Evidence map›Paper›PMID 40131300›Full record

ArticleAnalytical chemistry2025

Plasmonic Geometry-Induced Viscoelastic Biocomplex Formation with Optical Concealment, Liquid Slips, and Soundscapes in Bioassays.

Zoe Bradley, Nikhil Bhalla

Abstract read
In one paragraph

Article in Analytical chemistry, 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

2 authors.

Zoe BradleyNanotechnology and Integrated Bioengineering Centre (NIBEC), School of Engineering, Ulster University, 2-24 York Street, Belfast BT15 1AP, United Kingdom.
Nikhil BhallaNanotechnology and Integrated Bioengineering Centre (NIBEC), School of Engineering, Ulster University, 2-24 York Street, Belfast BT15 1AP, United Kingdom.ORCID 0000-0002-4720-3679

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmonic nanoparticles (NPs), typically made up of gold or silver, are widely used in point-of-care bio- and chemical sensing due to their role in enhancing detection sensitivity. Key NP properties influencing sensing performance include the material type, NP size, and geometry. While much research has focused on material and size optimization, less attention has been given to understand NP geometry effects and interactions with biomolecules involved in the bioassay. In this context, we investigate the interfacial properties of the biocomplex formed by spherical-shaped gold nanoparticles (AuNPs) and gold nanostars (AuNSts) during a sandwich assay using localized surface plasmon resonance (LSPR) and quartz crystal microbalance with dissipation (QCM-D). The chosen model to study the biocomplex specifically detects interleukin-6 (IL-6). Our results show that AuNSts, with their anisotropic shape and higher surface area, form antibody-antigen complexes more effectively than AuNPs. AuNSts also create a softer, more hydrated layer due to their complex geometry, which leads to larger liquid slips. Lastly, we showed that AuNSts avoid optical concealment at high IL-6 concentrations, unlike AuNPs, making them more reliable for detecting a wider range of concentrations. These findings highlight the importance of optimizing NP geometry for improved bio/chemical sensor performance.

Indexed as

Biological AssayGoldInterleukin-6Metal NanoparticlesElasticityHumansParticle SizeQuartz Crystal Microbalance TechniquesSurface Plasmon ResonanceViscosityGoldInterleukin-6

Identifiers

PMID40131300
PMCPMC11983360

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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.