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Lung-Specific mRNA Delivery Enabled by Sulfonium Lipid Nanoparticles.
Popoola, David O; Cao, Zhi; Men, Yuqin; Li, Xinyuan; Viapiano, Mariano; Wilkens, Stephan; Luo, Juntao; Teng, Yong; Meng, Qinghe; Li, Yamin.
Afiliação
  • Popoola DO; Department of Pharmacology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.
  • Cao Z; Department of Pharmacology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.
  • Men Y; Department of Pharmacology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.
  • Li X; Department of Pharmacology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.
  • Viapiano M; Department of Neuroscience and Physiology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.
  • Wilkens S; Department of Biochemistry and Molecular Biology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.
  • Luo J; Department of Pharmacology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.
  • Teng Y; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia 30322, United States.
  • Meng Q; Department of Surgery, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.
  • Li Y; Department of Pharmacology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.
Nano Lett ; 24(26): 8080-8088, 2024 Jul 03.
Article em En | MEDLINE | ID: mdl-38888232
ABSTRACT
Among various mRNA carrier systems, lipid nanoparticles (LNPs) stand out as the most clinically advanced. While current clinical trials of mRNA/LNP therapeutics mainly address liver diseases, the potential of mRNA therapy extends far beyond─yet to be unraveled. To fully unlock the promises of mRNA therapy, there is an urgent need to develop safe and effective LNP systems that can target extrahepatic organs. Here, we report on the development of sulfonium lipid nanoparticles (sLNPs) for systemic mRNA delivery to the lungs. sLNP effectively and specifically delivered mRNA to the lungs following intravenous administration in mice. No evidence of lung and systemic inflammation or toxicity in major organs was induced by sLNP. Our findings demonstrated that the newly developed lung-specific sLNP platform is both safe and efficacious. It holds great promise for advancing the development of new mRNA-based therapies for the treatment of lung-associated diseases and conditions.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: RNA Mensageiro / Nanopartículas / Lipídeos / Pulmão Limite: Animals / Humans Idioma: En Revista: Nano Lett Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: RNA Mensageiro / Nanopartículas / Lipídeos / Pulmão Limite: Animals / Humans Idioma: En Revista: Nano Lett Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos