Continuous dielectrophoretic bacterial separation and concentration from physiological media of high conductivity

被引:187
作者
Park, Seungkyung [1 ,2 ]
Zhang, Yi [1 ]
Wang, Tza-Huei [1 ,3 ,4 ]
Yang, Samuel [2 ]
机构
[1] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Dept Emergency Med, Baltimore, MD USA
[3] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[4] Johns Hopkins Univ, Dept Mech Engn, Baltimore, MD USA
基金
美国国家科学基金会;
关键词
DIAGNOSTICS; FUTURE; TECHNOLOGIES; PARTICLES; DEVICES; HEALTH; BLOOD; CELLS;
D O I
10.1039/c1lc20307j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Biological sample processing involves purifying target analytes from various sample matrices and concentrating them to a small volume from a large volume of crude sample. This complex process is the major obstacle for developing a microfluidic diagnostic platform. In this study, we present a microfluidic device that can continuously separate and concentrate pathogenic bacterial cells from complex sample matrices such as cerebrospinal fluid and whole blood. Having overcome critical limitations of dielectrophoretic (DEP) operation in physiological media of high conductivity, we utilized target specific DEP techniques to incorporate cell separation, medium exchange, and target concentration into an integrated platform. The proposed microfluidic device can uptake mL volumes of crude biological sample and selectively concentrate target cells into a submicrolitre volume, providing similar to 10(4) fold of concentration. We designed the device based on the electrokinetic theory and electric field simulation, and tested the device performance with different sample types. The separation efficiency of the device was as high as 97.0% for a bead mixture in TAE buffer and 94.3% and 87.2% for E. coli in human cerebrospinal fluid and blood, respectively. A capture efficiency of 100% was achieved in the concentration chamber. With a relatively simple configuration, the proposed device provides a robust method of continuous sample processing, which can be readily integrated into a fully automated microfluidic diagnostic platform for pathogen detection and quantification.
引用
收藏
页码:2893 / 2900
页数:8
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