Fluorescence affinity sensing by using a self-contained fluid manoeuvring microfluidic chip

• Published in: Analyst (London) 2008-04, Vol.133 (4), p.499-504
• Main Authors: JUNG WOO HONG, KWANG HYO CHUNG, YOON, Hyun C
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Antigens - analysis; Biosensing Techniques; Chemistry; Chromatographic methods and physical methods associated with chromatography; Chromatography, Affinity - methods; Electrochemistry - instrumentation; Electrochemistry - methods; Equipment Design; Exact sciences and technology; Fluorescence; Humans; Microfluidic Analytical Techniques; Microspheres; Miscellaneous; Other chromatographic methods; Point-of-Care Systems; Spectrometric and optical methods
• ISSN: 0003-2654; 1364-5528
• DOI: 10.1039/b718750e

An application of a novel polymer microfluidic chip for sample exchange via natural capillary forces for immuno-analysis is described. The microfluidic device was designed to achieve sample replacement by capillary force only, which would therefore be suitable for point-of-care-testing. Complete and automatic replacement of the sample in the reaction chamber with another one makes the chip able to mimic affinity chromatography and immunoassay processes. The microfluidic chip was made using polymer replication techniques, which were suitable for fast and cheap fabrication. Micrometre-sized polystyrene beads were used for the functionalization of biomolecules. Dinitrophenyl (DNP) and anti-DNP antibody coordination was employed on the chip for fluorescence analysis. DNP was immobilized on the polymer beads via a pre-adsorbed dendrimer layer and the beads were placed in the reaction chamber. Fluorescein tagged anti-DNP was successfully observed by a fluorescence microscope after the completion of the entire flow sequence. A calibration curve was registered based on the anti-DNP concentration. A multiplex sensing was accomplished by adding biotin/streptavidin coordination to the system. DNP and biotin conjugated beads were placed in the reaction chamber in an ordered fashion and biospecific bindings of anti-DNP antibody and streptavidin were observed at their expected sites. A ratiometric analysis was carried out with different concentration ratios of anti-DNP/streptavidin. The microfluidic chip described in this work could be applied to various biological and chemical analyses using integrated washing steps or fluid replacement steps with minimum sample handling.