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Multi-analyte biosensor interface for real-time monitoring of 3D microtissue spheroids in hanging-drop networks

机译:多分析物生物传感器接口用于实时监测悬挂式网络中的3D微组织球体

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摘要

Microfluidics is becoming a technology of growing interest for building microphysiological systems with integrated read-out functionalities. Here we present the integration of enzyme-based multi-analyte biosensors into a multi-tissue culture platform for ‘body-on-a-chip’ applications. The microfluidic platform is based on the technology of hanging-drop networks, which is designed for the formation, cultivation, and analysis of fluidically interconnected organotypic spherical three-dimensional (3D) microtissues of multiple cell types. The sensor modules were designed as small glass plug-ins featuring four platinum working electrodes, a platinum counter electrode, and an Ag/AgCl reference electrode. They were placed directly into the ceiling substrate from which the hanging drops that host the spheroid cultures are suspended. The electrodes were functionalized with oxidase enzymes to enable continuous monitoring of lactate and glucose through amperometry. The biosensors featured high sensitivities of 322±41 nA mM−1 mm−2 for glucose and 443±37 nA mM−1 mm−2 for lactate; the corresponding limits of detection were below 10 μM. The proposed technology enabled tissue-size-dependent, real-time detection of lactate secretion from single human colon cancer microtissues cultured in the hanging drops. Furthermore, glucose consumption and lactate secretion were monitored in parallel, and the impact of different culture conditions on the metabolism of cancer microtissues was recorded in real-time.
机译:微流体技术正在成为构建具有集成读出功能的微生理系统的兴趣所在。在这里,我们介绍了基于酶的多分析物生物传感器到“单芯片”应用的多组织培养平台中的集成。微流体平台基于悬挂式网络技术,该技术旨在用于多种细胞类型的流体互连有机型球形三维(3D)微组织的形成,培养和分析。传感器模块设计为小型玻璃插件,具有四个铂工作电极,一个铂对电极和一个Ag / AgCl参比电极。将它们直接置于天花板基质中,宿主球状培养物的悬滴从中悬浮下来。电极被氧化酶功能化,从而能够通过安培法连续监测乳酸和葡萄糖。该生物传感器对葡萄糖具有322±41 nA mM −1 mm −2 的高灵敏度,并具有443±37 nA mM -1 mm −2 表示乳酸;相应的检出限在10μm以下。所提出的技术使组织大小依赖性的实时检测悬滴培养的单个人结肠癌微组织中的乳酸分泌成为可能。此外,同时监测葡萄糖消耗和乳酸分泌,并实时记录不同培养条件对癌症微组织代谢的影响。

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