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Polymer-Lipid Nanoparticles for Systemic Delivery of mRNA to the Lungs

Author(s)
Heartlein, Michael W.; DeRosa, Frank; Kaczmarek, James Cliff; Kauffman, Kevin John; Webber, Matthew; Anderson, Daniel Griffith; Patel, Asha; Fenton, Owen Shea; ... Show more Show less
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Abstract
Therapeutic nucleic acids hold great promise for the treatment of disease but require vectors for safe and effective delivery. Synthetic nanoparticle vectors composed of poly(β-amino esters) (PBAEs) and nucleic acids have previously demonstrated potential utility for local delivery applications. To expand this potential utility to include systemic delivery of mRNA, hybrid polymer–lipid nanoformulations for systemic delivery to the lungs were developed. Through coformulation of PBAEs with lipid–polyethylene glycol (PEG), mRNA formulations were developed with increased serum stability and increased in vitro potency. The formulations were capable of functional delivery of mRNA to the lungs after intravenous administration in mice. To our knowledge, this is the first report of the systemic administration of mRNA for delivery to the lungs using degradable polymer–lipid nanoparticles.
Date issued
2016-09
URI
http://hdl.handle.net/1721.1/107933
Department
Massachusetts Institute of Technology. Institute for Medical Engineering & Science; Harvard University--MIT Division of Health Sciences and Technology; Massachusetts Institute of Technology. Department of Chemical Engineering; Massachusetts Institute of Technology. Department of Chemistry; Koch Institute for Integrative Cancer Research at MIT
Journal
Angewandte Chemie International Edition
Publisher
Wiley Blackwell
Citation
Kaczmarek, James C. et al. “Polymer-Lipid Nanoparticles for Systemic Delivery of mRNA to the Lungs.” Angewandte Chemie International Edition 55.44 (2016): 13808–13812.
Version: Author's final manuscript
ISSN
1433-7851
1521-3773

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