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Molecular communication model of nanoparticle-body interactions in Particulate Drug Delivery Systems

机译:颗粒药物传递系统中纳米粒子与人体相互作用的分子通讯模型

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Existing work in pharmacokinetics, the study of the movement of drugs in the body, has largely focused on multicompartmental models, based on ordinary first-order equations with constant flow. Nano-scale Particulate Drug Delivery Systems (PDDS) require better computational models. PDDS has been previously abstracted by the same authors as Molecular Communication (MC) systems, by solving the advection-diffusion problem with time-varying flow. In this paper, this framework is extended to solve the nanoparticle-body interactions problem. The delay and path loss of the system are expressed analytically. The results are validated by finite-element simulations. This model will enable more thorough pharmacokinetics than multicompartmental models.
机译:现有的药代动力学研究是研究药物在体内的运动,该研究主要集中在多隔室模型上,该模型基于具有恒定流量的普通一阶方程。纳米级颗粒药物输送系统(PDDS)需要更好的计算模型。通过解决随时变流动的对流扩散问题,PDDS已由与分子通信(MC)系统相同的作者抽象出来。在本文中,扩展了该框架以解决纳米粒子与人体的相互作用问题。系统的时延和路径损耗用解析表示。通过有限元模拟验证了结果。与多隔室模型相比,该模型将实现更彻底的药代动力学。

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