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dc.contributor.author Lee, Yuhyun -
dc.contributor.author Seo, Hee Won -
dc.contributor.author Lee, Kyeong Jae -
dc.contributor.author Jang, Jae-Won -
dc.contributor.author Kim, Sohee -
dc.date.accessioned 2020-11-12T08:24:22Z -
dc.date.available 2020-11-12T08:24:22Z -
dc.date.created 2020-10-29 -
dc.date.issued 2020-10 -
dc.identifier.citation Sensors, v.20, no.20, pp.5903 - 15 -
dc.identifier.issn 1424-8220 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/12485 -
dc.description.abstract Along with the increasing popularity of larval zebrafish as an experimental animal in the fields of drug screening, neuroscience, genetics, and developmental biology, the need for tools to deal with multiple larvae has emerged. Microfluidic channels have been employed to handle multiple larvae simultaneously, even for sensing electroencephalogram (EEG). In this study, we developed a microfluidic chip capable of uniform and continuous drug infusion across all microfluidic channels during EEG recording. Owing to the modular design of the microfluidic channels, the number of animals under investigation can be easily increased. Using the optimized design of the microfluidic chip, liquids could be exchanged uniformly across all channels without physically affecting the larvae contained in the channels, which assured a stable environment maintained all the time during EEG recording, by eliminating environmental artifacts and leaving only biological effects to be seen. To demonstrate the usefulness of the developed system in drug screening, we continuously measured EEG from four larvae without and with pentylenetetrazole application, up to 60 min. In addition, we recorded EEG from valproic acid (VPA)-treated zebrafish and demonstrated the suppression of seizure by VPA. The developed microfluidic system could contribute to the mass screening of EEG for drug development to treat neurological disorders such as epilepsy in a short time, owing to its handy size, cheap fabrication cost, and the guaranteed uniform drug infusion across all channels with no environmentally induced artifacts. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. -
dc.language English -
dc.publisher Multidisciplinary Digital Publishing Institute (MDPI) -
dc.title A Microfluidic System for Stable and Continuous EEG Monitoring from Multiple Larval Zebrafish -
dc.type Article -
dc.identifier.doi 10.3390/s20205903 -
dc.identifier.wosid 000585578500001 -
dc.identifier.scopusid 2-s2.0-85093673537 -
dc.type.local Article(Overseas) -
dc.type.rims ART -
dc.description.journalClass 1 -
dc.citation.publicationname Sensors -
dc.contributor.nonIdAuthor Lee, Yuhyun -
dc.contributor.nonIdAuthor Seo, Hee Won -
dc.contributor.nonIdAuthor Lee, Kyeong Jae -
dc.contributor.nonIdAuthor Jang, Jae-Won -
dc.identifier.citationVolume 20 -
dc.identifier.citationNumber 20 -
dc.identifier.citationStartPage 5903 -
dc.identifier.citationEndPage 15 -
dc.identifier.citationTitle Sensors -
dc.type.journalArticle Article -
dc.embargo.liftdate 9999-12-31 -
dc.embargo.terms 9999-12-31 -
dc.description.isOpenAccess Y -
dc.subject.keywordAuthor larval zebrafish -
dc.subject.keywordAuthor electroencephalogram (EEG) -
dc.subject.keywordAuthor microfluidic channel -
dc.subject.keywordAuthor agarose-free -
dc.subject.keywordAuthor drug screening -
dc.subject.keywordAuthor anti-epileptic drugs -
dc.subject.keywordPlus EPILEPTIC SEIZURES -
dc.subject.keywordPlus MODEL -
dc.subject.keywordPlus IDENTIFY -
dc.subject.keywordPlus SCREEN -
dc.subject.keywordPlus FISH -
dc.subject.keywordPlus TOOL -
dc.contributor.affiliatedAuthor Lee, Yuhyun -
dc.contributor.affiliatedAuthor Seo, Hee Won -
dc.contributor.affiliatedAuthor Lee, Kyeong Jae -
dc.contributor.affiliatedAuthor Jang, Jae-Won -
dc.contributor.affiliatedAuthor Kim, Sohee -

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