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Non-positional cell microarray prepared by shape-coded polymeric microboards: A new microarray format for multiplex and high throughput cell-based assays

机译:由形状编码的聚合物微板制备的非定位细胞微阵列:一种用于多重和高通量基于细胞的测定的新微阵列格式

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摘要

A non-positional (or suspension) cell microarray was developed using shape-coded SU-8 photoresist microboards for potential application in multiplex and high-throughput cell-based assays. A conventional photolithography process on glass slides produced various shapes of SU-8 micropatterns that had a lateral dimension of 200 μm and a thickness of 40 μm. The resultant micropatterns were detached from the slides by sonication and named “microboards” due to the fact that had a much larger lateral dimension than thickness. The surfaces of the SU-8 microboards were modified with collagen to promote cell adhesion, and it was confirmed that collagen-coated SU-8 microboards supported cell adhesion and proliferation. Seeding of cells into poly(ethylene glycol)(PEG) hydrogel-coated well plates containing collagen-modified microboards resulted in selective cell adhesion onto the microboards due to the non-adhesiveness of PEG hydrogel toward cells, thereby creating non-positional arrays of microboards carrying cells. Finally, two different cell types (fibroblasts and HeLa cells) were separately cultured on different shapes of microboards and subsequently mixed together to create a non-positional cell microarray consisting of multiple cell types where each cell could be easily identified by the shape of the microboard to which they had adhered. Because numerous unique shapes of microboards can be fabricated using this method by simply changing the photomask designs, high throughput and multiplex cell-based assays would be easily achieved with this system in the future.
机译:使用形状编码的SU-8光刻胶微板开发了非位置(或悬浮)细胞微阵列,可潜在地用于基于多重和高通量细胞的测定中。在载玻片上的常规光刻工艺产生了各种形状的SU-8微图案,其横向尺寸为200μm,厚度为40μm。由于其横向尺寸比厚度大得多的事实,通过超声处理将所得的微图案从载玻片上分离,并命名为“微板”。 SU-8微板的表面经过胶原蛋白修饰,以促进细胞粘附,并且可以确定,胶原蛋白涂覆的SU-8微板支持细胞粘附和增殖。将细胞接种到含有胶原蛋白修饰的微板的聚(乙二醇)(PEG)水凝胶涂层的孔板上,由于PEG水凝胶对细胞的非粘附性,导致细胞选择性粘附在微板上,从而形成微板的非定位阵列携带细胞。最后,将两种不同的细胞类型(成纤维细胞和HeLa细胞)分别培养在不同形状的微板上,然后混合在一起以创建由多种细胞类型组成的非定位细胞微阵列,其中每个细胞都可以通过微板的形状轻松识别他们所坚持的。由于可以通过简单地改变光掩模的设计,使用这种方法制造出许多独特形状的微板,因此将来使用该系统可以轻松实现高通量和基于多细胞的检测。

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