Cohen‐Wolkowiez, Michael Hornik, Christoph P. Watt, Kevin M. Jamieson, Brian D. Gonzalez, Daniel |
author_sort | Salerno, Sara N. |
collection | PubMed |
description | Solithromycin is a fluoroketolide antibiotic under investigation for community‐acquired bacterial pneumonia (CABP). We developed a whole‐body physiologically based pharmacokinetic (PBPK) model for solithromycin in adults using PK‐Sim and MoBi version 6.2, which incorporated time‐dependent CYP3A4 auto‐inhibition. The model was developed and evaluated using plasma and epithelial lining fluid (ELF) concentration data from 100 healthy subjects and 22 patients with CABP (1,966 plasma, 30 ELF samples). We performed population simulations and calculated the number of observations falling outside the 90% prediction interval. For the oral regimen (800 mg on day 1 and 400 mg daily on days 2–5) that was evaluated in phase III studies, 11% and 23% of observations from healthy adults fell outside the 90% prediction interval for plasma and ELF, respectively. This regimen should be effective because ≥97% of simulated adults achieved area under the concentration vs. time curve (AUC) to minimum inhibitory concentration ratios associated with a log(10) colony forming unit reduction in ELF. |
format | Online Article Text |
id | pubmed-5744174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57441742018-01-03 Development of an Adult Physiologically Based Pharmacokinetic Model of Solithromycin in Plasma and Epithelial Lining Fluid Salerno, Sara N. Edginton, Andrea Cohen‐Wolkowiez, Michael Hornik, Christoph P. Watt, Kevin M. Jamieson, Brian D. Gonzalez, Daniel CPT Pharmacometrics Syst Pharmacol Original Articles Solithromycin is a fluoroketolide antibiotic under investigation for community‐acquired bacterial pneumonia (CABP). We developed a whole‐body physiologically based pharmacokinetic (PBPK) model for solithromycin in adults using PK‐Sim and MoBi version 6.2, which incorporated time‐dependent CYP3A4 auto‐inhibition. The model was developed and evaluated using plasma and epithelial lining fluid (ELF) concentration data from 100 healthy subjects and 22 patients with CABP (1,966 plasma, 30 ELF samples). We performed population simulations and calculated the number of observations falling outside the 90% prediction interval. For the oral regimen (800 mg on day 1 and 400 mg daily on days 2–5) that was evaluated in phase III studies, 11% and 23% of observations from healthy adults fell outside the 90% prediction interval for plasma and ELF, respectively. This regimen should be effective because ≥97% of simulated adults achieved area under the concentration vs. time curve (AUC) to minimum inhibitory concentration ratios associated with a log(10) colony forming unit reduction in ELF. John Wiley and Sons Inc. 2017-10-25 2017-12 /pmc/articles/PMC5744174/ /pubmed/29068158 http://dx.doi.org/10.1002/psp4.12252 Text en © 2017 The Authors CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Salerno, Sara N. Edginton, Andrea Cohen‐Wolkowiez, Michael Hornik, Christoph P. Watt, Kevin M. Jamieson, Brian D. Gonzalez, Daniel Development of an Adult Physiologically Based Pharmacokinetic Model of Solithromycin in Plasma and Epithelial Lining Fluid |
title | Development of an Adult Physiologically Based Pharmacokinetic Model of Solithromycin in Plasma and Epithelial Lining Fluid |
title_full | Development of an Adult Physiologically Based Pharmacokinetic Model of Solithromycin in Plasma and Epithelial Lining Fluid |
title_fullStr | Development of an Adult Physiologically Based Pharmacokinetic Model of Solithromycin in Plasma and Epithelial Lining Fluid |
title_full_unstemmed | Development of an Adult Physiologically Based Pharmacokinetic Model of Solithromycin in Plasma and Epithelial Lining Fluid |
title_short | Development of an Adult Physiologically Based Pharmacokinetic Model of Solithromycin in Plasma and Epithelial Lining Fluid |
title_sort | development of an adult physiologically based pharmacokinetic model of solithromycin in plasma and epithelial lining fluid |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744174/ https://www.ncbi.nlm.nih.gov/pubmed/29068158 http://dx.doi.org/10.1002/psp4.12252 |
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