Development and Application of an Additively Manufactured Calcium Chloride Nebulizer for Alginate 3D-Bioprinting Purposes

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dc.identifier.uri http://dx.doi.org/10.15488/4719
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/4761
dc.contributor.author Raddatz, Lukas ger
dc.contributor.author Lavrentieva, Antonina ger
dc.contributor.author Pepelanova, Iliyana ger
dc.contributor.author Bahnemann, Janina ger
dc.contributor.author Geier, Dominik ger
dc.contributor.author Becker, Thomas ger
dc.contributor.author Scheper, Thomas ger
dc.contributor.author Beutel, Sascha ger
dc.date.accessioned 2019-04-18T06:54:47Z
dc.date.available 2019-04-18T06:54:47Z
dc.date.issued 2018
dc.identifier.citation Raddatz, L. et al.: Development and Application of an Additively Manufactured Calcium Chloride Nebulizer for Alginate 3D-Bioprinting Purposes. In: Journal of Functional Biomaterials 9 (2018), Nr. 4, 63. DOI: https://doi.org/10.3390/jfb9040063 ger
dc.description.abstract Three-dimensional (3D)-bioprinting enables scientists to mimic in vivo micro-environments and to perform in vitro cell experiments under more physiological conditions than is possible with conventional two-dimensional (2D) cell culture. Cell-laden biomaterials (bioinks) are precisely processed to bioengineer tissue three-dimensionally. One primarily used matrix material is sodium alginate. This natural biopolymer provides both fine mechanical properties when gelated and high biocompatibility. Commonly, alginate is 3D bioprinted using extrusion based devices. The gelation reaction is hereby induced by a CaCl2 solution in the building chamber after material extrusion. This established technique has two main disadvantages: (1) CaCl2 can have toxic effects on the cell-laden hydrogels by oxygen diffusion limitation and (2) good printing resolution in the CaCl2 solution is hard to achieve, since the solution needs to be removed afterwards and substituted by cell culture media. Here, we show an innovative approach of alginate bioprinting based on a CaCl2 nebulizer. The device provides CaCl2 mist to the building platform inducing the gelation. The necessary amount of CaCl2 could be decreased as compared to previous gelation strategies and limitation of oxygen transfer during bioprinting can be reduced. The device was manufactured using the MJP-3D printing technique. Subsequently, its digital blueprint (CAD file) can be modified and additive manufactured easily and mounted in various extrusion bioprinters. With our approach, a concept for a more gentle 3D Bioprinting method could be shown. We demonstrated that the concept of an ultrasound-based nebulizer for CaCl2 mist generation can be used for 3D bioprinting and that the mist-induced polymerization of alginate hydrogels of different concentrations is feasible. Furthermore, different cell-laden alginate concentrations could be used: Cell spheroids (mesenchymal stem cells) and single cells (mouse fibroblasts) were successfully 3D printed yielding viable cells and stable hydrogels after 24 h cultivation. We suggest our work to show a different and novel approach on alginate bioprinting, which could be useful in generating cell-laden hydrogel constructs for e.g., drug screening or (soft) tissue engineering applications. ger
dc.language.iso eng ger
dc.publisher Basel : MDPI
dc.relation.ispartofseries Journal of Functional Biomaterials 9 (2018), Nr. 4 ger
dc.rights CC BY 4.0 Unported
dc.rights.uri http://creativecommons.org/licenses/by/4.0/
dc.subject 3D printing eng
dc.subject bioprinting eng
dc.subject alginate eng
dc.subject bioink eng
dc.subject cell culture technology eng
dc.subject rapid tooling eng
dc.subject hydrogels eng
dc.subject customizable labware eng
dc.subject.ddc 540 | Chemie ger
dc.subject.ddc 660 | Technische Chemie ger
dc.subject.ddc 570 | Biowissenschaften, Biologie ger
dc.title Development and Application of an Additively Manufactured Calcium Chloride Nebulizer for Alginate 3D-Bioprinting Purposes eng
dc.type Article ger
dc.type Text ger
dc.relation.issn 2079-4983
dc.relation.doi 10.3390/jfb9040063
dc.bibliographicCitation.firstPage 63
dc.description.version publishedVersion ger
tib.accessRights frei zug�nglich


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