Evidence map›Paper›PMID 38398978›Full record

ArticleMicromachines2024

Flexible Toolbox of High-Precision Microfluidic Modules for Versatile Droplet-Based Applications.

Mario Saupe, Stefan Wiedemeier, Gunter Gastrock, Robert Römer, Karen Lemke

Abstract read
In one paragraph

Article in Micromachines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Mario SaupeInstitute for Bioprocessing and Analytical Measurement Techniques e.V., 37308 Heilbad Heiligenstadt, Germany.
Stefan WiedemeierInstitute for Bioprocessing and Analytical Measurement Techniques e.V., 37308 Heilbad Heiligenstadt, Germany.
Gunter GastrockInstitute for Bioprocessing and Analytical Measurement Techniques e.V., 37308 Heilbad Heiligenstadt, Germany.
Robert RömerInstitute for Bioprocessing and Analytical Measurement Techniques e.V., 37308 Heilbad Heiligenstadt, Germany.
Karen LemkeInstitute for Bioprocessing and Analytical Measurement Techniques e.V., 37308 Heilbad Heiligenstadt, Germany.

Funding

Thüringer Ministerium für Wirtschaft, Wissenschaft und Digitale Gesellschaft 2017 VF 0046Thüringer Ministerium für Wirtschaft, Wissenschaft und Digitale Gesellschaft Basic budget
6 · The paper itself

Abstract

Although the enormous potential of droplet-based microfluidics has been successfully demonstrated in the past two decades for medical, pharmaceutical, and academic applications, its inherent potential has not been fully exploited until now. Nevertheless, the cultivation of biological cells and 3D cell structures like spheroids and organoids, located in serially arranged droplets in micro-channels, has a range of benefits compared to established cultivation techniques based on, e.g., microplates and microchips. To exploit the enormous potential of the droplet-based cell cultivation technique, a number of basic functions have to be fulfilled. In this paper, we describe microfluidic modules to realize the following basic functions with high precision: (i) droplet generation, (ii) mixing of cell suspensions and cell culture media in the droplets, (iii) droplet content detection, and (iv) active fluid injection into serially arranged droplets. The robustness of the functionality of the Two-Fluid Probe is further investigated regarding its droplet generation using different flow rates. Advantages and disadvantages in comparison to chip-based solutions are discussed. New chip-based modules like the gradient, the piezo valve-based conditioning, the analysis, and the microscopy module are characterized in detail and their high-precision functionalities are demonstrated. These microfluidic modules are micro-machined, and as the surfaces of their micro-channels are plasma-treated, we are able to perform cell cultivation experiments using any kind of cell culture media, but without needing to use surfactants. This is even more considerable when droplets are used to investigate cell cultures like stem cells or cancer cells as cell suspensions, as 3D cell structures, or as tissue fragments over days or even weeks for versatile applications.

Indexed as

active fluid injectioncell-based assaydroplet-based microfluidicsdroplet content analysisdroplet generationhigh throughputmergingmixing

Identifiers

PMID38398978
PMCPMC10891953

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.