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dc.contributor.authorGranfeldt, Daniel
dc.contributor.authorJohansson, Marie-Louise
dc.contributor.authorSinclair, Jon
dc.contributor.authorPihl, Johan
dc.contributor.authorKarlsson, Mattias
dc.date.accessioned2015-10-07T07:44:34Z
dc.date.available2015-10-07T07:44:34Z
dc.date.issued2006
dc.identifier.issn1730-2366
dc.identifier.urihttp://hdl.handle.net/11089/12207
dc.description.abstractIon channels are transm embrane proteins, found in virtually all cell types throughout the human body. Ion channels underlie neural communication, memory, behavior, every movement and heartbeat, and are as such prone to cause disease if malfunctioning. Therefore ion channels are very important targets in drug discovery. The gold standard technique for obtaining information on ion channel function with high information content and temporal resolution is patch-clamp. The technique measures the minute currents originating from the movement of ions across the cellular membrane, and enables determination of the potency and efficacy of a drug. However, patch-clamp suffers from serious throughput restrictions due to its laborious nature. To address the throughput problems we have developed a microfluidic chip containing 48 microchannels for an extremely rapid, sequential delivery of a large number of completely controlled solution environments to a lifted, patch-clamped cell. In this way, throughput is increased drastically compared to classical patch-clamp perfusion set-ups, with uncompromised data quality. The 48-microchannel chip has been used for the characterization of drugs affecting ligand-gated ion channels including agonists, antagonists and positive modulators with positive effects on both throughput and data quality.pl_PL
dc.description.sponsorshipZadanie pt. „Digitalizacja i udostępnienie w Cyfrowym Repozytorium Uniwersytetu Łódzkiego kolekcji czasopism naukowych wydawanych przez Uniwersytet Łódzki” nr 885/P-DUN/2014 dofinansowane zostało ze środków MNiSW w ramach działalności upowszechniającej naukę.pl_PL
dc.language.isoenpl_PL
dc.publisherWydawnictwo Uniwersytetu Łódzkiegopl_PL
dc.relation.ispartofseriesActa Universitatis Lodziensis. Folia Biologica et Oecologica;3
dc.subjecthigh throughputpl_PL
dc.subjection channel screeningpl_PL
dc.subjectpatch clamppl_PL
dc.subjectmicrofluidicspl_PL
dc.subjectGABAa receptorpl_PL
dc.titleDynaflow ™ 48, a microfluidic chip solution for increasing throughput and data quality in patch-clamp-based drug screeningpl_PL
dc.typeArticlepl_PL
dc.page.number223-230pl_PL
dc.contributor.authorAffiliationDaniel Granfeldt - Department of Chemistry and Bioscience and Microtechnology Centre, Chalmers University of Technology, SE-412 96 Göteborg, Swedenpl_PL
dc.contributor.authorAffiliationJon Sinclair - Department of Chemistry and Bioscience and Microtechnology Centre, Chalmers University of Technology, SE-412 96 Göteborg, Swedenpl_PL
dc.contributor.authorAffiliationJohan Pihl - 2Cellectricon AB, Fabriksgatan 7, SE-412 50 Göteborg, Swedenpl_PL
dc.contributor.authorAffiliationMattias Karlsson -Cellectricon AB, Fabriksgatan 7, SE-412 50 Göteborg, Swedenpl_PL
dc.contributor.authorAffiliationMarie-Louise Johansson - Cellectricon AB, Fabriksgatan 7, SE-412 50 Göteborg, Swedenpl_PL
dc.contributor.authorAffiliationJohan Pihl - Cellectricon AB, Fabriksgatan 7, SE-412 50 Göteborg, Swedenpl_PL


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