Computation of Electromagnetic Fields in Assemblages of Biological Cells using a Modified Finite-Difference Time-Domain Scheme

Yes === When modeling objects that are small compared with the wavelength, e.g., biological cells at radio frequencies, the standard finite-difference time-domain (FDTD) method requires extremely small time-step sizes, which may lead to excessive computation times. The problem can be overcome by imp...

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Main Authors: Abd-Alhameed, Raed A., Excell, Peter S., See, Chan H.
Language:en
Published: 2009
Subjects:
Online Access:http://hdl.handle.net/10454/4171
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spelling ndltd-BRADFORD-oai-bradscholars.brad.ac.uk-10454-41712019-08-31T03:02:04Z Computation of Electromagnetic Fields in Assemblages of Biological Cells using a Modified Finite-Difference Time-Domain Scheme Abd-Alhameed, Raed A. Excell, Peter S. See, Chan H. Electromagnetic Fields Biological Cells Standard Finite-Difference Time-Domain FDTD Yes When modeling objects that are small compared with the wavelength, e.g., biological cells at radio frequencies, the standard finite-difference time-domain (FDTD) method requires extremely small time-step sizes, which may lead to excessive computation times. The problem can be overcome by implementing a quasi-static approximate version of FDTD based on transferring the working frequency to a higher frequency and scaling back to the frequency of interest after the field has been computed. An approach to modeling and analysis of biological cells, incorporating a generic lumped-element membrane model, is presented here. Since the external medium of the biological cell is lossy material, a modified Berenger absorbing boundary condition is used to truncate the computation grid. Linear assemblages of cells are investigated and then Floquet periodic boundary conditions are imposed to imitate the effect of periodic replication of the assemblages. Thus, the analysis of a large structure of cells is made more computationally efficient than the modeling of the entire structure. The total fields of the simulated structures are shown to give reasonable and stable results at 900,1800, and 2450 MHz. This method will facilitate deeper investigation of the phenomena in the interaction between electromagnetic fields and biological systems. 2009-12-18T09:21:14Z 2009-12-18T09:21:14Z 2007 Article published version paper Abd-Alhamee, R.A., Excell, P.S. and See, C.H. (2007). Computation of Electromagnetic Fields in Assemblages of Biological Cells using a Modified Finite-Difference Time-Domain Scheme. IEEE Transactions on Microwave Theory and Techniques. Vol. 55, No. 9, pp. 1986-1994. http://hdl.handle.net/10454/4171 en http://dx.doi.org/10.1109/TMTT.2007.904064 Copyright © 2007 IEEE. Reprinted from IEEE Transactions on Microwave Theory and Techniques, Vol. 55, No. 9. This material is posted here with permission of the IEEE. Such permission of the IEEE does not in any way imply IEEE endorsement of any of the University of Bradford's products or services. Internal or personal use of this material is permitted. However, permission to reprint/republish this material for advertising or promotional purposes or for creating new collective works for resale or redistribution must be obtained from the IEEE by writing to pubs-permissions@ieee.org. By choosing to view this document, you agree to all provisions of the copyright laws protecting it.
collection NDLTD
language en
sources NDLTD
topic Electromagnetic Fields
Biological Cells
Standard Finite-Difference Time-Domain
FDTD
spellingShingle Electromagnetic Fields
Biological Cells
Standard Finite-Difference Time-Domain
FDTD
Abd-Alhameed, Raed A.
Excell, Peter S.
See, Chan H.
Computation of Electromagnetic Fields in Assemblages of Biological Cells using a Modified Finite-Difference Time-Domain Scheme
description Yes === When modeling objects that are small compared with the wavelength, e.g., biological cells at radio frequencies, the standard finite-difference time-domain (FDTD) method requires extremely small time-step sizes, which may lead to excessive computation times. The problem can be overcome by implementing a quasi-static approximate version of FDTD based on transferring the working frequency to a higher frequency and scaling back to the frequency of interest after the field has been computed. An approach to modeling and analysis of biological cells, incorporating a generic lumped-element membrane model, is presented here. Since the external medium of the biological cell is lossy material, a modified Berenger absorbing boundary condition is used to truncate the computation grid. Linear assemblages of cells are investigated and then Floquet periodic boundary conditions are imposed to imitate the effect of periodic replication of the assemblages. Thus, the analysis of a large structure of cells is made more computationally efficient than the modeling of the entire structure. The total fields of the simulated structures are shown to give reasonable and stable results at 900,1800, and 2450 MHz. This method will facilitate deeper investigation of the phenomena in the interaction between electromagnetic fields and biological systems.
author Abd-Alhameed, Raed A.
Excell, Peter S.
See, Chan H.
author_facet Abd-Alhameed, Raed A.
Excell, Peter S.
See, Chan H.
author_sort Abd-Alhameed, Raed A.
title Computation of Electromagnetic Fields in Assemblages of Biological Cells using a Modified Finite-Difference Time-Domain Scheme
title_short Computation of Electromagnetic Fields in Assemblages of Biological Cells using a Modified Finite-Difference Time-Domain Scheme
title_full Computation of Electromagnetic Fields in Assemblages of Biological Cells using a Modified Finite-Difference Time-Domain Scheme
title_fullStr Computation of Electromagnetic Fields in Assemblages of Biological Cells using a Modified Finite-Difference Time-Domain Scheme
title_full_unstemmed Computation of Electromagnetic Fields in Assemblages of Biological Cells using a Modified Finite-Difference Time-Domain Scheme
title_sort computation of electromagnetic fields in assemblages of biological cells using a modified finite-difference time-domain scheme
publishDate 2009
url http://hdl.handle.net/10454/4171
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