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A capillary-driven microfluidic device for performing spatial multiplex PCR

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dc.contributor.authorWiederkehr, Rodrigo Sergio
dc.contributor.authorMarchal, Elisabeth
dc.contributor.authorFauvart, Maarten
dc.contributor.authorForceville, Tomas
dc.contributor.authorTaher, Ahmed
dc.contributor.authorSteylaerts, Tim
dc.contributor.authorChoe, YoungJae
dc.contributor.authorDusar, Hans
dc.contributor.authorLenci, Silvia
dc.contributor.authorSiouti, Eleni
dc.contributor.authorPotsika, Vassiliki T.
dc.contributor.authorAndreakos, Evangelos
dc.contributor.authorStakenborg, Tim
dc.contributor.imecauthorWiederkehr, Rodrigo S.
dc.contributor.imecauthorMarchal, Elisabeth
dc.contributor.imecauthorFauvart, Maarten
dc.contributor.imecauthorForceville, Tomas
dc.contributor.imecauthorTaher, Ahmed
dc.contributor.imecauthorSteylaerts, Tim
dc.contributor.imecauthorChoe, Youngjae
dc.contributor.imecauthorDusar, Hans
dc.contributor.imecauthorLenci, Silvia
dc.contributor.imecauthorStakenborg, Tim
dc.contributor.orcidimecFauvart, Maarten::0000-0002-6256-9193
dc.contributor.orcidimecForceville, Tomas::0000-0003-1045-4965
dc.contributor.orcidimecSteylaerts, Tim::0000-0002-2168-9033
dc.contributor.orcidimecDusar, Hans::0000-0002-7577-2078
dc.contributor.orcidimecLenci, Silvia::0000-0002-9622-0133
dc.contributor.orcidimecStakenborg, Tim::0000-0001-9878-9078
dc.date.accessioned2025-04-01T06:43:17Z
dc.date.available2025-04-01T06:43:17Z
dc.date.issued2025-JUN
dc.description.abstractMultiplex polymerase chain reaction (PCR) tests multiple biomarkers or pathogens that cause overlapping symptoms, making it an essential tool in syndromic testing. To achieve a multiplex PCR on chip, a design based on capillary-driven fluidic actuation is proposed. Our silicon chip features 22 reaction chambers and allows primers and probes to be pre-spotted in the reaction chambers prior to use. The design facilitates rapid sample loading through a common inlet channel, delivering reagents to all reaction chambers in less than 10 s. A custom clamping mechanism combined with a double depth cavity design ensures proper sealing during temperature cycling without the need for extra reagents like oil. Temperature cycling and fluorescence imaging were performed using custom-made hardware. As a proof of concept, two single nucleotide polymorphisms (SNPs), CyP2C19*2 and PCSK9 were detected. These results demonstrate the feasibility of on-chip multiplex PCR, compatible with different assays in parallel and requiring only a single pipetting step for reagent loading, without active fluidic actuation like pumping.
dc.description.wosFundingTextThis work was funded by European Union Horizon 2020 Research Innovation Programme (Project Taxinomisis, Grant number: 755320).
dc.identifier.doi10.1007/s10544-025-00745-2
dc.identifier.issn1387-2176
dc.identifier.pmidMEDLINE:40140106
dc.identifier.urihttps://imec-publications.be/handle/20.500.12860/45472
dc.publisherSPRINGER
dc.source.issue2
dc.source.journalBIOMEDICAL MICRODEVICES
dc.source.numberofpages11
dc.source.volume27
dc.subject.keywordsREAL-TIME PCR
dc.subject.keywordsSYSTEM
dc.subject.keywordsCHIP
dc.title

A capillary-driven microfluidic device for performing spatial multiplex PCR

dc.typeJournal article
dspace.entity.typePublication
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