Evidence map›Paper›PMID 24099566›Full record

ArticleAnalytical chemistry2013

Membrane-based, sedimentation-assisted plasma separator for point-of-care applications.

Changchun Liu, Michael Mauk, Robert Gross, Frederic D Bushman, Paul H Edelstein, Ronald G Collman, Haim H Bau

Open access · greenAbstract read
In one paragraph

Article in Analytical chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 117 citations in OpenAlex.

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  16. Thermally Responsive Alkane Partitions for Assay Automation.ACS applied materials & interfaces · 2022
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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

7 authors at 1 institution in 1 country.

Changchun LiuDepartment of Mechanical Engineering and Applied Mechanics, ‡Center for Clinical Epidemiology and Biostatistics, §Department of Microbiology, ∇Department of Pathology and Laboratory Medicine, and ⊥Department of Medicine University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
Michael Mauk
Robert Gross
Frederic D Bushman
Paul H Edelstein
Ronald G Collman
Haim H Bau
University of Pennsylvania · US

Funding

Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROBERT GROSS · 1999 to 2026
$78.6M
Fully-Integrated, Non-Instrumented Device for Molecular DiagnosticsK25AI099160 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI LIU, CHANGCHUN · 2012 to 2016
$642k
NIAID NIH HHS AI045008NIAID NIH HHS K25 AI099160NIAID NIH HHS K25AI099160NIAID NIH HHS P30 AI045008
6 · The paper itself

Abstract

Often, high-sensitivity, point-of-care (POC) clinical tests, such as HIV viral load, require large volumes of plasma. Although centrifuges are ubiquitously used in clinical laboratories to separate plasma from whole blood, centrifugation is generally inappropriate for on-site testing. Suitable alternatives are not readily available to separate the relatively large volumes of plasma from milliliters of blood that may be needed to meet stringent limit-of-detection specifications for low-abundance target molecules. We report on a simple-to-use, low-cost, pump-free, membrane-based, sedimentation-assisted plasma separator capable of separating a relatively large volume of plasma from undiluted whole blood within minutes. This plasma separator consists of an asymmetric, porous, polysulfone membrane housed in a disposable chamber. The separation process takes advantage of both gravitational sedimentation of blood cells and size exclusion-based filtration. The plasma separator demonstrated a "blood in-plasma out" capability, consistently extracting 275 ± 33.5 μL of plasma from 1.8 mL of undiluted whole blood within less than 7 min. The device was used to separate plasma laden with HIV viruses from HIV virus-spiked whole blood with recovery efficiencies of 95.5% ± 3.5%, 88.0% ± 9.5%, and 81.5% ± 12.1% for viral loads of 35,000, 3500, and 350 copies/mL, respectively. The separation process is self-terminating to prevent excessive hemolysis. The HIV-laden plasma was then injected into our custom-made microfluidic chip for nucleic acid testing and was successfully subjected to reverse-transcriptase loop-mediated isothermal amplification (RT-LAMP), demonstrating that the plasma is sufficiently pure to support high-efficiency nucleic acid amplification.

Indexed as

Membranes, ArtificialPlasmaPoint-of-Care SystemsHIVHumansMembranes, Artificial

Identifiers

PMID24099566
PMCPMC3897712
OpenAlexW1970275997

What OpenQuestion holds

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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.