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Microfluidic one-step synthesis of alginate microspheres immobilized with antibodies
Author(s) -
Wanyu Chen,
JongHoon Kim,
Di Zhang,
Kyong-Hoon Lee,
Gerard A. Cangelosi,
Scott D. Soelberg,
Clement E. Furlong,
Jae-Hyun Chung,
Amy Q. Shen
Publication year - 2013
Publication title -
journal of the royal society interface
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 139
eISSN - 1742-5689
pISSN - 1742-5662
DOI - 10.1098/rsif.2013.0566
Subject(s) - microbead (research) , microfluidics , microsphere , nanotechnology , chemistry , fluorescence , chromatography , microparticle , materials science , chemical engineering , biochemistry , physics , quantum mechanics , engineering
Micrometre- and submicrometre-size functionalized beads are frequently used to capture targets of interest from a biological sample for biological characterizations and disease diagnosis. The main challenge of the microbead-based assay is in the immobilization of probe molecules onto the microbead surfaces. In this paper, we report a versatile droplet microfluidics method to fabricate alginate microspheres while simultaneously immobilizing anti-Mycobacterium tuberculosis complex IgY and anti-Escherichia coli IgG antibodies primarily on the porous alginate carriers for specific binding and binding affinity tests. The binding affinity of antibodies is directly measured by fluorescence intensity of stained target bacteria on the microspheres. We demonstrate that the functionalized alginate microspheres yield specificity comparable with an enzyme-linked immunosorbent assay. The high surface area-to-volume ratio of the functionalized porous alginate microspheres improves the detection limit. By using the droplet microfluidics, we can easily modify the size and shape of alginate microspheres, and increase the concentration of functionalized alginate microspheres to further enhance binding kinetics and enable multiplexing.

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