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在微腔芯片上捕获的3D体外组织上进行药物测试。

Drug testing on 3D in vitro tissues trapped on a microcavity chip.

作者信息

Kloss Daniel, Fischer Michael, Rothermel Andrée, Simon Jan C, Robitzki Andrea A

机构信息

Center for Biotechnology and Biomedicine (BBZ), University of Leipzig, Division of Molecular Biological-Biochemical Processing Technology, Deutscher Platz 5, 04103, Leipzig, Germany.

出版信息

Lab Chip. 2008 Jun;8(6):879-84. doi: 10.1039/b800394g. Epub 2008 Apr 11.

Abstract

Close to realistic responses to anti-cancer drugs are not adequately provided in monolayer or single cells assays. 3-dimensional multicellular cultures (spheroids) mimicking in vivo-like conditions are established as cell biological models for microtumors/metastases. For a non-invasive real-time monitoring of the electrical parameters of such spheroid cultures we designed, fabricated and tested a 3D multifunctional electrode-based microcavity array. In a non-adherent assay acute tests with tumor spheroids were done maintaining their spherical shape and cellular arrangement. The sensor chip with 15 individual square microcavities containing four gold electrodes each was used for impedance spectroscopy to analyze the tissue models in terms of morphological and structural changes. Cell type specific differences in the spectra and varying responses to several anti-tumor drugs were found. Further development of the prototype will provide a promising tool for the use in pharmacological high-throughput studies.

摘要

单层或单细胞分析无法充分提供接近抗癌药物实际反应的结果。模拟体内样条件的三维多细胞培养物(球体)被确立为微肿瘤/转移灶的细胞生物学模型。为了对这种球体培养物的电学参数进行非侵入性实时监测,我们设计、制造并测试了一种基于三维多功能电极的微腔阵列。在非贴壁分析中,对肿瘤球体进行了急性测试,保持其球形形状和细胞排列。具有15个独立方形微腔、每个微腔包含四个金电极的传感器芯片用于阻抗谱分析,以根据形态和结构变化来分析组织模型。发现了光谱中的细胞类型特异性差异以及对几种抗肿瘤药物的不同反应。该原型的进一步开发将为药理学高通量研究提供一个有前景的工具。

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