Evidence map›Paper›PMID 31035747›Full record

ArticleAnalytical chemistry2019

PolyJet 3D-Printed Enclosed Microfluidic Channels without Photocurable Supports.

Andre D Castiaux, Cody W Pinger, Elizabeth A Hayter, Marcus E Bunn, R Scott Martin, Dana M Spence

Open access · greenAbstract read
In one paragraph

Article in Analytical chemistry, 2019. 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
4.9field-weighted citation impact, top 4% 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, 97 citations in OpenAlex.

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  11. 3D printed microfluidic devices with electrodes for electrochemical analysis.Analytical methods : advancing methods and applications · 2024
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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 2 institutions in 1 country.

Andre D CastiauxDepartment of Chemistry , Saint Louis University , 3501 Laclede Ave. , St. Louis , Missouri 63103 , United States.
Cody W PingerDepartment of Biomedical Engineering, Institute for Quantitative Health Science & Engineering , Michigan State University , East Lansing , Michigan 48824 , United States.
Elizabeth A HayterDepartment of Chemistry , Saint Louis University , 3501 Laclede Ave. , St. Louis , Missouri 63103 , United States.
Marcus E BunnDepartment of Biomedical Engineering, Institute for Quantitative Health Science & Engineering , Michigan State University , East Lansing , Michigan 48824 , United States.
R Scott MartinDepartment of Chemistry , Saint Louis University , 3501 Laclede Ave. , St. Louis , Missouri 63103 , United States.ORCID 0000-0002-6952-1408
Dana M SpenceDepartment of Biomedical Engineering, Institute for Quantitative Health Science & Engineering , Michigan State University , East Lansing , Michigan 48824 , United States.ORCID 0000-0002-4754-6671
Michigan State University · USSaint Louis University · US

Funding

From single molecule to microfluidic 3D tissue platforms: novel multiscale tools to investigate hyper-stimulated immune cells in the circulationR01NS105888 · NINDS · MICHIGAN STATE UNIVERSITY · PI Lane A. Baker, ROBERT Scott MARTIN · 2018 to 2026
$4.0M
NINDS NIH HHS R01 NS105888
6 · The paper itself

Abstract

Microfluidic devices have historically been prepared using fabrication techniques that often include photolithography and/or etching. Recently, additive manufacturing technologies, commonly known as 3D-printing, have emerged as fabrication tools for microfluidic devices. Unfortunately, PolyJet 3D-printing, which utilizes a photocurable resin that can be accurately printed, requires the use of support material for any designed void space internal to the model. Removing the support material from the printed channels is difficult in small channels with single dimensions of less than ∼200 μm and nearly impossible to remove from designs that contain turns or serpentines. Here, we describe techniques for printing channels ranging in cross sections from 0.6 cm × 1.5 cm to 125 μm × 54 μm utilizing commercially available PolyJet printers that require minimal to no postprocessing to form sealed channels. Specifically, printer software manipulation allows printing of one model with an open channel or void that is sealed with either a viscous liquid or a polycarbonate membrane (no commercially available support material). The printer stage is then adjusted and a second model is printed directly on top of the first model with the selected support system. Both the liquid-fill and the membrane method have enough structural integrity to support the printing resin while it is being cured. Importantly, such complex channel geometries as serpentine and Y-mixers can be designed, printed, and in use in under 2 h. We demonstrate device utility by measuring ATP release from flowing red blood cells using a luciferin/luciferase chemiluminescent assay that involves on-chip mixing and optical detection.

Indexed as

Lab-On-A-Chip DevicesPrinting, Three-Dimensional2-PropanolAdenosine TriphosphateEpoprostenolErythrocytesGlycerolHumansMicrofluidic Analytical TechniquesSoftware2-PropanolAdenosine TriphosphateEpoprostenolGlyceroltreprostinil

Identifiers

PMID31035747
PMCPMC7172018
OpenAlexW2943677326

What OpenQuestion holds

Textmetadata
LicenceTDM
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.