Evidence map›Paper›PMID 38873552›Full record

ArticleRSC advances2024

A enzyme-free fluorescence quenching sensor for amplified detection of kanamycin in milk based on competitive triggering strategies.

Yangyinchun Bao, Yidan Sang, Xuemei Yan, Mengyang Hu, Na Wang, Yafei Dong, Luhui Wang

Abstract read
In one paragraph

Article in RSC advances, 2024. 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. Review
  2. Article
  3. Chemiluminescence detection of kanamycin by DNA aptamer regulating peroxidase-like activity of CoAnalytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2025
    Article
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

7 authors.

Yangyinchun BaoCollege of Life Science, Shaanxi Normal University Xi'an Shaanxi 710119 PR China dongyf@snnu.edu.cn.ORCID https://orcid.org/0009-0000-6846-845X
Yidan SangCollege of Life Science, Shaanxi Normal University Xi'an Shaanxi 710119 PR China dongyf@snnu.edu.cn.
Xuemei YanCollege of Life Science, Shaanxi Normal University Xi'an Shaanxi 710119 PR China dongyf@snnu.edu.cn.
Mengyang HuCollege of Life Science, Shaanxi Normal University Xi'an Shaanxi 710119 PR China dongyf@snnu.edu.cn.ORCID https://orcid.org/0000-0002-9804-150X
Na WangCollege of Life Science, Shaanxi Normal University Xi'an Shaanxi 710119 PR China dongyf@snnu.edu.cn.ORCID https://orcid.org/0009-0007-4732-1388
Yafei DongCollege of Life Science, Shaanxi Normal University Xi'an Shaanxi 710119 PR China dongyf@snnu.edu.cn.
Luhui WangCollege of Life Science, Shaanxi Normal University Xi'an Shaanxi 710119 PR China dongyf@snnu.edu.cn.ORCID https://orcid.org/0000-0002-3582-7265

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this work, we constructed a FAM fluorescence quenching biosensor based on an aptamer competition recognition and enzyme-free amplification strategy. We design a competing unit consisting of an aptamer chain and a complementary chain, and a catalytic hairpin self-assembly (CHA) unit consisting of two hairpins in which the complementary chain can trigger the catalytic hairpin self-assembly. In the initial state, the aptamer chain is combined with the complementary chain, the catalytic hairpin self-assembly unit is inhibited, the FAM fluorescence group was far away from the BHQ1 quenching group, and the fluorescence is turn-on. In the presence of kanamycin, the aptamer chain recognizes kanamycin and doesn't form double chains, resulting in the free complementary chain triggering hairpin 1 (H1), and then H1 triggering hairpin 2 (H2), FAM fluorophore is close to the BHQ1 quenching group, and the fluorescence is off-on. When H1 and H2 form a cyclic reaction, enzyme-free amplification is achieved and there is significant output of the fluorescence signal. Therefore, the biosensor has good performance in detecting kanamycin, the detection line is 54 nM, the linear range is 54 nM-0.9 μM, and it can achieve highly selective detection of kanamycin. Kanamycin residue may cause serious harm to human health. The high sensitivity detection of kanamycin is urgent, so this project has a great application potential for food detection.

Identifiers

PMID38873552
PMCPMC11172409

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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.