Evidence map›Paper›PMID 32290165›Full record

ArticleMicromachines2020

Microfluidic Chamber Design for Controlled Droplet Expansion and Coalescence.

Mark Kielpinski, Oliver Walther, Jialan Cao, Thomas Henkel, J Michael Köhler, G Alexander Groß

Abstract read
In one paragraph

Article in Micromachines, 2020. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Microfluidics for Peptidomics, Proteomics, and Cell Analysis.Nanomaterials (Basel, Switzerland) · 2021
    Review
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.

Mark KielpinskiMicrofluidics Group, Institute for Photonic Technologies, IPHT-Jena, Albert-Einstein-Str. 9, Jena 07745, Germany.
Oliver WaltherDepartment of Physical Chemistry and Microreaction Technologies, Institute of Chemistry and Biotechnology, Technische Universität Ilmenau, Prof.-Schmidt-Straße 26, Ilmenau 98693, Germany.
Jialan CaoDepartment of Physical Chemistry and Microreaction Technologies, Institute of Chemistry and Biotechnology, Technische Universität Ilmenau, Prof.-Schmidt-Straße 26, Ilmenau 98693, Germany.
Thomas HenkelMicrofluidics Group, Institute for Photonic Technologies, IPHT-Jena, Albert-Einstein-Str. 9, Jena 07745, Germany.
J Michael KöhlerDepartment of Physical Chemistry and Microreaction Technologies, Institute of Chemistry and Biotechnology, Technische Universität Ilmenau, Prof.-Schmidt-Straße 26, Ilmenau 98693, Germany.
G Alexander GroßDepartment of Physical Chemistry and Microreaction Technologies, Institute of Chemistry and Biotechnology, Technische Universität Ilmenau, Prof.-Schmidt-Straße 26, Ilmenau 98693, Germany.

Funding

Bundesministerium für Bildung und Forschung 031A161A
6 · The paper itself

Abstract

The defined formation and expansion of droplets are essential operations for droplet-based screening assays. The volumetric expansion of droplets causes a dilution of the ingredients. Dilution is required for the generation of concentration graduation which is mandatory for many different assay protocols. Here, we describe the design of a microfluidic operation unit based on a bypassed chamber and its operation modes. The different operation modes enable the defined formation of sub-µL droplets on the one hand and the expansion of low nL to sub-µL droplets by controlled coalescence on the other. In this way the chamber acts as fluidic interface between two fluidic network parts dimensioned for different droplet volumes. Hence, channel confined droplets of about 30-40 nL from the first network part were expanded to cannel confined droplets of about 500 to about 2500 nL in the second network part. Four different operation modes were realized: (a) flow rate independent droplet formation in a self-controlled way caused by the bypassed chamber design, (b) single droplet expansion mode, (c) multiple droplet expansion mode, and (d) multiple droplet coalescence mode. The last mode was used for the automated coalescence of 12 droplets of about 40 nL volume to produce a highly ordered output sequence with individual droplet volumes of about 500 nL volume. The experimental investigation confirmed a high tolerance of the developed chamber against the variation of key parameters of the dispersed-phase like salt content, pH value and fluid viscosity. The presented fluidic chamber provides a solution for the problem of bridging different droplet volumes in a fluidic network.

Indexed as

bypassbypassed chamberchannel confinedcompact disk CD-productiondisposabledropletelectrocoalescencehigh-integratedlabdisclayoutmicrofluidic laboratory discmicrofluidicsnetwork interfacesegmented flowself-controlledvolume bridging

Identifiers

PMID32290165
PMCPMC7231328

What OpenQuestion holds

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LicenceCC BY
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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.