Evidence map›Paper›PMID 40454076›Full record

ArticleACS omega2025

Fabrication of MIP-based sensors for femtomolar detection of kynurenic acid for early diagnosis of neurodegenerative diseases.

Kübra Turan, Gözde Aydoğdu TiĞ

Abstract read
In one paragraph

Article in ACS omega, 2025. 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.

Kübra TuranAnkara University, Faculty of Science, Department of Chemistry, Ankara 06100, Türkiye.ORCID https://orcid.org/0000-0001-9661-3394
Gözde Aydoğdu TiĞAnkara University, Faculty of Science, Department of Chemistry, Ankara 06100, Türkiye.ORCID https://orcid.org/0000-0001-6959-4298

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodegenerative diseases (NDDs), among which Alzheimer's disease (AD) is one of the most significant medical and societal challenges of this century due to its increasing prevalence, require early diagnosis through reliable biomarkers to improve disease management. Among several biomarkers, kynurenic acid (KYNA) has emerged as a newly found metabolite, identified as a sensitive and selective blood-based biomarker, with its levels increasing in the early stages of AD. In this study, we aim to develop a low detection limit, stable, low-cost, and reliable molecularly imprinted polymer-based electrochemical biosensor for the rapid, selective, and sensitive detection of KYNA, a promising biomarker for AD. For this purpose, the glassy carbon electrode was first modified with copper-silver bimetallic structures (Cu-Ag BS). Then, a 3,4-ethylene-dioxythiophene (EDOT) monomer was electropolymerized on the Cu-Ag BS/GCE in the presence of the KYNA analyte. The introduced sensor was characterized through field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), differential pulse voltammetry (DPV), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). The effect of electrodeposition parameters was optimized. This is the first time the proposed MIP sensor allowed KYNA detection in a wide linear range of 1.0 fM-500 nM with a limit of detection (LOD) of 0.278 fM. Furthermore, the MIP layer provides highly selective binding by forming KYNA-specific recognition cavities. Notably, the sensor has been successfully validated in complex biological media, including fetal bovine serum and human serum, achieving high recovery values. The proposed sensor could potentially be utilized in the future design of a diagnostic kit for the early diagnosis of neurodegenerative diseases.

Identifiers

PMID40454076
PMCPMC12120629

What Socratic holds

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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 Socratic graph.