Evidence map›Paper›PMID 41354821›Full record

ArticleJournal of nanobiotechnology2025

Charge-mediated directed assembly of Pt nanoshell on PDA: colorimetric-catalytic co-enhanced lateral flow immunoassay for point-of-care testing.

Xingsheng Yang, Lei Ren, Jing Liang, Jiaojiao Gao, Chongwen Wang, Xiaoxian Liu, Xiaojing Wang, Rui Xiao

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Xingsheng Yang *Anhui Province Key Laboratory of Respiratory Tumor and Infectious Disease, Molecular Diagnosis Center, First Affiliated Hospital of Bengbu Medical University, Bengbu, 233004, China.
Lei Ren *Department of Pharmacy, Air Force Medical Center, Air Force Medical University, Beijing, 100142, China.
Jing Liang *State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, 100071, China.
Jiaojiao GaoAnhui Province Key Laboratory of Respiratory Tumor and Infectious Disease, Molecular Diagnosis Center, First Affiliated Hospital of Bengbu Medical University, Bengbu, 233004, China.
Chongwen WangDepartment of Clinical Laboratory Medicine, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510006, China.
Xiaoxian LiuState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, 100071, China. lxxawesome@126.com.
Xiaojing WangAnhui Province Key Laboratory of Respiratory Tumor and Infectious Disease, Molecular Diagnosis Center, First Affiliated Hospital of Bengbu Medical University, Bengbu, 233004, China. wangxiaojing8888@163.com.
Rui XiaoState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, 100071, China. xiaorui@bmi.ac.cn.

Funding

Anhui Provincial Major Science and Technology Project for Key Laboratory S202305a12020038Longhu Talent Project of Bengbu Medical University LH250104009Research Funds of Joint Research Center for Regional Diseases of Institute of Health and Medicine (IHM), Hefei Comprehensive National Science Center 2023bydjk001Scientific and Technological Research on Major Issues in Aviation Medicine of Air Force Medical University 2022ZZXM030The First Affiliated Hospital of Bengbu Medical University Foundation for Excellent Young Scholars 2025byyfyyq04
6 · The paper itself

Abstract

Effectively enhancing the detection sensitivity of lateral flow immunoassay (LFIA) without dependence on instruments has crucial implications for point-of-care diagnostics. Herein, we introduce a core-shell structured polydopamine (PDA)@platinum (Pt) nanozyme that boosts the colorimetric signal and amplifies the catalytic signal output of LFIA test strips, significantly enhancing the performance of visual detection. The synthesis of PDA@Pt employs a polyethyleneimine-mediated one-step reduction method, which simply controls the growth of Pt particles on the PDA surface, thereby forming a uniform Pt shell layer and providing enhanced chromatic catalytic synergistic effects. The newly developed PDA@Pt nanozyme exhibits dual functionality for visualization and catalytic enhancement, demonstrating favorable stability and reproducibility in complex samples, along with excellent flow characteristics within the LFIA system. Based on these advantages, we further developed a LFIA for detecting the influenza A virus using PDA@Pt nanozyme, achieving direct colorimetric detection within 12 min and enhanced colorimetric results through a 2 min additional catalytic reaction that increased sensitivity by 100-fold. The detection limits of PDA@Pt-LFIA in colorimetric and catalytic modes reached 0.5 and 0.005 ng/mL, which were 2 and 200 times lower than those of traditional AuNP-based LFIA, respectively. Furthermore, during testing with actual clinical samples, this technology exhibited 100% consistency with qPCR results, highlighting its considerable potential for practical pathogen detection.

Indexed as

ColorimetryIndolesNanoshellsPlatinumPoint-of-Care TestingPolymersCatalysisHumansImmunoassayLimit of DetectionReproducibility of ResultsIndolesPlatinumpolydopaminePolymersComposite nanozymesDual-functional nanoparticleIn situ reductionLateral flow immunoassaySignal amplification

Identifiers

PMID41354821
PMCPMC12683860

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.