类有机物
药物发现
个性化医疗
药品
诱导多能干细胞
人脑
多电极阵列
神经科学
药物反应
精密医学
电生理学
计算生物学
药物开发
医学
药理学
计算机科学
功效
药物
高含量筛选
微电极
生物
人体生理学
微流控
HEK 293细胞
毒品检测
微流控芯片
脑病
生物信息学
切片制备
脑功能
药物治疗
生物医学工程
电池类型
作者
Hyogeun Shin,Yeonjoo An,Ju‐Hyun Lee,Ji Hun Kim,Renuka Prasad,Keun‐Tae Kim,Hoon‐Chul Kang,Woong Sun,Seung‐Woo Cho,Il‐Joo Cho
标识
DOI:10.1002/advs.202504913
摘要
Human-induced pluripotent stem cell (iPSC)-derived brain organoids have attracted significant attention as promising models for drug screening owing to their remarkable resemblance to the human brain. The advent of disease model organoids, derived from patient's cells, has further elevated expectations for drug screening and personalized medicine. Nevertheless, the absence of a comprehensive platform for administering drugs and assessing their efficacy based on functional changes in brain organoids has remained a challenge. In this study, we introduce a one-step drug screening system designed designed to investigate functional changes induced by diverse drug doses in multiple brain organoids, utilizing electrophysiological signal measurements. Our system comprises a specialized culture chamber with a microfluidic chip capable of accommodating 10 organoids and delivering varying doses of two drugs to each organoid. Additionally, we integrate a three dimentional microelectrode array (3D MEA) with ten shanks, enabling functional assessment of 10 brain organoids. This approach facilitates dose-dependent drug screening across multiple organoids. We demonstrate the effectiveness of our system through real-time analysis of neural activity changes triggered by different doses of pottassium chloride (KCl). Furthermore, sodium channel protein type 2 subunit alpha (SCN2A)-epileptic organoids to demonstrate utility in disease-model-based drug screening. Our platform enables functional screening and personalized medicine using brain organoids.
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