Red blood cells do not attenuate the SPCE fluorescence in surface assays
Journal article, 2007

We describe the positive effect of surface plasmon-coupled fluorescence emission (SPCE) on the detection of a signal from a surface immunoassay in highly absorbing or/and scattering samples. A model immunoassay using fluorescently labeled anti-rabbit antibodies that bind to rabbit immunoglobulin on a silver surface was performed, and the signal was detected in the presence of various highly absorbing and/or scattering solutions or suspensions, such as hemoglobin solution, plastic beads, and red blood cells. The results showed that a highly absorbing solution consisting of small molecules (dye, hemoglobin) attenuates the SPCE signal approximately 2-3-fold. In contrast, suspensions with the same absorption containing large particles (large beads, red blood cell suspension) attenuate the SPCE signal only slightly, approximately 5-10%. Also, a suspension of large undyed, highly scattering beads does not reduce the SPCE signal. The effects on the immunoassay signal of the sample background absorption and scattering, the size of the background particles, and the geometry of the experimental set-up are discussed. We believe that SPCE is a promising technique in the development of biosensors utilized for surface-based assays, as well as any assays performed directly in highly absorbing and/or scattering solutions without washing or separation procedures.

fluorescence immunoassays

immunoassay

emission

background

enhanced fluorescence

total internal-reflection

high-sensitivity

suppression

planar wave-guides

hemoglobin

c-reactive protein

plasmon-coupled emission

directional

whole-blood

excitation

surface plasmon-coupled emission

red blood cells

Author

E. G. Matveeva

University of North Texas

I. Gryczynski

University of North Texas

A. Barnett

Macquarie University

Nils Calander

Chalmers, Applied Physics, Physical Electronics

Z. Gryczynski

University of North Texas

Analytical and Bioanalytical Chemistry

1618-2642 (ISSN) 1618-2650 (eISSN)

Vol. 388 5-6 1127-1135

Subject Categories

Physical Chemistry

Analytical Chemistry

DOI

10.1007/s00216-007-1322-z

More information

Created

10/7/2017