Evidence map›Paper›PMID 36140090›Full record

ArticleBiosensors2022

Hundreds-Dollar-Level Multiplex Integrated RT-qPCR Quantitative System for Field Detection.

Zhihao Lan, Yu Guo, Kangning Wang, Yipeng Zhang, Youyun Chen, Dezhou Zheng, Xiaolong Xu, Wenming Wu

Abstract read
In one paragraph

Article in Biosensors, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
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  4. 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.

Zhihao LanInstitute of Biological and Medical Engineering, Guangdong Academy of Sciences, Guangzhou 510075, China.ORCID 0000-0002-0464-3236
Yu GuoSchool of Mechanical and Electrical Engineering, Guangdong University of Technology, Guangzhou 510006, China.
Kangning WangInstitute of Biological and Medical Engineering, Guangdong Academy of Sciences, Guangzhou 510075, China.
Yipeng ZhangInstitute of Biological and Medical Engineering, Guangdong Academy of Sciences, Guangzhou 510075, China.
Youyun ChenInstitute of Biological and Medical Engineering, Guangdong Academy of Sciences, Guangzhou 510075, China.
Dezhou ZhengCollege of Applied Physics and Materials, Wuyi University, Jiangmen 529000, China.
Xiaolong XuSchool of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529000, China.ORCID 0000-0001-5899-4018
Wenming WuInstitute of Biological and Medical Engineering, Guangdong Academy of Sciences, Guangzhou 510075, China.ORCID 0000-0003-4793-6132

Funding

Guangdong Academy of Sciences (2022GDASZH-2022010110)
6 · The paper itself

Abstract

The COVID-19 pandemic poses a threat to global health. Due to its high sensitivity, specificity, and stability, real-time fluorescence quantitative (real-time PCR) detection has become the most extensively used approach for diagnosing SARS-CoV-2 pneumonia. According to a report from the World Health Organization, emerging and underdeveloped nations lack nucleic acid detection kits and polymerase chain reaction (PCR) instruments for molecular biological detection. In addition, sending samples to a laboratory for testing may result in considerable delays between sampling and diagnosis, which is not favorable to the timely prevention and control of new crown outbreaks. Concurrently, there is an urgent demand for accurate PCR devices that do not require a laboratory setting, are more portable, and are capable of completing testing on-site. Hence, we report on HDLRT-qPCR, a new, low-cost, multiplexed real-time fluorescence detection apparatus that we have developed for on-site testing investigations of diverse diseases in developing nations. This apparatus can complete on-site testing rapidly and sensitively. The entire cost of this instrument does not exceed USD 760. In order to demonstrate the applicability of our PCR instrument, we conducted testing that revealed that we achieved gradient amplification and melting curves comparable to those of commercially available equipment. Good consistency characterized the testing outcomes. The successful detection of target genes demonstrates the reliability of our inexpensive PCR diagnostic technique. With this apparatus, there is no need to transport samples to a central laboratory; instead, we conduct testing at the sampling site. This saves time on transportation, substantially accelerates overall testing speed, and provides results within 40 min.

Indexed as

COVID-19Nucleic AcidsClinical Laboratory TechniquesCOVID-19 TestingHumansPandemicsReal-Time Polymerase Chain ReactionReproducibility of ResultsSARS-CoV-2Sensitivity and SpecificityNucleic AcidsASFCOVID-19fluorescence detectionlow coston-site testingreal-time PCR

Identifiers

PMID36140090
PMCPMC9496240

What OpenQuestion holds

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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.