Programme

Unfurtunately the monastery Irsee has been closed by the Bavarian government due to the corona virus.

Therefore we have decided to offer the conference as a web conference only.

In those unpredictable times, protecting our participants’ health has the highest priority for us!

The scientific exchange must not come to a complete standstill and we believe that with this web solution we have found a way to keep the scientific community going.

In order to participate in the livestream of the conference as easy as possible and to give your presentation, we recommend the use of the web browsers Google Chrome or Microsoft Edge.

Here you can find detailed instructions for using the livestream.

As a participant of the Bioinspired 2020 you have received an e-mail containing the login data for the web conference.

The login data for the sessions are provided daily.

In order to allow all conference participants access to the posters, we ask you to upload your poster by login on the conference homepage and clicking on the button "My Submission" in the upper right corner of the conference homepage. Then select the submission to which you want to upload the poster and upload the poster at the bottom of the page.

Furthermore we would like to ask all poster authors to prepare 4 PowerPoint slides to present your poster to the audience.
Please also include your contact details on the digital poster to allow participants to reach you with questions.

Please note that your poster will be pictured publically.

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Click on "My Submissions" in the upper right corner at the homepage.

Poster documents can be found by opening the respective abstract in the online programme.
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Back to overview

Special Poster Session Biofabrication

Cell-loaded Microgels as mechanical Protection and controlled Microenvironment for Cells in Bioinks

Tuesday (17.03.2020)
17:43 - 17:46

Bioprinting of larger tissues and eventually organs presents a tremendous opportunity to challenge the status quo for medical treatments of all kinds of illnesses. Necessary for the successful implementation of bioprinting is improving the cell survival during the printing process, where cells are subjected to significant shear forces. A possible way to improve cell viability and to expand the bioprinting window is the encapsulation of cells in hydrogels, which can be done using microfluidics[1].

Poly(2-oxazolines) possess unique properties making them an ideal synthetic polymer for the stable encapsulation of cells. They are biocompatible[2], while providing excellent opportunities for a functionalization at the side chain and both termini of the polymer. Several different modifications, for example free thiol groups at the side chain, are available which allow covalent crosslinking via thiol-ene reaction[3] or Michael addition[4]. To obtain POx-based hydrogel precursors 2-ethyl-2-oxazoline was randomly copolymerized with 2-(3-butenyl)-2-oxazoline, which were then functionalized with free thiol groups for hydrogel formation via thiol-ene reaction. Combining these two polymers with double three-dimensional flow focusing microfluidic chips allows the production of droplets of varying sizes with high uniformity. The first 3D channel intersection can be used for flow focusing and/or mixing of A/B components, while the second 3D intersection is used for stable droplet production. A 3D contoured narrowing allows for precise control of achieved droplet sizes. After production, the droplets can be crosslinked on demand either using UV irradiation or visible light, depending on the chosen radical initiator. This allows to tailor the system towards specific needs of cells as well as further production parameters. The final droplets can then be used either as bioink alone or as additive in conventional bioinks to ensure cellular protection.

 

[1] E. Tumarkin, E. Kumacheva, Chem. Soc. Rev. 2009, 38, 2161.

[2] B. Verbraeken, B. D. Monnery, K. Lava, R. Hoogenboom, Eur. Polym. J. 2017, 88, 451.

[3] J. Blöhbaum, I. Paulus, A. Pöppler, J. Tessmar, J. Groll, J. Mater. Chem. B. 2019, 7, 178.

[4] D. P. Nair, M. Podgórski, S. Chatani, T. Gong, W. Xi, C. R. Fenoli, C. N. Bowman, Chem. Mater. 2014, 26, 724.

 

This research has received funding by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) – project number 326998133 – TRR 225 (subproject A06).

Speaker:
Ilona Paulus
University Hospital Würzburg
Additional Authors:
  • Benjamin Reineke
    Forschungszentrum Jülich GmbH
  • Dr. Stephan Hauschild
    Forschungszentrum Jülich GmbH
  • Prof. Dr. Stephan Förster
    Forschungszentrum Jülich GmbH
  • Prof. Dr. Jürgen Groll
    University of Würzburg