Digital Microfluidic Magnetic Separation for Particle-Based Immunoassays

被引:162
作者
Ng, Alphonsus H. C. [1 ,3 ]
Choi, Kihwan [2 ,3 ]
Luoma, Robert P. [4 ]
Robinson, John M. [5 ]
Wheeler, Aaron R. [1 ,2 ,3 ]
机构
[1] Univ Toronto, Inst Biomat & Biomed Engn, Toronto, ON M5S 3G9, Canada
[2] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
[3] Donnelly Ctr Cellular & Biomol Res, Toronto, ON M5S 3E1, Canada
[4] Abbott Diagnost, Irving, TX 75038 USA
[5] Abbott Diagnost, Abbott Pk, IL 60064 USA
基金
加拿大自然科学与工程研究理事会;
关键词
ELECTROWETTING-BASED ACTUATION; PLURONIC ADDITIVES; DROPLETS; PLATFORM; ELISA;
D O I
10.1021/ac3020627
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We introduce a new format for particle-based immunoassays relying on digital microfluidics (DMP) and magnetic forces to separate and resuspend antibody-coated paramagnetic particles. In DMF, fluids are electrostatically controlled as discrete droplets (picoliters to microliters) on an array of insulated electrodes. By applying appropriate sequences of potentials to these electrodes, multiple droplets can be manipulated simultaneously and various droplet operations can be achieved using the same device design. This flexibility makes DMF well-suited for applications that require complex, multistep protocols such as immunoassays. Here, we report the first particle-based immunoassay on DMF without the aid of oil carrier fluid to enable droplet movement (i.e., droplets are surrounded by air instead of oil). This new format allowed the realization of a novel on-chip particle separation and resuspension method capable of removing greater than 90% of unbound reagents in one step. Using this technique, we developed methods for noncompetitive and competitive immunoassays, using thyroid stimulating hormone (TSH) and 17 beta-estradiol (E2) as model analytes, respectively. We show that, compared to conventional methods, the new DMF approach reported here reduced reagent volumes and analysis time by 100-fold and 10-fold, respectively, while retaining a level of analytical performance required for clinical screening. Thus, we propose that the new technique has great potential for eventual use in a fast, low-waste, and inexpensive instrument for the quantitative analysis of proteins and small molecules in low sample volumes.
引用
收藏
页码:8805 / 8812
页数:8
相关论文
共 42 条
[1]   The Digital Revolution: A New Paradigm for Microfluidics [J].
Abdelgawad, Mohamed ;
Wheeler, Aaron R. .
ADVANCED MATERIALS, 2009, 21 (08) :920-925
[2]   Three-Dimensional Magnetic Focusing of Superparamagnetic Beads for On-Chip Agglutination Assays [J].
Afshar, R. ;
Moser, Y. ;
Lehnert, T. ;
Gijs, M. A. M. .
ANALYTICAL CHEMISTRY, 2011, 83 (03) :1022-1029
[3]   A New Angle on Pluronic Additives: Advancing Droplets and Understanding in Digital Microfluidics [J].
Au, Sam H. ;
Kumar, Paresh ;
Wheeler, Aaron R. .
LANGMUIR, 2011, 27 (13) :8586-8594
[4]   A microfluidic platform for complete mammalian cell culture [J].
Barbulovic-Nad, Irena ;
Au, Sam H. ;
Wheeler, Aaron R. .
LAB ON A CHIP, 2010, 10 (12) :1536-1542
[5]   The clinical significance of subclinical thyroid dysfunction [J].
Biondi, Bernadette ;
Cooper, David S. .
ENDOCRINE REVIEWS, 2008, 29 (01) :76-131
[6]   Creating, transporting, cutting, and merging liquid droplets by electrowetting-based actuation for digital microfluidic circuits [J].
Cho, SK ;
Moon, HJ ;
Kim, CJ .
JOURNAL OF MICROELECTROMECHANICAL SYSTEMS, 2003, 12 (01) :70-80
[7]   Digital Microfluidics [J].
Choi, Kihwan ;
Ng, Alphonsus H. C. ;
Fobel, Ryan ;
Wheeler, Aaron R. .
ANNUAL REVIEW OF ANALYTICAL CHEMISTRY, VOL 5, 2012, 5 :413-440
[8]   Digital microfluidics: is a true lab-on-a-chip possible? [J].
Fair, R. B. .
MICROFLUIDICS AND NANOFLUIDICS, 2007, 3 (03) :245-281
[9]   Microfluidic Applications of Magnetic Particles for Biological Analysis and Catalysis [J].
Gijs, Martin A. M. ;
Lacharme, Frederic ;
Lehmann, Ulrike .
CHEMICAL REVIEWS, 2010, 110 (03) :1518-1563
[10]   Least detectable concentration and dynamic range of three immunoassay systems using the same antibody [J].
Glass, Thomas R. ;
Ohmura, Naoya ;
Saiki, Hiroshi .
ANALYTICAL CHEMISTRY, 2007, 79 (05) :1954-1960