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引用次数: 0

摘要

连续血糖监测和胰岛素控制算法的发展使得闭环人工胰腺技术的发展成为可能。然而,尽管取得了这些进展,葡萄糖传感器在生理条件下和长时间监测下的准确性和可靠性仍然是实现真正闭环人工胰腺的限制因素。为了改进传感器技术,需要在生理条件下准确地模拟葡萄糖传感器的动态和性能。建立了三维氢基葡萄糖传感器模型,用于预测传感器的稳态性能。在COMSOL Multiphysics软件上建立了包含三电极体系和相关电化学反应的有限元模型,用于电化学电流计算。使用实验装置测量了从5毫米到35毫米的各种过氧化氢浓度,结果得到了验证。该模型预测了电流从5美元到35毫米之间的线性关系。1美元到35美元。8 \mu A$表示上述葡萄糖浓度。实验数据表明,在相同的范围内,过氧化氢浓度与当前的测量值之间存在线性关系,范围从$9。4美元到60美元。6 \mu A$。模型和实验数据在所有浓度测试中始终存在40- 46%之间的百分比差异。这种一致的标度误差可归因于电极几何面积和电化学活性面积的差异。模型的未来迭代必须考虑有效电极面积。
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Preliminary Finite Element Model for Hydrogen Peroxide-based Glucose Sensors.
The development of continuous glucose monitoring and insulin control algorithms have enabled the recent development of closed-loop artificial pancreas technology. However, despite these advancements, glucose sensor accuracy and reliability under physiologic conditions and over long periods of monitoring continue to be limiting factors in achieving a truly closed-loop artificial pancreas. To develop improved sensor technology, glucose sensor dynamics and performance need to be modeled accurately under physiologic conditions. A three dimensional hydrogen-based glucose sensor model was developed to predict steady-state sensor performance. The finite element model, which included a three-electrode system and relevant electrochemical reactions for electrochemical current calculation, was developed on COMSOL Multiphysics software. The results were validated using an experimental setup measuring various hydrogen peroxide concentrations ranging from 5 mM to 35 mM. The model predicted a linear relationship between current ranging from $5 . 1 \mu A$ to $35 . 8 \mu A$ for the aforementioned glucose concentrations. Experimental data demonstrated a linear relationship between hydrogen peroxide concentration within the same range, and current measurements ranging from $9 . 4 \mu A$ to $60 . 6 \mu A$. The model and experimental data differed consistently by percentages between 40-46 % for all concentrationstested. This consistent scaling error can be attributed to the difference in electrode geometric area and electrochemical active area. Future iterations of the model must take into consideration the effective electrode area.
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