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Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties

The pathophysiology of obstructive pulmonary diseases, such as cystic fibrosis (CF), leads to the development of chronic infections in the respiratory tract. Thus, the symptomatic management of the disease requires, in particular, repetitive antibiotherapy. Besides these antibacterial treatments, ce...

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Autores principales: Mottais, Angélique, Le Gall, Tony, Sibiril, Yann, Ravel, Julian, Laurent, Véronique, d’Arbonneau, Frédérique, Montier, Tristan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691145/
https://www.ncbi.nlm.nih.gov/pubmed/29046368
http://dx.doi.org/10.1042/BSR20160618
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author Mottais, Angélique
Le Gall, Tony
Sibiril, Yann
Ravel, Julian
Laurent, Véronique
d’Arbonneau, Frédérique
Montier, Tristan
author_facet Mottais, Angélique
Le Gall, Tony
Sibiril, Yann
Ravel, Julian
Laurent, Véronique
d’Arbonneau, Frédérique
Montier, Tristan
author_sort Mottais, Angélique
collection PubMed
description The pathophysiology of obstructive pulmonary diseases, such as cystic fibrosis (CF), leads to the development of chronic infections in the respiratory tract. Thus, the symptomatic management of the disease requires, in particular, repetitive antibiotherapy. Besides these antibacterial treatments, certain pathologies, such as CF or chronic obstructive pulmonary disease (COPD), require the intake of many drugs. This simultaneous absorption may lead to undesirable drug interactions. For example, Orkambi® (lumacaftor/Ivacaftor, Vertex), a pharmacological drug employed to treat F508del patients, cannot be used with antibiotics such as rifampicin or rifabutin (rifamycin family) which are necessary to treat Mycobacteriaceae. As far as gene therapy is concerned, bacteria and/or biofilm in the airways present an additional barrier for gene transfer. Thus, aerosol administration of nanoparticles have to overcome many obstacles before allowing cellular penetration of therapeutic compounds. This review focusses on the development of aerosol formulations adapted to the respiratory tract and its multiple barriers. Then, formulations that are currently used in clinical applications are summarized depending on the active molecule delivered. Finally, we focus on new therapeutic approaches to reduce possible drug interactions by transferring the antibacterial activity to the nanocarrier while ensuring the transfection efficiency.
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spelling pubmed-56911452017-11-28 Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties Mottais, Angélique Le Gall, Tony Sibiril, Yann Ravel, Julian Laurent, Véronique d’Arbonneau, Frédérique Montier, Tristan Biosci Rep Review Articles The pathophysiology of obstructive pulmonary diseases, such as cystic fibrosis (CF), leads to the development of chronic infections in the respiratory tract. Thus, the symptomatic management of the disease requires, in particular, repetitive antibiotherapy. Besides these antibacterial treatments, certain pathologies, such as CF or chronic obstructive pulmonary disease (COPD), require the intake of many drugs. This simultaneous absorption may lead to undesirable drug interactions. For example, Orkambi® (lumacaftor/Ivacaftor, Vertex), a pharmacological drug employed to treat F508del patients, cannot be used with antibiotics such as rifampicin or rifabutin (rifamycin family) which are necessary to treat Mycobacteriaceae. As far as gene therapy is concerned, bacteria and/or biofilm in the airways present an additional barrier for gene transfer. Thus, aerosol administration of nanoparticles have to overcome many obstacles before allowing cellular penetration of therapeutic compounds. This review focusses on the development of aerosol formulations adapted to the respiratory tract and its multiple barriers. Then, formulations that are currently used in clinical applications are summarized depending on the active molecule delivered. Finally, we focus on new therapeutic approaches to reduce possible drug interactions by transferring the antibacterial activity to the nanocarrier while ensuring the transfection efficiency. Portland Press Ltd. 2017-11-17 /pmc/articles/PMC5691145/ /pubmed/29046368 http://dx.doi.org/10.1042/BSR20160618 Text en © 2017 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Articles
Mottais, Angélique
Le Gall, Tony
Sibiril, Yann
Ravel, Julian
Laurent, Véronique
d’Arbonneau, Frédérique
Montier, Tristan
Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties
title Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties
title_full Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties
title_fullStr Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties
title_full_unstemmed Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties
title_short Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties
title_sort enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691145/
https://www.ncbi.nlm.nih.gov/pubmed/29046368
http://dx.doi.org/10.1042/BSR20160618
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