Tom�s Sou
Model-based drug development in pulmonary delivery: pharmacokinetic analysis of novel drug candidates for treatment of Pseudomonas aeruginosa lung infection
Sou, Tom�s; Kukavica-Ibrulj, Irena; Soukarieh, Fadi; Halliday, Nigel; Levesque, Roger C.; Williams, Paul; Stocks, Michael; C�mara, Miguel; Friberg, Lena E.; Bergstr�m, Christel A.S.
Authors
Irena Kukavica-Ibrulj
Dr FADI SOUKARIEH Fadi.Soukarieh@nottingham.ac.uk
RESEARCH FELLOW
Nigel Halliday
Roger C. Levesque
Professor PAUL WILLIAMS PAUL.WILLIAMS@NOTTINGHAM.AC.UK
PROFESSOR OF MOLECULAR MICROBIOLOGY
Professor MICHAEL STOCKS MICHAEL.STOCKS@NOTTINGHAM.AC.UK
PROFESSOR OF MEDICINAL CHEMISTRY AND DRUG DISCOVERY
Professor MIGUEL CAMARA MIGUEL.CAMARA@NOTTINGHAM.AC.UK
PROFESSOR OF MOLECULAR MICROBIOLOGY
Lena E. Friberg
Christel A.S. Bergstr�m
Abstract
Antibiotic resistance is a major public health threat worldwide. In particular, about 80% of cystic fibrosis patients have chronic Pseudomonas aeruginosa (PA) lung infection resistant to many current antibiotics. We are therefore developing a novel class of anti-virulence agents, quorum sensing inhibitors (QSIs), which inhibit biofilm formation and sensitise PA to antibiotic treatments. For respiratory conditions, targeted delivery to the lung could achieve higher local concentrations with reduced risk of adverse systemic events. In this study, we report the pharmacokinetics of three prototype QSIs after pulmonary delivery, and the simultaneous analysis of the drug concentration-time profiles from bronchoalveolar lavage, lung homogenate and plasma samples, using a modelling approach. In addition to facilitating the direct comparison and selection of drug candidates, the developed model was used for dosing simulation studies to predict in vivo exposure following different dosing scenarios. The results suggest that systemic clearance has limited impact on local drug exposure in the lung after pulmonary delivery. Therefore, we believe that novel QSIs designed for pulmonary delivery as targeted treatment for respiratory conditions should ideally have a long residence time in the lung for local efficacy with rapid clearance after systemic absorption for reduced risk of adverse systemic events.
Citation
Sou, T., Kukavica-Ibrulj, I., Soukarieh, F., Halliday, N., Levesque, R. C., Williams, P., Stocks, M., Cámara, M., Friberg, L. E., & Bergström, C. A. (2019). Model-based drug development in pulmonary delivery: pharmacokinetic analysis of novel drug candidates for treatment of Pseudomonas aeruginosa lung infection. Journal of Pharmaceutical Sciences, 108(1), 630-640. https://doi.org/10.1016/j.xphs.2018.09.017
Journal Article Type | Article |
---|---|
Acceptance Date | Sep 17, 2018 |
Online Publication Date | Sep 23, 2018 |
Publication Date | 2019-01 |
Deposit Date | Oct 2, 2018 |
Publicly Available Date | Jan 9, 2019 |
Journal | Journal of Pharmaceutical Sciences |
Print ISSN | 0022-3549 |
Electronic ISSN | 1520-6017 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 108 |
Issue | 1 |
Pages | 630-640 |
DOI | https://doi.org/10.1016/j.xphs.2018.09.017 |
Keywords | pulmonary drug delivery; pharmacometrics; PK/PD modeling; preclinical pharmacokinetics;absorption; solubility; metabolic clearance; distribution; disposition; simulations |
Public URL | https://nottingham-repository.worktribe.com/output/1142576 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S0022354918305446 |
Contract Date | Oct 2, 2018 |
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Model-Based Drug Development in Pulmonary Delivery: Pharmacokinetic Analysis of Novel Drug Candidates for Treatment of Pseudomonas aeruginosa Lung Infection
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Publisher Licence URL
https://creativecommons.org/licenses/by-nc-nd/4.0/
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