Evidence map›Paper›PMID 34502513›Full record

ArticleInternational journal of molecular sciences2021

Functional Polyglycidol-Based Block Copolymers for DNA Complexation.

Radostina Kalinova, Miroslava Valchanova, Ivaylo Dimitrov, Sevdalina Turmanova, Iva Ugrinova, Maria Petrova, Zlatina Vlahova, Stanislav Rangelov

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

8 authors at 2 institutions in 1 country.

Radostina KalinovaInstitute of Polymers, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.ORCID 0000-0001-8849-8787
Miroslava ValchanovaDepartment of Material Science and Technology, University "Prof. Assen Zlatarov", 8010 Burgas, Bulgaria.
Ivaylo DimitrovInstitute of Polymers, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Sevdalina TurmanovaDepartment of Material Science and Technology, University "Prof. Assen Zlatarov", 8010 Burgas, Bulgaria.
Iva UgrinovaInstitute of Molecular Biology, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.ORCID 0000-0002-0116-0079
Maria PetrovaInstitute of Molecular Biology, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Zlatina VlahovaInstitute of Molecular Biology, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Stanislav RangelovInstitute of Polymers, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Bulgarian Academy of Sciences · BGProf. Assen Zlatarov University · BG

Funding

Ministry of Education and Science of the Republic of Bulgaria supported by National Program "Innovative Low-Toxic and Biologically Active Means for Precision Medicine" Д01-217/30.11.2018Operational Program ''Science and Education for Smart Growth" 2014-2020, co-financed by European Union through the European Structural and Investment Funds BG05M2OP001-1.002-0012
6 · The paper itself

Abstract

Gene therapy is an attractive therapeutic method for the treatment of genetic disorders for which the efficient delivery of nucleic acids into a target cell is critical. The present study is aimed at evaluating the potential of copolymers based on linear polyglycidol to act as carriers of nucleic acids. Functional copolymers with linear polyglycidol as a non-ionic hydrophilic block and a second block bearing amine hydrochloride pendant groups were prepared using previously synthesized poly(allyl glycidyl ether)-b-polyglycidol block copolymers as precursors. The amine functionalities were introduced via highly efficient radical addition of 2-aminoethanethiol hydrochloride to the alkene side groups. The modified copolymers formed loose aggregates with strongly positive surface charge in aqueous media, stabilized by the presence of dodecyl residues at the end of the copolymer structures and the hydrogen-bonding interactions in polyglycidol segments. The copolymer aggregates were able to condense DNA into stable and compact nanosized polyplex particles through electrostatic interactions. The copolymers and the corresponding polyplexes showed low to moderate cytotoxicity on a panel of human cancer cell lines. The cell internalization evaluation demonstrated the capability of the polyplexes to successfully deliver DNA into the cancer cells.

Indexed as

Cell LineDNADrug Delivery SystemsGenetic TherapyGenetic VectorsGene Transfer TechniquesHumansPolymersPropylene GlycolsTransfectionDNApolyglycidolPolymersPropylene Glycolscationic copolymerscell internalizationcytotoxicityDNA complexationgene deliverynon-viral vectorspolyglycidol copolymerspolyplex formation

Identifiers

PMID34502513
PMCPMC8431755
OpenAlexW3197690679

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.