Evidence map›Paper›PMID 41548134›Full record

ArticleMacromolecular rapid communications2026

Bioinspired, Guanidinium, and Indole Modified Poly(glycidyl ether)s as Highly Efficient Vectors for Polyplex-Mediated Gene Delivery.

Markus Kötzsche, Andreas Dzierza, Lennert Sölter, Jan Egger, Kjell Cornelis, Andreas Stihl, Felix H Schacher, Dagmar Fischer, Kalina Peneva

Abstract read
In one paragraph

Article in Macromolecular rapid communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Markus KötzscheFriedrich Schiller University Jena, Institute of Organic and Macromolecular Chemistry (IOMC), Jena, Germany.
Andreas DzierzaFriedrich-Alexander-Universität Erlangen-Nürnberg, Division of Pharmaceutical Technology and Biopharmacy, Erlangen, Germany.
Lennert SölterFriedrich Schiller University Jena, Institute of Organic and Macromolecular Chemistry (IOMC), Jena, Germany.
Jan EggerFriedrich-Alexander-Universität Erlangen-Nürnberg, Division of Pharmaceutical Technology and Biopharmacy, Erlangen, Germany.ORCID https://orcid.org/0009-0009-7589-6984
Kjell CornelisFriedrich Schiller University Jena, Institute of Organic and Macromolecular Chemistry (IOMC), Jena, Germany.
Andreas StihlFriedrich Schiller University Jena, Institute of Organic and Macromolecular Chemistry (IOMC), Jena, Germany.
Felix H SchacherFriedrich Schiller University Jena, Institute of Organic and Macromolecular Chemistry (IOMC), Jena, Germany.
Dagmar FischerFriedrich-Alexander-Universität Erlangen-Nürnberg, Division of Pharmaceutical Technology and Biopharmacy, Erlangen, Germany.
Kalina PenevaFriedrich Schiller University Jena, Institute of Organic and Macromolecular Chemistry (IOMC), Jena, Germany.ORCID https://orcid.org/0000-0001-5578-3266

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allyl glycidyl ether and 2-methoxyethyl glycidyl ether were copolymerized via anionic ring-opening polymerization and subsequently functionalized with guanidinium and indole groups through a post-polymerization thiol-ene reaction. This modular approach yielded eight polymers with systematically varied hydrophilic-hydrophobic balance, carrying 50-92 mol% guanidinium and 0-22 mol% indole. The polymers featured molar masses between 10.1 and 15.7 kg/mol with a dispersity of around 1.3. Polyplexes were formulated using plasmid DNA and characterized with respect to their physicochemical properties including DNA binding affinity, surface charge, and particle size as well as their transfection efficiencies and polymer in vitro cytotoxicity. All polymers were able to form stable complexes and protected their cargo against enzymatic degradation. An additional hydrophilic monomer did not influence physicochemical characteristics, but increased polymer cytotoxicity. Transfection studies in CHO-K1 cells revealed a strong dependence on polymer hydrophobicity: polymers with medium indole content outperformed both more hydrophilic and more hydrophobic analogues, reaching efficiencies above the gold standard poly(ethylene imine). These results underline the critical role of balancing hydrophilic and hydrophobic groups in side-chain functionalized poly(glycidyl ether)s for safe and effective gene delivery.

Indexed as

Epoxy CompoundsGene Transfer TechniquesGuanidineIndolesPolymersAnimalsCHO CellsCricetulusDNAHydrophobic and Hydrophilic InteractionsParticle SizePlasmidsPolyether CompoundsTransfectionDNAEpoxy CompoundsGuanidineindoleIndolesPolyether CompoundsPolymersgene deliveryguanidiniumhydrophilic‐hydrophobic balanceindolepolyplexes

Identifiers

PMID41548134
PMCPMC13003722

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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.