| Literature DB >> 32293134 |
Hui-Yu Liu1, Claudia Koch2, Anna Haller3, Simon A Joosse2, Ravi Kumar1, Michael J Vellekoop4, Ludwig J Horst2, Laura Keller2, Anna Babayan2, Antonio Virgilio Failla5, Jana Jensen2, Sven Peine6, Franz Keplinger3, Harald Fuchs1,7, Klaus Pantel2, Michael Hirtz1.
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.Entities:
Keywords: breast cancer; circulating tumor cells; microfluidics; polymer pen lithography; staggered herringbone design
Mesh:
Year: 2019 PMID: 32293134 DOI: 10.1002/adbi.201900162
Source DB: PubMed Journal: Adv Biosyst ISSN: 2366-7478