Evidence map›Paper›PMID 33676500›Full record

ArticleJournal of nanobiotechnology2021

Improved gene delivery to K-562 leukemia cells by lipoic acid modified block copolymer micelles.

Friederike Richter, Prosper Mapfumo, Liam Martin, Jana I Solomun, Franziska Hausig, Jochen J Frietsch, Thomas Ernst, Stephanie Hoeppener, Johannes C Brendel, Anja Traeger

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Article
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  7. Review
  8. Efficient Transient Expression of Plasmid DNA Using Poly (2-(Frontiers in bioengineering and biotechnology · 2022
    Article
  9. 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

10 authors at 2 institutions in 1 country.

Friederike Richter *Laboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstrasse 10, 07743, Jena, Germany.
Prosper Mapfumo *Laboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstrasse 10, 07743, Jena, Germany.
Liam MartinLaboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstrasse 10, 07743, Jena, Germany.
Jana I SolomunLaboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstrasse 10, 07743, Jena, Germany.
Franziska HausigLaboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstrasse 10, 07743, Jena, Germany.
Jochen J FrietschKlinik für Innere Medizin II, Abteilung Hämatologie und Internistische Onkologie, Universitätsklinikum Jena, Am Klinikum 1, 07747, Jena, Germany.ORCID https://orcid.org/0000-0002-1476-8059
Thomas ErnstKlinik für Innere Medizin II, Abteilung Hämatologie und Internistische Onkologie, Universitätsklinikum Jena, Am Klinikum 1, 07747, Jena, Germany.
Stephanie HoeppenerLaboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstrasse 10, 07743, Jena, Germany.
Johannes C BrendelLaboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstrasse 10, 07743, Jena, Germany.ORCID https://orcid.org/0000-0002-1206-1375
Anja TraegerLaboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstrasse 10, 07743, Jena, Germany. anja.traeger@uni-jena.de.ORCID http://orcid.org/0000-0001-7734-2293
Friedrich Schiller University Jena · DEJena University Hospital · DE

Funding

Bundesministerium für Bildung und Forschung #13XP5034ADeutsche Forschungsgemeinschaft 316213987Deutsche Forschungsgemeinschaft 358263073
6 · The paper itself

Abstract

Although there has been substantial progress in the research field of gene delivery, there are some challenges remaining, e.g. there are still cell types such as primary cells and suspension cells (immune cells) known to be difficult to transfect. Cationic polymers have gained increasing attention due to their ability to bind, condense and mask genetic material, being amenable to scale up and highly variable in their composition. In addition, they can be combined with further monomers exhibiting desired biological and chemical properties, such as antioxidative, pH- and redox-responsive or biocompatible features. By introduction of hydrophobic monomers, in particular as block copolymers, cationic micelles can be formed possessing an improved chance of transfection in otherwise challenging cells. In this study, the antioxidant biomolecule lipoic acid, which can also be used as crosslinker, was incorporated into the hydrophobic block of a diblock copolymer, poly{[2-(dimethylamino)ethyl methacrylate]

Indexed as

Gene Transfer TechniquesMicellesAnimalsAntioxidantsCationsCell Line, TumorDNAHEK293 CellsHumansHydrophobic and Hydrophilic InteractionsLeukemiaMethacrylatesMicePlasmidsPolymersThioctic Acid2-(dimethylamino)ethyl methacrylateAntioxidantsbutyl methacrylateCationsDNAMethacrylatesMicellesPolymersThioctic AcidCationic polymerGene deliveryK-562 cellsLipoic acidMicelleTransfection

Identifiers

PMID33676500
PMCPMC7936509
OpenAlexW3135456539

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.