阻抗光谱法测定胰岛素吸收。可行性研究

G. Annuzzi, P. Arpaia, L. Bozzetto, Giusy Carleo, O. Cuomo, Francesca Mancino, N. Moccaldi, P. Ramos, M. Taglialatela
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引用次数: 2

摘要

提出了一种基于生物阻抗光谱的皮下胰岛素吸收监测芯片传感器。阻抗变化的测量允许检测药物从给药部位消失,从而提供药物吸收的间接测量。在本文的第一部分,介绍了传感器的硬件、固件和软件。然后,报告了对茄子的测试结果,比较了它们对车辆和胰岛素管理的电反应。当溶液量增加时,胰岛素对阻抗变化的影响小于对照。事实上,以胰岛素为例,阻抗大小和相位的敏感性分别为62.88 ml-1和44.07 ml-1。以车辆为例,阻抗幅值的灵敏度为171.21 ml-1,阻抗相位的灵敏度为88.91 ml-1。尽管存在这些差异,但阻抗大小相同,相位单调。在体外实验的基础上,对人体进行了初步实验,以研究由于吸收剂引起的组织阻抗变化。给药后注射部位的阻抗减小。在给药后,阻抗值有恢复到基线值的趋势。本研究通过阻抗变化测量药物从给药部位消失的量,证明了间接药物吸收评价的可行性。
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Measuring insulin absorption by impedance spectroscopy. A feasibility study
An on chip-transducer based on bioimpedance spectroscopy for monitoring insulin absorption after subcutaneous administration is presented. The measurement of impedance variation allows to detect the disappearance of the drug from administration site, thus providing an indirect measure of drug absorption. In the first part of this paper, the hardware, firmware, and software of the transducer are presented. Then, the results from tests on eggplants are reported comparing their electrical response to vehicle and insulin administration. When the amount of solution increased, impedance variation was lower with insulin compared to vehicle. As matter of fact, in case of insulin, a sensitivity of 62.88 ml-1 and 44.07 ml-1was calculated for impedance magnitude and phase, respectively. In case of vehicle, a sensitivity of 171.21 ml-1 was calculated for impedance magnitude, whereas, a variation of 88.91 ml-1was observed for the impedance phase. Despite these differences, the same impedance magnitude and phase monotonous trend emerged. Based on the evidence emerged from in-vitro test, a preliminary experimental on a human subject was performed to investigate tissue impedance variation due to vehicle absorption. Vehicle administration produced a decrease in impedance magnitude of the injection site. After vehicle administration, the impedance magnitude showed a tendency to return to the baseline value. This study demonstrated the feasibility of indirect drug absorption assessment by measuring the amount of drug disappearing from the site of administration in terms of impedance variation.
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