Evidence map›Paper›PMID 41090690›Full record

ArticleACS applied materials & interfaces2025

Polydopamine-Functionalized Magnetoliposomes as Magnetic Probes for Lectin-Glycan Interaction Analysis through Brownian Relaxation.

Adira N Ryofi, Kyohei Okubo, Akito Nunome, Tsung-Che Chang, Katsunori Tanaka, Yoshitaka Kitamoto

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 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

6 authors.

Adira N RyofiDepartment of Materials Science and Engineering, School of Materials and Chemical Technology, Institute of Science Tokyo, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.
Kyohei OkuboDepartment of Materials Science and Engineering, School of Materials and Chemical Technology, Institute of Science Tokyo, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.ORCID 0000-0001-5744-3679
Akito NunomeDepartment of Chemical Science and Engineering, School of Materials and Chemical Technology, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8552, Japan.
Tsung-Che ChangBiofunctional Synthetic Chemistry Laboratory, RIKEN Pioneering Research Institute, 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan.
Katsunori TanakaDepartment of Chemical Science and Engineering, School of Materials and Chemical Technology, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8552, Japan.
Yoshitaka KitamotoDepartment of Materials Science and Engineering, School of Materials and Chemical Technology, Institute of Science Tokyo, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.ORCID 0000-0002-5051-6668

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polydopamine-coated magnetoliposomes (PDA-MLs) are adhesive biocomposite nanomaterials commonly employed in intracellular applications such as controlled drug delivery, theranostics, and biosensing. However, the influence of their adhesive properties on lectin-glycan interactions remains unexplored. In this study, we developed PDA-MLs as magnetic sensing labels for the rapid detection of lectin-glycan binding using alternating current (AC) magnetization measurements in liquid media. The adhesive PDA-ML surface enables facile biomolecule adsorption, facilitating their integration into biosensors. The effects of dopamine-polymerization time on the morphological and functional properties of PDA-MLs were systematically investigated. Extended polymerization resulted in a thicker PDA layer that enhanced lectin immobilization on the ML surface. Multivalent N-glycan-clustered albumin facilitated cross-linking among lectin-immobilized PDA-MLs, leading to remarkable changes in the AC magnetization, compared with interactions with monovalent Gal-N-glycan and Sia-N-glycan. Specific lectin-glycan pairs produced distinct changes in AC magnetization spectra, whereas mismatched combinations showed minimal changes. These findings reveal that structure-property relationships are critical to the design of PDA-ML-based biorecognition systems, highlighting their potential in biosensing and bioanalytical applications.

Indexed as

IndolesLectinsLiposomesPolymersPolysaccharidesBiosensing TechniquesIndolesLectinsLiposomespolydopaminePolymersPolysaccharidesBrownian relaxationlectinliposomesmagnetoliposomesmultivalent glycansuperparamagnetic iron-oxide nanoparticles

Identifiers

PMID41090690
PMCPMC12581113

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.