Evidence map›Paper›PMID 34841143›Full record

ArticleACS omega2021

Quench-Release-Based Fluorescent Immunosensor for the Rapid Detection of Tumor Necrosis Factor α.

Haimei Li, Xinyu Li, Limei Chen, Baowei Li, Hang Dong, Hongying Liu, Xueying Yang, Hiroshi Ueda, Jinhua Dong

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
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

7 citing papers in PubMed, 21 citations in OpenAlex.

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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

9 authors at 3 institutions in 2 countries.

Haimei LiKey Laboratory for Biological Medicine in Shandong Universities, Weifang Key Laboratory for Antibody Medicine, School of Life Science and Technology, Weifang Medical University, Weifang 261053, China.ORCID https://orcid.org/0000-0003-2029-7553
Xinyu LiKey Laboratory for Biological Medicine in Shandong Universities, Weifang Key Laboratory for Antibody Medicine, School of Life Science and Technology, Weifang Medical University, Weifang 261053, China.
Limei ChenKey Laboratory for Biological Medicine in Shandong Universities, Weifang Key Laboratory for Antibody Medicine, School of Life Science and Technology, Weifang Medical University, Weifang 261053, China.
Baowei LiKey Laboratory for Biological Medicine in Shandong Universities, Weifang Key Laboratory for Antibody Medicine, School of Life Science and Technology, Weifang Medical University, Weifang 261053, China.
Hang DongSchool of Basic Medical Sciences, Peking University, Beijing 100191, China.
Hongying LiuKey Laboratory for Biological Medicine in Shandong Universities, Weifang Key Laboratory for Antibody Medicine, School of Life Science and Technology, Weifang Medical University, Weifang 261053, China.
Xueying YangKey Laboratory for Biological Medicine in Shandong Universities, Weifang Key Laboratory for Antibody Medicine, School of Life Science and Technology, Weifang Medical University, Weifang 261053, China.
Hiroshi UedaWorld Research Hub Initiative, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama 226-8503, Japan.ORCID https://orcid.org/0000-0001-8849-4217
Jinhua DongKey Laboratory for Biological Medicine in Shandong Universities, Weifang Key Laboratory for Antibody Medicine, School of Life Science and Technology, Weifang Medical University, Weifang 261053, China.ORCID https://orcid.org/0000-0002-7417-1932
Weifang Medical University · CNTokyo Institute of Technology · JPPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor α (TNF-α) is used as a biomarker for the diagnosis of various inflammatory and autoimmune diseases. In recent years, numerous approaches have been used for the qualitative and quantitative analyses of TNF-α. However, these methods have several drawbacks, such as a tedious and time-consuming process, high pH and temperature sensitivity, and increased chances of denaturation in vitro. Quenchbody (Q-body) is a fluorescence immunoprobe that functions based on the principle of photoinduced electron transfer and has been successful in detecting various substances. In this study, we constructed two Q-bodies based on a therapeutic antibody, adalimumab, to rapidly detect human TNF-α. Both sensors could detect TNF-α within 5 min. The results showed that the limit of detection (LOD) of TNF-α was as low as 0.123 ng/mL with a half-maximal effective concentration (EC

Identifiers

PMID34841143
PMCPMC8613823
OpenAlexW3213522700

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.