贴壁细胞培养检测用圆形贴片谐振器的设计与响应分析

S. Carraro, L. D’Alvia, Francesca Cerminara, Z. Prete, E. Rizzuto
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引用次数: 3

摘要

电磁波与物质相互作用的研究在检测被测材料中起着至关重要的作用。近年来,射频(RF)平面谐振器探头已被用于通过评估其介电特性来表征mut。许多研究提出这些器件作为生物传感器,特别是用于活细胞悬浮液甚至单细胞的介电测量。然而,尽管这些细胞应用代表了医学诊断改进的起点,但它们没有考虑细胞相互作用和粘附。我们提出了一个初步的研究,设计一个圆形贴片谐振器,以检测贴壁细胞培养。不同的配置,包括一个小,等于和大于标准培养皿的补丁进行了分析。并将仿真结果与应用圆形微带天线经验方程得到的理论结果进行了比较。结果表明,模拟结果与理论结果相差不到1.5%。最后,一旦确定了最佳贴片直径,就进行另外两个仿真集来评估天线的灵敏度。在第一组中,我们模拟了四种不同体积的培养基(从1.50 ml到6.00 ml)对天线的响应,在第二组中,我们模拟了在固定体积(1.5 ml)的培养基中不同水平的C2C12细胞融合对天线的响应。结果表明,所设计的探针可以根据培养基和C2C12培养细胞介电常数的变化来区分培养基和C2C12培养细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design and response analysis of a circular patch resonator for adherent cell culture detection
The study of the interaction between electromagnetic waves and matter plays a crucial role in detecting materials under test (MUTs). Recently, radiofrequency (RF) planar resonator probes have been used to characterize MUTs by evaluating their dielectric properties. Many studies proposed these devices as biosensors, especially for dielectric measurement of living cellular suspension or even single cell. However, even though these cellular applications represent a starting point for medical diagnostic improvement, they do not consider cell interaction and adhesion. We proposed a preliminary study to design a circular patch resonator to detect adherent cell cultures in this work. Different configurations comprising a patch smaller, equal and greater than that of a standard culture Petri dish have been analyzed. The simulation results were then compared with the theoretical ones obtained applying the circular microstrip antenna’s empirical equation. Results showed that the simulation outcomes differed from the theoretical ones less than 1.5%. Finally, once the best patch diameter was identified, two other simulation sets were carried out to evaluate the antenna’s sensitivity. In the first set, we simulated the antenna response to four different volumes of culture medium (from 1.50 ml to 6.00 ml), while in the second one, we simulated the antenna response to different levels of C2C12 cell confluence in a fixed volume (1.5 ml) of culture medium. The results showed that the designed probe could discriminate between medium and C2C12 culture cells based on their permittivity change.
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