Evidence map›Paper›PMID 26223817›Full record

ArticleJournal of biomedical materials research. Part A2016

Controlled release of an anthrax toxin-neutralizing antibody from hydrolytically degradable polyethylene glycol hydrogels.

Yingkai Liang, Megan V Coffin, Slobodanka D Manceva, Jessica A Chichester, R Mark Jones, Kristi L Kiick

Abstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 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

6 authors.

Yingkai LiangDepartment of Materials Science and Engineering, University of Delaware, Newark, Delaware, 19716.
Megan V CoffinFraunhofer USA, Center for Molecular Biotechnology, 9 Innovation Way, Newark, DE, 19711.
Slobodanka D MancevaFraunhofer USA, Center for Molecular Biotechnology, 9 Innovation Way, Newark, DE, 19711.
Jessica A ChichesterFraunhofer USA, Center for Molecular Biotechnology, 9 Innovation Way, Newark, DE, 19711.
R Mark JonesFraunhofer USA, Center for Molecular Biotechnology, 9 Innovation Way, Newark, DE, 19711.
Kristi L KiickDepartment of Materials Science and Engineering, University of Delaware, Newark, Delaware, 19716.

Funding

Pilot Research Subproject ProgramP30GM110758 · NIGMS · UNIVERSITY OF DELAWARE · PI BEEBE, THOMAS PAUL · 2014 to 2018
$5.8M
NIGMS NIH HHS 1 P30 GM110758-01NIGMS NIH HHS P30 GM110758
6 · The paper itself

Abstract

In this study, hydrophilic and hydrolytically degradable poly (ethylene glycol) (PEG) hydrogels were formed via Michael-type addition and employed for sustained delivery of a monoclonal antibody against the protective antigen of anthrax. Taking advantage of the PEG-induced precipitation of the antibody, burst release from the matrix was avoided. These hydrogels were able to release active antibodies in a controlled manner from 14 days to as long as 56 days in vitro by varying the polymer architectures and molecular weights of the precursors. Analysis of the secondary and tertiary structure and the in vitro activity of the released antibody showed that the encapsulation and release did not affect the protein conformation or functionality. The results suggest the promise for developing PEG-based carriers for sustained release of therapeutic antibodies against toxins in various applications.

Indexed as

Antibodies, NeutralizingAntigens, BacterialBacterial ToxinsChromatography, GelCircular DichroismDelayed-Action PreparationsElectrophoresis, Polyacrylamide GelGlycosylationHydrogelsHydrolysisPolyethylene GlycolsProtein Conformationanthrax toxinAntibodies, NeutralizingAntigens, BacterialBacterial ToxinsDelayed-Action PreparationsHydrogelsPolyethylene Glycolsanthraxcontrolled releasemonoclonal antibodyPEG hydrogelprotective antigen

Identifiers

PMID26223817
PMCPMC4933017

What OpenQuestion holds

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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.