S. Nomura, Li Liu, Yong Chen, H. Maruyama, F. Arai
{"title":"Giant liposome sorting/collection device: For individual analysis of artificial cell-models","authors":"S. Nomura, Li Liu, Yong Chen, H. Maruyama, F. Arai","doi":"10.1109/MHS.2009.5352048","DOIUrl":null,"url":null,"abstract":"In this report, we will present a novel liposome handling method on microfluidic channel. For the quantitative analysis of individual giant liposomes, a microfluidic device with multi-pillar was designed. Liposomes suspension from neutral phospholipids prepared by natural swelling method was introduced into the separation device. As a result, giant liposomes are safely trapped in the microscope viewfield along with the internal pillar within a weak flow. In the condition, small solutes (excess dye molecules, small liposomes) are washed away through the pillars. This system should be useful for time-course analysis of individual cell-sized liposomes.","PeriodicalId":344667,"journal":{"name":"2009 International Symposium on Micro-NanoMechatronics and Human Science","volume":"5 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2009-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2009 International Symposium on Micro-NanoMechatronics and Human Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/MHS.2009.5352048","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
In this report, we will present a novel liposome handling method on microfluidic channel. For the quantitative analysis of individual giant liposomes, a microfluidic device with multi-pillar was designed. Liposomes suspension from neutral phospholipids prepared by natural swelling method was introduced into the separation device. As a result, giant liposomes are safely trapped in the microscope viewfield along with the internal pillar within a weak flow. In the condition, small solutes (excess dye molecules, small liposomes) are washed away through the pillars. This system should be useful for time-course analysis of individual cell-sized liposomes.