Dihydroxy-Substituted Coumarins as Fluorescent Probes for Nanomolar-Level Detection of the 4-Amino-TEMPO Spin Label.

Krzysztof Żamojć,Paweł Błażej Rudnicki-Velasquez,Lech Chmurzyński,Magdalena Zdrowowicz,Maciej Witwicki,Aleksandra Hać,Dariusz Wyrzykowski,Wiesław Wiczk

doi:10.3390/ijms20153802

Krzysztof Żamojć, Paweł Błażej Rudnicki-Velasquez + Show 6 more

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https://doi.org/10.3390/ijms20153802

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Abstract

This paper reports on dihydroxycoumarins as fluorescent probes suitable for the detection and determination of the nitroxide radical, namely 4-amino-TEMPO. Since 4-amino-TEMPO is used as a spin label for the detection of various radicals and damage caused by these species, its determination under physiological conditions might help us to understand the mechanism of the oxidative stress. Among different coumarins studied, only dihydroxy-substituted derivatives show high sensitivity, specificity, and selectivity for the nitroxide radical. In this assay, dihydroxy-substituted coumarins under the action of 4-amino-TEMPO show a very fast and significant increase in fluorescence intensity and lifetime. Among them 6,7-dihydroxycoumarin (esculetin) exhibits the strongest fluorescence enhancement (up to 40 times), with an estimated limit of detection equal to 16.7 nM—a significantly lower value when compared with UV-Vis or electron paramagnetic resonance (EPR) spectroscopy. The method is characterized by an easy procedure of sample preparation and very short time of analysis. The mechanism of the interaction between 6,7-dihydroxycoumarin and 4-amino-TEMPO has been examined with the use of a series of complementary techniques, such as steady-state and time-resolved fluorescence spectroscopy, UV-Vis spectroscopy, electron paramagnetic resonance spectroscopy, potentiometric titration, and high-performance liquid chromatography. It has been proven that the only route of the reaction in the system studied is a proton transfer from the molecule of esculetin to the amino group of the nitroxide. Biological studies performed on prostate cancer cells, breast cancer cells, and normal skin fibroblasts revealed significant anticancer properties of 6,7-dihydroxycoumarin, which caused a considerable decrease in the viability and number of cancer cells, and affected their morphology, contrary to normal fibroblasts. Furthermore, the experiment performed on prostate cancer cells showed that fluorescence emission of esculetin is closely related to intracellular pH—the higher pH, the higher observed fluorescence intensity (in accordance with a chemical experiment). On the other hand, the studies performed in different pH levels revealed that when pH of the solution increases, the observed fluorescence intensity enhancement under the action of 4-amino-TEMPO decreases (better sensing properties of esculetin towards the nitroxide in lower pH).

Highlights

Reactive oxygen and nitrogen species (RONS), e.g., superoxide, hydroxyl radical, singlet oxygen, nitric oxide, nitrogen dioxide, peroxynitrite, and hydrogen peroxide, are powerful oxidants that may damage cellular targets non-selectively [1]
In case of monohydroxy-substituted coumarins as well as dihydroxy-substituted derivatives without neighbouring hydroxyl groups, in case of which the formation of intramolecular hydrogen bond does not occur, deprotonation may be responsible for the observed shifts—the deprotonation leads to a significant increase of HOMO energy in 7-hydroxycoumarins and to bathochromic band shifts in their electronic absorption spectra [41]
The use of a series of complementary techniques enabled us to prove that the mechanism of the interaction between 6,7-dihydroxycoumarin and 4-amino-TEMPO is based on a proton transfer from the molecule of esculetin to the amino group of the nitroxide radical

Summary

Introduction

Reactive oxygen and nitrogen species (RONS), e.g., superoxide, hydroxyl radical, singlet oxygen, nitric oxide, nitrogen dioxide, peroxynitrite, and hydrogen peroxide, are powerful oxidants that may damage cellular targets non-selectively [1]. Radicals, including RONS, represent a broad range of short-lived and chemically distinct individuals [2]. They are very difficult to detect in dynamic environments such as biological media, where the presence of a variety of endogenous antioxidants complicates their determination [3]. A variety of TEMPO derivatives are used as spin labels for supramolecular complexes [5]; reversible inhibitors for nitroxide-mediated polymerization [6]; probes for the detection of various radicals and the damage mediated by these species [7,8,9,10,11,12]; prefluorescent probes [13,14]; and as superoxide dismutase mimetics for the protection of biomolecules against oxidative stress [15,16]. Derivatives of TEMPO can act as radical scavenging, anti-oxidant stabilizers for polymers, improving durability and aesthetic properties throughout their service lifetime [4]

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