Evidence map›Paper›PMID 32869628›Full record

ArticleAnalytical chemistry2020

Facile Coupling of Droplet Magnetofluidic-Enabled Automated Sample Preparation for Digital Nucleic Acid Amplification Testing and Analysis.

David E Gaddes, Pei-Wei Lee, Alexander Y Trick, Pornpat Athamanolap, Christine M O'Keefe, Chris Puleo, Kuangwen Hsieh, Tza-Huei Wang

Abstract read
In one paragraph

Article in Analytical chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Advances in methods for rapid detection of Staphylococcus aureus and methicillin-resistant S. aureus.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. 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

8 authors.

David E GaddesDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.ORCID 0000-0001-7196-3750
Pei-Wei LeeDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Alexander Y TrickDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21205, United States.
Pornpat AthamanolapDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21205, United States.
Christine M O'KeefeDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21205, United States.
Chris PuleoElectronics Organization, GE Global Research Center, Niskayuna, New York 12309, United States.
Kuangwen HsiehDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.ORCID 0000-0003-3730-4406
Tza-Huei WangDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.ORCID 0000-0002-3540-9354

Funding

A Droplet-based single cell platform for pathogen identification and ASTR01AI117032 · NIAID · JOHNS HOPKINS UNIVERSITY · PI LIAO, JOSEPH C, WANG, TZA-HUEI JEFF · 2015 to 2019
$5.7M
Technology development for point-of-care detection and antimicrobial susceptibility testing of Neisseria gonorrhoeaeR01AI138978 · NIAID · JOHNS HOPKINS UNIVERSITY · PI WANG, TZA-HUEI JEFF · 2018 to 2021
$5.1M
A "Culture" Shift: Integrated Bacterial Screening and Antibacterial Susceptibility Test on Microfluidic Digital Array for Bloodstream InfectionsR01AI137272 · NIAID · JOHNS HOPKINS UNIVERSITY · PI WANG, TZA-HUEI JEFF, YANG, SAMUEL · 2018 to 2022
$3.6M
Acquisition of GE Typhoon FLA9500 Variable Mode ImagerS10OD021567 · OD · JOHNS HOPKINS UNIVERSITY · PI MCCAFFERY, J. MICHAEL · 2017 to 2017
$147k
NIAID NIH HHS R01 AI117032NIAID NIH HHS R01 AI137272NIAID NIH HHS R01 AI138978
6 · The paper itself

Abstract

Digital nucleic acid amplification testing (dNAAT) and analysis techniques, such as digital polymerase chain reaction (PCR), have become useful clinical diagnostic tools. However, nucleic acid (NA) sample preparation preceding dNAAT is generally laborious and performed manually, thus creating the need for a simple sample preparation technique and a facile coupling strategy for dNAAT. Therefore, we demonstrate a simple workflow which automates magnetic bead-based extraction of NAs with a one-step transfer to dNAAT. Specifically, we leverage droplet magnetofluidics (DM) to automate the movement of magnetic beads between small volumes of reagents commonly employed for NA extraction and purification. Importantly, the buffer typically used to elute the NAs off the magnetic beads is replaced by a carefully selected PCR solution, enabling direct transfer from sample preparation to dNAAT. Moreover, we demonstrate the potential for multiplexing using a digital high-resolution melt (dHRM) after the digital PCR (dPCR). The utility of this workflow is demonstrated with duplexed detection of bacteria in a sample imitating a coinfection. We first purify the bacterial DNA into a PCR solution using our DM-based sample preparation. We then transfer the purified bacterial DNA to our microfluidic nanoarray to amplify 16S rRNA using dPCR and then perform dHRM to identify the two bacterial species.

Indexed as

AutomationNucleic Acid Amplification TechniquesPolymerase Chain ReactionEscherichia coliParticle SizeRNA, Ribosomal, 16SStaphylococcus aureusSurface PropertiesRNA, Ribosomal, 16S

Identifiers

PMID32869628
PMCPMC8549765

What OpenQuestion holds

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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.