Evidence map›Paper›PMID 41087332›Full record

ArticleMicrosystems & nanoengineering2025

A fully automated rotary microfluidic platform for high-throughput multiplex detection of respiratory tract pathogens.

Daoguangyao Zhang, Anyi Li, Chuanlong Li, Pei Ren, Liming Zhang, Bin Liu, Shiyong Yu, Xuefei Lv, Wenzhe Si, Yulin Deng

Abstract read
In one paragraph

Article in Microsystems & nanoengineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

10 authors.

Daoguangyao Zhang *Beijing Key Laboratory for Separation and Analysis in Biomedicine and Pharmaceuticals, School of medical Technology, Beijing institute of Technology, Beijing, China.
Anyi Li *Beijing Key Laboratory for Separation and Analysis in Biomedicine and Pharmaceuticals, School of medical Technology, Beijing institute of Technology, Beijing, China.ORCID http://orcid.org/0009-0008-1092-0157
Chuanlong LiBIT&GS Technology Co. Ltd, Beijing, China.
Pei RenBIT&GS Technology Co. Ltd, Beijing, China.
Liming ZhangBIT&GS Technology Co. Ltd, Beijing, China.
Bin LiuBIT&GS Technology Co. Ltd, Beijing, China.
Shiyong YuBIT&GS Technology Co. Ltd, Beijing, China.
Xuefei LvBeijing Key Laboratory for Separation and Analysis in Biomedicine and Pharmaceuticals, School of medical Technology, Beijing institute of Technology, Beijing, China.
Wenzhe SiDepartment of Laboratory Medicine, Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, State Key Laboratory of Vascular Homeostasis and Remodeling, Peking University Third Hospital, Beijing, China. wenzhesi@bjmu.edu.cn.
Yulin DengBeijing Key Laboratory for Separation and Analysis in Biomedicine and Pharmaceuticals, School of medical Technology, Beijing institute of Technology, Beijing, China. deng@bit.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rapid, high-throughput, timely, multiplex diagnosis of respiratory-tract infections still relies on laboratory infrastructure, sequential assays, and trained personnel, thereby delaying targeted therapy and outbreak containment. In this study, a Fully Automated rotary microfluidic platform (FA-RMP) for high-throughput multiplex respiratory tract pathogens detection was presented. FA-RMP enables a true "sample-in, result-out" workflow through the integration of swab lysis, reagent partitioning, lyophilized reverse transcription loop-mediated isothermal amplification (RT-LAMP), and moving-probe fluorescence read-out, all encapsulated with a disposable microfluidic cartridge and paired with a 9 kg, four-channel benchtop reader. The FA-RMP enables parallel processing of 16 independent reactions within 30 min, supporting simultaneous detection of up to 4 distinct clinical samples. Analytical validation using serially diluted Mycoplasma pneumoniae (MP) DNA established a limit of detection (LoD) of 50 copies µL

Identifiers

PMID41087332
PMCPMC12521484

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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.