Evidence map›Paper›PMID 40998404›Full record

ArticleACS sensors2025

Interpretating SPR-Derived Reaction Kinetics via Self-Organizing Maps for Diagnostic Applications.

Jaqueline Volpe, Floriatan S Costa, Beatriz Sachuk, Isabela Camilo, Angélica Faria, Hélida M de Andrade, Saimon M Silva, Dênio Souto

Abstract read
In one paragraph

Article in ACS sensors, 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. Review
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

8 authors.

Jaqueline VolpeLaboratório de Espectrometria, Sensores e Biossensores─Department of Chemistry, Federal University of Paraná (UFPR), Curitiba, Paraná 81530-900, Brazil.
Floriatan S CostaLaboratório de Espectrometria, Sensores e Biossensores─Department of Chemistry, Federal University of Paraná (UFPR), Curitiba, Paraná 81530-900, Brazil.
Beatriz SachukLaboratório de Espectrometria, Sensores e Biossensores─Department of Chemistry, Federal University of Paraná (UFPR), Curitiba, Paraná 81530-900, Brazil.
Isabela CamiloLaboratório de Espectrometria, Sensores e Biossensores─Department of Chemistry, Federal University of Paraná (UFPR), Curitiba, Paraná 81530-900, Brazil.
Angélica FariaDepartamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas (UNIFAL), Alfenas, Minas Gerais 37130-001, Brazil.
Hélida M de AndradeLaboratório de Leishmanioses, Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais 31270-901, Brazil.
Saimon M SilvaBiomedical and Environmental Sensor Technology (BEST) Research Centre, La Trobe Institute for Molecular Science (LIMS), Department of Biochemistry and Chemistry, School of Agriculture, Biomedicine and Environment, La Trobe University, Melbourne, Victoria 3086, Australia.ORCID 0000-0001-6119-4417
Dênio SoutoLaboratório de Espectrometria, Sensores e Biossensores─Department of Chemistry, Federal University of Paraná (UFPR), Curitiba, Paraná 81530-900, Brazil.ORCID 0000-0003-3276-8797

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biosensors emerge as promising, cost-effective infectious disease diagnostics in resource-limited settings, requiring neither laboratory infrastructure nor specialized personnel. Surface plasmon resonance (SPR)-based biosensors remain preeminent for label-free, real-time analysis of biological interactions and kinetic parameter determination. Integrating Artificial Intelligence (AI), particularly self-organizing maps (SOMs), automates infection screening by projecting high-dimensional data onto topology-preserving 2D maps, offering advantages in diagnostic strategies by enabling efficient classification of infected vs healthy patients. This study presents an SPR biosensor with SOM analysis to enhance serodiagnosis of canine visceral leishmaniasis (CVL), a neglected tropical disease, whose delayed and inadequate detection in human and canine populations compromises effective disease control. The reaction kinetics of PQ20, a multiepitope chimeric protein with 20 B- and T-cell epitopes, with anti-PQ20 was evaluated. The proposed mechanism suggests two immunodominant epitopes of PQ20 through its reaction with polyclonal antibodies of

Indexed as

Biosensing TechniquesDog DiseasesLeishmaniasis, VisceralSurface Plasmon ResonanceAnimalsArtificial IntelligenceDogsHumansKineticscanine visceral leishmaniasiskinetic approachmachine learningmultiepitope proteinself-organizing mapsurface plasmon resonance

Identifiers

PMID40998404
PMCPMC12560123

What OpenQuestion holds

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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.