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本文引用的文献

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Computational methods for predicting drug transport in anisotropic and heterogeneous brain tissue.预测药物在各向异性和异质性脑组织中转运的计算方法。
J Biomech. 2008 Jul 19;41(10):2176-87. doi: 10.1016/j.jbiomech.2008.04.025. Epub 2008 Jun 11.
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Prediction of convection-enhanced drug delivery to the human brain.对流增强药物输送至人脑部的预测。
J Theor Biol. 2008 Jan 7;250(1):125-38. doi: 10.1016/j.jtbi.2007.09.009. Epub 2007 Sep 14.
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A biphasic model for micro-indentation of a hydrogel-based contact lens.一种基于水凝胶的隐形眼镜微压痕的双相模型。
J Biomech Eng. 2007 Apr;129(2):156-63. doi: 10.1115/1.2472373.
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Interstitial transport and transvascular fluid exchange during infusion into brain and tumor tissue.向脑和肿瘤组织输注期间的间质转运和跨血管液体交换
Microvasc Res. 2007 Jan;73(1):58-73. doi: 10.1016/j.mvr.2006.07.001. Epub 2006 Oct 25.
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Computational model of interstitial transport in the spinal cord using diffusion tensor imaging.利用扩散张量成像的脊髓间质转运计算模型
Ann Biomed Eng. 2006 Aug;34(8):1304-21. doi: 10.1007/s10439-006-9135-3. Epub 2006 Jul 11.
6
Fabrication and characterization of microfluidic probes for convection enhanced drug delivery.用于对流增强药物递送的微流体探针的制备与表征
J Control Release. 2006 Apr 10;111(3):252-62. doi: 10.1016/j.jconrel.2005.11.018. Epub 2006 Feb 14.
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Direct interstitial infusion of NK1-targeted neurotoxin into the spinal cord: a computational model.将靶向NK1的神经毒素直接间质内注入脊髓:一种计算模型。
Am J Physiol Regul Integr Comp Physiol. 2003 Jul;285(1):R243-54. doi: 10.1152/ajpregu.00472.2002.
8
A computational model of direct interstitial infusion of macromolecules into the spinal cord.一种将大分子直接间质内注入脊髓的计算模型。
Ann Biomed Eng. 2003 Apr;31(4):448-61. doi: 10.1114/1.1558032.
9
Diffusion-tensor MRI: theory, experimental design and data analysis - a technical review.扩散张量磁共振成像:理论、实验设计与数据分析——技术综述
NMR Biomed. 2002 Nov-Dec;15(7-8):456-67. doi: 10.1002/nbm.783.
10
Successful and safe perfusion of the primate brainstem: in vivo magnetic resonance imaging of macromolecular distribution during infusion.灵长类动物脑干的成功安全灌注:输注过程中大分子分布的体内磁共振成像
J Neurosurg. 2002 Oct;97(4):905-13. doi: 10.3171/jns.2002.97.4.0905.

直接注入白质后大鼠脊髓间质转运的体素化模型。

Voxelized model of interstitial transport in the rat spinal cord following direct infusion into white matter.

作者信息

Kim Jung Hwan, Astary Garrett W, Chen Xiaoming, Mareci Thomas H, Sarntinoranont Malisa

机构信息

Department of Mechanical and Aerospace Engineering, University of Florida, Gainesville, FL 32611, USA.

出版信息

J Biomech Eng. 2009 Jul;131(7):071007. doi: 10.1115/1.3169248.

DOI:10.1115/1.3169248
PMID:19640132
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2906454/
Abstract

Direct tissue infusion, e.g., convection-enhanced delivery (CED), is a promising local delivery technique for treating diseases of the central nervous system. Predictive models of spatial drug distribution during and following direct tissue infusion are necessary for treatment optimization and planning of surgery. In this study, a 3D interstitial transport modeling approach in which tissue properties and anatomical boundaries are assigned on a voxel-by-voxel basis using tissue alignment data from diffusion tensor imaging (DTI) is presented. The modeling approach is semi-automatic and utilizes porous media transport theory to estimate interstitial transport in isotropic and anisotropic tissue regions. Rat spinal cord studies compared predicted distributions of albumin tracer (for varying DTI resolution) following infusion into the dorsal horn with tracer distributions measured by Wood et al. in a previous study. Tissue distribution volumes compared favorably for small infusion volumes (<4 microl). The presented DTI-based methodology provides a rapid means of estimating interstitial flows and tracer distributions following CED into the spinal cord. Quantification of these transport fields provides an important step toward development of drug-specific transport models of infusion.

摘要

直接组织灌注,例如对流增强递送(CED),是一种用于治疗中枢神经系统疾病的很有前景的局部递送技术。在直接组织灌注期间及之后进行空间药物分布的预测模型对于治疗优化和手术规划是必要的。在本研究中,提出了一种三维间质运输建模方法,该方法使用来自扩散张量成像(DTI)的组织对齐数据,逐体素地分配组织特性和解剖边界。该建模方法是半自动的,并利用多孔介质传输理论来估计各向同性和各向异性组织区域中的间质运输。大鼠脊髓研究将注入背角后白蛋白示踪剂的预测分布(针对不同的DTI分辨率)与伍德等人在先前研究中测量的示踪剂分布进行了比较。对于小灌注体积(<4微升),组织分布体积具有良好的一致性。所提出的基于DTI的方法提供了一种快速估计CED注入脊髓后间质流动和示踪剂分布的方法。对这些运输场的量化为开发特定药物的灌注运输模型迈出了重要一步。