Selective and sensitive ratiometric fluorescent probe for copper(II) cations in an aqueous solution based on resonance energy transfer and “1,8-naphthalimide–styrylpyridine” dyad bearing dipicolylamine receptor

Abstract

Development of ratiometric fluorescent probes for Cu²⁺ in aqueous solutions and biological systems remains the challenging task, given that Cu²⁺ commonly acts as an efficient fluorescence quencher. In this work, a novel dyad compound NI-SP bearing energy donor naphthalimide and energy acceptor styrylpyridine chromophore has been prepared using azide-alkyne click reaction. The photophysical properties of NI-SP and its coordination with Cu²⁺ have been investigated by the absorption and fluorescent spectroscopy. Upon addition of Cu²⁺ to a solution of NI-SP, the long wavelength emission peak of styrylpyridine (600 nm) was quenched, whereas the fluorescence of naphthalimide (450 nm) was enhanced due to a decrease in resonance energy transfer efficiency between the chromophores in the (NI-SP)·Cu²⁺ complex. The observed spectral changes enable ratiometric detection of Cu²⁺ by the registration of the ratio of fluorescence intensities I₄₅₀/I₆₀₀. The probe exhibited high selectivity toward Cu²⁺ in the tested conditions. The detection limit was determined at 120 nmol·L^–1, and the stability constant for (NI-SP)·Cu²⁺ was found to be 3.0 × 10⁶ L·mol^–1. Bioimaging experiments showed the NI-SP could penetrate human lung adenocarcinoma A549 cells, accumulate in mitochondria, and respond to the presence of Cu²⁺ via the changes in the fluorescence intensity of styrylpyridine fragment.

Graphical abstract

Keywords

chemosensor / fluorescence imaging / human lung adenocarcinoma A549 cells / resonance energy transfer / intramolecular charge transfer

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