Maskless direct cell patterning by laser writing

J.Y. Cheng, Hsueh-Yi Lee, M. Yen, T. Young
{"title":"Maskless direct cell patterning by laser writing","authors":"J.Y. Cheng, Hsueh-Yi Lee, M. Yen, T. Young","doi":"10.1109/MMB.2006.251550","DOIUrl":null,"url":null,"abstract":"A simple and effective method for patterning cell on glass substrate is reported. A passivation layer that is capable of preventing cell adhesion was first coated onto glass surface. The passivation coatings that were tested include 3-[Bis(2-hydroxyethyl)amino]propyl-triethoxysilane, 3-Aminopropyltriethoxysilane, 1H, 1H, 2H, 2H-Perfluorodecyl-triethoxysilane, 3 -Glycidyloxypropyltriethoxysilane, Octade cyltrimethoxysilane, and Octadecyltrichlorosilane. A CO2 laser and a UV laser were used to remove the passivation layer and define patterns according to user design. Cell arrays and arbitrary pattern were demonstrated. The minimal feature attainable by the CO2 laser is about 100 mum. The minimal feature for reliable cell adhesion is found to be about 25 mum. Cells adhere and grow cleanly in the laser defined pattern. The pattern can be re-designed and fabricated easily and rapidly. Living cell staining by CMFDA and antibody staining for epidermal growth factor receptor (EGFR) detection were successfully performed on the surface bound cells. This method can be very useful for developing drug screening tools that utilize cell-based detection","PeriodicalId":170356,"journal":{"name":"2006 International Conference on Microtechnologies in Medicine and Biology","volume":"39 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2006-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2006 International Conference on Microtechnologies in Medicine and Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/MMB.2006.251550","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

A simple and effective method for patterning cell on glass substrate is reported. A passivation layer that is capable of preventing cell adhesion was first coated onto glass surface. The passivation coatings that were tested include 3-[Bis(2-hydroxyethyl)amino]propyl-triethoxysilane, 3-Aminopropyltriethoxysilane, 1H, 1H, 2H, 2H-Perfluorodecyl-triethoxysilane, 3 -Glycidyloxypropyltriethoxysilane, Octade cyltrimethoxysilane, and Octadecyltrichlorosilane. A CO2 laser and a UV laser were used to remove the passivation layer and define patterns according to user design. Cell arrays and arbitrary pattern were demonstrated. The minimal feature attainable by the CO2 laser is about 100 mum. The minimal feature for reliable cell adhesion is found to be about 25 mum. Cells adhere and grow cleanly in the laser defined pattern. The pattern can be re-designed and fabricated easily and rapidly. Living cell staining by CMFDA and antibody staining for epidermal growth factor receptor (EGFR) detection were successfully performed on the surface bound cells. This method can be very useful for developing drug screening tools that utilize cell-based detection
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
激光书写的无掩模直接细胞图案
本文报道了一种简单有效的在玻璃基板上对电池进行图像化的方法。首先在玻璃表面涂上一层能防止细胞粘附的钝化层。测试的钝化涂层包括3-[双(2-羟乙基)氨基]丙基三乙基氧基硅烷、3-氨基丙基三乙基氧基硅烷、1H、1H、2H、2H-全氟癸基三乙基氧基硅烷、3-缩水氧基氧基三乙基氧基硅烷、八烷基三甲氧基硅烷和十八烷基三氯硅烷。使用CO2激光器和UV激光器去除钝化层并根据用户设计定义图案。证明了细胞阵列和任意模式。CO2激光器可达到的最小特性约为100毫微米。可靠的细胞粘附的最小特征约为25 μ m。细胞在激光定义的模式中粘附和生长干净。该图案可以方便、快速地重新设计和制作。对表面结合细胞进行CMFDA活细胞染色和表皮生长因子受体(EGFR)抗体染色。这种方法对于开发基于细胞检测的药物筛选工具非常有用
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
PDF Not Yet Available In IEEE Xplore Two-Compartments Microbioreactor with Integrated Magnetic Stirrer Pump for Measurement of Transmembrane Transport of Caco-2 Cells 3D Microelectrodes for Coulometric Screening in Microfabricated Lab-on-a-Chip Devices A Silicon-Based Single-Cell Electroporation Microchip for Gene Transfer Adsorption-induced inactivation of heavy meromyosin on polymer surfaces imposes effective drag force on sliding actin filaments in vitro
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1