Evidence map›Paper›PMID 28190039›Full record

ArticleJournal of visualized experiments : JoVE2017

Multi-step Variable Height Photolithography for Valved Multilayer Microfluidic Devices.

Kara Brower, Adam K White, Polly M Fordyce

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

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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

3 authors.

Kara BrowerDepartment of Bioengineering, Stanford University; Microfluidic Foundry, Stanford University; Chem-H Institute, Stanford University.
Adam K WhiteDepartment of Bioengineering, Stanford University; Microfluidic Foundry, Stanford University.
Polly M FordyceDepartment of Bioengineering, Stanford University; Microfluidic Foundry, Stanford University; Department of Genetics, Stanford University; Chem-H Institute, Stanford University; pfordyce@stanford.edu.

Funding

Leveraging spectral encoding for high dimensional biological multiplexingDP2GM123641 · NIGMS · STANFORD UNIVERSITY · PI FORDYCE, POLLY MORRELL · 2016 to 2016
$2.4M
Spectrum Stanford Center for Clinical and Translational Research and EducationTL1TR001084 · NCATS · STANFORD UNIVERSITY · PI CULLEN, MARK RICHARD, GREENBERG, HARRY BERNARD · 2013 to 2017
$1.1M
NCATS NIH HHS TL1 TR001084NIGMS NIH HHS DP2 GM123641
6 · The paper itself

Abstract

Microfluidic systems have enabled powerful new approaches to high-throughput biochemical and biological analysis. However, there remains a barrier to entry for non-specialists who would benefit greatly from the ability to develop their own microfluidic devices to address research questions. Particularly lacking has been the open dissemination of protocols related to photolithography, a key step in the development of a replica mold for the manufacture of polydimethylsiloxane (PDMS) devices. While the fabrication of single height silicon masters has been explored extensively in literature, fabrication steps for more complicated photolithography features necessary for many interesting device functionalities (such as feature rounding to make valve structures, multi-height single-mold patterning, or high aspect ratio definition) are often not explicitly outlined. Here, we provide a complete protocol for making multilayer microfluidic devices with valves and complex multi-height geometries, tunable for any application. These fabrication procedures are presented in the context of a microfluidic hydrogel bead synthesizer and demonstrate the production of droplets containing polyethylene glycol (PEG diacrylate) and a photoinitiator that can be polymerized into solid beads. This protocol and accompanying discussion provide a foundation of design principles and fabrication methods that enables development of a wide variety of microfluidic devices. The details included here should allow non-specialists to design and fabricate novel devices, thereby bringing a host of recently developed technologies to their most exciting applications in biological laboratories.

Indexed as

Lab-On-A-Chip DevicesComputer-Aided DesignDimethylpolysiloxanesHydrogelsMicrofluidicsPolyethylene GlycolsSiliconUltraviolet RaysbaysilonDimethylpolysiloxanesHydrogelsPolyethylene GlycolsSilicon

Identifiers

PMID28190039
PMCPMC5352304

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.