Evidence map›Paper›PMID 33829677›Full record

ArticleChemistryOpen2021

A Novel Graphene Quantum Dot-Based mRNA Delivery Platform.

Ya Liu, Changhong Zhao, Alan Sabirsh, Lilei Ye, Xiaoqiu Wu, Hongbin Lu, Johan Liu

Abstract read
In one paragraph

Article in ChemistryOpen, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Cellular functions and biomedical applications of circular RNAs.Acta biochimica et biophysica Sinica · 2024
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. mRNA Delivery: Challenges and Advances through Polymeric Soft Nanoparticles.International journal of molecular sciences · 2024
    Review
  12. Research progress in mRNA drug modification and delivery systems.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2023
    Review
  13. Article
  14. Article
  15. Nanotechnology-based mRNA vaccines.Nature reviews. Methods primers · 2023
    Article
  16. Review
  17. Review
  18. Article
  19. Article
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

7 authors.

Ya LiuDepartment of Microtechnology and Nanoscience, Chalmers University of Technology, 9 Kemivägen, Gothenborg, 412 96, Sweden.
Changhong ZhaoDepartment of Microtechnology and Nanoscience, Chalmers University of Technology, 9 Kemivägen, Gothenborg, 412 96, Sweden.
Alan SabirshAdvanced Drug Delivery, Pharmaceutical Sciences, R&D AstraZeneca, 1 Pepparedsleden, Mölndal, 431 50, Sweden.
Lilei YeSHT Smart High Tech AB, 6 Kemivägen, Gothenburg, 412 58, Sweden.
Xiaoqiu WuAdvanced Drug Delivery, Pharmaceutical Sciences, R&D AstraZeneca, 1 Pepparedsleden, Mölndal, 431 50, Sweden.
Hongbin LuDepartment of Macromolecular Science, Collaborative Innovation Center of Polymers and Polymer Composites, Fudan University, 2005 Songhu Road, Shanghai, 200433, China.
Johan LiuDepartment of Microtechnology and Nanoscience, Chalmers University of Technology, 9 Kemivägen, Gothenborg, 412 96, Sweden.ORCID 0000-0001-9931-1439

Funding

Formas FR-2017/0009National Natural Science Foundation of China 51872182Shanghai International Collaboration research project 19520713900State Key Laboratory of Molecular Engineering of Polymers at Fudan UniversitySTINT DD2016-6502Swedish Board for Strategic Research SE13-0061Swedish National Science Foundation 621-2007-4660
6 · The paper itself

Abstract

During the last decades, there has been growing interest in using therapeutic messager RNA (mRNA) together with drug delivery systems. Naked, unformulated mRNA is, however, unable to cross the cell membrane and is susceptible to degradation. Here we use graphene quantum dots (GQDs) functionalized with polyethyleneimine (PEI) as a novel mRNA delivery system. Our results show that these modified GQDs can be used to deliver intact and functional mRNA to Huh-7 hepatocarcinoma cells at low doses and, that the GQDs are not toxic, although cellular toxicity is a problem for these first-generation modified particles. Functionalized GQDs represent a potentially interesting delivery system that is easy to manufacture, stable and effective.

Indexed as

Cell Line, TumorCell Membrane PermeabilityCell SurvivalFluorescent DyesGraphiteHumansOptical ImagingPolyethyleneimineQuantum DotsRNA, MessengerTransfectionFluorescent DyesGraphitePolyethyleneimineRNA, Messengerdrug deliveryfunctionalizationgraphene quantum dotshepatocarcinomamRNA

Identifiers

PMID33829677
PMCPMC8248920

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.