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Development of Liposomal Ciprofloxacin to Treat Lung Infections

Except for management of Pseudomonas aeruginosa (PA) in cystic fibrosis, there are no approved inhaled antibiotic treatments for any other diseases or for infections from other pathogenic microorganisms such as tuberculosis, non-tuberculous mycobacteria, fungal infections or potential inhaled biowar...

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Autores principales: Cipolla, David, Blanchard, Jim, Gonda, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810082/
https://www.ncbi.nlm.nih.gov/pubmed/26938551
http://dx.doi.org/10.3390/pharmaceutics8010006
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author Cipolla, David
Blanchard, Jim
Gonda, Igor
author_facet Cipolla, David
Blanchard, Jim
Gonda, Igor
author_sort Cipolla, David
collection PubMed
description Except for management of Pseudomonas aeruginosa (PA) in cystic fibrosis, there are no approved inhaled antibiotic treatments for any other diseases or for infections from other pathogenic microorganisms such as tuberculosis, non-tuberculous mycobacteria, fungal infections or potential inhaled biowarfare agents including Francisella tularensis, Yersinia pestis and Coxiella burnetii (which cause pneumonic tularemia, plague and Q fever, respectively). Delivery of an antibiotic formulation via the inhalation route has the potential to provide high concentrations at the site of infection with reduced systemic exposure to limit side effects. A liposomal formulation may improve tolerability, increase compliance by reducing the dosing frequency, and enhance penetration of biofilms and treatment of intracellular infections. Two liposomal ciprofloxacin formulations (Lipoquin(®) and Pulmaquin(®)) that are in development by Aradigm Corporation are described here.
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spelling pubmed-48100822016-04-04 Development of Liposomal Ciprofloxacin to Treat Lung Infections Cipolla, David Blanchard, Jim Gonda, Igor Pharmaceutics Review Except for management of Pseudomonas aeruginosa (PA) in cystic fibrosis, there are no approved inhaled antibiotic treatments for any other diseases or for infections from other pathogenic microorganisms such as tuberculosis, non-tuberculous mycobacteria, fungal infections or potential inhaled biowarfare agents including Francisella tularensis, Yersinia pestis and Coxiella burnetii (which cause pneumonic tularemia, plague and Q fever, respectively). Delivery of an antibiotic formulation via the inhalation route has the potential to provide high concentrations at the site of infection with reduced systemic exposure to limit side effects. A liposomal formulation may improve tolerability, increase compliance by reducing the dosing frequency, and enhance penetration of biofilms and treatment of intracellular infections. Two liposomal ciprofloxacin formulations (Lipoquin(®) and Pulmaquin(®)) that are in development by Aradigm Corporation are described here. MDPI 2016-03-01 /pmc/articles/PMC4810082/ /pubmed/26938551 http://dx.doi.org/10.3390/pharmaceutics8010006 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Cipolla, David
Blanchard, Jim
Gonda, Igor
Development of Liposomal Ciprofloxacin to Treat Lung Infections
title Development of Liposomal Ciprofloxacin to Treat Lung Infections
title_full Development of Liposomal Ciprofloxacin to Treat Lung Infections
title_fullStr Development of Liposomal Ciprofloxacin to Treat Lung Infections
title_full_unstemmed Development of Liposomal Ciprofloxacin to Treat Lung Infections
title_short Development of Liposomal Ciprofloxacin to Treat Lung Infections
title_sort development of liposomal ciprofloxacin to treat lung infections
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810082/
https://www.ncbi.nlm.nih.gov/pubmed/26938551
http://dx.doi.org/10.3390/pharmaceutics8010006
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