Evidence map›Paper›PMID 40136975›Full record

ArticleBiosensors2025

Evaluation of Preferential Cytokine Adsorption onto Biosensing Surface Modified with Glycopolymer.

Yuhei Terada, Masayuki Futamata, Kaori Tsutsui, Hiroshi Aoki

Abstract read
In one paragraph

Article in Biosensors, 2025. 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

4 authors.

Yuhei TeradaEnvironmental Management Research Institute (EMRI), National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba 305-8569, Japan.ORCID 0000-0001-8554-9964
Masayuki FutamataEnvironmental Management Research Institute (EMRI), National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba 305-8569, Japan.
Kaori TsutsuiEnvironmental Management Research Institute (EMRI), National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba 305-8569, Japan.
Hiroshi AokiEnvironmental Management Research Institute (EMRI), National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba 305-8569, Japan.ORCID 0000-0002-0975-2116

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For the improvement of biosensor performance, the development of a molecular recognition material as well as a sensor platform is necessary. A glycopolymer is a molecular recognition material capable of recognizing specific proteins as natural glycans. However, the target molecules for biosensors using glycopolymers are limited to lectins that are already known for their specific interactions with glycan residues. The aim of this study is to investigate a glycopolymer-modified (GM) surface capable of recognizing non-lectin proteins. As non-lectin proteins, we focused on cytokines, in which the interaction preference to glycopolymers is unknown. The cytokine adsorption onto the GM surfaces was evaluated using a surface plasmon resonance imaging technique as a biosensing tool. Differences in cytokine adsorption onto the different glycan residues were revealed, which will be important for selective cytokine detection. This study indicates the possibility of a biosensing surface modified with glycopolymers for the detection of non-lectin proteins. The results are beneficial for expanding the use of glycopolymers as a molecular recognition material for future applications such as cell analysis and diagnostic devices.

Indexed as

Biosensing TechniquesCytokinesPolysaccharidesAdsorptionPolymersSurface Plasmon ResonanceSurface PropertiesCytokinesPolymersPolysaccharidescytokineglycanglycopolymermolecular recognitionpolymer-modified surfacesurface plasmon resonance imaging

Identifiers

PMID40136975
PMCPMC11940340

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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.