Nonviral siRNA Delivery to the Lung: Investigation of PEG−PEI Polyplexes and Their In Vivo Performance Olivia M. Merkel Andrea Beyerle Damiano Librizzi Andreas Pfestroff Thomas M. Behr Brian Sproat Peter J. Barth Thomas Kissel 10.1021/mp900107v.s001 https://acs.figshare.com/articles/media/Nonviral_siRNA_Delivery_to_the_Lung_Investigation_of_PEG_PEI_Polyplexes_and_Their_In_Vivo_Performance/2839669 This study describes the physicobiological characterization of PEI− and PEG−PEI polyplexes containing partially 2′-OMe modified 25/27mer dicer substrate siRNAs (DsiRNAs) and their in vivo behavior regarding biodistribution and systemic bioavailability after pulmonary application as well as their ability to knock down gene expression in the lung. Biophysical characterization included circular dichroism of siRNA in polyplexes, condensation efficiency of polymers and in vitro stability. After in vivo application, biodistribution and kinetics of radiolabeled polyplexes were quantified and recorded over time in three-dimensional SPECT images and by end point scintillation counting. The influence on lung tissue and on the humoral and cellular immunosystem was investigated, and finally knockdown of endogenous gene expression in the lung was determined qualitatively. While all of the polymers used in our study were proven to effectively condense siRNA, stability of the complexes depended on the PEG grafting degree. Interestingly, PEI 25 kDa, which showed the least interaction with mucin or surfactant in vitro, performed poorly in vivo. Our nuclear imaging approach enabled us to follow biodistribution of the instilled nanocarriers over time and indicated that PEGylated nanocarriers are more suitable for lung application. While moderate proinflammatory effects were attributed to PEI25k−PEG(2k)<sub>10</sub> nanocarriers, none of the treatments caused histological abnormalities. Our preliminary in vivo knockdown experiment suggests that PEG−PEI/siRNA complexes are promising nanomedicines for pulmonary siRNA delivery. These results encouraged us to further investigate possible adverse effects and to quantify in vivo gene silencing in the lung after intratracheal instillation of PEG−PEI/siRNA complexes. 2009-08-03 00:00:00 stability biodistribution PEI 25k nanocarriers gene expression characterization PEG Nonviral siRNA Delivery polyplexe end point scintillation Vivo PerformanceThis study vivo knockdown experiment polymer application complex PEI 25 kDa SPECT