Spectroscopic studies on the interaction of fluorescein and safranine T in PC liposomes

In this study, the fluorescence quenching of fluorescein by safranine T in liposome media had been investigated systematically by fluorescence spectroscopy, UV–vis absorption spectroscopy and fluorescence decay lifetime measurements. The spectroscopic data were analyzed using a Stern–Volmer equation to determine the quenching process. The experimental results showed that the intrinsic fluorescence of fluorescein was strongly quenched by safranine T, and that the quenching mechanism was considered as static quenching by forming a ground-complex. The Stern–Volmer quenching constant Ksv, and the bimolecular quenching constant Kq were estimated. The distances between the donor (fluorescein) and the acceptor (safranine T) were calculated according to the Förster non-radiation energy transfer theory. In addition, the partition coefficient of the safranine T (Kp) in the L-egg lecithin phosphatidylcholine liposomes was also calculated by utilizing the fluorescence quenching.

The fluorescence quenching of fluorescein by safranine T in liposome media had been investigated systematically by spectroscopic techniques.Figure optionsDownload as PowerPoint slideHighlights
► We explored the interaction of fluorescein and safranine T by spectroscopic methods.
► The fluorescence quenching mechanism is static quenching.
► The distances between the donor and the acceptor were calculated.
► The partition coefficient of safranine T (Kp) in PC liposomes was calculated.