T. Kurakazu, K. Kuribayashi, Y. Tsuda, H. Kimura, T. Fujii, Y. Sakai, S. Takeuchi
{"title":"一种用于电池阵列应用的使用电解产生气泡的选择性释放方法","authors":"T. Kurakazu, K. Kuribayashi, Y. Tsuda, H. Kimura, T. Fujii, Y. Sakai, S. Takeuchi","doi":"10.1109/SENSOR.2009.5285447","DOIUrl":null,"url":null,"abstract":"This paper describes a method of selective release of particles/cells by bubbles generated by electrolysis. The particles/cells trapped into microchambers that were produced with SU-8 on the top of an electrode of indium tin oxide (ITO) patterned on glass. The bubbles of oxygen and chlorine (or hydrogen) were selectively generated in a target chamber by applying voltage through the electrodes. We successfully released a microbead (100 µm in diameter) confined in the microchamber. Since this method is gentle enough to maintain the cellular activity, we believe that this method will be useful for quantitative analysis of cells in a microarray.","PeriodicalId":247826,"journal":{"name":"TRANSDUCERS 2009 - 2009 International Solid-State Sensors, Actuators and Microsystems Conference","volume":"20 5-6","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2009-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A selective release method using electrolytically generated bubbles for cell array applications\",\"authors\":\"T. Kurakazu, K. Kuribayashi, Y. Tsuda, H. Kimura, T. Fujii, Y. Sakai, S. Takeuchi\",\"doi\":\"10.1109/SENSOR.2009.5285447\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This paper describes a method of selective release of particles/cells by bubbles generated by electrolysis. The particles/cells trapped into microchambers that were produced with SU-8 on the top of an electrode of indium tin oxide (ITO) patterned on glass. The bubbles of oxygen and chlorine (or hydrogen) were selectively generated in a target chamber by applying voltage through the electrodes. We successfully released a microbead (100 µm in diameter) confined in the microchamber. Since this method is gentle enough to maintain the cellular activity, we believe that this method will be useful for quantitative analysis of cells in a microarray.\",\"PeriodicalId\":247826,\"journal\":{\"name\":\"TRANSDUCERS 2009 - 2009 International Solid-State Sensors, Actuators and Microsystems Conference\",\"volume\":\"20 5-6\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-06-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"TRANSDUCERS 2009 - 2009 International Solid-State Sensors, Actuators and Microsystems Conference\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/SENSOR.2009.5285447\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"TRANSDUCERS 2009 - 2009 International Solid-State Sensors, Actuators and Microsystems Conference","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/SENSOR.2009.5285447","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A selective release method using electrolytically generated bubbles for cell array applications
This paper describes a method of selective release of particles/cells by bubbles generated by electrolysis. The particles/cells trapped into microchambers that were produced with SU-8 on the top of an electrode of indium tin oxide (ITO) patterned on glass. The bubbles of oxygen and chlorine (or hydrogen) were selectively generated in a target chamber by applying voltage through the electrodes. We successfully released a microbead (100 µm in diameter) confined in the microchamber. Since this method is gentle enough to maintain the cellular activity, we believe that this method will be useful for quantitative analysis of cells in a microarray.