Evidence map›Paper›PMID 35548880›Full record

ArticleLab on a chip2022

Quantitative isothermal amplification on paper membranes using amplification nucleation site analysis.

Benjamin P Sullivan, Yu-Shan Chou, Andrew T Bender, Coleman D Martin, Zoe G Kaputa, Hugh March, Minyung Song, Jonathan D Posner

Open access · greenAbstract read
In one paragraph

Article in Lab on a chip, 2022. 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 27% 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, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Benjamin P SullivanDepartment of Mechanical Engineering, University of Washington, Stevens Way, Box 352600, Seattle, WA 98195, Washington, USA. jposner@uw.edu.ORCID 0000-0002-3520-1684
Yu-Shan ChouDepartment of Chemical Engineering, University of Washington, Seattle, Washington, USA.
Andrew T BenderDepartment of Mechanical Engineering, University of Washington, Stevens Way, Box 352600, Seattle, WA 98195, Washington, USA. jposner@uw.edu.ORCID 0000-0003-4349-4488
Coleman D MartinDepartment of Chemical Engineering, University of Washington, Seattle, Washington, USA.ORCID 0000-0003-4931-7677
Zoe G KaputaPaul G. Allen School of Computer Science & Engineering, University of Washington, Seattle, Washington, USA.
Hugh MarchPaul G. Allen School of Computer Science & Engineering, University of Washington, Seattle, Washington, USA.
Minyung SongDepartment of Mechanical Engineering, University of Washington, Stevens Way, Box 352600, Seattle, WA 98195, Washington, USA. jposner@uw.edu.
Jonathan D PosnerDepartment of Mechanical Engineering, University of Washington, Stevens Way, Box 352600, Seattle, WA 98195, Washington, USA. jposner@uw.edu.ORCID 0000-0001-8860-050X
University of Washington · US

Funding

NRSA Training CoreTL1TR002318 · NCATS · UNIVERSITY OF WASHINGTON · PI Megan Moore · 2017 to 2026
$8.4M
Electrokinetic paper diagnostic platform: 15-minute, quantitative nucleic acidamplification for viral pathogens in whole bloodR01EB022630 · NIBIB · UNIVERSITY OF WASHINGTON · PI POSNER, JONATHAN D · 2017 to 2020
$2.2M
NCATS NIH HHS TL1 TR002318NIBIB NIH HHS R01 EB022630
6 · The paper itself

Abstract

Quantitative nucleic acid amplification tests (qNAATs) are critical in treating infectious diseases, such as in HIV viral load monitoring or SARS-CoV-2 testing, in which viral load indicates viral suppression or infectivity. Quantitative PCR is the gold standard tool for qNAATs; however, there is a need to develop point-of-care (POC) qNAATs to manage infectious diseases in outpatient clinics, low- and middle-income countries, and the home. Isothermal amplification methods are an emerging tool for POC NAATs as an alternative to traditional PCR-based workflows. Previous works have focused on relating isothermal amplification bulk fluorescence signals to input copies of target nucleic acids for sample quantification with limited success. In this work, we show that recombinase polymerase amplification (RPA) reactions on paper membranes exhibit discrete fluorescent amplification nucleation sites. We demonstrate that the number of nucleation sites can be used to quantify HIV-1 DNA and viral RNA in less than 20 minutes. An image-analysis algorithm quantifies nucleation sites and determines the input nucleic acid copies in the range of 67-3000 copies per reaction. We demonstrate a mobile phone-based system for image capture and onboard processing, illustrating that this method may be used at the point-of-care for qNAATs with minimal instrumentation.

Indexed as

COVID-19Nucleic AcidsCOVID-19 TestingHumansNucleic Acid Amplification TechniquesReal-Time Polymerase Chain ReactionRNA, ViralSARS-CoV-2Nucleic AcidsRNA, Viral

Identifiers

PMID35548880
PMCPMC9202034
OpenAlexW4226381515

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.