Evidence map›Paper›PMID 33350825›Full record

ArticleBiomacromolecules2021

Comparative Study of the Cellular Uptake and Intracellular Behavior of a Library of Cyclic Peptide-Polymer Nanotubes with Different Self-Assembling Properties.

Sean H Ellacott, Carlos Sanchez-Cano, Edward D H Mansfield, Julia Y Rho, Ji-Inn Song, Raoul Peltier, Sébastien Perrier

Abstract read
In one paragraph

Article in Biomacromolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

7 authors.

Sean H EllacottDepartment of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.
Carlos Sanchez-CanoDepartment of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.ORCID 0000-0002-9522-0019
Edward D H MansfieldDepartment of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.
Julia Y RhoDepartment of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.
Ji-Inn SongDepartment of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.
Raoul PeltierDepartment of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.
Sébastien PerrierDepartment of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, U.K.ORCID 0000-0001-5055-9046

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Particle shape has been described as a key factor in improving cell internalization and biodistribution among the different properties investigated for drug-delivery systems. In particular, tubular structures have been identified as promising candidates for improving drug delivery. Here, we investigate the influence of different design elements of cyclic peptide-polymer nanotubes (CPNTs) on cellular uptake including the nature and length of the polymer and the cyclic peptide building block. By varying the composition of these cyclic peptide-polymer conjugates, a library of CPNTs of lengths varying from a few to over a 150 nm were synthesized and characterized using scattering techniques (small-angle neutron scattering and static light scattering). In vitro studies with fluorescently labeled CPNTs have shown that nanotubes comprised of a single polymer arm with a size between 8 and 16 nm were the most efficiently taken up by three different mammalian cell lines. A mechanistic study on multicellular tumor spheroids has confirmed the ability of these compounds to penetrate to their core. Variations in the proportion of paracellular and transcellular uptake with the self-assembling potential of the CPNT were also observed, giving key insights about the behavior of CPNTs in cellular systems.

Indexed as

NanotubesNanotubes, PeptideAnimalsPeptides, CyclicPolymersTissue DistributionNanotubes, PeptidePeptides, CyclicPolymers

Identifiers

PMID33350825
PMCPMC8243322

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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.