A versatile and robust method for the determination of DNA and PCR products ( (dsDNA, ssDNA or circular DNA), the quenched luminescence is reinstated, AO and EB intercalating into DNA, which removes the interaction with the complexes. The best results are obtained with with detections limits in the range ; detection limits for the system are slightly larger; simpler monometallic complexes with dipicolinate derivatives do not follow suit in that they decompose in the presence of DNA. The method is shown to be pH insensitive in the range 3–10; furthermore it is essentially insensitive to 1000-fold excesses of potential interfering substances, e.g. BSA, glucose, chelating agents and anions, alkaline earth and transition metal cations, variations in luminescence intensity being < 5%, (10 analytes) or 5–10% (4 analytes); only and interfere substantially.
Rosario Scopelliti, Kay Severin, Farzaneh Fadaei Tirani, Paul Varava, Wolfram Feuerstein