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聚二甲基硅氧烷微通道中接枝聚 N-异丙基丙烯酰胺的温敏细胞培养/收获。

Thermomodulated cell culture∕harvest in polydimethylsiloxane microchannels with poly(N-isopropylacrylamide)-grafted surface.

机构信息

Department of Chemistry, The Institute of Micro-analytical Systems, Zhejiang University, Zijin'gang Campus, Hangzhou 310058, China.

出版信息

Biomicrofluidics. 2010 Nov 19;4(4):44107. doi: 10.1063/1.3516038.

DOI:10.1063/1.3516038
PMID:21151579
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3000856/
Abstract

Cell culture and harvest are the most upstream operation for a completely integrated cell assay chip. In our previous work, thermoresponsive poly(N-isopropylacrylamide) (PNIPAAm) was successfully grafted onto polydimethylsiloxane (PDMS) surface via benzophenone-initiated photopolymerization. In the present work, the PNIPAAm-grafted-PDMS (PNIPAAm-g-PDMS) surface was explored for thermomodulated cell culture and noninvasive harvest in microfluidic channels. Using COS 7 fibroblast from African green monkey kidney as the model cells, the thermomodulated adhering and detaching behaviors of the cells on the PNIPAAm-g-PDMS surfaces were optimized with respect to PNIPAAm-grafting yields and gelatin modification. The viability of the cells cultured on and harvested from the PNIPAAm-g-PDMS surface with the thermomodulated noninvasive protocol was estimated against the traditional cell culture∕harvest method involving trypsin digestion. The configuration of the microchannel on the PNIPAAm-g-PDMS chip was evaluated for static cell culture. Using a pipette-shaped PNIPAAm-g-PDMS microchannel, long-term cell culture could be achieved at 37 °C with periodic change of the culture medium every 12 h. After moving the microchip from the incubator set at 37 °C to the room temperature, the proliferated cells could be spontaneously detached from the PNIPAAm-g-PDMS surface of the upstream chamber and transferred by a gentle fluid flow to the downstream chamber, wherein the transferred cells could be subcultured. The thermomodulated cell culture, harvest, and passage operations on the PNIPAAm-g-PDMS microfluidic channels were demonstrated.

摘要

细胞培养和收获是完全集成的细胞分析芯片最上游的操作。在我们之前的工作中,通过苯甲酮引发的光聚合成功地将温敏性聚(N-异丙基丙烯酰胺)(PNIPAAm)接枝到聚二甲基硅氧烷(PDMS)表面上。在本工作中,探索了 PNIPAAm 接枝 PDMS(PNIPAAm-g-PDMS)表面用于微流控通道中的热调节细胞培养和非侵入式收获。使用来自非洲绿猴肾的 COS 7 成纤维细胞作为模型细胞,优化了细胞在 PNIPAAm-g-PDMS 表面上的热调节粘附和脱落行为,具体取决于 PNIPAAm 接枝产率和明胶修饰。使用传统的细胞培养∕收获方法(涉及胰蛋白酶消化),评估了根据热调节非侵入性方案在 PNIPAAm-g-PDMS 表面上培养和收获的细胞的活力。评估了 PNIPAAm-g-PDMS 芯片上微通道的配置用于静态细胞培养。使用管形 PNIPAAm-g-PDMS 微通道,可以在 37°C 下进行长期细胞培养,每隔 12 小时周期性地更换培养基。将微芯片从设置在 37°C 的孵育器移动到室温后,增殖的细胞可以从上游腔室的 PNIPAAm-g-PDMS 表面自动脱落,并通过温和的流体流转移到下游腔室,其中转移的细胞可以进行传代培养。在 PNIPAAm-g-PDMS 微流控通道上演示了热调节细胞培养、收获和传代操作。