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Abstract We performed the transport of a breast cancer cell (MB231-TGFb) in a microvessel using high-resolution simulations. Using open-source imaging software Slicer3D and Meshmixer, the 3D surface mesh forming the cell membrane was reconstructed from confocal microscopic images. The Dissipative Particle Dynamics method is used to model the cell membrane. The extracellular fluid flow is modeled with the Immersed Boundary Method to solve the governing equations of the blood plasma. The unsteady flow is applied at the inlet of the microchannel with an oscillatory pattern. Our results showed that the extracellular flow patterns are highly dependent on the waveform profile. The oscillatory flow showed the creation of vortices that influence the cellular deformations in the microchannel. These results could have implications on the destination of the cancer cells during transport in physiological flows.
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Migration of Leukocytes in Shear Flows: Insights from Simulations
Abstract The objective of this study is to investigate the rolling dynamics of leukocytes in microchannel flows using a hybrid continuum-particle approach. Leukocytes play an essential role in the immune system, and their margination behavior has been extensively studied both experimentally and numerically. In this study, we have developed a series of numerical experiments using a hybrid DPD-CFD solver with the membrane stiffness of the modeled leukocytes as the primary investigation subject. Our results show that increasing the stiffness of the cell's membrane influences its deformability and trajectory in microchannel flows. The results obtained from this study could be valuable in designing next-generation micro-carriers for targeted drug delivery systems, which mimic the margination behavior of leukocytes.
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- Award ID(s):
- 1946202
- PAR ID:
- 10579309
- Publisher / Repository:
- American Society of Mechanical Engineers
- Date Published:
- ISBN:
- 978-0-7918-8775-2
- Format(s):
- Medium: X
- Location:
- Minneapolis, MN, USA
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Conference Paper:
- https://doi.org/10.1115/dmd2024-1076
