Evidence map›Paper›PMID 19350094›Full record

ArticleLab on a chip2009

Rapid and inexpensive fabrication of polymeric microfluidic devices via toner transfer masking.

Christopher J Easley, Richard K P Benninger, Jesse H Shaver, W Steven Head, David W Piston

Abstract read
In one paragraph

Article in Lab on a chip, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 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

5 authors.

Christopher J EasleyDepartment of Molecular Physiology, Vanderbilt University Medical Center, Vanderbilt University, 747D Light Hall, 21st Avenue South, Nashville, TN 37232-0615, USA.
Richard K P Benninger
Jesse H Shaver
W Steven Head
David W Piston

Funding

DYNAMICS OF PANCREATIC ISLET FUNCTIONR01DK053434 · NIDDK · VANDERBILT UNIVERSITY · PI PISTON, DAVID W · 1998 to 2010
$3.1M
Probes:Quantitative Optical and Electron Microscopy(RMI)P20GM072048 · NIGMS · VANDERBILT UNIVERSITY · PI PISTON, DAVID W. · 2004 to 2007
$2.7M
Inter-islet insulin dynamics measured via controlled microfluidic stimulationF32DK079644 · NIDDK · VANDERBILT UNIVERSITY · PI EASLEY, CHRISTOPHER J · 2007 to 2008
$53k
NIDDK NIH HHS F32DK07964NIDDK NIH HHS F32 DK079644NIDDK NIH HHS R01 DK053434NIDDK NIH HHS R01DK053434NIGMS NIH HHS P20 GM072048NIGMS NIH HHS P20GM072048
6 · The paper itself

Abstract

An alternative fabrication method is presented for production of masters for single- or multi-layer polymeric microfluidic devices in a standard laboratory environment, precluding the need for a cleanroom. This toner transfer masking (TTM) method utilizes an office laser printer to generate a toner pattern which is thermally transferred to a metal master to serve as a mask for etching. With master fabrication times as little as one hour (depending on channel depth) using commercially-available equipment and supplies, this approach should make microfluidic technology more widely accessible to the non-expert-even the non-scientist. The cost of fabrication consumables was estimated to be < $1 per master, over an order of magnitude decrease in consumable costs compared to standard photolithography. In addition, the use of chemical etching allows accurate control over the height of raised features (i.e., channel depths), allowing the flexibility to fabricate multiple depths on a single master with little added time. Resultant devices are shown capable of pneumatic valving, three-dimensional channel formation (using layer-connecting vias), droplet fluidics, and cell imaging and staining. The multiple-depth capabilities of the method are proven useful for cellular analysis by fabrication of handheld, disposable devices used for trapping and imaging of live murine pancreatic islets. The precise fluidic control provided by the microfluidic platform allows subsequent fixing and staining of these cells without significant movement, thus spatial correlation of imaging and staining is attainable-even with rare alpha cells that constitute only approximately 10% of the islet cells.

Indexed as

AnimalsCell Culture TechniquesCells, CulturedCost-Benefit AnalysisDimethylpolysiloxanesEquipment DesignIslets of LangerhansMiceMicrofluidic Analytical TechniquesPrintingTime FactorsbaysilonDimethylpolysiloxanes

Identifiers

PMID19350094
PMCPMC2752280

What OpenQuestion holds

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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.