Evidence map›Paper›PMID 37105997›Full record

ArticleScientific reports2023

Lipid-coated mesoporous silica nanoparticles for anti-viral applications via delivery of CRISPR-Cas9 ribonucleoproteins.

Annette E LaBauve, Edwin A Saada, Iris K A Jones, Richard Mosesso, Achraf Noureddine, Jessica Techel, Andrew Gomez, Nicole Collette, Michael B Sherman, Rita E Serda and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

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  19. Expanding the CRISPR/Cas toolkit: applications in proteomics and theranostics.Frontiers in bioengineering and biotechnology · 2025
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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

15 authors at 5 institutions in 1 country.

Annette E LaBauve *Department of Biotechnology and Bioengineering, Sandia National Laboratories, Livermore, USA.
Edwin A Saada *Department of Systems Biology, Sandia National Laboratories, Livermore, USA.
Iris K A JonesDepartment of Systems Biology, Sandia National Laboratories, Livermore, USA.
Richard MosessoDepartment of Systems Biology, Sandia National Laboratories, Livermore, USA.
Achraf NoureddineChemical and Biological Engineering, University of New Mexico, Albuquerque, USA.
Jessica TechelDepartment of Biotechnology and Bioengineering, Sandia National Laboratories, Livermore, USA.
Andrew GomezDepartment of Active Ceramics Value Stream, Sandia National Laboratories, Albuquerque, USA.
Nicole ColletteBiotechnology and Biosciences Division, Physical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, USA.
Michael B ShermanSealy Center for Structural Biology and Molecular Biophysics, University of Texas Medical Branch, Galveston, USA.
Rita E SerdaDepartment of Internal Medicine, Health Sciences Center, University of New Mexico, Albuquerque, USA.
Kimberly S ButlerDepartment of Molecular and Microbiology, Sandia National Laboratories, Albuquerque, USA.
C Jeffery BrinkerChemical and Biological Engineering, University of New Mexico, Albuquerque, USA.
Joseph S SchoenigerDepartment of Systems Biology, Sandia National Laboratories, Livermore, USA.
Darryl SasakiDepartment of Biotechnology and Bioengineering, Sandia National Laboratories, Livermore, USA.
Oscar A NegreteDepartment of Systems Biology, Sandia National Laboratories, Livermore, USA. onegrete@sandia.gov.
Sandia National Laboratories California · USUniversity of New Mexico · USLawrence Livermore National Laboratory · USSandia National Laboratories · USThe University of Texas Medical Branch at Galveston · US

Funding

A Targeted Nanomedicine Prototype Against Enzalutamide-resistant Prostate CancerR01CA226537 · NCI · RBHS -CANCER INSTITUTE OF NEW JERSEY · PI ARAP, WADIH, BRINKER, C JEFFREY · 2018 to 2022
$3.2M
NCI NIH HHS R01 CA226537
6 · The paper itself

Abstract

Emerging and re-emerging viral pathogens present a unique challenge for anti-viral therapeutic development. Anti-viral approaches with high flexibility and rapid production times are essential for combating these high-pandemic risk viruses. CRISPR-Cas technologies have been extensively repurposed to treat a variety of diseases, with recent work expanding into potential applications against viral infections. However, delivery still presents a major challenge for these technologies. Lipid-coated mesoporous silica nanoparticles (LCMSNs) offer an attractive delivery vehicle for a variety of cargos due to their high biocompatibility, tractable synthesis, and amenability to chemical functionalization. Here, we report the use of LCMSNs to deliver CRISPR-Cas9 ribonucleoproteins (RNPs) that target the Niemann-Pick disease type C1 gene, an essential host factor required for entry of the high-pandemic risk pathogen Ebola virus, demonstrating an efficient reduction in viral infection. We further highlight successful in vivo delivery of the RNP-LCMSN platform to the mouse liver via systemic administration.

Indexed as

CRISPR-Cas SystemsNanoparticlesAnimalsAntiviral AgentsGene EditingLipidsMiceRibonucleoproteinsAntiviral AgentsLipidsRibonucleoproteins

Identifiers

PMID37105997
PMCPMC10133914
OpenAlexW4367173578

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.