Evidence map›Paper›PMID 34046699›Full record

ArticleAnalytical and bioanalytical chemistry2021

Wicking microfluidic approach to separate blood plasma from whole blood to facilitate downstream assays.

Gayan C Bandara, Linus J Unitan, Matthew H Kremer, Owen T Shellhammer, Shay Bracha, Vincent T Remcho

Abstract read
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In one paragraph

Article in Analytical and bioanalytical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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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

6 authors at 1 institution in 1 country.

Gayan C BandaraDepartment of Chemistry, Oregon State University, 153 Gilbert Hall, Corvallis, OR, 97331, USA.
Linus J UnitanDepartment of Chemistry, Oregon State University, 153 Gilbert Hall, Corvallis, OR, 97331, USA.
Matthew H KremerMaterials Science Program, College of Engineering, Oregon State University, Corvallis, OR, 97331, USA.
Owen T ShellhammerDepartment of Chemistry, Oregon State University, 153 Gilbert Hall, Corvallis, OR, 97331, USA.
Shay BrachaCarlson College of Veterinary Medicine, Oregon State University, Corvallis, OR, 97331, USA.
Vincent T RemchoDepartment of Chemistry, Oregon State University, 153 Gilbert Hall, Corvallis, OR, 97331, USA. vince.remcho@oregonstate.edu.
Oregon State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Separation of blood plasma or serum from blood is essential for accurate analysis. Conventional blood separation requires instrumentation, reagents, and large sample volumes, limiting this process to laboratory environments with trained personnel. Full implementation of effective blood separation and analysis on microliter sample volumes for point of care (POC) diagnostics has proven extremely challenging resulting in a growing market demand, with common challenges such as expensive device fabrication processes or devices being comprised of materials which are not easily disposable. We developed a membrane-based wicking microfluidic device which is made using a simple fabrication process. This device uses a unique 3D flow channel geometry, fabricated in a polycaprolactone-filled glass microfiber membrane, to efficiently separate microliter sample volumes of blood. Colorimetric assay chemistries were integrated to demonstrate utility of these devices in POC diagnostics. The devices are capable of separating both fresh and anticoagulant-treated blood at microscale sample volumes (<15.0 μL). Modifications to the base device are also reported herein which increased sample volume capacity and separation efficiency. Integrated colorimetric assay enabled semi-quantitative detection of conjugated bilirubin in real blood samples (1.0-1.5 mg/dL). These blood separation devices, fabricated on polycaprolactone-filled glass microfiber, enabled effective blood plasma (anticoagulant-treated blood) and serum (fresh blood) separation with microscale sample volumes. Sample volume capacity and separation efficiency are customizable for specific applications and devices can be integrated with downstream assay chemistries to develop complete POC devices that offer blood separation and diagnostics at the same time on a single membrane.

Indexed as

Point-of-Care TestingBilirubinColorimetryEquipment DesignHumansLimit of DetectionMicrofluidic Analytical TechniquesPlasmaPolyestersSerumBilirubinpolycaprolactonePolyestersBlood separationGlass microfiberPlasmaPoint of care diagnosticsPolycaprolactoneSerum

Identifiers

PMID34046699
OpenAlexW3164193787

What OpenQuestion holds

Textmetadata
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.