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使用无支架球形肿瘤微组织进行自动化生产和药物敏感性测试。

Towards automated production and drug sensitivity testing using scaffold-free spherical tumor microtissues.

机构信息

InSphero AG, Zürich, Switzerland.

出版信息

Biotechnol J. 2011 Dec;6(12):1488-96. doi: 10.1002/biot.201100290. Epub 2011 Nov 21.

DOI:10.1002/biot.201100290
PMID:22102438
Abstract

Although the relevance of three-dimensional (3-D) culture has been recognized for years and exploited at an academic level, its translation to industrial applications has been slow. The development of reliable high-throughput technologies is clearly a prerequisite for the industrial implementation of 3-D models. In this study the robustness of spherical microtissue production and drug testing in a 96-well hanging-drop multiwell plate format was assessed on a standard 96-well channel robotic platform. Microtissue models derived from six different cell lines were produced and characterized according to their growth profile and morphology displaying high-density tissue-like reformation and growth over at least 15 days. The colon cancer cell line HCT116 was chosen as a model to assess microtissue-based assay reproducibility. Within three individual production batches the size variations of the produced microtissues were below 5%. Reliability of the microtissue-based assay was tested using two reference compounds, staurosporine and chlorambucil. In four independent drug testings the calculated IC(50) values were benchmarked against 2-D multiwell testings displaying similar consistency. The technology presented here for the automated production of a variety of microtissues for efficacy testing in a standard 96-well format will aid the implementation of more organotypic models at an early time point in the drug discovery process.

摘要

虽然三维(3-D)培养已经得到了多年的认可,并在学术层面得到了应用,但其向工业应用的转化却一直较为缓慢。可靠的高通量技术的发展显然是将 3-D 模型应用于工业的前提。在这项研究中,我们在标准的 96 孔通道机器人平台上评估了在 96 孔悬挂滴板多微孔板格式下进行球形微组织生产和药物测试的稳健性。根据细胞生长曲线和形态学特征,我们从六种不同的细胞系中生产和表征了微组织模型,这些模型显示出高密度的组织样重构和生长,至少持续 15 天。我们选择结肠癌细胞系 HCT116 作为模型来评估基于微组织的测定重现性。在三个独立的生产批次中,所产生的微组织的大小变化均低于 5%。我们使用两种参考化合物,即星形孢菌素和苯丁酸氮芥,测试了基于微组织的测定的可靠性。在四个独立的药物测试中,计算得出的 IC50 值与 2-D 微孔板测试进行了基准比较,显示出相似的一致性。本文介绍的这项技术可用于自动化生产各种微组织,以便在药物发现过程的早期阶段在标准的 96 孔格式中进行功效测试,将有助于更多器官样模型的实施。

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