Evaluation of Microfluidic Ceiling Designs for the Capture of Circulating Tumor Cells on a Microarray Platform. Issue 2 (23rd December 2019)

• Record Type: Journal Article
• Authors: Liu, Hui‐Yu; Koch, Claudia; Haller, Anna; Joosse, Simon A.; Kumar, Ravi; Vellekoop, Michael J.; Horst, Ludwig J.; Keller, Laura; Babayan, Anna; Failla, Antonio Virgilio; Jensen, Jana; Peine, Sven; Keplinger, Franz; Fuchs, Harald; Pantel, Klaus; Hirtz, Michael
• Is Part Of: Advanced biosystems. Volume 4:Issue 2(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2019-12-23
• Subjects: breast cancer -- circulating tumor cells -- microfluidics -- polymer pen lithography -- staggered herringbone design; Biological systems -- Periodicals; Biotechnology -- Periodicals; Bioengineering -- Periodicals; Biomedical engineering -- Periodicals; Biological Science Disciplines; Periodicals; Periodicals; 660.6
• DOI: 10.1002/adbi.201900162
• Languages: English
• ISSNs: 2366-7478

Abstract

Abstract: The capture of circulating tumor cells (CTCs) is still a challenging application for microfluidic chips, as these cells are rare and hidden in a huge background of blood cells. Here, different microfluidic ceiling designs in regard to their capture efficiency for CTCs in model experiments and more realistic conditions of blood samples spiked with a clinically relevant amount of tumor cells are evaluated. An optimized design for the capture platform that allows highly efficient recovery of CTCs from size‐based pre‐enriched samples under realistic conditions is obtained. Furthermore, the viability of captured tumor cells as well as single cell recovery for downstream genomic analysis is demonstrated. Additionally, the authors' findings underline the importance of evaluating rational design rules for microfluidic devices based on theoretical models by application‐specific experiments. Abstract : Different types of ceiling design are evaluated for their efficiency in a microfluidic chip for the capture of circulating tumor cells. In experiments with realistic blood samples spiked with tumor cells, an optimized layout of the platform is obtained and single cell recovery for downstream genomic analysis is demonstrated.