Evidence map›Paper›PMID 40760206›Full record

ArticleMikrochimica acta2025

Ultra-fast, palm-sized platform for visual point-of-care virus detection using convective PCR with gold nanoparticle probes.

Jingwen Shan, Kerui Shi, Yuanmeng Wang, Tao Zhang, Chen Chen, Likun Zhang, Yanan Chu, Xueping Ma, Xiu Han, Haiping Wu and 1 more

Abstract read
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In one paragraph

Article in Mikrochimica acta, 2025. 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

11 authors.

Jingwen ShanDepartment of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, 210002, Nanjing, China.
Kerui ShiSchool of Pharmaceutical Sciences, Southern Medical University, Guangzhou, 510515, China.
Yuanmeng WangDepartment of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, 210002, Nanjing, China.
Tao ZhangSchool of Pharmaceutical Sciences, Southern Medical University, Guangzhou, 510515, China.
Chen ChenDepartment of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, 210002, Nanjing, China.
Likun ZhangDepartment of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, 210002, Nanjing, China.
Yanan ChuDepartment of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, 210002, Nanjing, China.
Xueping MaDepartment of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, 210002, Nanjing, China.
Xiu HanThe Key Laboratory of the Jiangsu Higher Education Institutions for Nucleic Acid & Cell Fate Regulation, School of Medicine, Yangzhou University, Yangzhou, 225001, China.
Haiping WuDepartment of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, 210002, Nanjing, China. wuhaiping@smu.edu.cn.
Guohua ZhouDepartment of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, 210002, Nanjing, China. ghzhou@nju.edu.cn.

Funding

the Project of Invigorating Health Care through Science, Technology and Education, Jiangsu Provincial Key Medical Discipline Cultivation Unit JSDW202250
6 · The paper itself

Abstract

Convective PCR (cPCR) offers rapid and efficient DNA amplification in as little as 10 min, presenting a promising alternative to traditional PCR. However, current palm-sized cPCR devices fail to achieve one-pot visual detection, limiting their utility for point-of-care testing. Here, we present a visual convective PCR (Vis-cPCR) assay that integrates reverse transcription, ultra-fast cPCR, nested invasive reactions, and gold nanoparticle probes (AuNPs)-based colorimetric detection into a single-tube, one-pot system. This assay eliminates the need for time-consuming nucleic acid extraction and purification by employing a room-temperature chemical lysis step, which rapidly releases viral RNA from pharyngeal swabs in just 2 min and is fully compatible with downstream detection. The palm-sized cPCR device enables the entire process-including reverse transcription, DNA amplification, amplicon identification, and visual signal generation-to be completed in approximately 30 min. The Vis-cPCR assay demonstrates high sensitivity (as low as 10 copies) and specificity for detecting a panel of viruses, including SARS-CoV-2, influenza A/B, western equine encephalitis virus, tick-borne encephalitis virus, chikungunya virus, and Zika virus. Validation using 30 clinical pharyngeal swab samples and 42 artificially prepared arboviral RNA samples showed 100% agreement with RT-qPCR results. By combining rapid sample preparation, ultra-fast amplification, and visual detection, Vis-cPCR represents a significant advancement in point-of-care diagnostics, offering a simple, cost-effective, and highly efficient tool for on-site pathogen screening in resource-limited settings and emergency situations.

Indexed as

GoldMetal NanoparticlesPoint-of-Care SystemsPolymerase Chain ReactionColorimetryCOVID-19HumansLimit of DetectionPoint-of-Care TestingRNA, ViralSARS-CoV-2Zika VirusGoldRNA, ViralConvective PCRGold nanoparticle probesNucleic acid detectionPoint-of-care testing

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Registered trials

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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.