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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/35501
Title: Evaluation of agglutination strength by a flow-induced cell movement assay based surface plasmon resonance (SPR) technique
Authors: Krisda Sudprasert
Patjaree Peungthum
Apirom Vongsakulyanon
Ratthasart Amarit
Armote Somboonkaew
Boonsong Sutapun
Pimpun Kitpoka
Mongkol Kunakorn
Toemsak Srikhirin
Mahidol University
Thailand National Electronics and Computer Technology Center
Suranaree University of Technology
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry;Environmental Science
Issue Date: 7-Feb-2015
Citation: Analyst. Vol.140, No.3 (2015), 880-888
Abstract: © The Royal Society of Chemistry 2015. A flow-induced cell movement assay combined with a surface plasmon resonance (SPR) technique was developed to quantify the agglutination strength, derived from the standard tube-agglutination test. Red blood cells (RBCs), based on the ABO blood group system, were specifically captured by anti-A and/or anti-B antibodies immobilized on a sensor surface. The agglutination strength corresponds to the amount of antigen-antibody interactions or the strength of RBC adhesion. Under a shear flow, the adherent RBCs were forced to move out of the region of interest with different average cell velocities (vc) depending upon the adhesion strength and wall shear stress (WSS). That is, a higher adhesion strength (higher agglutination strength) or lower WSS represents a lower vcor vice versa. In this work, the agglutination strength was derived from the vcthat was calculated from the time derivative of the relative SPR signal by using a simple model of cell movement response, whose validity was verified. The vcvalues of different samples were correlated with their agglutination strengths at a given WSS and antibody surface density. The vcdecreased as the agglutination strength increased, which can be considered as a linear regression. The coefficient of variation of the calculated vcdecreased to 0.1 as vcincreased to 30 μm min-1. The sensitivity of this assay can be controlled by optimizing the antibody surface density or the WSS. This assay has the capability to resolve the antigen density of A1and B RBCs from that of A1B RBCs.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84921448103&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/35501
ISSN: 13645528
00032654
Appears in Collections:Scopus 2011-2015

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