Evidence map›Paper›PMID 32528558›Full record

ArticleAnalytical methods : advancing methods and applications2019

Droplet Incubation and Splitting in Open Microfluidic Channels.

Samuel B Berry, Jing J Lee, Jean Berthier, Erwin Berthier, Ashleigh B Theberge

Abstract read
In one paragraph

Article in Analytical methods : advancing methods and applications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Interfacial tension driven open droplet microfluidics.Advanced materials interfaces · 2023
    Article
  8. Article
  9. Cell-Free Production Systems in Droplet Microfluidics.Advances in biochemical engineering/biotechnology · 2023
    Review
  10. Article
  11. Review
  12. Article
  13. Recent progress of microfluidic chips in immunoassay.Frontiers in bioengineering and biotechnology · 2022
    Review
  14. 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

5 authors.

Samuel B BerryDepartment of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195, USA.
Jing J LeeDepartment of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195, USA.
Jean BerthierDepartment of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195, USA.
Erwin BerthierDepartment of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195, USA.
Ashleigh B ThebergeDepartment of Chemistry, University of Washington, Box 351700, Seattle, Washington 98195, USA.

Funding

Theberge Admin Supp Undergraduate Summer Research ExperiencesR35GM128648 · NIGMS · UNIVERSITY OF WASHINGTON · PI Ashleigh Brooks Theberge · 2018 to 2026
$4.7M
NIGMS NIH HHS R35 GM128648
6 · The paper itself

Abstract

Droplet-based microfluidics enables compartmentalization and controlled manipulation of small volumes. Open microfluidics provides increased accessibility, adaptability, and ease of manufacturing compared to closed microfluidic platforms. Here, we begin to build a toolbox for the emerging field of open channel droplet-based microfluidics, combining the ease of use associated with open microfluidic platforms with the benefits of compartmentalization afforded by droplet-based microfluidics. We develop fundamental microfluidic features to control droplets flowing in an immiscible carrier fluid within open microfluidic systems. Our systems use capillary flow to move droplets and carrier fluid through open channels and are easily fabricated through 3D printing, micromilling, or injection molding; further, droplet generation can be accomplished by simply pipetting an aqueous droplet into an empty open channel. We demonstrate on-chip incubation of multiple droplets within an open channel and subsequent transport (using an immiscible carrier phase) for downstream experimentation. We also present a method for tunable droplet splitting in open channels driven by capillary flow. Additional future applications of our toolbox for droplet manipulation in open channels include cell culture and analysis, on-chip microscale reactions, and reagent delivery.

Identifiers

PMID32528558
PMCPMC7289158

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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.