Evidence map›Paper›PMID 39943569›Full record

ArticleSensors (Basel, Switzerland)2025

An Attomolar-Level Optical Device for Monitoring Receptor-Analyte Interactions Without Functionalization Steps: A Case Study of Cytokine Detection.

Nunzio Cennamo, Francesco Arcadio, Chiara Marzano, Rosalba Pitruzzella, Mimimorena Seggio, Maria Pesavento, Stefano Toldo, Antonio Abbate, Luigi Zeni

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Nunzio CennamoDepartment of Engineering, University of Campania Luigi Vanvitelli, Via Roma 29, 81031 Aversa, Italy.ORCID 0000-0001-7769-0984
Francesco ArcadioDepartment of Engineering, University of Campania Luigi Vanvitelli, Via Roma 29, 81031 Aversa, Italy.ORCID 0000-0001-7863-743X
Chiara MarzanoDepartment of Engineering, University of Campania Luigi Vanvitelli, Via Roma 29, 81031 Aversa, Italy.
Rosalba PitruzzellaDepartment of Engineering, University of Campania Luigi Vanvitelli, Via Roma 29, 81031 Aversa, Italy.ORCID 0009-0003-7257-0694
Mimimorena SeggioDepartment of Engineering, University of Campania Luigi Vanvitelli, Via Roma 29, 81031 Aversa, Italy.ORCID 0000-0002-8193-5873
Maria PesaventoOptosensing Srl, Via Carlo de Marco 69F, 80137 Naples, Italy.ORCID 0000-0002-2927-6065
Stefano ToldoBerne Cardiovascular Research Center and Division of Cardiovascular Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Antonio AbbateBerne Cardiovascular Research Center and Division of Cardiovascular Medicine, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0002-1930-785X
Luigi ZeniDepartment of Engineering, University of Campania Luigi Vanvitelli, Via Roma 29, 81031 Aversa, Italy.ORCID 0000-0001-8356-7480

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A plastic optical fiber (POF)-based device for biosensing strategies has been developed to monitor several protein-protein interactions at ultra-low concentrations without functionalization processes, exploiting plasmonic phenomena. In this work, novel tests were applied to different kinds of analyte-receptor interactions, such as interleukins, where the bioreceptor's (protein antibody) molecular weight is roughly ten times that of the analyte (protein interleukin), while intracellular bioreceptors and small molecules at low molecular weight interactions have already been demonstrated via the same point-of-care test (POCT). The POCT was implemented by a white light source and a spectrometer connected via two POF-based chips connected in series: an innovative microcuvette chip and a D-shaped POF surface plasmon resonance (SPR) probe. In particular, the POF microcuvette chip was achieved by drilling three micro holes in the core of a modified POF. Instead of performing a functionalization step, the micro holes were filled with a specific receptor solution for the analyte (one microliter at the femtomolar level), which selectively captured the target (e.g., cytokine) when the samples were dropped over the filled micro holes (twenty microliters at the attomolar level). Three interleukins, IL-1β, IL-17A, and IL-18, were detected in the attomolar concentrations range by monitoring the resonance wavelength shift over time due to the cytokine/antibody (protein-protein) interaction. The POF-based device was proven to be effective for detecting several interleukins at the attomolar level in a few minutes and without functionalization processes.

Indexed as

Biosensing TechniquesCytokinesOptical DevicesHumansOptical FibersSurface Plasmon ResonanceCytokinesattomolar-level detectioncytokine monitoringoptical biosensorsplasmonic sensorsplastic optical fibers (POFs)receptor–analyte interactionssurface plasmon resonance (SPR)

Identifiers

PMID39943569
PMCPMC11820668

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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.