Evidence map›Paper›PMID 32912236›Full record

ArticleJournal of nanobiotechnology2020

Duplex Shiny app quantification of the sepsis biomarkers C-reactive protein and interleukin-6 in a fast quantum dot labeled lateral flow assay.

Christoph Ruppert, Lars Kaiser, Lisa Johanna Jacob, Stefan Laufer, Matthias Kohl, Hans-Peter Deigner

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Optical Bionanosensors for Sepsis Diagnostics.Small (Weinheim an der Bergstrasse, Germany) · 2025
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Sensitive Colorimetric Detection of Interleukin-6Frontiers in bioengineering and biotechnology · 2021
    Article
  14. Nanotools for Sepsis Diagnosis and Treatment.Advanced healthcare materials · 2021
    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

6 authors.

Christoph RuppertMedical and Life Sciences Faculty, Furtwangen University, Jakob-Kienzle Str. 17, 78054, Villingen-Schwenningen, Germany.
Lars KaiserMedical and Life Sciences Faculty, Furtwangen University, Jakob-Kienzle Str. 17, 78054, Villingen-Schwenningen, Germany.
Lisa Johanna JacobMedical and Life Sciences Faculty, Furtwangen University, Jakob-Kienzle Str. 17, 78054, Villingen-Schwenningen, Germany.
Stefan LauferDepartment of Pharmaceutical Chemistry, Pharmaceutical Institute, University of Tuebingen, Auf der Morgenstelle 8, 72076, Tübingen, Germany.
Matthias KohlMedical and Life Sciences Faculty, Furtwangen University, Jakob-Kienzle Str. 17, 78054, Villingen-Schwenningen, Germany. kohl@hs-furtwangen.de.
Hans-Peter DeignerMedical and Life Sciences Faculty, Furtwangen University, Jakob-Kienzle Str. 17, 78054, Villingen-Schwenningen, Germany. dei@hs-furtwangen.de.ORCID http://orcid.org/0000-0002-7745-0152

Funding

Bundesministerium für Bildung und Forschung 03FH046PX4Bundesministerium für Bildung und Forschung 13FH121PX8
6 · The paper itself

Abstract

Fast point-of-care (POC) diagnostics represent an unmet medical need and include applications such as lateral flow assays (LFAs) for the diagnosis of sepsis and consequences of cytokine storms and for the treatment of COVID-19 and other systemic, inflammatory events not caused by infection. Because of the complex pathophysiology of sepsis, multiple biomarkers must be analyzed to compensate for the low sensitivity and specificity of single biomarker targets. Conventional LFAs, such as gold nanoparticle dyed assays, are limited to approximately five targets-the maximum number of test lines on an assay. To increase the information obtainable from each test line, we combined green and red emitting quantum dots (QDs) as labels for C-reactive protein (CRP) and interleukin-6 (IL-6) antibodies in an optical duplex immunoassay. CdSe-QDs with sharp and tunable emission bands were used to simultaneously quantify CRP and IL-6 in a single test line, by using a single UV-light source and two suitable emission filters for readout through a widely available BioImager device. For image and data processing, a customized software tool, the MultiFlow-Shiny app was used to accelerate and simplify the readout process. The app software provides advanced tools for image processing, including assisted extraction of line intensities, advanced background correction and an easy workflow for creation and handling of experimental data in quantitative LFAs. The results generated with our MultiFlow-Shiny app were superior to those generated with the popular software ImageJ and resulted in lower detection limits. Our assay is applicable for detecting clinically relevant ranges of both target proteins and therefore may serve as a powerful tool for POC diagnosis of inflammation and infectious events.

Indexed as

AntibodiesBetacoronavirusBiomarkersCoronavirus InfectionsCOVID-19C-Reactive ProteinHumansImmunoassayInterleukin-6Limit of DetectionPandemicsPneumonia, ViralPoint-of-Care SystemsQuantum DotsSARS-CoV-2SepsisAntibodiesBiomarkersC-Reactive ProteinInterleukin-6Conjugation chemistryDuplex lateral flow assayImage processingMultiplexingNanoparticlesPoint-of-care diagnosticsQuantum dotsR-packageSandwich immunoassayShiny app

Identifiers

PMID32912236
PMCPMC7481553

What OpenQuestion holds

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LicenceCC BY
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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.