Evidence map›Paper›PMID 23924216›Full record

ArticleMolecular pharmaceutics2013

RNA replicon delivery via lipid-complexed PRINT protein particles.

Jing Xu, J Christopher Luft, Xianwen Yi, Shaomin Tian, Gary Owens, Jin Wang, Ashley Johnson, Peter Berglund, Jonathan Smith, Mary E Napier and 1 more

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2013. 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
–field-weighted citation impact
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.

  1. Review
  2. Review
  3. Self-amplifying mRNA-Based Vaccine Technology and Its Mode of Action.Current topics in microbiology and immunology · 2022
    Article
  4. A Review of Nanotechnology for Treating Dysfunctional Placenta.Frontiers in bioengineering and biotechnology · 2022
    Review
  5. Review
  6. Recent advances in nanotheranostics for triple negative breast cancer treatment.Journal of experimental & clinical cancer research : CR · 2019
    Review
  7. Review
  8. Delivering the Messenger: Advances in Technologies for Therapeutic mRNA Delivery.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Control of polymeric nanoparticle size to improve therapeutic delivery.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  14. Biomimetic particles as therapeutics.Trends in biotechnology · 2015
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
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

11 authors.

Jing XuDepartment of Chemistry, △Department of Pharmacology, ∥UNC Eshelman School of Pharmacy, †Carolina Center of Cancer Nanotechnology Excellence, ⊥Institute for Advanced Materials, #Institute for Nanomedicine, ¶Lineberger Comprehensive Cancer Center, and ■Department of Biochemistry and Biophysics, University of North Carolina , Chapel Hill, North Carolina 27599, United States.
J Christopher Luft
Xianwen Yi
Shaomin Tian
Gary Owens
Jin Wang
Ashley Johnson
Peter Berglund
Jonathan Smith
Mary E Napier
Joseph M DeSimone

Funding

Translational Nanosystems for Improved Lung Cancer Treatment with Small MoleculesU54CA151652 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAROON, ZISHAN A, TEPPER, JOEL E · 2010 to 2014
$12.1M
Delivery of Biological Therapeutics: Using Engineered Particles and Novel DeliverDP1OD006432 · OD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DESIMONE, JOSEPH M. · 2009 to 2011
$2.2M
Engineered Organic Particles of Controlled Size, Shape and Surface Chemistry for R01EB009565 · NIBIB · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DESIMONE, JOSEPH M. · 2009 to 2012
$1.3M
NCI NIH HHS U54 CA151652NIBIB NIH HHS R01 EB009565NIBIB NIH HHS R01EB009565NIH HHS 1DP1OD006432NIH HHS DP1 OD006432
6 · The paper itself

Abstract

Herein we report the development of a nonviral lipid-complexed PRINT (particle replication in nonwetting templates) protein particle system (LPP particle) for RNA replicon delivery with a view toward RNA replicon-based vaccination. Cylindrical bovine serum albumin (BSA) particles (diameter (d) 1 μm, height (h) 1 μm) loaded with RNA replicon and stabilized with a fully reversible disulfide cross-linker were fabricated using PRINT technology. Highly efficient delivery of the particles to Vero cells was achieved by complexing particles with a mixture of 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) and 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE) lipids. Our data suggest that (1) this lipid-complexed protein particle is a promising system for delivery of RNA replicon-based vaccines and (2) it is necessary to use a degradable cross-linker for successful delivery of RNA replicon via protein-based particles.

Indexed as

Cell LineFatty Acids, MonounsaturatedGene Transfer TechniquesHumansLipidsPhosphatidylethanolaminesQuaternary Ammonium CompoundsRNASerum Albumin, Bovine1,2-dioleoyl-glycero-3-phosphatidyl ethanolamine1,2-dioleoyloxy-3-(trimethylammonium)propaneFatty Acids, MonounsaturatedLipidsPhosphatidylethanolaminesQuaternary Ammonium CompoundsRNASerum Albumin, Bovine

Identifiers

PMID23924216
PMCPMC3948333

What OpenQuestion holds

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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.