Evidence map›Paper›PMID 30960067›Full record

ArticlePolymers2019

Polyelectrolyte Complexation of Oligonucleotides by Charged Hydrophobic-Neutral Hydrophilic Block Copolymers.

Alexander E Marras, Jeffrey R Vieregg, Jeffrey M Ting, Jack D Rubien, Matthew V Tirrell

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2019. 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
2.7field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 56 citations in OpenAlex.

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  10. Recent Advances in DNA Nanomaterials.Nanomaterials (Basel, Switzerland) · 2023
    Review
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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

5 authors at 3 institutions in 1 country.

Alexander E MarrasInstitute for Molecular Engineering, University of Chicago, Chicago, IL 60637, USA. marras@uchicago.edu.ORCID 0000-0001-8972-9532
Jeffrey R ViereggInstitute for Molecular Engineering, University of Chicago, Chicago, IL 60637, USA. jvieregg@uchicago.edu.ORCID 0000-0002-4786-5867
Jeffrey M TingInstitute for Molecular Engineering, University of Chicago, Chicago, IL 60637, USA. jting1@uchicago.edu.ORCID 0000-0001-7816-3326
Jack D RubienDepartments of Biology and Physics, Swarthmore College, Swarthmore, PA 19081, USA. jrubien@uchicago.edu.
Matthew V TirrellInstitute for Molecular Engineering, University of Chicago, Chicago, IL 60637, USA. mtirrell@uchicago.edu.
Argonne National Laboratory · USUniversity of Chicago · USSwarthmore College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyelectrolyte complex micelles (PCMs, core-shell nanoparticles formed by complexation of a polyelectrolyte with a polyelectrolyte-hydrophilic neutral block copolymer) offer a solution to the critical problem of delivering therapeutic nucleic acids, Despite this, few systematic studies have been conducted on how parameters such as polycation charge density, hydrophobicity, and choice of charged group influence PCM properties, despite evidence that these strongly influence the complexation behavior of polyelectrolyte homopolymers. In this article, we report a comparison of oligonucleotide PCMs and polyelectrolyte complexes formed by poly(lysine) and poly((vinylbenzyl) trimethylammonium) (PVBTMA), a styrenic polycation with comparatively higher charge density, increased hydrophobicity, and a permanent positive charge. All of these differences have been individually suggested to provide increased complex stability, but we find that PVBTMA in fact complexes oligonucleotides more weakly than does poly(lysine), as measured by stability versus added salt. Using small angle X-ray scattering and electron microscopy, we find that PCMs formed from both cationic blocks exhibit very similar structure-property relationships, with PCM radius determined by the cationic block size and shape controlled by the hybridization state of the oligonucleotides. These observations narrow the design space for optimizing therapeutic PCMs and provide new insights into the rich polymer physics of polyelectrolyte self-assembly.

Indexed as

complex coacervationnanoparticlesoligonucleotidesphase separationpolyelectrolytes

Identifiers

PMID30960067
PMCPMC6402004
OpenAlexW2906780606

What OpenQuestion holds

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LicenceCC BY
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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.