O. Gaillard et al., TIME-RESOLVED FLUOROMETRY - PRINCIPLES AN D APPLICATIONS IN CLINICAL-CHEMISTRY, Annales de biologie clinique, 52(11), 1994, pp. 751-755
Time-resolved fluorometric assay is based on lanthanide fluorescence.
This time-resolved fluorescence has a narrow-band emission line whose
wavelength differs from that of emission-pulsed light and has a long d
ecay-time. These characteristics make it possible to avoid background
interference from sample constituents (protein, light-scattering parti
cles, etc). Europium and its chelates are the most commonly used lanth
anides. The europium-labeling of antigens or antibodies is followed by
immunoassay. In the final step, fluorescence is measured, after enhan
cement, as counts per second. This assay has several advantages, inclu
ding a wide working range, high sensitivity and good practicability. T
he method has widespread applications in the field of immunoassays in
both clinical and research laboratories. The use of non-radioactive eu
ropium-labelled probes and the development of simultaneous multiple te
sts are possible future orientations.