Evidence map›Paper›PMID 35334778›Full record

ArticleMicromachines2022

Characterization of a Centrifugal Microfluidic Orthogonal Flow Platform.

Michael Shane Woolf, Leah M Dignan, Scott M Karas, Hannah M Lewis, Kevyn C Hadley, Aeren Q Nauman, Marcellene A Gates-Hollingsworth, David P AuCoin, Heather R Green, Geoffrey M Geise and 1 more

Open access · goldAbstract read
In one paragraph

Article in Micromachines, 2022. 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
0.2field-weighted citation impact, top 55% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 2 institutions in 1 country.

Michael Shane WoolfDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.ORCID 0000-0001-8722-5410
Leah M DignanDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
Scott M KarasDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.ORCID 0000-0002-3564-7432
Hannah M LewisDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
Kevyn C HadleyDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
Aeren Q NaumanDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
Marcellene A Gates-HollingsworthDepartment of Chemical Engineering, University of Virginia, Charlottesville, VA 22904, USA.
David P AuCoinDepartment of Chemical Engineering, University of Virginia, Charlottesville, VA 22904, USA.
Heather R GreenDepartment of Chemical Engineering, University of Virginia, Charlottesville, VA 22904, USA.
Geoffrey M GeiseDepartment of Chemical Engineering, University of Virginia, Charlottesville, VA 22904, USA.ORCID 0000-0002-5439-272X
James P LandersDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
University of Virginia · USUniversity of Nevada, Reno · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To bring to bear the power of centrifugal microfluidics on vertical flow immunoassays, control of flow orthogonally through nanoporous membranes is essential. The on-disc approach described here leverages the rapid print-cut-laminate (PCL) disc fabrication and prototyping method to create a permanent seal between disc materials and embedded nanoporous membranes. Rotational forces drive fluid flow, replacing capillary action, and complex pneumatic pumping systems. Adjacent microfluidic features form a flow path that directs fluid orthogonally (vertically) through these embedded membranes during assay execution. This method for membrane incorporation circumvents the need for solvents (e.g., acetone) to create the membrane-disc bond and sidesteps issues related to undesirable bypass flow. In other recently published work, we described an orthogonal flow (OF) platform that exploited embedded membranes for automation of enzyme-linked immunosorbent assays (ELISAs). Here, we more fully characterize flow patterns and cellulosic membrane behavior within the centrifugal orthogonal flow (cOF) format. Specifically, high-speed videography studies demonstrate that sample volume, membrane pore size, and ionic composition of the sample matrix significantly impact membrane behavior, and consequently fluid drainage profiles, especially when cellulosic membranes are used. Finally, prototype discs are used to demonstrate proof-of-principle for sandwich-type antigen capture and immunodetection within the cOF system.

Indexed as

centrifugaldecay constantembedded membraneexponential decaymembrane deswellingmicrofluidicorthogonal flow

Identifiers

PMID35334778
PMCPMC8950265
OpenAlexW4221049294

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.