Zhou Meijun, Urrutia Gomez Joaquin E, Mandsberg Nikolaj K, Liu Sida, Schmidt Sabine, Meier Matthias, Levkin Pavel A, Jahnke Heinz-Georg, Popova Anna
Institute of Biological and Chemical Systems - Functional Molecular Systems (IBCS-FMS), Karlsruhe Institute of Technology, Kaiserstrasse 12, 76131, Karlsruhe, Germany.
Karlsruhe Institute of Technology (KIT), Institute of Automation and Applied Informatics (IAI) Eggenstein-Leopoldshafen, 76344, Karlsruhe, Germany.
Adv Healthc Mater. 2025 Jan;14(3):e2402046. doi: 10.1002/adhm.202402046. Epub 2024 Oct 15.
Label-free real-time monitoring of cellular behavior using impedance spectroscopy is important for drug development and toxicological assessments. Parallelization and miniaturization of such experiments are essential for increasing throughput and enabling experiments with low abundant stem or primary cells. Traditional methods are not miniaturized and require large volumes of reagents and number of cells, limiting their suitability for cost effective high-throughput screening of cells of limited availability. Here, the fabrication, optimization, and application of a bioelectrical signaling monitoring system - electrode droplet microarray (eDMA) are demonstrated. The eDMA platform is based on preparation of a hydrophilic-superhydrophobic patterns covering an array of individually addressable microelectrodes, which confines cells to individual microelectrodes, allowing for parallel, real-time, and label-free detection of cellular responses to drug treatments in nanoliter droplets. The real-time monitoring of cytotoxic effect of an anticancer drug is demonstrated over 48 h with real-time calculation of the half-inhibitory concentration (IC50) values through impedance spectroscopy. This demonstrates eDMA's ability to dynamically assess responses to various drugs in parallel at any given time point, which is crucial for functional personalized oncology. Specifically, the platform can be employed for monitoring anticancer drug toxicity using limited patient samples, where the miniaturization provided by eDMA is essential.
使用阻抗谱对细胞行为进行无标记实时监测对于药物开发和毒理学评估至关重要。此类实验的并行化和小型化对于提高通量以及开展针对低丰度干细胞或原代细胞的实验至关重要。传统方法未实现小型化,需要大量试剂和细胞数量,限制了它们对有限可用细胞进行经济高效高通量筛选的适用性。在此,展示了一种生物电信号监测系统——电极液滴微阵列(eDMA)的制造、优化及应用。eDMA平台基于制备覆盖一系列可单独寻址微电极的亲水 - 超疏水图案,这将细胞限制在各个微电极上,从而能够对纳升级液滴中细胞对药物处理的反应进行并行、实时且无标记检测。通过阻抗谱实时计算半抑制浓度(IC50)值,展示了对一种抗癌药物细胞毒性效应长达48小时的实时监测。这证明了eDMA在任何给定时间点并行动态评估对各种药物反应的能力,这对于功能性个性化肿瘤学至关重要。具体而言,该平台可用于使用有限的患者样本监测抗癌药物毒性,其中eDMA提供的小型化至关重要。