Evidence map›Paper›PMID 42455338›Full record

ArticleMikrochimica acta2026

Aptamer-based colorimetric assay on poly(allylamine)-blended polycaprolactone electrospun nanofibers for CD36 detection.

Zeynep Elcim Koru, Dilek Odaci

Abstract read
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In one paragraph

Article in Mikrochimica acta, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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.

Zeynep Elcim KoruBiochemistry Department Faculty of Science, Ege University, Bornova, Izmir, 35100, Türkiye.
Dilek OdaciBiochemistry Department Faculty of Science, Ege University, Bornova, Izmir, 35100, Türkiye. dilek.odaci.demirkol@ege.edu.tr.

Funding

Ege Üniversitesi 31999Türkiye Bilimsel ve Teknolojik Araştırma Kurumu 2210/C National MSc/MA Scholarship Program
6 · The paper itself

Abstract

A new bioanalytical system was designed to provide colorimetric determination on nanofibers for the determination of CD36, a biomarker of atherosclerosis. First, electrospun nanofibers (ENFs) with a bead-free morphology and hydrophilic surface were produced using electrospinning with polycaprolactone (PCL) and poly(allylamine) hydrochloride (PAH) polymers. Bioconjugates were prepared using CD36-specific aptamers and gold nanoparticles (AuNPs) for the determination of CD36. Aptamer-AuNPs bioconjugates were incubated with various concentrations of CD36. Then, mixtures of CD36 and Aptamer-AuNPs bioconjugates were applied on NaCl-pretreated PCL-PAH ENFs. Visible color changes occurred on the PCL-PAH ENFs in proportion to the increasing CD36 concentrations. Each color intensity was recorded using a smartphone camera. The linear range of the colorimetric bioassay designed on the PCL-PAH ENFs was found to be 25-400 ng•mL

Indexed as

Aptamers, NucleotideBiosensing TechniquesCD36 AntigensColorimetryNanofibersPolyaminesPolyestersGoldHumansLimit of DetectionMetal NanoparticlesAptamers, NucleotideCD36 AntigensGoldpolyallylaminePolyaminespolycaprolactonePolyestersAptamerCD36Colorimetric detectionElectrospun nanofiberGold nanoparticlesSmartphone-assisted color detectionSpot tests

Identifiers

PMID42455338

What Socratic holds

Textmetadata
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Registered trials

None linked

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.