Surface Morphology Control and Amino Functionalization of Silicon Nanoparticles for Enhanced Antibody Immobilization.

Myat Endra Swe, Yoshinobu Manome, Akinori Ueno, Keisuke Sato

Abstract read

In one paragraph

Article in Materials (Basel, Switzerland), 2026. 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.

Myat Endra SweDepartment of Electrical and Electronic Engineering, Tokyo Denki University, 5 Senju-Asahi-cho, Adachi-ku, Tokyo 120-8551, Japan.ORCID 0009-0004-9997-4493

Yoshinobu ManomeCore Research Facilities, Jikei University School of Medicine, 3-25-8 Nishi-Shinbashi, Minato-ku, Tokyo 105-8461, Japan.ORCID 0000-0002-8755-8976

Akinori UenoDepartment of Electrical and Electronic Engineering, Tokyo Denki University, 5 Senju-Asahi-cho, Adachi-ku, Tokyo 120-8551, Japan.ORCID 0000-0002-5710-1721

Keisuke SatoDepartment of Electrical and Electronic Engineering, Tokyo Denki University, 5 Senju-Asahi-cho, Adachi-ku, Tokyo 120-8551, Japan.

Funding

Tokyo Denki University Q24DS-02

6 · The paper itself

Abstract

The large specific surface area of nanoparticles makes them an attractive platform for antibody immobilization in immunoassays, but the combined effects of their surface structuring and chemical functionalization on properties relevant to antibody immobilization have not yet been clarified. Here, porous and spiky silicon nanoparticles (SiNPs) were fabricated by metal-assisted chemical etching, and the relationships among specific surface area, amino functionalization, and the JT-95-related ELISA signal following BS3-mediated immobilization were investigated. The formation of the porous and spiky surface structures was confirmed by scanning electron microscopy, including quantitative image analysis, and nitrogen adsorption analysis revealed that the specific surface area increased from 62.3 m

Indexed as

amino functionalizationantibody immobilizationimmunoassaymetal-assisted chemical etchingsilicon nanoparticlesspecific surface area

Identifiers

PMID42882570

DOI10.3390/ma19194069

PMCPMC13666502

What OpenQuestion holds

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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.