The objective of this work is to develop a series of fluorescent stains suitable for the simultaneous multiple labelling of cytological specimens for flow analysis. While these stains are primarily intended for cancer screening and detection, their usefulness extends to any area of citology where multiple fluorescent staining might be advantageous. The key requisites of these stains are high fluorescence intensity, very narrow emission bands, and chemical stability in aqueous media. Two lanthanide ions, europium(III) and terbium(III), are known to exhibit monochromatic light-excited luminescence in the visible region. This luminescence is sensitized when the metal ions are coordinated to rigidly chelating ?-bonded O-donor and N-donor ligands, such as the anions of ?-diketones and 1,10-phenanthroline. To take advantage of this effect and to enhance the stability of the fluorochromes in solution through the formation of fused polychelated species, various tris-?-diketones (LH3) containing a benzene bridgehead have been synthesized. Depending on the reaction conditions, these ligands yield either monomeric or polymeric complexes with the Eu(III) and Tb(III) ions; the polymeric species, {ML}n, are anhydrous and do not show any tendency to bind additional O-donor or N-donor hetero-ligands. The absorption, emission, and excitation spectral properties of the complexes have been investigated; the unusual features observed for the excitation spectra of these and other tris-?-diketonato complexes will be discussed.
Development of fluorescent stains containing a lanthanide chelate as the light-emitting center
Mauro Bassetti;
1984
Abstract
The objective of this work is to develop a series of fluorescent stains suitable for the simultaneous multiple labelling of cytological specimens for flow analysis. While these stains are primarily intended for cancer screening and detection, their usefulness extends to any area of citology where multiple fluorescent staining might be advantageous. The key requisites of these stains are high fluorescence intensity, very narrow emission bands, and chemical stability in aqueous media. Two lanthanide ions, europium(III) and terbium(III), are known to exhibit monochromatic light-excited luminescence in the visible region. This luminescence is sensitized when the metal ions are coordinated to rigidly chelating ?-bonded O-donor and N-donor ligands, such as the anions of ?-diketones and 1,10-phenanthroline. To take advantage of this effect and to enhance the stability of the fluorochromes in solution through the formation of fused polychelated species, various tris-?-diketones (LH3) containing a benzene bridgehead have been synthesized. Depending on the reaction conditions, these ligands yield either monomeric or polymeric complexes with the Eu(III) and Tb(III) ions; the polymeric species, {ML}n, are anhydrous and do not show any tendency to bind additional O-donor or N-donor hetero-ligands. The absorption, emission, and excitation spectral properties of the complexes have been investigated; the unusual features observed for the excitation spectra of these and other tris-?-diketonato complexes will be discussed.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
