Evidence map›Paper›PMID 35748772›Full record

ArticleBiomacromolecules2022

Controlled Bioactive Delivery Using Degradable Electroactive Polymers.

Mark D Ashton, Patricia A Cooper, Sofia Municoy, Martin F Desimone, David Cheneler, Steven D Shnyder, John G Hardy

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Biomacromolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Mark D AshtonDepartment of Chemistry, Faculty of Science and Technology, Lancaster University, Bailrigg, Lancaster LA1 4YB, U.K.ORCID 0000-0003-2199-6057
Patricia A CooperInstitute of Cancer Therapeutics, School of Pharmacy and Medical Sciences, Faculty of Life Sciences, University of Bradford, Bradford BD7 1DP, U.K.
Sofia MunicoyInstituto de Química y Metabolismo del Fármaco (IQUIMEFA), Facultad de Farmacia y Bioquímica, Consejo Nacional de Investigaciones, Científicas y Técnicas (CONICET), Universidad de Buenos Aires, Junín 956, Piso 3° (1113), Buenos Aires 1113, Argentina.
Martin F DesimoneInstituto de Química y Metabolismo del Fármaco (IQUIMEFA), Facultad de Farmacia y Bioquímica, Consejo Nacional de Investigaciones, Científicas y Técnicas (CONICET), Universidad de Buenos Aires, Junín 956, Piso 3° (1113), Buenos Aires 1113, Argentina.
David ChenelerDepartment of Engineering, Faculty of Science and Technology, Lancaster University, Bailrigg, Lancaster LA1 4YW, U.K.ORCID 0000-0003-1353-0329
Steven D ShnyderInstitute of Cancer Therapeutics, School of Pharmacy and Medical Sciences, Faculty of Life Sciences, University of Bradford, Bradford BD7 1DP, U.K.
John G HardyDepartment of Chemistry, Faculty of Science and Technology, Lancaster University, Bailrigg, Lancaster LA1 4YB, U.K.ORCID 0000-0003-0655-2167
Lancaster University · GBConsejo Nacional de Investigaciones Científicas y Técnicas · ARUniversity of Bradford · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L0137971/1
6 · The paper itself

Abstract

Biomaterials capable of precisely controlling the delivery of agrochemicals/biologics/drugs/fragrances have significant markets in the agriscience/healthcare industries. Here, we report the development of degradable electroactive polymers and their application for the controlled delivery of a clinically relevant drug (the anti-inflammatory dexamethasone phosphate, DMP). Electroactive copolymers composed of blocks of polycaprolactone (PCL) and naturally occurring electroactive pyrrole oligomers (e.g., bilirubin, biliverdin, and hemin) were prepared and solution-processed to produce films (optionally doped with DMP). A combination of in silico/in vitro/in vivo studies demonstrated the cytocompatibility of the polymers. The release of DMP in response to the application of an electrical stimulus was observed to be enhanced by ca. 10-30% relative to the passive release from nonstimulated samples in vitro. Such stimuli-responsive biomaterials have the potential for integration devices capable of delivering a variety of molecules for technical/medical applications.

Indexed as

Biocompatible MaterialsPolymersElectricityPyrrolesBiocompatible MaterialsPolymersPyrroles

Identifiers

PMID35748772
PMCPMC9277582
OpenAlexW4283362019

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.