向病变组织输送药物的可逆电穿孔模型

IF 2.3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nilay Mondal, D C Dalal
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引用次数: 0

摘要

通过电穿孔给药对治疗人体内不同类型的病变组织大有裨益。在这项研究中,我们提出了一个可逆组织电穿孔数学模型,用于向病变细胞注射药物。该模型强调了作为点源注入药物的组织边界。此外,还详细研究了药物在组织边界通过细胞外空间流失的影响。采用多个脉冲将足量的药物注入靶细胞。对模拟物理环境的微分方程组进行了数值求解。该模型通过孔隙率系数和药物渗透性得出传质系数(MTC),从而控制药物从细胞外向细胞内的传输。在应用不同的脉冲时,药物在整个组织中的渗透情况被捕捉到。本研究强调了药物浓度的边界效应。所提倡的模型能够将药物均匀地输送到细胞内,从而使受影响的组织得到完全治疗。该模型可用于优化临床实验,避免了冗长而昂贵的体内和体外实验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Model for Reversible Electroporation to Deliver Drugs into Diseased Tissues.

A Model for Reversible Electroporation to Deliver Drugs into Diseased Tissues.

Drug delivery through electroporation could be highly beneficial for the treatment of different types of diseased tissues within the human body. In this work, a mathematical model of reversible tissue electroporation is presented for injecting drug into the diseased cells. The model emphasizes the tissue boundary where the drug is injected as a point source. In addition, the effect of drug loss at tissue boundaries through extracellular space is studied elaborately. Multiple pulses are applied to deliver a sufficient amount of drug into the targeted cells. The set of differential equations that model the physical circumstances are solved numerically. This model obtains a mass transfer coefficient (MTC), in terms of pore fraction coefficient and drug permeability that controls the drug transport from extracellular to intracellular space. The drug penetration throughout the tissue is captured for the application of different pulses. The boundary effects on drug concentration are highlighted in this study. The advocated model is able to perform homogeneous drug transport into the cells so that the affected tissue is treated completely. This model can be applied to optimize clinical experiments by avoiding the lengthy and costly in vivo and in vitro experiments.

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来源期刊
Journal of Membrane Biology
Journal of Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
4.20%
发文量
63
审稿时长
6-12 weeks
期刊介绍: The Journal of Membrane Biology is dedicated to publishing high-quality science related to membrane biology, biochemistry and biophysics. In particular, we welcome work that uses modern experimental or computational methods including but not limited to those with microscopy, diffraction, NMR, computer simulations, or biochemistry aimed at membrane associated or membrane embedded proteins or model membrane systems. These methods might be applied to study topics like membrane protein structure and function, membrane mediated or controlled signaling mechanisms, cell-cell communication via gap junctions, the behavior of proteins and lipids based on monolayer or bilayer systems, or genetic and regulatory mechanisms controlling membrane function. Research articles, short communications and reviews are all welcome. We also encourage authors to consider publishing ''negative'' results where experiments or simulations were well performed, but resulted in unusual or unexpected outcomes without obvious explanations. While we welcome connections to clinical studies, submissions that are primarily clinical in nature or that fail to make connections to the basic science issues of membrane structure, chemistry and function, are not appropriate for the journal. In a similar way, studies that are primarily descriptive and narratives of assays in a clinical or population study are best published in other journals. If you are not certain, it is entirely appropriate to write to us to inquire if your study is a good fit for the journal.
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