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dc.contributor.authorZhao, Xinyan
dc.contributor.authorDong, Tao
dc.date.accessioned2017-12-19T14:15:13Z
dc.date.available2017-12-19T14:15:13Z
dc.date.created2014-01-10T14:09:33Z
dc.date.issued2013
dc.identifier.citationSensors. 2013, 13 (11), 14570-14582.nb_NO
dc.identifier.issn1424-8220
dc.identifier.urihttp://hdl.handle.net/11250/2473026
dc.description.abstractMood disorders are common mental diseases, but physiological diagnostic methods are still lacking. Since much evidence has implied a relationship between mood disorders and the protein composition of blood sera, it is conceivable to develop a serological criterion for assisting diagnosis of mood disorders, based on a correlative database with enough capacity and high quality. In this pilot study, a low-cost microfluidic microarray device for quantifying at most 384 serological biomarkers at the same time was designed for the data acquisition of the serological study. The 1,536-chamber microfluidic device was modeled on a 1,536-well microtiter plate in order to employ a common microplate reader as the detection module for measuring the chemiluminescent immunoassay tests on the chips. The microfluidic microarrays were rapidly fabricated on polymethylmethacrylate slides using carbon dioxide laser ablation, followed by effective surface treatment processing. Sixteen types of different capture antibodies were immobilized on the chips to test the corresponding hormones and cytokines. The preliminary tests indicated that the signal-to-noise ratio and the limit of detection of microfluidic microarrays have reached the level of standard ELISA tests, whereas the operation time of microfluidic microarrays was sharply reduced.nb_NO
dc.language.isoengnb_NO
dc.relation.urihttp://www.mdpi.com/1424-8220/13/11/14570
dc.rightsNavngivelse 3.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/deed.no*
dc.titleDesign and fabrication of low-cost 1536-chamber microfluidic microarrays for mood-disorders-related serological studiesnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.rights.holder© 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).nb_NO
dc.source.pagenumber14570-14582nb_NO
dc.source.volume13nb_NO
dc.source.journalSensorsnb_NO
dc.source.issue11nb_NO
dc.identifier.doi10.3390/s131114570
dc.identifier.cristin1087626
dc.relation.projectNorges forskningsråd: 197411nb_NO
dc.relation.projectAndre: Oslofjorfondet 220635nb_NO
dc.relation.projectAndre: Oslofjorfondet 229857nb_NO
cristin.unitcode222,58,4,0
cristin.unitnameInstitutt for mikrosystemer
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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