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High-throughput 3D spheroid culture and drug testing using a 384 hanging drop array

机译:使用384悬滴阵列进行高通量3D球体培养和药物测试

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摘要

Culture of cells as three-dimensional (3D) aggregates can enhance in vitro tests for basic biological research as well as for therapeutics development. Such 3D culture models, however, are often more complicated, cumbersome, and expensive than two-dimensional (2D) cultures. This paper describes a 384-well format hanging drop culture plate that makes spheroid formation, culture, and subsequent drug testing on the obtained 3D cellular constructs as straightforward to perform and adapt to existing high-throughput screening (HTS) instruments as conventional 2D cultures. Using this platform, we show that drugs with different modes of action produce distinct responses in the physiological 3D cell spheroids compared to conventional 2D cell monolayers. Specifically, the anticancer drug 5-fluorouracil (5-FU) has higher anti-proliferative effects on 2D cultures whereas the hypoxia activated drug commonly referred to as tirapazamine (TPZ) are more effective against 3D cultures. The multiplexed 3D hanging drop culture and testing plate provides an efficient way to obtain biological insights that are often lost in 2D platforms.
机译:将细胞培养为三维(3D)聚集体可增强基础生物学研究以及治疗方法开发的体外测试。但是,此类3D文化模型通常比二维(2D)文化更复杂,麻烦且昂贵。本文介绍了一种384孔格式的悬滴培养板,该培养板可对获得的3D细胞构建体进行球体的形成,培养和后续药物测试,与常规2D培养一样,可以直接执行并适应现有的高通量筛选(HTS)仪器。使用该平台,我们显示与传统的2D细胞单层相比,具有不同作用方式的药物在生理3D细胞球体中产生不同的响应。具体而言,抗癌药物5-氟尿嘧啶(5-FU)对2D培养物具有较高的抗增殖作用,而通常称为替拉帕明(TPZ)的低氧激活药物对3D培养物更有效。多重3D悬滴式培养和测试板提供了一种有效的方法来获取通常在2D平台中丢失的生物学见解。

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