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用于量子胞吐测量的细胞对氮掺杂类金刚石碳(DLC:N)的优先附着。

Preferential cell attachment to nitrogen-doped diamond-like carbon (DLC:N) for the measurement of quantal exocytosis.

作者信息

Sen Atanu, Barizuddin Syed, Hossain Maruf, Polo-Parada Luis, Gillis Kevin D, Gangopadhyay Shubhra

机构信息

Department of Biological Engineering, University of Missouri-Columbia, Columbia, MO 65211, USA.

出版信息

Biomaterials. 2009 Mar;30(8):1604-12. doi: 10.1016/j.biomaterials.2008.11.039. Epub 2009 Jan 4.

Abstract

Electrochemical measurement of transmitter or hormone release from individual cells on microchips has applications both in basic science and drug screening. High-resolution measurement of quantal exocytosis requires the working electrode to be small (cell-sized) and located in immediate proximity to the cell. We examined the ability of candidate electrode materials to promote the attachment of two hormone-secreting cell types as a mechanism for targeting cells for to recording electrodes with high precision. We found that nitrogen-doped diamond-like carbon (DLC:N) promoted cell attachment relative to other materials tested in the rank order of DLC:N>In(2)O(3)/SnO(2) (ITO), Pt>Au. In addition, we found that treating candidate electrode materials with polylysine did not increase attachment of chromaffin cells to DLC:N, but promoted cell attachment to the other tested materials. We found that hormone-secreting cells did not attach readily to Teflon AF as a potential insulating material, and demonstrated that patterning of Teflon AF leads to selective cell targeting to DLC:N "docking sites". These results will guide the design of the next generation of biochips for automated and high-throughput measurement of quantal exocytosis.

摘要

在微芯片上对单个细胞释放递质或激素进行电化学测量在基础科学和药物筛选方面都有应用。对量子性胞吐作用进行高分辨率测量要求工作电极尺寸小(细胞大小)且紧邻细胞放置。我们研究了候选电极材料促进两种激素分泌细胞类型附着的能力,以此作为将细胞高精度靶向记录电极的一种机制。我们发现,相对于测试的其他材料,氮掺杂类金刚石碳(DLC:N)促进细胞附着的能力按以下顺序排列:DLC:N>In(2)O(3)/SnO(2)(ITO)、Pt>Au。此外,我们发现用聚赖氨酸处理候选电极材料不会增加嗜铬细胞对DLC:N的附着,但会促进细胞对其他测试材料的附着。我们发现,作为一种潜在的绝缘材料,激素分泌细胞不容易附着在聚四氟乙烯AF上,并证明聚四氟乙烯AF的图案化会导致细胞选择性地靶向DLC:N“对接位点”。这些结果将指导下一代生物芯片的设计,用于对量子性胞吐作用进行自动化和高通量测量。

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