Cited by 1,800RNA Interference and Gene DeliveryNanoparticle-Based Drug DeliveryDendrimers and Hyperbranched Polymers

Delivery materials for siRNA therapeutics

Kanasty, Rosemary, Dorkin, Joseph Robert, Vegas, Arturo, Anderson, Daniel·2013·Nature Materials

Abstract

RNA interference (RNAi) has broad potential as a therapeutic to reversibly silence any gene. To achieve the clinical potential of RNAi, delivery materials are required to transport short interfering RNA (siRNA) to the site of action in the cells of target tissues. This Review provides an introduction to the biological challenges that siRNA delivery materials aim to overcome, as well as a discussion of the way that the most effective and clinically advanced classes of siRNA delivery systems, including lipid nanoparticles and siRNA conjugates, are designed to surmount these challenges. The systems that we discuss are diverse in their approaches to the delivery problem, and provide valuable insight to guide the design of future siRNA delivery materials.

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Crossref · 10.1038/nmat3765

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112 of 112 references verified0 citation errors · 0 not checkable

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  • Several miRNAs and antisense oligonucleotides (ASOs) are currently under investigation in clinical trials for various diseases.

    “Several miRNAs and antisense oligonucleotides (ASOs) are currently under investigation in clinical trials for various diseases (Kanasty et al., 2013;van Rooij and Kauppinen, 2014;Gaudet et al., 2015).”

    From microRNA-33 Regulates ApoE Lipidation and Amyloid-β Metabolism in the Brain (2015) · cites this paper as Kanasty et al., 2013

  • The main role of PEGylated lipid in LNPs is to reduce aggregation and non-specific uptake by immune cells.

    “The main role of PEGylated lipid in LNPs is to reduce aggregation and non-specific uptake by immune cells.304–306”

    From Advances in COVID-19 mRNA vaccine development (2022) · cites this paper as [306]

  • CRISPR-Cas9-mediated correction may be translatable to humans.

    “we believe that recent advances in the delivery of nucleic acid therapeutics provide hope that CRISPR-Cas9–mediated correction may be translatable to humans15.”

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Authors
Kanasty, R., Dorkin, J. R., Vegas, A., & Anderson, D.
Affiliations
  • Koch Institute for Integrative Cancer Research At MIT (US)
  • Boston Children's Hospital (US)
Corresponding author
Anderson, Daniel
Venue
Nature Materials
Published
2013-10-23
Volume
12
Issue
11
Pages
967-977
ISSN
  • 1476-1122 (ISSN-L)
  • 1476-4660
OpenAlex
W1995770815
Cited by
1,800
References
113
Citations by year
2026: 77 · 2025: 103 · 2024: 111 · 2023: 138 · 2022: 139 · 2021: 148 · 2020: 159 · 2019: 129 · 2018: 164 · 2017: 151 · 2016: 183 · 2015: 179 · 2014: 114 · 2013: 4 · 2012: 1
FWCI
15.04
Type
journal article
Language
en
Open access
closed
Locations
  • Nature Materials (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
  • Physical Sciences › Materials Science › Polymers and Plastics › Dendrimers and Hyperbranched Polymers
Keywords
siRNA delivery, RNA interference therapy, lipid nanoparticles, siRNA conjugates, gene silencing, drug delivery materials
MeSH terms
Animals, Drug Carriers, Humans, RNA, Small Interfering, Nanoparticles

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