Ion-selective reversing aggregation-caused quenching - Maximizing optodes signal stability.

An alternative optical signal transduction mechanism for ion-selective optodes is proposed. The nanostructural sensors benefit from ion-selective reversing aggregation caused quenching yielding turn-on, bright and highly stable optical signals. Selective incorporation of analyte results in transformation of the polymer dye from aggregate to a micelle structure, affecting spatial arrangement of chromophore groups in the nanostructure. Formation of micelles, induced by ion-selective interactions, is coupled with pronounced increase of emission due to decrease of aggregation caused quenching, characteristic for dispersed phase formation. The formed micelles are highly stable in solution, offering constant in time (days scale) emission signal. The important difference from other known systems is that the analyte binding induced change does not affect the chromophore group, but occurs in distant, terminal position of the side chain of the polymer. As a model system calcium selective optodes have been prepared. Thus obtained probes were characterized with broad analyte concentration range (from 10-7 to 10-3 M) emission signal increase. The turn-on response was observed within broad range of pH (6.3-8.9), with no sign of optical signal deterioration during 5 days contact with the analyte or more than two weeks storage.