Enhancement of lung gene delivery after aerosol: a new strategy using non-viral complexes with antibacterial properties
Author(s) -
Angélique Mottais,
Tony Le Gall,
Y. Sibiril,
Julian Ravel,
Véronique Laurent,
Frédérique d’Arbonneau,
Tristan Montier
Publication year - 2017
Publication title -
bioscience reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 77
eISSN - 1573-4935
pISSN - 0144-8463
DOI - 10.1042/bsr20160618
Subject(s) - ivacaftor , rifabutin , medicine , drug , cystic fibrosis , rifamycin , antibiotics , nanocarriers , respiratory tract , copd , drug delivery , pulmonary disease , rifampicin , pharmacology , biology , respiratory system , nanotechnology , microbiology and biotechnology , materials science , cystic fibrosis transmembrane conductance regulator , clarithromycin
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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