Capillary-driven multiparametric microfluidic chips for one-step immunoassays

被引:75
作者
Gervais, Luc [1 ]
Hitzbleck, Martina [1 ]
Delamarche, Emmanuel [1 ]
机构
[1] IBM Res Zurich, CH-8803 Ruschlikon, Switzerland
关键词
Microfluidics; Point-of-care; Diagnostics; Immunoassays; Lab-on-a-chip; BLOOD-VISCOSITY; FLOW; MICROCHANNELS; TECHNOLOGIES; CHEMISTRY; NETWORKS; SYSTEMS; PROTEIN; MIXER;
D O I
10.1016/j.bios.2011.06.016
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Here we present a capillary-driven microfluidic chip for "one-step" immunoassays. The chip allows for easy modification of several assay parameters such as the flow rates of sample, the volumes of samples for tests, and the type of reagents and receptors for detecting analytes. We therefore term such a chip a multiparametric chip and illustrate this concept with the integration and release of anti-C-reactive protein (CRP) detection antibodies (dAbs) together with splitting flow of samples containing CRP across lines of anti-CRP capture antibodies (cAbs). The microfluidic chip is fabricated in Si and is sealed with polydimethylsiloxane (PDMS) patterned with cAbs. The microfluidic chip is similar to 1.7 x 3.4 cm(2) and is capable of analyzing 20 mu L of human serum in 6 parallel flow paths with a range of flow rates from 3.3 nL s(-1) to 0.46 nL s(-1). An inkjet spotter was used to deposit 10.6 nL of dAb solution in a structure vicinal to the main flow path of the chip. The consequent asymmetric release of dAbs in a stream of human serum is compensated by a Dean flow mixer having 9 mixing loops and a footprint of 2.8 mm x 0.78 mm. The quantity of dAb present in the half of the flow path close to the spotting region decreases from 83% at the entrance of the mixer to 52% in the region after the mixer. The sample is then equally split into 6 reaction chambers and proceeds via connecting channels to 2 mu L capillary pumps. The hydraulic resistance of the connecting channels is designed to vary flow rates, and therefore the kinetics of capture of CRP-dAb complexes, from 10 min to 72 min. The increased incubation time leads to a fourfold increase in detection signal in the reaction chamber with the longer incubation time. The concept presented here is flexible and suited for implementing various surface fluorescence immunoassays on a capillary-driven microfluidic chip. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 70
页数:7
相关论文
共 33 条
[1]   Optical sectioning for microfluidics: secondary flow and mixing in a meandering microchannel [J].
Ahn, Yeh-Chan ;
Jung, Woonggyu ;
Chen, Zhongping .
LAB ON A CHIP, 2008, 8 (01) :125-133
[2]  
Apple FS, 1999, CLIN CHEM, V45, P199
[3]   Polymer microfabrication technologies for microfluidic systems [J].
Becker, Holger ;
Gaertner, Claudia .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2008, 390 (01) :89-111
[4]   Diagnosing infections--current and anticipated technologies for point-of-care diagnostics and home-based testing [J].
Bissonnette, L. ;
Bergeron, M. G. .
CLINICAL MICROBIOLOGY AND INFECTION, 2010, 16 (08) :1044-1053
[5]  
Buechler K.F., 1995, U.S. Patent, Patent No. 5458852
[6]   Microfluidic networks for chemical patterning of substrate: Design and application to bioassays [J].
Delamarche, E ;
Bernard, A ;
Schmid, H ;
Bietsch, A ;
Michel, B ;
Biebuyck, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (03) :500-508
[7]   Continuous inertial focusing, ordering, and separation of particles in microchannels [J].
Di Carlo, Dino ;
Irimia, Daniel ;
Tompkins, Ronald G. ;
Toner, Mehmet .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (48) :18892-18897
[8]   Health benefits of saliva: a review [J].
Dodds, MWJ ;
Johnson, DA ;
Yeh, CK .
JOURNAL OF DENTISTRY, 2005, 33 (03) :223-233
[9]   Clinical Chemistry: Challenges for Analytical Chemistry and the Nanosciences from Medicine [J].
Durner, Juergen .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (06) :1026-1051
[10]   Controlled microfluidic reconstitution of functional protein from an anhydrous storage depot [J].
Garcia, E ;
Kirkham, JR ;
Hatch, AV ;
Hawkins, KR ;
Yager, P .
LAB ON A CHIP, 2004, 4 (01) :78-82