Evidence map›Paper›PMID 39227738›Full record

ArticleCommunications chemistry2024

Controlling enzyme hydrolysis of branched polymers synthesised using transfer-dominated branching radical telomerisation via telogen and taxogen selection.

Samuel Mckeating, Oliver B Penrhyn-Lowe, Sean Flynn, Savannah R Cassin, Sarah Lomas, Christopher Fidge, Paul Price, Stephen Wright, Pierre Chambon, Steve P Rannard

Abstract read
In one paragraph

Article in Communications chemistry, 2024. 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

10 authors.

Samuel MckeatingDepartment of Chemistry & Materials Innovation Factory, University of Liverpool, Crown Street, Liverpool, L69 7ZD, UK.
Oliver B Penrhyn-LoweDepartment of Chemistry & Materials Innovation Factory, University of Liverpool, Crown Street, Liverpool, L69 7ZD, UK.
Sean FlynnDepartment of Chemistry & Materials Innovation Factory, University of Liverpool, Crown Street, Liverpool, L69 7ZD, UK.
Savannah R CassinDepartment of Chemistry & Materials Innovation Factory, University of Liverpool, Crown Street, Liverpool, L69 7ZD, UK.
Sarah LomasDepartment of Chemistry & Materials Innovation Factory, University of Liverpool, Crown Street, Liverpool, L69 7ZD, UK.
Christopher FidgeUnilever R&D, Port Sunlight Laboratory, Quarry Road East, Bebington, Wirral, CH63, 3JW, UK.
Paul PriceUnilever R&D, Port Sunlight Laboratory, Quarry Road East, Bebington, Wirral, CH63, 3JW, UK.
Stephen WrightDepartment of Chemistry & Materials Innovation Factory, University of Liverpool, Crown Street, Liverpool, L69 7ZD, UK.
Pierre ChambonDepartment of Chemistry & Materials Innovation Factory, University of Liverpool, Crown Street, Liverpool, L69 7ZD, UK.
Steve P RannardDepartment of Chemistry & Materials Innovation Factory, University of Liverpool, Crown Street, Liverpool, L69 7ZD, UK. srannard@liverpool.ac.uk.ORCID http://orcid.org/0000-0002-6946-1097

Funding

RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/R010544/1
6 · The paper itself

Abstract

With the ever-growing reliance on polymeric materials for numerous applications, new avenues to induce, design and control degradation are clearly important. Here, we describe a previously unreported approach to controlling enzymatic hydrolysis of high molecular weight branched polymers formed from the new free-radical polymer synthesis strategy transfer-dominated branching radical telomerisation (TBRT). Modifying the chemical nature of TBRT polymers may be accomplished through telogen selection and multi-vinyl taxogen (MVT) design, and we show telogen-driven control of enzyme-catalysed hydrolysis and the impact of careful placement of hydrolytically susceptible groups within readily synthesised MVTs. Our results indicate that utilising conventional free-radical chemistries and unsaturated monomers as feedstocks for highly branched polymer architectures has considerable potential for the design of future materials that degrade into very low molecular weight byproducts at variable and controllable rates.

Identifiers

PMID39227738
PMCPMC11372115

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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.