Evidence map›Paper›PMID 35218106›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2022

Anionic Lipid Nanoparticles Preferentially Deliver mRNA to the Hepatic Reticuloendothelial System.

Roy Pattipeiluhu, Gabriela Arias-Alpizar, Genc Basha, Karen Y T Chan, Jeroen Bussmann, Thomas H Sharp, Mohammad-Amin Moradi, Nico Sommerdijk, Edward N Harris, Pieter R Cullis and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 1 pooled it
14.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

83 citing papers in PubMed, 1 synthesis or guideline pooled it, 173 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Decoding Undesirable Inflammatory Responses of Nucleic Acid-Delivering Lipid Nanoparticles.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Advancements in CRISPR-basedFrontiers in genome editing · 2026
    Review
  16. Emerging nanomedicine for liver diseases treatment.Journal of nanobiotechnology · 2025
    Review
  17. Article
  18. Glycolipid nanoparticles target the spleen and detarget the liver without charge.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  19. Review
  20. Review

23 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 3 countries.

Roy PattipeiluhuSupramolecular and Biomaterials Chemistry, Leiden Institute of Chemistry, Leiden University, Leiden, 2333 CC, The Netherlands.ORCID https://orcid.org/0000-0001-7195-5099
Gabriela Arias-AlpizarSupramolecular and Biomaterials Chemistry, Leiden Institute of Chemistry, Leiden University, Leiden, 2333 CC, The Netherlands.ORCID https://orcid.org/0000-0002-3149-3368
Genc BashaNanoMedicines Research Group, Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, V6T 1Z3, Canada.ORCID https://orcid.org/0000-0003-0471-2892
Karen Y T ChanNanoMedicines Research Group, Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, V6T 1Z3, Canada.
Jeroen BussmannDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, Leiden, 2333 CC, The Netherlands.ORCID https://orcid.org/0000-0003-2814-3305
Thomas H SharpBioNanoPatterning, Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, 2333 RC, The Netherlands.ORCID https://orcid.org/0000-0002-1990-2333
Mohammad-Amin MoradiMaterials and Interface Chemistry, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, Eindhoven, 5600 MB, The Netherlands.
Nico SommerdijkDepartment of Biochemistry, Institute of Molecular Life Sciences, Radboud University Medical Center, Nijmegen, 6500 HB, The Netherlands.ORCID https://orcid.org/0000-0002-8956-195X
Edward N HarrisDepartment of Biochemistry, University of Nebraska, Lincoln, NE, 68588, USA.ORCID https://orcid.org/0000-0001-7045-1040
Pieter R CullisNanoMedicines Research Group, Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, V6T 1Z3, Canada.ORCID https://orcid.org/0000-0001-9586-2508
Alexander KrosSupramolecular and Biomaterials Chemistry, Leiden Institute of Chemistry, Leiden University, Leiden, 2333 CC, The Netherlands.ORCID https://orcid.org/0000-0002-3983-3048
Dominik WitzigmannNanoMedicines Research Group, Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, V6T 1Z3, Canada.ORCID https://orcid.org/0000-0002-8197-8558
Frederick CampbellSupramolecular and Biomaterials Chemistry, Leiden Institute of Chemistry, Leiden University, Leiden, 2333 CC, The Netherlands.ORCID https://orcid.org/0000-0001-9029-6885
Leiden University · NLUniversity of British Columbia · CAEindhoven University of Technology · NLLeiden University Medical Center · NLRadboud University Nijmegen · NLUniversity of Nebraska–Lincoln · US

Funding

Liver-Mediated Clearance of Low Molecular Weight HeparinsR01HL130864 · NHLBI · UNIVERSITY OF NEBRASKA LINCOLN · PI HARRIS, EDWARD N · 2016 to 2019
$1.6M
European Regional Development Fund Site Drug 2S07-033M-ERA.NET : MediSURFNational Institute of Health HL130864Netherlands Organization for Scientific Research 724.014.001NHLBI NIH HHS R01 HL130864Swiss National Science Foundation 186741
6 · The paper itself

Abstract

Lipid nanoparticles (LNPs) are the leading nonviral technologies for the delivery of exogenous RNA to target cells in vivo. As systemic delivery platforms, these technologies are exemplified by Onpattro, an approved LNP-based RNA interference therapy, administered intravenously and targeted to parenchymal liver cells. The discovery of systemically administered LNP technologies capable of preferential RNA delivery beyond hepatocytes has, however, proven more challenging. Here, preceded by comprehensive mechanistic understanding of in vivo nanoparticle biodistribution and bodily clearance, an LNP-based messenger RNA (mRNA) delivery platform is rationally designed to preferentially target the hepatic reticuloendothelial system (RES). Evaluated in embryonic zebrafish, validated in mice, and directly compared to LNP-mRNA systems based on the lipid composition of Onpattro, RES-targeted LNPs significantly enhance mRNA expression both globally within the liver and specifically within hepatic RES cell types. Hepatic RES targeting requires just a single lipid change within the formulation of Onpattro to switch LNP surface charge from neutral to anionic. This technology not only provides new opportunities to treat liver-specific and systemic diseases in which RES cell types play a key role but, more importantly, exemplifies that rational design of advanced RNA therapies must be preceded by a robust understanding of the dominant nano-biointeractions involved.

Indexed as

LipidsNanoparticlesAnimalsLiposomesLiverMiceMononuclear Phagocyte SystemRNA, MessengerRNA, Small InterferingTissue DistributionZebrafishLipid NanoparticlesLipidsLiposomesRNA, MessengerRNA, Small Interferingembryonic zebrafishlipid nanoparticlesmRNA deliveryreticuloendothelial systemstabilin-2

Identifiers

PMID35218106
PMCPMC9461706
OpenAlexW4214591749

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.