Evidence map›Paper›PMID 34671697›Full record

ArticleArXiv2021

Quantum Optical Immunoassay: Upconversion Nanoparticle-based Neutralizing Assay for COVID-19.

Navid Rajil, Shahriar Esmaeili, Benjamin W Neuman, Reed Nessler, Hung-Jen Wu, Zhenhuan Yi, Robert W Brick, Alexei V Sokolov, Philip R Hemmer, Marlan O Scully

Open access · greenAbstract readPreprint
In one paragraph

Article in ArXiv, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Navid RajilInstitute for Quantum Science and Engineering, Texas A&M university, TX 77843, US.
Shahriar EsmaeiliInstitute for Quantum Science and Engineering, Texas A&M university, TX 77843, US.
Benjamin W NeumanInstitute for Quantum Science and Engineering, Texas A&M university, TX 77843, US.
Reed NesslerInstitute for Quantum Science and Engineering, Texas A&M university, TX 77843, US.
Hung-Jen WuDepartment of Chemical Engineering, Texas A&M University, College Station, TX 77843, US.
Zhenhuan YiInstitute for Quantum Science and Engineering, Texas A&M university, TX 77843, US.
Robert W BrickInstitute for Quantum Science and Engineering, Texas A&M university, TX 77843, US.
Alexei V SokolovInstitute for Quantum Science and Engineering, Texas A&M university, TX 77843, US.
Philip R HemmerInstitute for Quantum Science and Engineering, Texas A&M university, TX 77843, US.
Marlan O ScullyInstitute for Quantum Science and Engineering, Texas A&M university, TX 77843, US.

Funding

Design of hetero-multivalent targeted liposome for combating intracellular Mycobacterium tuberculosisR21AI149383 · NIAID · TEXAS ENGINEERING EXPERIMENT STATION · PI CIRILLO, JEFFREY D., WU, HUNG-JEN · 2020 to 2021
$416k
Study the interaction between Lipopolysaccharide-Binding Protein and Immune Cell MembranesR03AI139650 · NIAID · TEXAS ENGINEERING EXPERIMENT STATION · PI JAYARAMAN, ARUL, WU, HUNG-JEN · 2019 to 2020
$149k
NIAID NIH HHS R03 AI139650NIAID NIH HHS R21 AI149383
6 · The paper itself

Abstract

In a viral pandemic, a few important tests are required for successful containment of the virus and reduction in severity of the infection. Among those tests, a test for the neutralizing ability of an antibody is crucial for assessment of population immunity gained through vaccination, and to test therapeutic value of antibodies made to counter the infections. Here, we report a sensitive technique to detect the relative neutralizing strength of various antibodies against the SARS-CoV-2 virus. We used bright, photostable, background-free, fluorescent upconversion nanoparticles conjugated with SARS-CoV-2 receptor binding domain as a phantom virion. A glass bottom plate coated with angiotensin-converting enzyme 2 (ACE-2) protein imitates the target cells. When no neutralizing IgG antibody was present in the sample, the particles would bind to the ACE-2 with high affinity. In contrast, a neutralizing antibody can prevent particle attachment to the ACE-2-coated substrate. A prototype system consisting of a custom-made confocal microscope was used to quantify particle attachment to the substrate. The sensitivity of this assay can reach 4.0 ng/ml and the dynamic range is from 1.0 ng/ml to 3.2 {\mu}g/ml. This is to be compared to 19 ng/ml sensitivity of commercially available kits.

Identifiers

PMID34671697
PMCPMC8528078
OpenAlexW4213460525

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.