Evidence map›Paper›PMID 36760606›Full record

ArticlePolymer chemistry2023

How does the polymer architecture and position of cationic charges affect cell viability?

Joana S Correia, Sofía Mirón-Barroso, Charlotte Hutchings, Silvia Ottaviani, Birsen Somuncuoğlu, Leandro Castellano, Alexandra E Porter, Jonathan Krell, Theoni K Georgiou

Abstract read
In one paragraph

Article in Polymer chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Charge-Shifting Copolymers of 2‑(ACS applied polymer materials · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
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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.

Joana S CorreiaDepartment of Materials, Imperial College London London UK t.georgiou@imperial.ac.uk.ORCID https://orcid.org/0000-0003-0092-0328
Sofía Mirón-BarrosoDepartment of Materials, Imperial College London London UK t.georgiou@imperial.ac.uk.
Charlotte HutchingsDepartment of Materials, Imperial College London London UK t.georgiou@imperial.ac.uk.
Silvia OttavianiThe John van Geest Cancer Research Centre, School of Science and Technology, Nottingham Trent University Nottingham NG11 8NS UK.ORCID https://orcid.org/0000-0002-8830-9947
Birsen SomuncuoğluDepartment of Materials, Imperial College London London UK t.georgiou@imperial.ac.uk.ORCID https://orcid.org/0000-0003-4933-5621
Leandro CastellanoDepartment of Surgery and Cancer, Division of Cancer, Imperial College London, Imperial Centre for Translational and Experimental Medicine (ICTEM) London W12 0NN UK.
Alexandra E PorterDepartment of Materials, Imperial College London London UK t.georgiou@imperial.ac.uk.ORCID https://orcid.org/0000-0003-1295-105X
Jonathan KrellDepartment of Surgery & Cancer, Imperial College London UK.ORCID https://orcid.org/0000-0002-9835-9227
Theoni K GeorgiouDepartment of Materials, Imperial College London London UK t.georgiou@imperial.ac.uk.ORCID https://orcid.org/0000-0003-4474-6931

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polymer chemistry, composition and molar mass are factors that are known to affect cytotoxicity, however the influence of polymer architecture has not been investigated systematically. In this study the influence of the position of the cationic charges along the polymer chain on cytotoxicity was investigated while keeping constant the other polymer characteristics. Specifically, copolymers of various architectures, based on a cationic pH responsive monomer, 2-(dimethylamino)ethyl methacrylate (DMAEMA) and a non-ionic hydrophilic monomer, oligo(ethylene glycol)methyl ether methacrylate (OEGMA) were engineered and their toxicity towards a panel of cell lines investigated. Of the seven different polymer architectures examined, the block-like structures were less cytotoxic than statistical or gradient/tapered architectures. These findings will assist in developing future vectors for nucleic acid delivery.

Identifiers

PMID36760606
PMCPMC9846193

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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.