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Thiophenol (PhSH), a highly reactive aromatic thiol, plays an essential role as a common industrial raw material in food, pesticides, pharmaceuticals, and cosmetics. In this work, we designed and constructed two fluorescent probes CM-PhSH and CM-Ratio-PhSH by a rational strategy. Specifically, coumarin fluorophores with excellent optical properties were modified, and olefinic unsaturated bonds served as reaction sites for the detection of PhSH. Based on this, the introduction of the nitro group at specific positions of the CM-PhSH changed the fluorescence emission of the CM-Ratio-PhSH, eventually obtaining a novel ratiometric fluorescent probe CM-Ratio-PhSH for PhSH detection. Surprisingly, these two probes exhibited advantages such as high specificity and low limit of detection (LOD) for CM-PhSH 32.3 nM and CM-Ratio-PhSH 40.2 nM, respectively. Furthermore, subsequent experiments demonstrated CM-PhSH and CM-Ratio-PhSH could be successfully used for highly selective and rapid detection of PhSH in aqueous solutions, live cells, and complex food samples., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

For the early diagnosis and effective evaluation of treatment effects of inflammation, a de novo bioanalytical method is urgently needed to monitor the metabolite nitric oxide (NO) associated with inflammatory diseases. However, developing a reliable detection method with excellent water solubility, biocompatibility, long retention time, and blood circulation is still challenging. In this work, we reported for the first time a de novo host-guest self-assembled nanosensor CTA for the quantitative detection and visualization of NO levels in inflammatory models. CTA mainly consists of two parts: (i) an adamantyl-labeled guest small-molecule RN-adH containing a classical response moiety o- phenylenediamine for a chemical-specific response toward NO and fluorophore rhodamine B with excellent optical properties as an internal reference for self-calibration and (ii) a remarkable water-soluble and biocompatible supramolecular β-cyclodextrin polymer (Poly-β-CD) host. In the presence of NO, the o- phenylenediamine unit was reacted with NO at a low pH value of ∼7.0, accompanied by changes in the intensity of the two emission peaks corrected for each other and the change in fluorescence color of the CTA solution from fuchsia to pink. Furthermore, CTA was an effective tool for NO detection with a fast response time (∼60 s), high selectivity, and sensitivity (LOD: 22.3 nM). Impressively, the CTA nanosensor has successfully achieved the targeted imaging of NO in living inflammatory RAW 264.7 cells and mice models with satisfactory results, which can provide a powerful molecular tool for the visualization and assessment of the occurrence and development of NO-related inflammatory diseases in complex biosystems.

Carbon monoxide (CO) is a vital endogenous gaseous transmitter molecule involved in the regulation of various physiological and pathological processes in living biosystems. In order to investigate the biological function of CO, many technologies have been developed to monitor the level of endogenous CO in biosystems. Among them, the fluorescence detection technology based on the fluorescent probe has the advantages of high sensitivity, excellent selectivity, simple operation, especially non-invasive damage to biological samples, and the possibility of real-time in situ detection, etc., which is considered to be one of the most effective and applicable detection techniques. Therefore, in the last few years, a lot of work has been carried out on the design, synthesis and in vivo fluorescence imaging studies of CO fluorescent probes. Furthermore, using fluorescent probes to detect the changes in CO concentrations in living cells and tissues as well as in organisms has been one of the hot research topics in recent years. However, it is still a challenge to rationally design CO fluorescent probe with excellent optical performance, structural stability, low background interference, good biocompatibility, and excellent water solubility. Therefore, this review focuses on the research progress of CO fluorescent probes in the detection mechanism and biological applications in recent years. However, this popular and leading topic has rarely been summarized comprehensively to date. Thus, the research progress of CO fluorescent probes in recent years is reviewed in terms of their design concept, detection mechanism, and their biological applications. In addition, the relationship between the structure and performance of the probes was also discussed. More significantly, we hope that more excellent optical properties fluorescent probes for gaseous transmitter molecule CO detection and imaging will overcome the current problems of high biotoxicity and limited water solubility in future.

Liver injury poses a serious threat to human health and growing evidence suggests that it is closely associated with a biomarker (peroxynitrite, ONOO - ). Therefore, considering that the relationship of ONOO - levels with the occurrence and development of liver injury disease remains a challenge, an urgent need exists to develop a reliable and robust tool for its visual rapid diagnosis and assessment. Herein, a two-photon near-infrared (TP-NIR) ratiometric fluorescent nanoprobe ( NTC ) based on a fluorescence resonance energy transfer (FRET) strategy was designed, synthesized, and characterized, which had the advantages of good water solubility, low background interference, deep tissue penetration, and high imaging resolution. Specially, NTC was constructed by self-assembly of an alkynyl group of a small-molecule fluorescent probe (NR) via click chemistry grafting onto azide chitosan (natural polymeric nanomaterial). NR contained acceptor 1 (NIR fluorophore) and donor 3 ( D -π- A structure of naphthalimide derivative fluorophore) with outstanding TP properties that could be activated by ONOO - for the ratiometric detection of ONOO - . Furthermore, in the presence of ONOO - , NTC exhibited a short response time (∼10 s) and high selectivity and sensitivity toward ONOO - with an excellent detection limit as low as 15.3 nM over other reactive oxygen/nitrogen species. Notably, NTC has been successfully employed for ONOO - detection and imaging in living HepG2 cells, liver injury mice tissues, and mice models with satisfactory results. Thus, the construction of this NTC nanoprobe can provide a robust molecule tool for enabling early diagnosis and assessment of liver injury in the future.

Thiophenol and hydrosulphite are a group of toxic environmental pollutants, which contaminate land, water and food exhibiting a serious risk to human health. Herein, we reported a xanthene dye-based sensor (DSF) with dual well-known response sites for visual detecting PhSH and HSO 3 - . Specifically, when DSF reacted with PhSH firstly, the color of the solution changed to blue with bright red fluorescence emission. After added with HSO 3 - , the color of the solution became yellow, and emitted yellow fluorescence signal. However, DSF was first added with HSO 3 - , the color of the solution changed to purple with no-fluorescence emission, and then PhSH was added, the color of the solution changed to yellow with a bright yellow fluorescence. Notably, DSF exhibited high sensitivity and selectivity for PhSH and HSO 3 - detection with a very low detection limits of 2.27 nM and 22.91 nM, respectively. More importantly, DSF could detect PhSH and HSO 3 - in water, real-food and biological systems. Therefore, the experimental results showed DSF as a robust new logical monitoring tool for the detection of PhSH and HSO 3 - in water, real-food samples and biological systems., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Bisulfite (HSO 3 - ) is usually widely added to tap water and food because it has antibacterial, bleaching, and antioxidant effects. However, its abnormal addition would cause a series of serious diseases related to it. Therefore, development of an effective method for HSO 3 - detection was of great significance to human health. In this work, a new reaction-based ratiometric fluorescent probe KQ-SO 2 was rationally designed, which could be used for the highly selective detection of HSO3 - in tap water, real food samples, onion tissues, and zebrafish. Specifically, a positively charged benzo[ e ]indolium moiety and a carbazole group through a condensation reaction resulted in KQ-SO 2 , which displayed two well-resolved emission bands separated by 225 nm, fast response (1 min), and high selectivity and sensitivity toward HSO3 - upon undergoing the Michael addition reaction, as well as low cytotoxicity in vitro. In addition, KQ-SO 2 has been successfully applied for the detection of HSO 3 - in tap water, real food samples, onion tissues, and zebrafish with satisfactory results. We predict that KQ-SO 2 could be used as a powerful tool to reveal the relationship between HSO3 - and the human health.

Fluorescence imaging plays an increasingly important role in biomedicine field due to its superior sensitivity and selectivity along with dynamic, real-time, in situ monitoring the occurrence and development of biological events. Therefore, it is crucial to construct a near-infrared (NIR) fluorescent molecule with excellent optical properties. Herein a NIR robust out mitochondria-targeting dye NN has been designed, synthesized and characterized, whose fluorescence properties are easily adjusted by changing the substitution position of the nitro group at the benzene ring in this fluorescent dye. NN was a unique fluorescence-enhanced nitro dye with high fluorescence quantum yields∼0.17, a large Stokes shift∼120 nm and stable chemical structure. Encouraged by this, a novel fluorescent probe NN - Sec based on intramolecular charge transfer (ICT) was constructed by grafting NN with a selenocysteine (Sec) recognition group 2,4-dinitrobenzenesulfonyl (DNBS), and it exhibited a targeted ability with great sensitivity and selectivity. Subsequently, the probe was used for NIR imaging in living cells and mice, and deep imaging results further illustrate its potential application in biosystems. The successful design of NN and NN - Sec offer a valuable theoretical basis and technical support for investigating the occurrence and development of Sec-related diseases. • A novel NIR fluorescent dye NN bearing nitro was reported with an enhanced fluorescence quantum yields. • The recognition group 2,4-dinitrobenzenesulfonyl of Sec was grafted with dye NN to synthesize fluorescent probe NN-Sec. • ANN-Sec can detect Sec in live cells and mice by high sensitivity and selectivity, accompanied by bright NIR emission. [ABSTRACT FROM AUTHOR]