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A red-emitting fluorescent probe with large Stokes shift for real-time tracking of cysteine over glutathione and homocysteine in living cells
摘要： Fluorescent probes with high quality for highly selective detection of cysteine (Cys) are still urgently in demand because of the indispensable roles Cys plays in the biological systems. Herein, a red-emitting fluorescent probe CP was developed for the highly selective detection of Cys over glutathione (GSH) and homocysteine (Hcy) by incorporating the recognition unit into the 2-(2-(4-hydroxystyryl)-6-methyl-4H-pyran-4-ylidene) malononitrile (P-OH) fluorophore which is characterized by red emission, noteworthy Stokes shift, and appreciable photostability. Basically, CP demonstrated appreciable sensing performance toward Cys including short response time of 4 min, high sensitivity with approximately 147-fold emission enhancement, low detection limit of 41.696 nM, and good selectivity both in the solution and living cells, indicating its promising potential of visualizing Cys in biological systems.
关键词： Large Stokes shift,Fluorescence imaging,Cysteine detection,Fluorescent probe
更新于2025-11-19 16:56:35
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A Glucose Oxidase-Instructed Fluorescence Amplification Strategy for Intracellular Glucose Detection
摘要： The accurate detection of glucose in the cellular level remains a big challenge. In this study, a signal amplification strategy mediated by silver nanocube (AgNC), glucose oxidase (GOx) and silver ion fluorescence probe (denoted as AgNC-GOx/Ag+-FP) is proposed for amplified intracellular glucose detection. The AgNC is oxidized into Ag+ by H2O2 generated from the GOx-catalyzed glucose oxidation reaction, and Ag+ remarkably enhances the red fluorescence of Ag+-FP. Our results show that the AgNC-GOx/Ag+-FP is highly sensitive and specific to glucose and H2O2. Afterwards, the feasibility of using AgNC-GOx/Ag+-FP to detect intracellular glucose is verified in five different cell lines. In summary, a sensitive and specific fluorescence amplification strategy has been developed for intracellular glucose detection.
关键词： intracellular glucose,silver nanocube,fluorescence probe,glucose oxidase,signal amplification
更新于2025-11-19 16:56:35
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Two pH-responsive fluorescence probes based on indole derivatives
摘要： Two new pH ?uorescent probes 2,8-bis((E)-2-(1,1-dimethyl-1H-benzo[e]indol-2-yl)vinyl)-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocine (1) and 2,8-bis((E)-2-(3,3-dimethyl-3H-indol-2-yl)vinyl)-6H,12H-5,11-methanodibenzo[b,f] [1,5]diazocine (2) were designed and synthesized via ethylene bridging of the Tr?ger's Base (TB) framework and indole derivatives. As the protonation of nitrogen atoms of indole derivatives, both probes displayed the signi?cant pH-dependent spectral properties. The probing behavior toward pH variations indicated that probes exhibited excellent pH dependent behavior in the pH ranges of 2.07–7.01 (1) and 1.96–7.01 (2), especially possessing good linear response in the pH ranges of 2.50–4.00. The emissions of 1 can be reversibly switched between brilliant yellow and dark states by protonation and deprotonation. Also, the yellow-green ?uorescence emission of 2 could be quenched upon protonation. Such behaviors enable them to work as turn-o? ?uorescent pH sensors in the solution state. Furthermore, protonation and deprotonation on indole moiety nitrogen of the probe 1 and 2 provided a sensing mechanism for pH changes. In addition, both probes performed good photostability, high selectivity and excellent reversibility.
关键词： Sensors,Fluorescent probe,pH detection,Luminescence,Indole derivatives
更新于2025-11-19 16:56:35
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A mitochondria-targeted ratiometric fluorescent probe for detection of SO2 derivatives in living cells and in vivo
摘要： A new near-infrared (NIR) ?uorescent probe for colorimetric and ratiometric detection of SO2 derivatives was developed based on conjugated hybrid coumarin-hemicyanine. The probe can detect HSO3?/SO32? in HEPES bu?er (10 mM, pH 7.4, with 10% DMF, v/v) with a large emission shift (259 nm). Importantly, it was successfully used for ?uorescence imaging of endogenous bisul?te in BT-474 cells and zebra?sh.
关键词： Near-infrared ?uorescent probe,SO2 derivatives,Mitochondria-targeted,Ratiometric,Colorimetric
更新于2025-11-19 16:56:35
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An AND logic gate-based fluorescence probe for the detection of homovanillic acid, an indicator of the tumor
摘要： Homovanillic acid (HVA) is one of the major metabolites of catecholamine in human. An elevated level of HVA in urine and blood has been associated with many diseases, including catecholamine-secreting tumors. Consequently, detection of the biomarker HVA in urine is an effective strategy to detect cancer precursors and early stage cancers. In this study, a fluorescence probe is designed and fabricated by integrating lanthanide ions with metal-organic frameworks (MOFs). The fluorescence probe shows distinguished response toward HVA and exhibits ratiometric detection of HVA, rendering it an excellent candidate for sensing devices. Thus, we have designed logic gate operation integrating the probe with logical operations for the intelligent sensing of HVA. Furthermore, this type of luminesce based sensors integrated with logic gate augur for the further application in real-time early diagnosis of tumors in the future.
关键词： Rare earth,Homovanillic acid,Fluorescent probe,Logic gate,Ratiometric sensing,Metal-organic frameworks
更新于2025-11-19 16:56:35
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A novel rhodamine-based turn-on probe for fluorescent detection of Au3+ and colorimetric detection of Cu2+
摘要： In this work, we design and synthesize the novel probe RC through introduction the 1-aza-4,13-dithia-15-crown-5 ring into the structure of rhodamine 6G hydrazide, where the N atom of crown ring is responsible for quenching of rhodamine fluorescence. The compound obtained behaves as multifunctional cation sensor providing selective fluorescent response to Au3+ and selective colorimetric response to Cu2+ ions in aqueous acetonitrile (1/1, v/v) at pH 7.0. The use of 10-5 M RC solution allowed reliable determination of target cations in the presence of a wide range of environmentally relevant ions with detection limits of 2×10-6 M and 5×10-7 M for gold and copper, respectively.
关键词： Colorimetric probe,Cu,Sensor,Rhodamine,Fluorescent probe,Au
更新于2025-11-19 16:46:39
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A Red Emitting Fluorescent Probe for Imaging Mitochondrial Hydrogen Polysulfide in Living Cells and Tissues
摘要： Hydrogen polysulfide (H2Sn) has attracted increasing attention since H2Sn instead of H2S has been shown to be the actual signaling molecule in physiological and pathological processes. Thus, developing accurate and sensitive assays for H2Sn detection is urgently needed in biological science. In this work, we developed a red emitting mitochondria-targeting fluorescent probe, HQO-PSP, that is capable of tracking H2Sn. With low cytotoxicity, good selectively and high sensitively, HQO-PSP was able to detect H2Sn in living cells. Furthermore, we also demonstrated that HQO-PSP could also be successfully applied to recognize H2Sn in living tissues.
关键词： Hydrogen polysulfide,Fluorescent probe,Lung tissues,Living cells
更新于2025-11-19 16:46:39
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FRET-based dual channel fluorescent probe for detecting endogenous/exogenous H2O2/H2S formation through multicolor images
摘要： We have developed a FRET-based fluorescent probe (PHS1) as a combination of two different fluorophores (coumarin and naphthalimide); which can detect both exogenous and endogenous H2S and H2O2 in live cells through multicolor images. The precise overlap between UV-absorption of naphthalimide and the emission band of coumarin in probe PHS1 allows the acquisition of the self-calibrated information of dual analytes through FRET-based imaging. The UV–Vis absorption (λabs 390 nm) and fluorescence emission (λem 460 nm) of probe PHS1 in the presence of H2O2 are increased ∽35- fold and ∽15-fold respectively. It also allows the estimation of the levels of H2S through enhancement of emission intensity at 550 nm. The probe PHS1 exhibits high stability against various analytes, including various pH (4–9.5). The cell viability assay data indicate that the probe is not harmful to the cancer cells. The nontoxic nature of the probe PHS1 encourages application for cancer cell labeling. The probe PHS1 can detect the level of endogenous H2O2, H2S, and H2O2/H2S in cancer cells through blue, green and FRET-based green channel imaging. PHS1 is a unique probe, has potential application for diagnosing cancer by providing information on the level of dual analytes (H2S, H2O2) in cancer cells.
关键词： FRET-based fluorescent probe,Naphthalimide,Endogenous H2O2,Endogenous H2S,Coumarin
更新于2025-11-19 16:46:39
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Water-sensitive ratiometric fluorescent probes and application to test strip for rapid and reversible detection of water
摘要： Naphthalimide-decorated fluorinated acetamides 1 and 2 were developed as solvent-sensitive dual emissive fluorescence probes. Particularly, 1 exhibited dual emission with a large Stokes shift for water, DMF, and DMSO solvents over other various organic solvents. The dual emission might be due to the increase of intramolecular charge transfer (ICT) of the naphthalimide moiety through the association of the difluorinated acetamide group with the solvent molecules. The 1 can give rise to a ratiometric change in the dual emission and a visual fluorescent color change depending on the water contents in organic solvents, including ethanol, methanol, acetonitrile and DMF solvents. Moreover, the 1-impregnated paper strips showed a rapid and easy-to-visualize fluorescent color change enabling water detection in organic solvents. These simple-to-use paper strips were also found to be reusable over 20 times.
关键词： Naphthalimide,Ratiometric fluorescence probe,Reusable test strip,Intramolecular charge transfer (ICT),Water detection
更新于2025-11-19 16:46:39
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Multifunctional N,S co-doped carbon dots for sensitive probing of temperature, ferric ion, and methotrexate
摘要： In this paper, we have presented a facile method to fabricate nitrogen and sulfur co-doped carbon dots (N,S-CDs) for blood methotrexate (MTX) sensing applications. The N,S-CDs with quantum yield up to 75% were obtained by one-step hydrothermal carbonization, using reduced glutathione and citric acid as the precursors. With this approach, the formation and the surface passivation of N,S-CDs were carried out simultaneously, resulting in intrinsic fluorescence emission. Owing to their pronounced temperature dependence of the fluorescence emission spectra, resultant N,S-CDs can work as versatile nanothermometry devices by taking advantage of the temperature sensitivity of their emission intensity. In addition, the obtained N,S-CDs facilitated high selectivity detection of Fe3+ ions with a detection limit as low as 0.31 μM and a wide linear range from 3.33 to 99.90 μM. More importantly, the added MTX selectively led to the fluorescence quenching of the N,S-CDs. Such fluorescence responses were used for well quantifying MTX in the range of 2.93 to 117.40 μM, and the detection limit was down to 0.95 μM. Due to Binert^ surface, the N,S-CDs well resisted the interferences from various biomolecules and exhibited excellent selectivity. The proposed sensing system was successfully used for the assay of MTX in human plasma. Due to simplicity, sensitivity, selectivity, and low cost, it exhibits great promise as a practical platform for MTX sensing in biological samples.
关键词： Hydrothermal carbonization,Doped carbon dots,Excitation-independent emission,Multifunctional probe,Methotrexate,Surface passivation
更新于2025-11-19 16:46:39