4.8 Article

Non-viral vectors for RNA delivery

Journal

JOURNAL OF CONTROLLED RELEASE
Volume 342, Issue -, Pages 241-279

Publisher

ELSEVIER
DOI: 10.1016/j.jconrel.2022.01.008

Keywords

RNA drugs; Non-viral vector; Biological barrier; Control release; Gene therapy

Funding

  1. National Natural Science Foundation of China [81773650, 81690264, 81973259]
  2. Beijing Natural Science Foundation [J200018]
  3. National Key New Drug Creation and Manufacturing Program, Ministry of Science and Technology of China [2018ZX09721003-004]

Ask authors/readers for more resources

RNA-based therapy is a promising strategy for disease treatment, and recent advances in non-viral delivery systems have shown potential in protecting RNA, facilitating cell internalization, and controlled release of therapeutics.
RNA-based therapy is a promising and potential strategy for disease treatment by introducing exogenous nucleic acids such as messenger RNA (mRNA), small interfering RNA (siRNA), microRNA (miRNA) or antisense oligonucleotides (ASO) to modulate gene expression in specific cells. It is exciting that mRNA encoding the spike protein of COVID-19 (coronavirus disease 2019) delivered by lipid nanoparticles (LNPs) exhibits the efficient protection of lungs infection against the virus. In this review, we introduce the biological barriers to RNA delivery in vivo and discuss recent advances in non-viral delivery systems, such as lipid-based nanoparticles, polymeric nanoparticles, N-acetylgalactosamine (GalNAc)-siRNA conjugate, and biomimetic nanovectors, which can protect RNAs against degradation by ribonucleases, accumulate in specific tissue, facilitate cell internalization, and allow for the controlled release of the encapsulated therapeutics.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available