Evidence map›Paper›PMID 35333430›Full record

ArticleAngewandte Chemie (International ed. in English)2022

Under-5-Minute Immunoblot Assays by Vortex Fluidic Device Acceleration.

Emily C Sanders, Sanjana R Sen, Aidan A Gelston, Alicia M Santos, Xuan Luo, Keertna Bhuvan, Derek Y Tang, Colin L Raston, Gregory A Weiss

Open access · hybridAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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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

9 authors at 2 institutions in 2 countries.

Emily C SandersDepartments of Chemistry, Molecular Biology and Biochemistry, and Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697-2025, USA.ORCID 0000-0003-1043-5772
Sanjana R SenDepartments of Chemistry, Molecular Biology and Biochemistry, and Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697-2025, USA.ORCID 0000-0002-1535-814X
Aidan A GelstonDepartments of Chemistry, Molecular Biology and Biochemistry, and Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697-2025, USA.ORCID 0000-0002-7162-289X
Alicia M SantosDepartments of Chemistry, Molecular Biology and Biochemistry, and Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697-2025, USA.ORCID 0000-0002-0887-2140
Xuan LuoFlinders Institute for Nanoscale Sciences and Technology, Flinders University, Adelaide, SA 5042, AU.ORCID 0000-0002-8811-3143
Keertna BhuvanDepartments of Chemistry, Molecular Biology and Biochemistry, and Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697-2025, USA.ORCID 0000-0001-8760-2570
Derek Y TangDepartments of Chemistry, Molecular Biology and Biochemistry, and Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697-2025, USA.ORCID 0000-0003-4424-5125
Colin L RastonFlinders Institute for Nanoscale Sciences and Technology, Flinders University, Adelaide, SA 5042, AU.ORCID 0000-0003-4753-0079
Gregory A WeissDepartments of Chemistry, Molecular Biology and Biochemistry, and Pharmaceutical Sciences, University of California, Irvine, Irvine, CA 92697-2025, USA.ORCID 0000-0003-0296-9846
University of California, Irvine · USFlinders University · AU

Funding

MARC U*STAR at the University of California, IrvineT34GM069337 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI BUCHMEIER, MICHAEL JOSEPH, DE LA CRUZ, MARLENE · 2005 to 2019
$8.2M
Monitoring Recurrent Bladder Cancer with Electro-Phage BiosensorsR33CA206955 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI WEISS, GREGORY A. · 2016 to 2018
$932k
NCI NIH HHS R33 CA206955NIGMS NIH HHS T34 GM069337
6 · The paper itself

Abstract

Unlocking the potential of personalized medicine in point-of-care settings requires a new generation of biomarker and proteomic assays. Ideally, assays could inexpensively perform hundreds of quantitative protein measurements in parallel at the bedsides of patients. This goal greatly exceeds current capabilities. Furthermore, biomarker assays are often challenging to translate from benchtop to clinic due to difficulties achieving and assessing the necessary selectivity, sensitivity, and reproducibility. To address these challenges, we developed an efficient (<5 min), robust (comparatively lower CVs), and inexpensive (decreasing reagent use and cost by >70 %) immunoassay method. Specifically, the immunoblot membrane is dotted with the sample and then developed in a vortex fluidic device (VFD) reactor. All assay steps-blocking, binding, and washing-leverage the unique thin-film microfluidics of the VFD. The approach can accelerate direct, indirect, and sandwich immunoblot assays. The applications demonstrated include assays relevant to both the laboratory and the clinic.

Indexed as

MicrofluidicsProteomicsAccelerationHumansImmunoassayReproducibility of ResultsDiagnosticsImmunoassayVortex Fluidics

Identifiers

PMID35333430
PMCPMC9156566
OpenAlexW4220795211

What OpenQuestion holds

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LicenceTDM
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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.