Luminescent oxygen channeling immunoassay: measurement of particle binding kinetics by chemiluminescence.

EF Ullman, H Kirakossian, S Singh… - Proceedings of the …, 1994 - National Acad Sciences
EF Ullman, H Kirakossian, S Singh, ZP Wu, BR Irvin, JS Pease, AC Switchenko, JD Irvine…
Proceedings of the National Academy of Sciences, 1994National Acad Sciences
A method for monitoring formation of latex particle pairs by chemiluminescence is described.
Molecular oxygen is excited by a photosensitizer and an antenna dye that are dissolved in
one of the particles. 1 delta gO2 diffuses to the second particle and initiates a high quantum
yield chemiluminescent reaction of an olefin that is dissolved in it. The efficiency of 1 delta
gO2 transfer between particles is approximately 3.5%. The technique permits real-time
measurement of particle binding kinetics. Second-order rate constants increase with the …
A method for monitoring formation of latex particle pairs by chemiluminescence is described. Molecular oxygen is excited by a photosensitizer and an antenna dye that are dissolved in one of the particles. 1 delta gO2 diffuses to the second particle and initiates a high quantum yield chemiluminescent reaction of an olefin that is dissolved in it. The efficiency of 1 delta gO2 transfer between particles is approximately 3.5%. The technique permits real-time measurement of particle binding kinetics. Second-order rate constants increase with the number of receptor binding sites on the particles and approach diffusion control. By using antibody-coated particles, a homogeneous immunoassay capable of detecting approximately 4 amol of thyroid-stimulating hormone in 12 min was demonstrated. Single molecules of analyte produce particle heterodimers that are detected even when no larger aggregates are formed.
National Acad Sciences