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dc.date.accessioned2021-02-06T20:35:36Z
dc.date.available2021-02-06T20:35:36Z
dc.date.created2021-01-22T14:35:41Z
dc.date.issued2021
dc.identifier.citationKohl, Yvonne Biehl, Margit Spring, Sarah Hesler, Michelle Ogourtsov, Vladimir Todorovic, Miomir Owen, Joshua Elje, Elisabeth Kopecka, Kristina Moriones, Oscar Hernando Bastus, Neus G. Simon, Peter Dubaj, Tibor Rundén-Pran, Elise Puntes, Victor William, Nicola von Briesen, Hagen Wagner, Sylvia Kapur, Nikil Mariussen, Espen Nelson, Andrew Gabelova, A Dusinska, Maria Velten, Thomas Knoll, Thorsten . Microfluidic In Vitro Platform for (Nano)Safety and (Nano)Drug Efficiency Screening. Small. 2021
dc.identifier.urihttp://hdl.handle.net/10852/82961
dc.description.abstractMicrofluidic technology is a valuable tool for realizing more in vitro models capturing cellular and organ level responses for rapid and animal‐free risk assessment of new chemicals and drugs. Microfluidic cell‐based devices allow high‐throughput screening and flexible automation while lowering costs and reagent consumption due to their miniaturization. There is a growing need for faster and animal‐free approaches for drug development and safety assessment of chemicals (Registration, Evaluation, Authorisation and Restriction of Chemical Substances, REACH). The work presented describes a microfluidic platform for in vivo‐like in vitro cell cultivation. It is equipped with a wafer‐based silicon chip including integrated electrodes and a microcavity. A proof‐of‐concept using different relevant cell models shows its suitability for label‐free assessment of cytotoxic effects. A miniaturized microscope within each module monitors cell morphology and proliferation. Electrodes integrated in the microfluidic channels allow the noninvasive monitoring of barrier integrity followed by a label‐free assessment of cytotoxic effects. Each microfluidic cell cultivation module can be operated individually or be interconnected in a flexible way. The interconnection of the different modules aims at simulation of the whole‐body exposure and response and can contribute to the replacement of animal testing in risk assessment studies in compliance with the 3Rs to replace, reduce, and refine animal experiments.
dc.languageEN
dc.publisherWiley - VCH Verlag GmbH
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleMicrofluidic In Vitro Platform for (Nano)Safety and (Nano)Drug Efficiency Screening
dc.typeJournal article
dc.creator.authorKohl, Yvonne
dc.creator.authorBiehl, Margit
dc.creator.authorSpring, Sarah
dc.creator.authorHesler, Michelle
dc.creator.authorOgourtsov, Vladimir
dc.creator.authorTodorovic, Miomir
dc.creator.authorOwen, Joshua
dc.creator.authorElje, Elisabeth
dc.creator.authorKopecka, Kristina
dc.creator.authorMoriones, Oscar Hernando
dc.creator.authorBastus, Neus G.
dc.creator.authorSimon, Peter
dc.creator.authorDubaj, Tibor
dc.creator.authorRundén-Pran, Elise
dc.creator.authorPuntes, Victor
dc.creator.authorWilliam, Nicola
dc.creator.authorvon Briesen, Hagen
dc.creator.authorWagner, Sylvia
dc.creator.authorKapur, Nikil
dc.creator.authorMariussen, Espen
dc.creator.authorNelson, Andrew
dc.creator.authorGabelova, A
dc.creator.authorDusinska, Maria
dc.creator.authorVelten, Thomas
dc.creator.authorKnoll, Thorsten
cristin.unitcode185,51,12,0
cristin.unitnameAvdeling for molekylærmedisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1877269
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Small&rft.volume=&rft.spage=&rft.date=2021
dc.identifier.jtitleSmall
dc.identifier.doihttps://doi.org/10.1002/smll.202006012
dc.identifier.urnURN:NBN:no-85754
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1613-6810
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/82961/1/Kohl%2Bet%2Bal_Small_2021.pdf
dc.type.versionPublishedVersion
cristin.articleid2006012
dc.relation.projectEC/H2020/857381
dc.relation.projectEC/H2020/685817
dc.relation.projectNFR/271075
dc.relation.projectNFR/246672
dc.relation.projectNFR/272412
dc.relation.projectNILU/117062
dc.relation.projectNILU/116073
dc.relation.projectNILU/119125
dc.relation.projectNILU/117048


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