Voxelized Model of Brain Infusion That Accounts for Small Feature Fissures: Comparison With Magnetic Resonance Tracer StudiesSource: Journal of Biomechanical Engineering:;2016:;volume( 138 ):;issue: 005::page 51007Author:Dai, Wei
,
Astary, Garrett W.
,
Kasinadhuni, Aditya K.
,
Carney, Paul R.
,
Mareci, Thomas H.
,
Sarntinoranont, Malisa
DOI: 10.1115/1.4032626Publisher: The American Society of Mechanical Engineers (ASME)
Abstract: Convection enhanced delivery (CED) is a promising novel technology to treat neural diseases, as it can transport macromolecular therapeutic agents greater distances through tissue by direct infusion. To minimize offtarget delivery, our group has developed 3D computational transport models to predict infusion flow fields and tracer distributions based on magnetic resonance (MR) diffusion tensor imaging data sets. To improve the accuracy of our voxelized models, generalized anisotropy (GA), a scalar measure of a higher order diffusion tensor obtained from high angular resolution diffusion imaging (HARDI) was used to improve tissue segmentation within complex tissue regions of the hippocampus by capturing small feature fissures. Simulations were conducted to reveal the effect of these fissures and cerebrospinal fluid (CSF) boundaries on CED tracer diversion and mistargeting. Sensitivity analysis was also conducted to determine the effect of dorsal and ventral hippocampal infusion sites and tissue transport properties on drug delivery. Predicted CED tissue concentrations from this model are then compared with experimentally measured MR concentration profiles. This allowed for more quantitative comparison between model predictions and MR measurement. Simulations were able to capture infusate diversion into fissures and other CSF spaces which is a major source of CED mistargeting. Such knowledge is important for proper surgical planning.
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contributor author | Dai, Wei | |
contributor author | Astary, Garrett W. | |
contributor author | Kasinadhuni, Aditya K. | |
contributor author | Carney, Paul R. | |
contributor author | Mareci, Thomas H. | |
contributor author | Sarntinoranont, Malisa | |
date accessioned | 2017-05-09T01:26:06Z | |
date available | 2017-05-09T01:26:06Z | |
date issued | 2016 | |
identifier issn | 0148-0731 | |
identifier other | bio_138_05_051007.pdf | |
identifier uri | http://yetl.yabesh.ir/yetl/handle/yetl/160381 | |
description abstract | Convection enhanced delivery (CED) is a promising novel technology to treat neural diseases, as it can transport macromolecular therapeutic agents greater distances through tissue by direct infusion. To minimize offtarget delivery, our group has developed 3D computational transport models to predict infusion flow fields and tracer distributions based on magnetic resonance (MR) diffusion tensor imaging data sets. To improve the accuracy of our voxelized models, generalized anisotropy (GA), a scalar measure of a higher order diffusion tensor obtained from high angular resolution diffusion imaging (HARDI) was used to improve tissue segmentation within complex tissue regions of the hippocampus by capturing small feature fissures. Simulations were conducted to reveal the effect of these fissures and cerebrospinal fluid (CSF) boundaries on CED tracer diversion and mistargeting. Sensitivity analysis was also conducted to determine the effect of dorsal and ventral hippocampal infusion sites and tissue transport properties on drug delivery. Predicted CED tissue concentrations from this model are then compared with experimentally measured MR concentration profiles. This allowed for more quantitative comparison between model predictions and MR measurement. Simulations were able to capture infusate diversion into fissures and other CSF spaces which is a major source of CED mistargeting. Such knowledge is important for proper surgical planning. | |
publisher | The American Society of Mechanical Engineers (ASME) | |
title | Voxelized Model of Brain Infusion That Accounts for Small Feature Fissures: Comparison With Magnetic Resonance Tracer Studies | |
type | Journal Paper | |
journal volume | 138 | |
journal issue | 5 | |
journal title | Journal of Biomechanical Engineering | |
identifier doi | 10.1115/1.4032626 | |
journal fristpage | 51007 | |
journal lastpage | 51007 | |
identifier eissn | 1528-8951 | |
tree | Journal of Biomechanical Engineering:;2016:;volume( 138 ):;issue: 005 | |
contenttype | Fulltext |