用于治疗血流动力学障碍给药系统的压电微泵的三维瞬态多场分析。

Asim Nisar, Nitin Afzulpurkar, Adisorn Tuantranont, Banchong Mahaisavariya
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引用次数: 18

摘要

在本文中,我们提出了一种经皮给药系统的设计,用于治疗心血管或血液动力学疾病,如高血压。该系统由微泵、微血压传感器和微针阵列等集成控制电子和微机电系统器件组成。目的是克服口服治疗的局限性,如吸收谱的变化和频繁给药的需要,通过制造一种安全、可靠和经济有效的透皮给药系统,通过皮肤分配各种药理学药物,治疗血液动力学功能障碍,如高血压。此外,提出了一种用于给药系统的压电驱动无阀微泵的优化设计。由于压电微泵分析的复杂性,涉及复杂几何布置下的结构和流场耦合,因此采用有限元数值模拟而非解析系统。首先通过压电分析研究了生物相容性聚二甲基硅氧烷膜压电致动器的性能。建立了无阀微泵的三维电-固-流模型,分析了无阀微泵的性能。采用多码耦合方法对无阀微泵进行瞬态分析,研究了几何尺寸对微泵特性和喷嘴/扩散器元件效率的影响。用多场码耦合分析得到的膜的变形结果与压电微泵的解析和单场码耦合分析结果吻合较好。分析表明,为了提高微泵的性能,需要对扩散器长度、扩散器颈宽和扩散器角度等几何尺寸进行优化。在10至200 Hz的低激励频率下,微泵流量不受强烈影响。与激励频率相比,激励电压是影响微泵流量的主要因素。然而,在超过8,000 Hz的极高激励频率下,由于膜呈现多个弯曲峰,流速下降,这对流体流动是不理想的。在广泛的数值分析之后,介绍了微泵的实际制造和性能表征。研究了微泵在不同运行参数下的压电致动器挠度和微泵流量对微泵性能的影响。在不同电压和激励频率下的偏转和流量的多场模拟和实验测量是电-固-流耦合场效应研究的重要进展,它允许对微泵进行瞬态、三维压电和流体分析,从而使多场分析更加真实。本研究结果也将有助于今后开展微泵微针阵列一体化给药装置的相关强度持续时间试验。
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Three dimensional transient multifield analysis of a piezoelectric micropump for drug delivery system for treatment of hemodynamic dysfunctions.

In this paper, we present design of a transdermal drug delivery system for treatment of cardiovascular or hemodynamic disorders such as hypertension. The system comprises of integrated control electronics and microelectromechanical system devices such as micropump, micro blood pressure sensor and microneedle array. The objective is to overcome the limitations of oral therapy such as variable absorption profile and the need for frequent dosing, by fabricating a safe, reliable and cost effective transdermal drug delivery system to dispense various pharmacological agents through the skin for treatment of hemodynamic dysfunction such as hypertension. Moreover, design optimization of a piezoelectrically actuated valveless micropump is presented for the drug delivery system. Because of the complexity in analysis of piezoelectric micropump, which involves structural and fluid field couplings in a complicated geometrical arrangement, finite element (FE) numerical simulation rather than an analytical system has been used. The behavior of the piezoelectric actuator with biocompatible polydimethylsiloxane membrane is first studied by conducting piezoelectric analysis. Then the performance of the valveless micropump is analyzed by building a three dimensional electric-solid-fluid model of the micropump. The effect of geometrical dimensions on micropump characteristics and efficiency of nozzle/diffuser elements of a valveless micropump is investigated in the transient analysis using multiple code coupling method. The deformation results of the membrane using multifield code coupling analysis are in good agreement with analytical as well as results of single code coupling analysis of a piezoelectric micropump. The analysis predicts that to enhance the performance of the micropump, diffuser geometrical dimensions such as diffuser length, diffuser neck width and diffuser angle need to be optimized. Micropump flow rate is not strongly affected at low excitation frequencies from 10 to 200 Hz. The excitation voltage is the more dominant factor that affects the flow rate of the micropump as compared with the excitation frequency. However, at extremely high excitation frequencies beyond 8,000 Hz, the flow rate drops as the membrane exhibits multiple bending peaks which is not desirable for fluid flow. Following the extensive numerical analysis, actual fabrication and performance characterization of the micropump is presented. The performance of the micropump is characterized in terms of piezoelectric actuator deflection and micropump flow rate at different operational parameters. The set of multifield simulations and experimental measurement of deflection and flow rate at varying voltage and excitation frequency is a significant advance in the study of the electric-solid-fluid coupled field effects as it allows transient, three dimensional piezoelectric and fluid analysis of the micropump thereby facilitating a more realistic multifield analysis. The results of the present study will also help to conduct relevant strength duration tests of integrated drug delivery device with micropump and microneedle array in future.

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