Evidence map›Paper›PMID 26835721›Full record

ArticleAnalytical chemistry2016

Investigation of Reagent Delivery Formats in a Multivalent Malaria Sandwich Immunoassay and Implications for Assay Performance.

Tinny Liang, Robert Robinson, Jared Houghtaling, Gina Fridley, Stephen A Ramsey, Elain Fu

Abstract read
In one paragraph

Article in Analytical chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Inkjet-printed point-of-care immunoassay on a nanoscale polymer brush enables subpicomolar detection of analytes in blood.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  11. 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.

Tinny LiangDepartment of Bioengineering, University of Washington , N107 Foege Building, Seattle, Washington 98195, United States.
Robert RobinsonSchool of Chemical, Biological, and Environmental Engineering, Oregon State University , 102 Gleeson Hall, Corvallis, Oregon 97331, United States.
Jared HoughtalingDepartment of Bioengineering, University of Washington , N107 Foege Building, Seattle, Washington 98195, United States.
Gina FridleyDepartment of Bioengineering, University of Washington , N107 Foege Building, Seattle, Washington 98195, United States.
Stephen A RamseyDepartment of Biomedical Sciences, Oregon State University , 106 Dryden Hall, Corvallis, Oregon 97331, United States.
Elain FuDepartment of Bioengineering, University of Washington , N107 Foege Building, Seattle, Washington 98195, United States.

Funding

A high-sensitivity low-cost multiplexed immunoassay platform based on 2-dimensionR01AI096184 · NIAID · UNIVERSITY OF WASHINGTON · PI YAGER, PAUL · 2011 to 2015
$5.2M
NIAID NIH HHS R01 AI096184NIAID NIH HHS R01AI096184
6 · The paper itself

Abstract

Conventional lateral flow tests (LFTs), the current standard bioassay format used in low-resource point-of-care (POC) settings, have limitations that have held back their application in the testing of low concentration analytes requiring high sensitivity and low limits of detection. LFTs use a premix format for a rapid one-step delivery of premixed sample and labeled antibody to the detection region. We have compared the signal characteristics of two types of reagent delivery formats in a model system of a sandwich immunoassay for malarial protein detection. The premix format produced a uniform binding profile within the detection region. In contrast, decoupling the delivery of sample and labeled antibody to the detection region in a sequential format produced a nonuniform binding profile in which the majority of the signal was localized to the upstream edge of the detection region. The assay response was characterized in both the sequential and premix formats. The sequential format had a 4- to 10-fold lower limit of detection than the premix format, depending on assay conjugate concentration. A mathematical model of the assay quantitatively reproduced the experimental binding profiles for a set of rate constants that were consistent with surface plasmon resonance measurements and absorbance measurements of the experimental multivalent malaria system.

Indexed as

AntibodiesAntigen-Antibody ReactionsAntigensImmunoassayIndicators and ReagentsMalariaProtozoan ProteinsAntibodiesAntigensIndicators and ReagentsProtozoan Proteins

Identifiers

PMID26835721
PMCPMC6387624

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.