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Licensed Unlicensed Requires Authentication Published by De Gruyter May 19, 2016

Guidelines for standardization of bioprinting: a systematic study of process parameters and their effect on bioprinted structures

  • Matti Kesti , Philipp Fisch , Marco Pensalfini , Edoardo Mazza and Marcy Zenobi-Wong EMAIL logo
From the journal BioNanoMaterials

Abstract

Biofabrication techniques including three-dimensional bioprinting could be used one day to fabricate living, patient-specific tissues and organs for use in regenerative medicine. Compared to traditional casting and molding methods, bioprinted structures can be much more complex, containing for example multiple materials and cell types in controlled spatial arrangement, engineered porosity, reinforcement structures and gradients in mechanical properties. With this complexity and increased function, however, comes the necessity to develop guidelines to standardize the bioprinting process, so printed grafts can safely enter the clinics. The bioink material must firstly fulfil requirements for biocompatibility and flow. Secondly, it is important to understand how process parameters affect the final mechanical properties of the printed graft. Using a gellan-alginate physically crosslinked bioink as an example, we show shear thinning and shear recovery properties which allow good printing resolution. Printed tensile specimens were used to systematically assess effect of line spacing, printing direction and crosslinking conditions. This standardized testing allowed direct comparison between this bioink and three commercially-available products. Bioprinting is a promising, yet complex fabrication method whose outcome is sensitive to a range of process parameters. This study provides the foundation for highly needed best practice guidelines for reproducible and safe bioprinted grafts.

Acknowledgments:

The work was funded by the Swiss National Science Foundation (grant number CR32I3_146338/1) and FIFA/F-MARC. Authors would like to thank Prof. André Studart, Complex Materials, ETH Zurich for use of equipment.

  1. Author’s statement

  2. Conflict of interest: Authors state no conflict of interest.

  3. Materials and methods

  4. Informed consent: Informed consent has been obtained from all individuals included in this study.

  5. Ethical approval: The research related to human use has been complied with all the relevant national regulations, institutional policies and in accordance the tenets of the Helsinki Declaration, and has been approved by the authors’ institutional review board or equivalent committee.

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Supplemental Material:

The online version of this article (DOI: 10.1515/bnm-2016-0004) offers supplementary material, available to authorized users.


Received: 2016-3-4
Accepted: 2016-4-25
Published Online: 2016-5-19
Published in Print: 2016-9-1

©2016 Walter de Gruyter GmbH, Berlin/Boston

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