Bubble collapse near a fluid-fluid interface using the spectral element marker particle method with applications in bioengineering

Christopher F. Rowlatt, Steven J. Lind

Research output: Contribution to journalArticle

Abstract

The spectral element marker particle (SEMP) method is a high-order numerical scheme for modelling multiphase flow where the governing equations are discretised using the spectral element method and the (compressible) fluid phases are tracked using marker particles. Thus far, the method has been successfully applied to two-phase problems involving the collapse of a two-dimensional bubble in the vicinity of a rigid wall. In this article, the SEMP method is extended to include a third fluid phase before being applied to bubble collapse problems near a fluid-fluid interface. Two-phase bubble collapse near a rigid boundary (where a highly viscous third phase approximates the rigid boundary) is considered as validation of the method. A range of fluid parameter values and geometric configurations are studied before a bioengineering application is considered. A simplified model of (micro)bubble-cell interaction is presented, with the aim of gaining initial insights into the flow mechanisms behind sonoporation and microbubble-enhanced targeted drug delivery. Results from this model indicate that the non-local cell membrane distortion (blebbing) phenomenon often observed experimentally may result from stress propagation along the cell surface and so be hydrodynamical in origin.
LanguageEnglish
Pages118-143
Number of pages26
JournalInternational Journal of Multiphase Flow
Volume90
Early online date1 Dec 2016
DOIs
Publication statusPublished - 30 Apr 2017

Fingerprint

bioengineering
markers
bubbles
Fluids
fluids
stress propagation
compressible fluids
multiphase flow
cells
Multiphase flow
Cell membranes
delivery
drugs
Bioengineering
configurations
interactions

Keywords

  • bubble dynamics
  • drug delivery
  • sonoporation
  • spectral element
  • marker particle method
  • bioengineering

Cite this

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title = "Bubble collapse near a fluid-fluid interface using the spectral element marker particle method with applications in bioengineering",
abstract = "The spectral element marker particle (SEMP) method is a high-order numerical scheme for modelling multiphase flow where the governing equations are discretised using the spectral element method and the (compressible) fluid phases are tracked using marker particles. Thus far, the method has been successfully applied to two-phase problems involving the collapse of a two-dimensional bubble in the vicinity of a rigid wall. In this article, the SEMP method is extended to include a third fluid phase before being applied to bubble collapse problems near a fluid-fluid interface. Two-phase bubble collapse near a rigid boundary (where a highly viscous third phase approximates the rigid boundary) is considered as validation of the method. A range of fluid parameter values and geometric configurations are studied before a bioengineering application is considered. A simplified model of (micro)bubble-cell interaction is presented, with the aim of gaining initial insights into the flow mechanisms behind sonoporation and microbubble-enhanced targeted drug delivery. Results from this model indicate that the non-local cell membrane distortion (blebbing) phenomenon often observed experimentally may result from stress propagation along the cell surface and so be hydrodynamical in origin.",
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author = "Rowlatt, {Christopher F.} and Lind, {Steven J.}",
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N2 - The spectral element marker particle (SEMP) method is a high-order numerical scheme for modelling multiphase flow where the governing equations are discretised using the spectral element method and the (compressible) fluid phases are tracked using marker particles. Thus far, the method has been successfully applied to two-phase problems involving the collapse of a two-dimensional bubble in the vicinity of a rigid wall. In this article, the SEMP method is extended to include a third fluid phase before being applied to bubble collapse problems near a fluid-fluid interface. Two-phase bubble collapse near a rigid boundary (where a highly viscous third phase approximates the rigid boundary) is considered as validation of the method. A range of fluid parameter values and geometric configurations are studied before a bioengineering application is considered. A simplified model of (micro)bubble-cell interaction is presented, with the aim of gaining initial insights into the flow mechanisms behind sonoporation and microbubble-enhanced targeted drug delivery. Results from this model indicate that the non-local cell membrane distortion (blebbing) phenomenon often observed experimentally may result from stress propagation along the cell surface and so be hydrodynamical in origin.

AB - The spectral element marker particle (SEMP) method is a high-order numerical scheme for modelling multiphase flow where the governing equations are discretised using the spectral element method and the (compressible) fluid phases are tracked using marker particles. Thus far, the method has been successfully applied to two-phase problems involving the collapse of a two-dimensional bubble in the vicinity of a rigid wall. In this article, the SEMP method is extended to include a third fluid phase before being applied to bubble collapse problems near a fluid-fluid interface. Two-phase bubble collapse near a rigid boundary (where a highly viscous third phase approximates the rigid boundary) is considered as validation of the method. A range of fluid parameter values and geometric configurations are studied before a bioengineering application is considered. A simplified model of (micro)bubble-cell interaction is presented, with the aim of gaining initial insights into the flow mechanisms behind sonoporation and microbubble-enhanced targeted drug delivery. Results from this model indicate that the non-local cell membrane distortion (blebbing) phenomenon often observed experimentally may result from stress propagation along the cell surface and so be hydrodynamical in origin.

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