4.8 Article

Co-delivery of mRNA and SPIONs through amino-este nanomaterials

期刊

NANO RESEARCH
卷 11, 期 10, 页码 5596-5603

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-018-2082-0

关键词

amino-ester nanomaterials; lipid-like nanoparticles (LLNs); dual-functional; superparamagnetic iron oxide nanoparticles (SPIONs); mRNA delivery; magnetic resonance imaging (MRI)

资金

  1. Early Career Investigator Award from the Bayer Hemophilia Awards Program
  2. Research Awards from the National PKU Alliance
  3. New Investigator Grant from the American Association of Pharmaceutical Scientists (AAPS) Foundation
  4. Maximizing Investigators' Research Award from the National Institute of General Medical Sciences [1R35GM119679]
  5. College of Pharmacy at The Ohio State University
  6. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R35GM119679] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Nanoparticles have been widely explored for combined therapeutic and diagnostic applications. For example, lipid-based nanoparticles have been used to encapsulate multiple types of agents and achieve multi-functions. Herein, we enabled a co-delivery of mRNA molecules and superparamagnetic iron oxide nanoparticles (SPIONs) by using an amino-ester lipid-like nanomaterial. An orthogonal experimental design was used to identify the optimal formulation. The optimal formulation, MPA-Ab-8 LLNs, not only showed high encapsulation of both mRNA and SPIONs, but also increased the r(2) relaxivity of SPIONs by more than 1.5-fold in vitro. MPA-Ab-8 LLNs effectively delivered mRNA and SPIONs into cells, and consequently induced high protein expression as well as strong MRI contrast. Consistent herewith, we observed both mRNA-mediated protein expression and an evident negative contrast enhancement of MRI signal in mice. In conclusion, amino-ester nanomaterials demonstrate great potential as delivery vehicles for theranostic applications.

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