Evidence map›Paper›PMID 31731709›Full record

ArticlePolymers2019

High-Throughput Production of Micrometer Sized Double Emulsions and Microgel Capsules in Parallelized 3D Printed Microfluidic Devices.

Alexander Jans, Jonas Lölsberg, Abdolrahman Omidinia-Anarkoli, Robin Viermann, Martin Möller, Laura De Laporte, Matthias Wessling, Alexander J C Kuehne

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
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

8 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Hydrogel Microparticles for Bone Regeneration.Gels (Basel, Switzerland) · 2023
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. 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

8 authors at 2 institutions in 1 country.

Alexander JansDWI-Leibniz Institute for Interactive Materials, Forckenbeckstraße 50, 52076 Aachen, Germany.
Jonas LölsbergDWI-Leibniz Institute for Interactive Materials, Forckenbeckstraße 50, 52076 Aachen, Germany.ORCID 0000-0003-0824-0976
Abdolrahman Omidinia-AnarkoliDWI-Leibniz Institute for Interactive Materials, Forckenbeckstraße 50, 52076 Aachen, Germany.
Robin ViermannDWI-Leibniz Institute for Interactive Materials, Forckenbeckstraße 50, 52076 Aachen, Germany.
Martin MöllerDWI-Leibniz Institute for Interactive Materials, Forckenbeckstraße 50, 52076 Aachen, Germany.
Laura De LaporteDWI-Leibniz Institute for Interactive Materials, Forckenbeckstraße 50, 52076 Aachen, Germany.
Matthias WesslingDWI-Leibniz Institute for Interactive Materials, Forckenbeckstraße 50, 52076 Aachen, Germany.
Alexander J C KuehneDWI-Leibniz Institute for Interactive Materials, Forckenbeckstraße 50, 52076 Aachen, Germany.ORCID 0000-0003-0142-8001
DWI – Leibniz Institute for Interactive Materials · DEUniversität Ulm · DE

Funding

Deutsche Forschungsgemeinschaft SFB 985EFRE 30 00 883 02European Commission EUSMI, 731019
6 · The paper itself

Abstract

Double emulsions are useful geometries as templates for core-shell particles, hollow sphere capsules, and for the production of biomedical delivery vehicles. In microfluidics, two approaches are currently being pursued for the preparation of microfluidic double emulsion devices. The first approach utilizes soft lithography, where many identical double-flow-focusing channel geometries are produced in a hydrophobic silicone matrix. This technique requires selective surface modification of the respective channel sections to facilitate alternating wetting conditions of the channel walls to obtain monodisperse double emulsion droplets. The second technique relies on tapered glass capillaries, which are coaxially aligned, so that double emulsions are produced after flow focusing of two co-flowing streams. This technique does not require surface modification of the capillaries, as only the continuous phase is in contact with the emulsifying orifice; however, these devices cannot be fabricated in a reproducible manner, which results in polydisperse double emulsion droplets, if these capillary devices were to be parallelized. Here, we present 3D printing as a means to generate four identical and parallelized capillary device architectures, which produce monodisperse double emulsions with droplet diameters in the range of 500 µm. We demonstrate high throughput synthesis of W/O/W and O/W/O double emulsions, without the need for time-consuming surface treatment of the 3D printed microfluidic device architecture. Finally, we show that we can apply this device platform to generate hollow sphere microgels.

Indexed as

3D printingcapillaryhollow microgelsmicrofluidicsrapid prototyping

Identifiers

PMID31731709
PMCPMC6918360
OpenAlexW2984044525

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.