Your browser doesn't support javascript.
loading
Inhalable Dry Powders for Lung mRNA Delivery.
Gordon, Akiva; Li, Bowen; Witten, Jacob; Nguyen, Hong; Anderson, Daniel G.
Affiliation
  • Gordon A; David H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
  • Li B; Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
  • Witten J; David H Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
  • Nguyen H; Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
  • Anderson DG; Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario, Canada.
Adv Healthc Mater ; : e2400509, 2024 Oct 01.
Article in En | MEDLINE | ID: mdl-39352052
ABSTRACT
Despite great promise, application of mRNA therapeutics in the lung has proven challenging. Many groups have reported success instilling liquid mRNA formulations in animal models, but direct intratracheal administration of large liquid quantities to the human lung presents significant safety and distribution concerns. To accomplish safe and effective mRNA delivery to the lung, formulations must be prepared for dosing via inhalation. An inhaled mRNA delivery system for the lung must be both robust enough to survive inhalation conditions and potent enough to deliver mRNA upon reaching the lung. In this work dry powder lipid nanoparticle formulations are developed, using spray-freeze-drying, to produce stable, biologically active, inhalable dry powders for mRNA delivery. The final powders have suitable aerosolization properties, with mean mass aerodynamic diameter (MMAD) of 3-4 microns, and fine particle fraction (FPF) ≈40%, allowing for efficient mRNA delivery to the deep lung following inhalation. Importantly, the formulations developed here are suitable for use with different ionizable lipids. Four different ionizable lipid-based formulations are evaluated as powders, and all exhibit in vivo pulmonary mRNA delivery equal to that of instilled liquid formulations. These results lay promising groundwork for the eventual development of an inhalable mRNA dry powder therapeutic.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Adv Healthc Mater Year: 2024 Document type: Article Affiliation country: United States Country of publication: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Adv Healthc Mater Year: 2024 Document type: Article Affiliation country: United States Country of publication: Germany