TY - JOUR
T1 - Magnetized aerosols comprising superparamagnetic iron oxide nanoparticles improve targeted drug and gene delivery to the lung
AU - Hasenpusch, Guenther
AU - Geiger, Johannes
AU - Wagner, Kai
AU - Mykhaylyk, Olga
AU - Wiekhorst, Frank
AU - Trahms, Lutz
AU - Heidsieck, Alexandra
AU - Gleich, Bernhard
AU - Bergemann, Christian
AU - Aneja, Manish K.
AU - Rudolph, Carsten
PY - 2012/5
Y1 - 2012/5
N2 - Purpose: Targeted delivery of aerosols could not only improve efficacy of inhaled drugs but also reduce side effects resulting from their accumulation in healthy tissue. Here we investigated the impact of magnetized aerosols on model drug accumulation and transgene expression in magnetically targeted lung regions of unanesthetized mice. Methods: Solutions containing superparamagnetic iron oxide nanoparticles (SPIONs) and model drugs (fluorescein or complexed plasmid DNA) were nebulized to unanesthetized mice under the influence of an external magnetic gradient directed to the lungs. Drug accumulation and transgene expression was subsequently measured at different time points. Results: We could demonstrate 2-3 fold higher accumulation of the model drug fluorescein and specific transgene expression in lung regions of mice which had been exposed to an external magnetic gradient during nebulization compared to the control mice without any exposure to magnetic gradient. Conclusions: Magnetized aerosols present themselves as an efficient approach for targeted pulmonary delivery of drugs and gene therapeutic agents in order to treat localized diseases of the deeper airways.
AB - Purpose: Targeted delivery of aerosols could not only improve efficacy of inhaled drugs but also reduce side effects resulting from their accumulation in healthy tissue. Here we investigated the impact of magnetized aerosols on model drug accumulation and transgene expression in magnetically targeted lung regions of unanesthetized mice. Methods: Solutions containing superparamagnetic iron oxide nanoparticles (SPIONs) and model drugs (fluorescein or complexed plasmid DNA) were nebulized to unanesthetized mice under the influence of an external magnetic gradient directed to the lungs. Drug accumulation and transgene expression was subsequently measured at different time points. Results: We could demonstrate 2-3 fold higher accumulation of the model drug fluorescein and specific transgene expression in lung regions of mice which had been exposed to an external magnetic gradient during nebulization compared to the control mice without any exposure to magnetic gradient. Conclusions: Magnetized aerosols present themselves as an efficient approach for targeted pulmonary delivery of drugs and gene therapeutic agents in order to treat localized diseases of the deeper airways.
KW - Aerosol
KW - Cancer
KW - Gene delivery
KW - Lung
KW - Magnetic drug targeting
UR - http://www.scopus.com/inward/record.url?scp=84862700846&partnerID=8YFLogxK
U2 - 10.1007/s11095-012-0682-z
DO - 10.1007/s11095-012-0682-z
M3 - Article
C2 - 22271050
AN - SCOPUS:84862700846
SN - 0724-8741
VL - 29
SP - 1308
EP - 1318
JO - Pharmaceutical Research
JF - Pharmaceutical Research
IS - 5
ER -