Centrifugo-Magnetophoretic Purification of CD4+Cells from Whole Blood Toward Future HIV/AIDS Point-of-Care Applications

被引:31
作者
Glynn, Macdara [1 ]
Kirby, Daniel [1 ]
Chung, Danielle [1 ]
Kinahan, David J. [1 ]
Kijanka, Gregor [1 ]
Ducree, Jens [1 ]
机构
[1] Dublin City Univ, Sch Phys Sci, Biomed Diagnost Inst, Natl Ctr Sensor Res, Dublin 9, Ireland
来源
JALA | 2014年 / 19卷 / 03期
基金
爱尔兰科学基金会;
关键词
centrifugal microfluidics; lab-on-a-disc; cell separation; cell purification; HIV; AIDS diagnostics; RESOURCE-POOR SETTINGS; DIAGNOSIS; CHIP; ENUMERATION; CAPTURE; CELLS; CD4;
D O I
10.1177/2211068213504759
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In medical diagnostics, detection of cells exhibiting specific phenotypes constitutes a paramount challenge. Detection technology must ensure efficient isolation of (often rare) targets while eliminating nontarget background cells. Technologies exist for such investigations, but many require high levels of expertise, expense, and multistep protocols. Increasing automation, miniaturization, and availability of such technologies is an aim of microfluidic lab-on-a-chip strategies. To this end, we present an integrated, dual-force cellular separation strategy using centrifugo-magnetophoresis. Whole blood spiked with target cells is incubated with (super-)paramagnetic microparticles that specifically bind phenotypic markers on target cells. Under rotation, all cells sediment into a chamber located opposite a co-rotating magnet. Unbound cells follow the radial vector, but under the additional attraction of the lateral magnetic field, bead-bound target cells are deflected to a designated reservoir. This multiforce separation is continuous and low loss. We demonstrate separation efficiently up to 92% for cells expressing the HIV/AIDS relevant epitope (CD4) from whole blood. Such highly selective separation systems may be deployed for accurate diagnostic cell isolations from biological samples such as blood. Furthermore, this high efficiency is delivered in a cheap and simple device, thus making it an attractive option for future deployment in resource-limited settings.
引用
收藏
页码:285 / 296
页数:12
相关论文
共 35 条
[1]   Point-of-care testing [J].
Anderson D.A. ;
Crowe S.M. ;
Garcia M. .
Current HIV/AIDS Reports, 2011, 8 (1) :31-37
[2]  
[Anonymous], 2009, Rapid Advice: Antiretroviral Therapy for HIV Infection in Adults and Adolescents
[3]  
Boettcher Michael, 2006, Biophysical Reviews and Letters, V1, P443, DOI 10.1142/S1793048006000306
[4]   Emerging technologies for point-of-care CD4 T-lymphocyte counting [J].
Boyle, David S. ;
Hawkins, Kenneth R. ;
Steele, Matthew S. ;
Singhal, Mitra ;
Cheng, Xuanhong .
TRENDS IN BIOTECHNOLOGY, 2012, 30 (01) :45-54
[5]   Centrifugal microfluidics for cell analysis [J].
Burger, Robert ;
Kirby, Daniel ;
Glynn, Macdara ;
Nwankire, Charles ;
O'Sullivan, Mary ;
Siegrist, Jonathan ;
Kinahan, David ;
Aguirre, Gerson ;
Kijanka, Gregor ;
Gorkin, Robert A., III ;
Ducree, Jens .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2012, 16 (3-4) :409-414
[6]  
Burger R, 2012, EXPERT REV MOL DIAGN, V12, P407, DOI [10.1586/ERM.12.28, 10.1586/erm.12.28]
[7]   Array-based capture, distribution, counting and multiplexed assaying of beads on a centrifugal microfluidic platform [J].
Burger, Robert ;
Reith, Patrick ;
Kijanka, Gregor ;
Akujobi, Victor ;
Abgrall, Patrick ;
Ducree, Jens .
LAB ON A CHIP, 2012, 12 (07) :1289-1295
[8]   National Cancer Institute-sponsored Working Group guidelines for chronic lymphocytic leukemia: Revised guidelines for diagnosis and treatment [J].
Cheson, BD ;
Bennett, JM ;
Grever, M ;
Kay, N ;
Keating, MJ ;
OBrien, S ;
Rai, KR .
BLOOD, 1996, 87 (12) :4990-4997
[9]   Commercialization of microfluidic point-of-care diagnostic devices [J].
Chin, Curtis D. ;
Linder, Vincent ;
Sia, Samuel K. .
LAB ON A CHIP, 2012, 12 (12) :2118-2134
[10]   STUDY ON MECHANISM OF INTERCELLULAR-ADHESION - EFFECTS OF NEURAMINIDASE, CALCIUM, AND TRYPSIN ON AGGREGATION OF SUSPENDED HELA-CELLS [J].
DEMAN, JJ ;
BRUYNEEL, EA ;
MAREEL, MM .
JOURNAL OF CELL BIOLOGY, 1974, 60 (03) :641-652