Evidence map›Paper›PMID 37355278›Full record

ArticleThe Journal of molecular diagnostics : JMD2023

A Novel Microfluidic Dielectrophoresis Technology to Enable Rapid Diagnosis of Mycobacteria tuberculosis in Clinical Samples.

Catherine M Moore, Jasvir Dhillon, Rebecca Flynn, Krzysztof Gizynski, Candice Adams, George Morgan, David McGurk, Eduardo Boada, Shireen Shabestary, Jonathan Peat and 4 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in The Journal of molecular diagnostics : JMD, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Future Research Directions on Mycobacterium tuberculosis Proteins.Advances in experimental medicine and biology · 2026
    Review
  4. Review
  5. Article
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Catherine M MooreInstitute for Infection and Immunity, St. George's University of London, London, United Kingdom.
Jasvir DhillonInstitute for Infection and Immunity, St. George's University of London, London, United Kingdom.
Rebecca FlynnInstitute for Infection and Immunity, St. George's University of London, London, United Kingdom.
Krzysztof GizynskiQuantuMDx Group Ltd., Newcastle upon Tyne, United Kingdom.
Candice AdamsQuantuMDx Group Ltd., Newcastle upon Tyne, United Kingdom.
George MorganQuantuMDx Group Ltd., Newcastle upon Tyne, United Kingdom.
David McGurkQuantuMDx Group Ltd., Newcastle upon Tyne, United Kingdom.
Eduardo BoadaQuantuMDx Group Ltd., Newcastle upon Tyne, United Kingdom.
Shireen ShabestaryQuantuMDx Group Ltd., Newcastle upon Tyne, United Kingdom.
Jonathan PeatQuantuMDx Group Ltd., Newcastle upon Tyne, United Kingdom.
Jonathan O'HalloranQuantuMDx Group Ltd., Newcastle upon Tyne, United Kingdom.
Neil G StokerInstitute for Infection and Immunity, St. George's University of London, London, United Kingdom.
Philip D ButcherInstitute for Infection and Immunity, St. George's University of London, London, United Kingdom. Electronic address: butcherp@sgul.ac.uk.
Heather MurtonQuantuMDx Group Ltd., Newcastle upon Tyne, United Kingdom. Electronic address: heather.danks@lexdiagnostics.com.
QuantuMDx (United Kingdom) · GBSt George's, University of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To achieve the global efforts to end tuberculosis, affordable diagnostics suitable for true point-of-care implementation are required to reach the missing millions. In addition, diagnostics with increased sensitivity and expanded drug susceptibility testing are needed to address drug resistance and to diagnose low-bacterial burden cases. The laboratory-on-a-chip technology described herein used dielectrophoresis to selectively isolate Mycobacterium tuberculosis from sputum samples, purifying the bacterial population ahead of molecular confirmation by multiplex real-time quantitative PCR. After optimization using a panel of 50 characterized sputum samples, the performance of the prototype was assessed against the current gold standards, screening 100 blinded sputum samples using characterized and biobanked sputum provided by Foundation for Innovative New Diagnostics. Concordance with culture diagnosis was 100% for smear-negative samples and 87% for smear-positive samples. Of the smear-positive samples, the high burden sample concordance was 100%. Samples were diagnosed on the basis of visual assessment of the dielectrophoresis array and by multiplex real-time quantitative PCR assay. The results described herein demonstrate the potential of the CAPTURE-XT technology to provide a powerful sample preparation tool that could function as a front-end platform for molecular detection. This versatile tool could equally be applied as a visual detection diagnostic, potentially associated with bacterial identification for low-cost screening or coupled with an expanded PCR assay for genotypic drug susceptibility testing.

Indexed as

Mycobacterium tuberculosisTuberculosisHumansMicrobial Sensitivity TestsMicrofluidicsMultiplex Polymerase Chain ReactionSensitivity and Specificity

Identifiers

PMID37355278
PMCPMC12179504
OpenAlexW4381616077

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.