Two-dimensional Finite Element Model of Breast Cancer Cell Motion Through a Microfluidic Channel

If you need an accessible version of this item, please email your request to digschol@iu.edu so that they may create one and provide it to you.
Date
2019-04
Language
English
Embargo Lift Date
Committee Members
Degree
Degree Year
Department
Grantor
Journal Title
Journal ISSN
Volume Title
Found At
Springer
Abstract

A two-dimensional model for red blood cell motion is adapted to consider the dynamics of breast cancer cells in a microfluidic channel. Adjusting parameters to make the membrane stiffer, as is the case with breast cancer cells compared with red blood cells, allows the model to produce reasonable estimates of breast cancer cell trajectories through the channel. In addition, the model produces estimates of quantities not as easily obtained from experiment such as velocity and stress field information throughout the fluid and on the cell membrane. This includes locations of maximum stress along the membrane wall. A sensitivity analysis shows that the model is capable of producing useful insights into various systems involving breast cancer cells. Current results suggest that dynamics taking place when cells are near other objects are most sensitive to membrane and cytoplasm elasticity, dynamics taking place when cells are not near other objects are most sensitive to cytoplasm viscosity, and dynamics are significantly affected by low membrane bending elasticity. These results suggest that continued calibration and application of this model can yield useful predictions in other similar systems.

Description
item.page.description.tableofcontents
item.page.relation.haspart
Cite As
Barber, J., & Zhu, L. (2019). Two-dimensional Finite Element Model of Breast Cancer Cell Motion Through a Microfluidic Channel. Bulletin of Mathematical Biology, 81(4), 1238–1259. https://doi.org/10.1007/s11538-018-00557-x
ISSN
Publisher
Series/Report
Sponsorship
Major
Extent
Identifier
Relation
Journal
Bulletin of Mathematical Biology
Source
Author
Alternative Title
Type
Article
Number
Volume
Conference Dates
Conference Host
Conference Location
Conference Name
Conference Panel
Conference Secretariat Location
Version
Author's manuscript
Full Text Available at
This item is under embargo {{howLong}}