Evidence map›Paper›PMID 41126667›Full record

ArticleNanomedicine (London, England)2026

Peptide nucleic acid-based biosensor for detection of

Nurullah Çiftçi, Zihni Onur Uygun

Abstract read
In one paragraph

Article in Nanomedicine (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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.

Nurullah ÇiftçiFaculty of Medicine, Department of Medical Microbiology, Kafkas University, Kars, Türkiye.
Zihni Onur UygunFaculty of Medicine, Department of Medical Biochemistry, Kafkas University, Kars, Türkiye.

Funding

Science Academy (TR)
6 · The paper itself

Abstract

aimsThis study aimed to develop a rapid and highly sensitive electrochemical biosensor for the sequence-specific detection of Escherichia coli 16S rRNA using a peptide nucleic acid (PNA) probe immobilized on a graphene - NH/gold-nanoparticle (GNH - AuNP) composite. MATERIALS &

methodsAn SH-terminated PNA probe was covalently attached to a GNH - AuNP nanocomposite layer deposited on gold screen-printed electrodes via 3-mercaptopropionic acid (MPA). The electrode assembly and hybridization processes were characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and X-ray photoelectron spectroscopy (XPS). Quantification was achieved using differential pulse voltammetry (DPV) with hexaammineruthenium(III) (RuHex) as an electrostatic redox indicator.

resultsHybridization of the target 16S rRNA sequence produced a distinct "signal-on" DPV response proportional to target concentration. The biosensor exhibited excellent linearity from 1 to 1000 pM (R

conclusionsThe PNA/GNH - AuNP interface enabled fast, stable, and highly sensitive E. coli detection. Its disposable electrode format and portable electrochemical readout make it suitable for on-site diagnostic and food-safety monitoring applications.

Indexed as

Biosensing TechniquesElectrochemical TechniquesEscherichia coliPeptide Nucleic AcidsElectrodesGoldGraphiteLimit of DetectionMetal NanoparticlesNanocompositesNucleic Acid HybridizationRNA, Ribosomal, 16SGoldGraphitePeptide Nucleic AcidsRNA, Ribosomal, 16SBiosensordifferential pulse voltammetryE. coligraphenepeptide nucleic acid

Identifiers

PMID41126667
PMCPMC12773554

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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.