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dc.contributor.authorRimann, Markus-
dc.contributor.authorGraf-Hausner, Ursula-
dc.contributor.authorPatocchi-Tenzer, Isabel-
dc.contributor.authorAngres, Brigitte-
dc.contributor.authorBraum, Susanne-
dc.date.accessioned2017-11-29T10:09:07Z-
dc.date.available2017-11-29T10:09:07Z-
dc.date.issued2014-
dc.identifier.issn2472-6303de_CH
dc.identifier.issn2472-6311de_CH
dc.identifier.urihttps://digitalcollection.zhaw.ch/handle/11475/1608-
dc.description.abstractDrug development relies on high-throughput screening involving cell-based assays. Most of the assays are still based on cells grown in monolayer rather than in three-dimensional (3D) formats, although cells behave more in vivo–like in 3D. To exemplify the adoption of 3D techniques in drug development, this project investigated the automation of a hydrogel-based 3D cell culture system using a liquid-handling robot. The hydrogel technology used offers high flexibility of gel design due to a modular composition of a polymer network and bioactive components. The cell inert degradation of the gel at the end of the culture period guaranteed the harmless isolation of live cells for further downstream processing. Human colon carcinoma cells HCT-116 were encapsulated and grown in these dextran-based hydrogels, thereby forming 3D multicellular spheroids. Viability and DNA content of the cells were shown to be similar in automated and manually produced hydrogels. Furthermore, cell treatment with toxic Taxol concentrations (100 nM) had the same effect on HCT-116 cell viability in manually and automated hydrogel preparations. Finally, a fully automated dose-response curve with the reference compound Taxol showed the potential of this hydrogel-based 3D cell culture system in advanced drug development.de_CH
dc.language.isoende_CH
dc.publisherSagede_CH
dc.relation.ispartofSLAS Technology: Translating Life Sciences Innovationde_CH
dc.rightsLicence according to publishing contractde_CH
dc.subject.ddc660.6: Biotechnologiede_CH
dc.titleAutomation of 3D cell culture using chemically defined hydrogelsde_CH
dc.typeBeitrag in wissenschaftlicher Zeitschriftde_CH
dcterms.typeTextde_CH
zhaw.departementLife Sciences und Facility Managementde_CH
zhaw.organisationalunitInstitut für Chemie und Biotechnologie (ICBT)de_CH
dc.identifier.doi10.1177/2211068213508651de_CH
zhaw.funding.euNode_CH
zhaw.issue2de_CH
zhaw.originated.zhawYesde_CH
zhaw.pages.end197de_CH
zhaw.pages.start191de_CH
zhaw.publication.statuspublishedVersionde_CH
zhaw.volume19de_CH
zhaw.publication.reviewPeer review (Publikation)de_CH
Appears in collections:Publikationen Life Sciences und Facility Management

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Rimann, M., Graf-Hausner, U., Patocchi-Tenzer, I., Angres, B., & Braum, S. (2014). Automation of 3D cell culture using chemically defined hydrogels. SLAS Technology: Translating Life Sciences Innovation, 19(2), 191–197. https://doi.org/10.1177/2211068213508651
Rimann, M. et al. (2014) ‘Automation of 3D cell culture using chemically defined hydrogels’, SLAS Technology: Translating Life Sciences Innovation, 19(2), pp. 191–197. Available at: https://doi.org/10.1177/2211068213508651.
M. Rimann, U. Graf-Hausner, I. Patocchi-Tenzer, B. Angres, and S. Braum, “Automation of 3D cell culture using chemically defined hydrogels,” SLAS Technology: Translating Life Sciences Innovation, vol. 19, no. 2, pp. 191–197, 2014, doi: 10.1177/2211068213508651.
RIMANN, Markus, Ursula GRAF-HAUSNER, Isabel PATOCCHI-TENZER, Brigitte ANGRES und Susanne BRAUM, 2014. Automation of 3D cell culture using chemically defined hydrogels. SLAS Technology: Translating Life Sciences Innovation. 2014. Bd. 19, Nr. 2, S. 191–197. DOI 10.1177/2211068213508651
Rimann, Markus, Ursula Graf-Hausner, Isabel Patocchi-Tenzer, Brigitte Angres, and Susanne Braum. 2014. “Automation of 3D Cell Culture Using Chemically Defined Hydrogels.” SLAS Technology: Translating Life Sciences Innovation 19 (2): 191–97. https://doi.org/10.1177/2211068213508651.
Rimann, Markus, et al. “Automation of 3D Cell Culture Using Chemically Defined Hydrogels.” SLAS Technology: Translating Life Sciences Innovation, vol. 19, no. 2, 2014, pp. 191–97, https://doi.org/10.1177/2211068213508651.


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