Evidence map›Paper›PMID 40146678›Full record

ArticleAnalytical chemistry2025

Metal-Ion Optical Fingerprinting Sensor Selection via an Analyte Classification and Feature Selection Algorithm.

Gabriel Petresky, Michael Faran, Verena Wulf, Gili Bisker

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. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Near-Infrared Fluorescent Single-Walled Carbon Nanotubes for Biosensing.Small (Weinheim an der Bergstrasse, Germany) · 2025
    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

4 authors.

Gabriel PetreskyDepartment of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv 6997801, Israel.ORCID 0009-0006-5493-5567
Michael FaranDepartment of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv 6997801, Israel.ORCID 0009-0001-7545-1477
Verena WulfDepartment of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv 6997801, Israel.ORCID 0000-0003-0155-9829
Gili BiskerDepartment of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv 6997801, Israel.ORCID 0000-0003-2592-7956

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate analyte classification remains a significant challenge in sensor technologies. We present the Analyte Classification and Feature Selection Algorithm (ACFSA), a computational tool designed to identify optimal sensor combinations from unique fingerprint patterns for analyte classification. We applied the ACFSA to a library of peptide-corona-functionalized single-walled carbon nanotubes (SWCNTs), developed as a near-infrared fluorescent, semiselective fingerprinting sensor set for detecting heavy metal ions. Inspired by natural metal-ion complexation sites, each SWCNT sensor in this library features a unique peptide sequence containing various amino acids for metal binding, revealing diverse optical response patterns to the various metal ions tested. The sensor library was further diversified using different SWCNT chiralities and photochemical modifications of the peptide coronae. The ACFSA was applied to the screening data of the fluorescence response of the 30 resulting SWCNT-peptide sensors to five metal-ion analytes. Through iterative dimensionality reduction and rational sensor selection, the algorithm identified the optimal fingerprinting sensors as a minimal two-sensor set with a 0.02% classification error. The final output of the ACFSA is thus an analyte classifier that serves as a unique analyte fingerprint pattern for the selected sensors. The developed peptide-SWCNT system serves as an effective proof-of-concept, illustrating the potential of our platform as a generally applicable tool for fingerprinting analytes and optimal sensor set selection in other sensor-analyte screening experiments.

Identifiers

PMID40146678
PMCPMC12044593

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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.