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首页> 外文期刊>RSC Advances >Efficient cell capture in an agarose–PDMS hybrid chip for shaped 2D culture under temozolomide stimulation
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Efficient cell capture in an agarose–PDMS hybrid chip for shaped 2D culture under temozolomide stimulation

机译:在替替莫唑胺刺激下,在琼脂糖-PDMS杂交芯片中捕获的高效细胞捕获

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In this work, hybrid microfluidic devices were fabricated by assembling a polydimethylsiloxane (PDMS) mold with an agarose microarray to realize cell capture and patterning in precisely controlled spatial distribution. Microwells with diameter varying from 15 to 30 μm were formed on the agarose hydrogel surface at 15 μm to 40 μm spacing. Cells were efficiently captured in microwells with nearly 100% occupancy, thus achieving cell manipulation in a semi-quantitative manner. The size of the cell population captured on the microwell array is proportional to the patterning area. Further study revealed that the capture process was mainly regulated by fluid dynamics, where liquid was absorbed by the highly permeable agarose substrate and carried target cells into microwells. Our method spared the complex chemical modification steps, and the agarose substrate promised good biocompatibility. By designing PDMS channels with different geometrical layouts, various cell patterning geometries were easily created. Cell culture models with controllable pattern area and population size were successfully developed for a temozolomide stimulation study for as long as 2 days. This work should benefit the study of cancer developing niche and provide a powerful platform for the direct and continuous observation of cell dynamics under drug stimulation.
机译:在这项工作中,通过用琼脂糖微阵列组装聚二甲基硅氧烷(PDMS)模具来制造杂化微流体装置,以实现细胞捕获和在精确控制的空间分布中进行图案化。在15μm至40μm间距的琼脂糖水凝胶表面上形成具有15至30μm的直径从15至30μm的微孔。细胞在微孔中有效地捕获,近100%占用,从而以半定量方式实现细胞操纵。在微孔阵列上捕获的细胞群的大小与图案化区域成比例。进一步的研究表明,捕获过程主要由流体动力学调节,其中液体被高度渗透的琼脂糖基质吸收并将靶细胞携带成微孔。我们的方法使复杂的化学改性步骤施加,琼脂糖基质承诺良好的生物相容性。通过设计具有不同几何布局的PDMS通道,容易创建各种细胞图案化几何形状。具有可控图案区域和群体规模的细胞培养模型对于替代粒衍生刺激研究成功开发,只需2天即可。这项工作应该有益于癌症发展利基的研究,并为药物刺激下的直接和连续观察细胞动力学提供强大的平台。

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