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使用可移动细胞捕获屏障的多细胞球体形成和提取芯片。

A multicellular spheroid formation and extraction chip using removable cell trapping barriers.

机构信息

Cell Bench Research Center, KAIST, 373-1 Guseong-dong, Yuseong-gu, Daejeon, Republic of Korea 305-701.

出版信息

Lab Chip. 2011 Jan 7;11(1):115-9. doi: 10.1039/c0lc00134a. Epub 2010 Nov 1.

Abstract

This paper presents a multicellular spheroid chip capable of forming and extracting three-dimensional (3D) spheroids using removable cell trapping barriers. Compared to the conventional macro-scale spheroid formation methods, including spinning, hanging-drop, and liquid-overlay methods, the recent micro-scale spheroid chips have the advantage of forming smaller spheroids with better uniformity. The recent micro spheroid chips, however, have difficulties in extracting the spheroids due to fixed cell trapping barriers. The present spheroid chip, having two PDMS layers, uses removable cell trapping barriers, thereby making it easy to form and extract uniform and small-sized spheroids. We have designed, fabricated and characterized a 4 × 1 spheroid chip, where membrane cell trapping barriers are inflated at a pressure of 50 kPa for spheroid formation and are deflated at zero gauge pressure for simple and safe extraction of the spheroids formed. In this experimental study, the cell suspension of non-small lung cancer cells, H1650, is supplied to the fabricated spheroid chip in the pressure range 145-155 Pa. The fabricated spheroid chips collect the cancer cells in the cell trapping regions from the cell suspension at a concentration of 2 × 10(6) ml(-1), thus forming uniform 3D spheroids with a diameter of 197.2 ± 11.7 μm, after 24 h incubation at 5% CO(2) and 37°C environment. After the removal of the cell trapping barriers, the spheroids formed were extracted through the outlet ports at a cell inlet pressure of 5 kPa. The cells in the extracted spheroids showed a viability of 80.3 ± 7.7%. The present spheroid chip offers a simple and effective method of obtaining uniform and small-sized 3D spheroids for the next stage of cell-based biomedical research, such as gene expression analysis and spheroid inoculation in animal models.

摘要

本文提出了一种使用可移动细胞捕获障碍形成和提取三维(3D)球体的多细胞球体芯片。与传统的宏观球体形成方法(包括旋转、悬滴和液滴覆盖方法)相比,最近的微尺度球体芯片具有形成更小、更均匀球体的优势。然而,最近的微球体芯片由于固定的细胞捕获障碍而难以提取球体。本研究提出的球体芯片具有两个 PDMS 层,使用可移动的细胞捕获障碍,从而可以轻松形成和提取均匀且小尺寸的球体。我们设计、制造并对 4×1 球体芯片进行了特征描述,其中膜细胞捕获障碍在 50 kPa 的压力下膨胀以形成球体,在零表压下放气以简单且安全地提取形成的球体。在这项实验研究中,非小细胞肺癌细胞 H1650 的细胞悬浮液在 145-155 Pa 的压力范围内供应到制造的球体芯片中。制造的球体芯片将细胞悬浮液中的癌细胞收集到细胞捕获区域,浓度为 2×10(6)ml(-1),然后在 5% CO(2)和 37°C 环境下孵育 24 h 后形成直径为 197.2±11.7μm 的均匀 3D 球体。在去除细胞捕获障碍后,通过入口压力为 5 kPa 的出口端口提取形成的球体。提取的球体中的细胞显示出 80.3±7.7%的活力。本研究提出的球体芯片为基于细胞的生物医学研究的下一阶段提供了一种简单有效的获得均匀且小尺寸 3D 球体的方法,例如基因表达分析和动物模型中的球体接种。

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