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A miniaturized nebulization catheter for improved gene delivery to the mouse lung
Author(s) -
KöpingHöggård Magnus,
Issa Mohamed M.,
Köhler Tamara,
Tronde Ann,
Vårum Kjell M.,
Artursson Per
Publication year - 2005
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.762
Subject(s) - gene delivery , in vivo , lung , transfection , chemistry , catheter , genetic enhancement , microbiology and biotechnology , biomedical engineering , pharmacology , biology , gene , medicine , surgery , biochemistry
Background The available methods for administration of gene delivery systems to the lungs of small animals via nebulization have several drawbacks. These include lack of control over the delivered dose and a negative impact on the stability of the formulation. This paper describes a new nebulization catheter device for the administration of plasmid‐based gene delivery systems (polyplexes) as aerosols to the mouse lung in vivo . Methods The physical stability of naked pDNA and polyplexes formulated with chitosan oligomers and PEI was examined following nebulization with the catheter device. We also examined the in vitro transfection efficiency of the polyplexes recovered after nebulization. Lung distribution and gene expression after administration of the selected gene delivery systems to the mouse lung were also investigated. Results In contrast to previously described nebulization methods, the structural integrity of the unprotected naked pDNA was maintained following nebulization by the catheter device, which indicates relatively mild nebulization conditions. In addition, the nebulization procedure did not affect the physical stability of the formulated polyplexes. Small volumes of the pDNA aerosol (10–20 µl) were delivered in a highly controlled and reproducible manner. The aerosol droplet size varied with the molecular weight of the polycations. Aerosol delivery via this method resulted in improved lung distribution of pDNA polyplexes and a six‐fold increase in the efficiency of gene delivery in vivo over that seen with the commonly used intratracheal instillation method. Conclusion The use of the nebulization catheter device provides a promising alternative for aerosol gene delivery to the mouse lung. Copyright © 2005 John Wiley & Sons, Ltd.

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