Publication:
A capillary-driven microfluidic device for performing spatial multiplex PCR
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| dc.contributor.author | Wiederkehr, Rodrigo Sergio | |
| dc.contributor.author | Marchal, Elisabeth | |
| dc.contributor.author | Fauvart, Maarten | |
| dc.contributor.author | Forceville, Tomas | |
| dc.contributor.author | Taher, Ahmed | |
| dc.contributor.author | Steylaerts, Tim | |
| dc.contributor.author | Choe, YoungJae | |
| dc.contributor.author | Dusar, Hans | |
| dc.contributor.author | Lenci, Silvia | |
| dc.contributor.author | Siouti, Eleni | |
| dc.contributor.author | Potsika, Vassiliki T. | |
| dc.contributor.author | Andreakos, Evangelos | |
| dc.contributor.author | Stakenborg, Tim | |
| dc.contributor.imecauthor | Wiederkehr, Rodrigo S. | |
| dc.contributor.imecauthor | Marchal, Elisabeth | |
| dc.contributor.imecauthor | Fauvart, Maarten | |
| dc.contributor.imecauthor | Forceville, Tomas | |
| dc.contributor.imecauthor | Taher, Ahmed | |
| dc.contributor.imecauthor | Steylaerts, Tim | |
| dc.contributor.imecauthor | Choe, Youngjae | |
| dc.contributor.imecauthor | Dusar, Hans | |
| dc.contributor.imecauthor | Lenci, Silvia | |
| dc.contributor.imecauthor | Stakenborg, Tim | |
| dc.contributor.orcidimec | Fauvart, Maarten::0000-0002-6256-9193 | |
| dc.contributor.orcidimec | Forceville, Tomas::0000-0003-1045-4965 | |
| dc.contributor.orcidimec | Steylaerts, Tim::0000-0002-2168-9033 | |
| dc.contributor.orcidimec | Dusar, Hans::0000-0002-7577-2078 | |
| dc.contributor.orcidimec | Lenci, Silvia::0000-0002-9622-0133 | |
| dc.contributor.orcidimec | Stakenborg, Tim::0000-0001-9878-9078 | |
| dc.date.accessioned | 2025-04-01T06:43:17Z | |
| dc.date.available | 2025-04-01T06:43:17Z | |
| dc.date.issued | 2025-JUN | |
| dc.description.abstract | Multiplex 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.wosFundingText | This work was funded by European Union Horizon 2020 Research Innovation Programme (Project Taxinomisis, Grant number: 755320). | |
| dc.identifier.doi | 10.1007/s10544-025-00745-2 | |
| dc.identifier.issn | 1387-2176 | |
| dc.identifier.pmid | MEDLINE:40140106 | |
| dc.identifier.uri | https://imec-publications.be/handle/20.500.12860/45472 | |
| dc.publisher | SPRINGER | |
| dc.source.issue | 2 | |
| dc.source.journal | BIOMEDICAL MICRODEVICES | |
| dc.source.numberofpages | 11 | |
| dc.source.volume | 27 | |
| dc.subject.keywords | REAL-TIME PCR | |
| dc.subject.keywords | SYSTEM | |
| dc.subject.keywords | CHIP | |
| dc.title | A capillary-driven microfluidic device for performing spatial multiplex PCR | |
| dc.type | Journal article | |
| dspace.entity.type | Publication | |
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