Automated and Flexible Liquid Manipulation Technique Based on Sequential Operation Droplet Array Str

来源 :第九届全国微全分析系统学术会议、第四届全国微纳尺度生物分离分析学术会议、2014国际微流控芯片与微纳尺度生物分离分析学术 | 被引量 : 0次 | 上传用户:liongliong501
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  In the past 20 years,microfluidic technique has undergone fast progress,and various manipulation techniques for microfluids have been developed,including hydrodynamic,electrokinetic,microvalve/pump,centrifugation,and electrowetting techniques.Despite the successful and broad applications of these techniques,automated and flexible liquid handling techniques with high versatility are still in urgent need.Recently,on the basis of the DropLab system [1],we developed a sequential operation droplet array(SODA)system for performing fully-automated picoliter to nanoliter-scale droplet manipulation,analysis and screening [2].The SODA system has a simple setup consisting of a tapered capillary-syringe pump module and a twodimensional oil-covered droplet array fixed on a x-y-z translational stage [2].An automated liquid handling strategy was developed with the SODA system using the programmable combination of the capillary-based liquid aspirating-depositing and the moving of the oil-covered droplet array,so-called “aspirating-depositing-moving”(ADM)mode.Complex and flexible liquid handling manipulations can be achieved with picoliter-scale precision,including liquid droplet assembling,generation,indexing,transferring,splitting and fusion.We applied the SODA system in screening of inhibitors for capases-1 from a chemical library.The consumptions of samples and reagents are only 60–180 pL for each droplet microreactor,which are commonly 3–5 orders of magnitude lower than those of conventional multi-well plate systems.We also applied the SODA system in cell-based schedule dependent drug combination screening with multi-step operations involving cell culture,medium changing,drug dosage and stimulation,and cell viability testing [3].Most recently,we applied the SODA system in large-scale screening of crystallization conditions of five soluble proteins and one membrane protein with 35–96 different crystallization conditions and droplet reactor volumes of 4–8 nL [4].The protein consumption significantly reduces 50–500 fold compared with current crystallization stations.The SODA systems use the different combination of simple unit operations(ADM)to automatically achieve complex droplet manipulations,which have provided a versatile and flexible platform for picoliter-scale liquid handling,analysis,and screening for multiple different samples.The SODA strategy may also provide a novel liquid manipulation technique for microfluidic systems,besides the previously-reported techniques.
其他文献
目的:利用自制微流控芯片(microchip)结合环介导等温扩增(LAMP)技术检测全血样本中JAK2 V617F基因突变,实现对骨髓增殖性肿瘤的分子诊断.方法:设计LAMP检测JAK2 V617F引物,建立并优化反应体系;检测HEL细胞株中JAK2 V617F突变DNA及野生型DNA,对LAMP扩增产物进行测序及酶切鉴定;LAMP检测JAK2 V617F突变率;设计微流控芯片,采用SU-8光刻胶
To develop the method for separation of epithelial cells and sperm in a microfludic chip,the glass-PDMS chip,which is easy to manufacture,was selected to separation of epithelial cells and sperm.Buffe
Rapid and accurate determination of veterinary drug residues and metabolites in animal tissues is important for human health.The major analytical challenges are extensive interferences with molecules
Glycosylation is one of the most common and complex post-translational modifications in biological systems.Information on glycan heterogeneity is increasingly recognized as crucial to understanding gl
Rapid mixing of high viscosity solutions is crucial for tracking the folding kinetics of macromolecules under molecular crowding conditions.In this paper,we design a three dimensional micromixer for r
量子点(QDs)是近年来发展起来的一种新型半导体纳米发光材料.与传统的有机荧光染料相比,量子点具有吸收光谱宽,发射光谱窄;量子产率高,荧光寿命长,抗漂白性能强等特点.作为一种新型的单分子荧光探针,其广泛应用于化学分析、生物传感、分子成像等领域.本文主要以宽场显微成像技术为主要手段,根据聚合体中各个量子点所表现出的光谱蓝移的不同步性以及漂白的差异性(如图1),来计算团聚体中量子点的个数,从而实现对蛋
A novel solid phase extration technique is described where oxytetracyline is bound and eluted from magnetic molecularly imprinted polymers(MMIPs)in a manner where efficiency is dependent on the magnet
Circulating tumor cells(CTCs)are cancer cells which are slip from either elementary tumor cells or distortional sites.[1] The major cause of death in cancer patients is distant metastasis.Cancer cell
A simple and effective method using capillary force for TiO2 nano particles patterned in microfluidic channel has been demonstrated.Due to the hydroxide groups on the particles surface,specific cancer
Pressure pinched injection can introduce well defined shape of sample plugs into the separation channel1.Proper difference in liquid levels among the reservoirs of a microchip is critical for the succ