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
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