N. M. Fuad, J. Skommer, Timo Friedrich, J. Kaslin, D. Wlodkowic
{"title":"An integrated micromechanical large particle in flow sorter (MILPIS)","authors":"N. M. Fuad, J. Skommer, Timo Friedrich, J. Kaslin, D. Wlodkowic","doi":"10.1117/12.2180691","DOIUrl":null,"url":null,"abstract":"At present, the major hurdle to widespread deployment of zebrafish embryo and larvae in large-scale drug development projects is lack of enabling high-throughput analytical platforms. In order to spearhead drug discovery with the use of zebrafish as a model, platforms need to integrate automated pre-test sorting of organisms (to ensure quality control and standardization) and their in-test positioning (suitable for high-content imaging) with modules for flexible drug delivery. The major obstacle hampering sorting of millimetre sized particles such as zebrafish embryos on chip-based devices is their substantial diameter (above one millimetre), mass (above one milligram), which both lead to rapid gravitational-induced sedimentation and high inertial forces. Manual procedures associated with sorting hundreds of embryos are very monotonous and as such prone to significant analytical errors due to operator’s fatigue. In this work, we present an innovative design of a micromechanical large particle in-flow sorter (MILPIS) capable of analysing, sorting and dispensing living zebrafish embryos for drug discovery applications. The system consisted of a microfluidic network, revolving micromechanical receptacle actuated by robotic servomotor and opto-electronic sensing module. The prototypes were fabricated in poly(methyl methacrylate) (PMMA) transparent thermoplastic using infrared laser micromachining. Elements of MILPIS were also fabricated in an optically transparent VisiJet resin using 3D stereolithography (SLA) processes (ProJet 7000HD, 3D Systems). The device operation was based on a rapidly revolving miniaturized mechanical receptacle. The latter function was to hold and position individual fish embryos for (i) interrogation, (ii) sorting decision-making and (iii) physical sorting..The system was designed to separate between fertilized (LIVE) and non-fertilized (DEAD) eggs, based on optical transparency using infrared (IR) emitters and receivers embedded in the system. Digital oscilloscope were used to distinguish the diffraction signals from IR sensors when both LIVE and DEAD embryos were flow through in the chip. Image process analysis were also used as detection module to track DEAD embryos as it flowed in the channel.","PeriodicalId":232941,"journal":{"name":"Microtechnologies for the New Millennium","volume":"77 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microtechnologies for the New Millennium","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1117/12.2180691","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
At present, the major hurdle to widespread deployment of zebrafish embryo and larvae in large-scale drug development projects is lack of enabling high-throughput analytical platforms. In order to spearhead drug discovery with the use of zebrafish as a model, platforms need to integrate automated pre-test sorting of organisms (to ensure quality control and standardization) and their in-test positioning (suitable for high-content imaging) with modules for flexible drug delivery. The major obstacle hampering sorting of millimetre sized particles such as zebrafish embryos on chip-based devices is their substantial diameter (above one millimetre), mass (above one milligram), which both lead to rapid gravitational-induced sedimentation and high inertial forces. Manual procedures associated with sorting hundreds of embryos are very monotonous and as such prone to significant analytical errors due to operator’s fatigue. In this work, we present an innovative design of a micromechanical large particle in-flow sorter (MILPIS) capable of analysing, sorting and dispensing living zebrafish embryos for drug discovery applications. The system consisted of a microfluidic network, revolving micromechanical receptacle actuated by robotic servomotor and opto-electronic sensing module. The prototypes were fabricated in poly(methyl methacrylate) (PMMA) transparent thermoplastic using infrared laser micromachining. Elements of MILPIS were also fabricated in an optically transparent VisiJet resin using 3D stereolithography (SLA) processes (ProJet 7000HD, 3D Systems). The device operation was based on a rapidly revolving miniaturized mechanical receptacle. The latter function was to hold and position individual fish embryos for (i) interrogation, (ii) sorting decision-making and (iii) physical sorting..The system was designed to separate between fertilized (LIVE) and non-fertilized (DEAD) eggs, based on optical transparency using infrared (IR) emitters and receivers embedded in the system. Digital oscilloscope were used to distinguish the diffraction signals from IR sensors when both LIVE and DEAD embryos were flow through in the chip. Image process analysis were also used as detection module to track DEAD embryos as it flowed in the channel.
目前,在大规模药物开发项目中广泛部署斑马鱼胚胎和幼虫的主要障碍是缺乏高通量的分析平台。为了以斑马鱼为模型率先进行药物发现,平台需要将生物的自动测试前分选(以确保质量控制和标准化)及其测试中定位(适用于高含量成像)与灵活的药物输送模块集成在一起。在基于芯片的设备上分选毫米大小的颗粒(如斑马鱼胚胎)的主要障碍是它们的巨大直径(超过1毫米)和质量(超过1毫克),这两者都会导致重力引起的快速沉降和高惯惯力。与数百个胚胎分选相关的人工程序非常单调,并且由于操作人员的疲劳,因此容易产生重大的分析错误。在这项工作中,我们提出了一种创新设计的微机械大颗粒流分选器(MILPIS),能够分析、分选和分配活斑马鱼胚胎,用于药物发现应用。该系统由微流控网络、由机器人伺服电机驱动的旋转微机械容器和光电传感模块组成。采用红外激光微加工技术在聚甲基丙烯酸甲酯(PMMA)透明热塑性塑料中制备了原型。MILPIS的元件也使用3D立体光刻(SLA)工艺(ProJet 7000HD, 3D Systems)在光学透明的VisiJet树脂中制造。该装置的操作是基于一个快速旋转的小型机械容器。后一种功能是保存和定位单个鱼胚胎,用于(i)询问,(ii)分类决策和(iii)物理分类。该系统设计用于区分受精卵(活)和未受精卵(死),基于光学透明度,使用嵌入系统的红外(IR)发射器和接收器。当活胚胎和死胚胎在芯片中流过时,用数字示波器区分红外传感器发出的衍射信号。图像处理分析也被用作检测模块,以跟踪在通道中流动的死亡胚胎。