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PMID: 25971361 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

A transfer function approach for predicting rare cell capture microdevice performance.

Biomedical microdevices ·Vol. 17 ·No. 3 ·2015-00-00 ·页码 9956

Smith JP, Kirby BJ

Abstract

Rare cells have the potential to improve our understanding of biological systems and the treatment of a variety of diseases; each of those applications requires a different balance of throughput, capture efficiency, and sample purity. Those challenges, coupled with the limited availability of patient samples and the costs of repeated design iterations, motivate the need for a robust set of engineering tools to optimize application-specific geometries. Here, we present a transfer function approach for predicting rare cell capture in microfluidic obstacle arrays. Existing computational fluid dynamics (CFD) tools are limited to simulating a subset of these arrays, owing to computational costs; a transfer function leverages the deterministic nature of cell transport in these arrays, extending limited CFD simulations into larger, more complicated geometries. We show that the transfer function approximation matches a full CFD simulation within 1.34 %, at a 74-fold reduction in computational cost. Taking advantage of these computational savings, we apply the transfer function simulations to simulate reversing array geometries that generate a "notch filter" effect, reducing the collision frequency of cells outside of a specified diameter range. We adapt the transfer function to study the effect of off-design boundary conditions (such as a clogged inlet in a microdevice) on overall performance. Finally, we have validated the transfer function's predictions for lateral displacement within the array using particle tracking and polystyrene beads in a microdevice.

MeSH 主题词
Animals Cell Physiological Phenomena Cell Separation/instrumentation Computer Simulation Computer-Aided Design Equipment Design Equipment Failure Analysis Flow Cytometry/instrumentation Humans Lab-On-A-Chip Devices Models, Biological Reproducibility of Results Sensitivity and Specificity
作者与单位
共 2 位作者,点击展开单位 / ORCID
Smith James P
Sibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, 14853, USA.
Kirby Brian J
Article Info
Journal
Biomedical microdevices
Abbr.
Biomed Microdevices
ISSN
1572-8781
Published
2015-00-00
页码
9956
Language
English
Country/Region
United States
NLM ID
100887374
基金资助
NCI NIH HHS · U54CA143876 · United States
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