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Proton Triggered Colorimetric and Fluorescence Response of a Novel Quinoxaline Compromising a Donor-Acceptor System
摘要： Quinoxaline-based novel acid-responsive probe Q1 was designed on the basis of a conjugated donor-acceptor (D-A) subunit. Q1 shows colorimetric and fluorometric changes through protonation and deprotonation in dichloromethane. With the addition of the trifluoroacetic acid (TFA), UV-vis absorption spectral changes in peak intensity of Q1 was observed. Moreover, the appearance of a new peaks at 284 nm 434 nm in absorption spectra with the addition of TFA indicating protonation of quinoxaline nitrogen and form Q1.H+ and Q1.2H+. The emission spectra display appearance of new emission peak at 515 nm. The optical property variations were supported by time resolved fluorescence studies. The energy band gap was calculated by employing cyclic voltammetry and density functional calculations. Upon addition of triethylamine (TEA) the fluorescence emission spectral changes of Q1 are found to be reversible. Q1 shows color changes from blue to green in basic and acidic medium, respectively. The paper strip test was developed for making Q1 a colorimetric and fluorometric indicator.
关键词： proton sensor,quinoxaline,fluorescent,colorimetric,reversible sensor
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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Ultrathin Ti3C2 Nanosheets based “off-on” Fluorescent nanoprobe for Rapid and Sensitive Detection of HPV Infection
摘要： MXenes as a new class of 2D materials have recently been widely applied in energy storage, electrocatalysis, sensors, adsorption, water purification, and so on, due to their tunable versatile properties. Herein, we demonstrate a simple, rapid and highly-sensitive sensing platform based on ultrathin two-dimensional MXene Ti3C2 nanosheets (Ti3C2 NSs) for selective analysis of Human papillomavirus (HPV), a major human pathogens and causative agents of cervical cancer. Ultrathin Ti3C2 NSs, obtained by exfoliating their layered HF-etched powder, exhibit high fluorescence quenching ability to dye-labeled single-stranded DNA (ssDNA) and different affinities for ssDNA and double-stranded DNA (dsDNA). Under the fluorescence quenching effect of Ti3C2 NSs, ssDNA probe (P) shows the minimal fluorescent emission. After the formation of duplex structure with its complementary target, ssDNA (T), the fluorescence intensity enhances evidently. Exonuclease III (Exo III) was used to improve the sensitivity by promoting more fluorescence enhancement. This magnified fluorescent sensor for HPV-18 detection shows a low detection limit of 100 pM and a high specificity. Furthermore, the developed DNA sensor can be employed to determine PCR amplified HPV-18 from cervical scrapes samples. It highlights ultrathin Ti3C2 NSs as a potential candidate for construction of fluorescence DNA biosensors with excellent performances.
关键词： DNA hybridization,Ti3C2 nanosheets,HPV,Fluorescent detection
更新于2025-11-19 16:46:39
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An Insight into the Mechanisms of the Scale Inhibition. A Case Study of a Novel Task-specific Fluorescent-tagged Scale Inhibitor Location on Gypsum Crystals
摘要： Scaling in reverse osmosis facilities, boilers, heat exchangers, evaporation plants, and oilfield applications is a serious problem worldwide. In order to provide a new insight into the mechanism of the scale formation and inhibition, a novel fluorescent-tagged 1-hydroxy-7-(6-methoxy-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)heptane-1,1-diyl-di(phosphonic acid), (HEDP-F) was synthesized and applied for the fluorescent microscope visualization of gypsum crystals formation in supersaturated aqueous solutions. The visualization of HEDP-F location at gypsum crystals, has demonstrated that the bisphosphonate molecules do not act as they are expected to do according to the current scale inhibition theory. At ambient temperature the gypsum macrocrystals are found to form, and then to grow without visible sorption of bisphosphonate on the crystal edges or any other gypsum crystal growth centers. A tentative nonconventional mechanism of scale inhibition in the bulk supersaturated aqueous solutions of gypsum is proposed.
关键词： crystal formation,scale formation,visualization,gypsum,mechanisms of scale inhibition,fluorescent-tagged bisphosphonate
更新于2025-11-19 16:46:39
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A sensitive polymer dots fluorescent sensor for determination of α-L-fucosidase activity in human serum
摘要： α-L-Fucosidase (AFu) is an important biomarker for early diagnosis of hepatocellular carcinoma and fucosidosis. In this study, a novel, sensitive and selective polymer dots (PDs) fluorescent sensing strategy based on inner filter effect was firstly developed for AFu activity determination. The PDs with a high quantum yield of 53.6% were synthesized by a mild one-pot method. The detection mechanism of this strategy was based on inner filter effect between PDs and p-nitrophenol (PNP) which was the hydrolyzate of 4-nitrophenyl-α-L-fucopyranoside (PNPF) catalyzed by AFu. The absorption of PNP overlapped the fluorescence excitation spectrum of the PDs, which resulted in a fluorescence quenching or weakening of PDs. The sensing system showed a good linear relationship within 0.01-0.9 U L-1 and provided a low AFu detection limit of 0.001 U L-1 (S/N=3). This PDs sensor were successfully applied for the determination of AFu in human serum samples.
关键词： Human serum,α-L-Fucosidase,Polymer dots,Inner filter effect,Fluorescent sensor
更新于2025-11-19 16:46:39
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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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Dopamine-functionalized upconversion nanoparticles as fluorescent sensors for organophosphorus pesticide analysis
摘要： Organophosphorus pesticide (OP) residues in agricultural products, herbal medicines and environment have attracted increasing concerns because they cause high healthy risk. Herein, a tyrosinase-mediated photoinduced electron transfer system was constructed for OPs analysis by using dopamine-functionalized upconversion nanoparticles (UCNPs) as fluorescent (FL) sensors. Dopamine quinone was produced by tyrosinase-mediated oxidation of dopamine on the surface of UCNPs, which acted as electron accepter to quench the FL emission of UCNPs. The FL quenching was inhibited by OP since it inhibited the activity of tyrosinase. Chlorpyrifos was used as a model analyte to investigate the feasibility of the FL sensor for the analysis of OPs. Under the optimal conditions, chlorpyrifos can be analysed in a wide range of 1.0 ? 1000 ng mL?1, with a detection limit of 0.38 ng mL?1 (3σ). Some other groups pesticides, including organonitrogen pesticide, organochlorine pesticide and chloronicotinyl insecticide all showed negligible interference. The proposed sensor was successfully used to analyse chlorpyrifos spiked in Balloonflower and Angelica with acceptable recovery values of 95.4–120.0%, demonstrating its application potential for real samples. It exhibits some advantages like low cost, high sensitivity and free of autofluorescent interference and photobleaching.
关键词： Tyrosinase,Photoinduced electron transfer,Fluorescent sensor,Organophosphorus pesticide,Upconversion nanoparticles,Chlorpyrifos
更新于2025-11-14 17:15:25
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Sulfur doped carbon nitride quantum dots with efficient fluorescent property and their application for bioimaging
摘要： Heteroatom doping can drastically alter electronic characteristics of carbon nitride quantum dots, thus resulting in unusual properties and related applications. Herein, we used sulfur as the doping element and investigated the influence of doping on the electronic distribution of carbon nitride and the corresponding fluorescent property. A simple synthetic strategy was applied to prepare sulfur-doped carbon nitride (S-g-C3N4) quantum dots through ultrasonic treatment of bulk S-g-C3N4. Characterization results demonstrated that the prepared S-g-C3N4 quantum dots with an average size of 2.0 nm were successfully prepared. Fluorescent properties indicated that S-g-C3N4 quantum dots have an emission peak at 460 nm and cover the emission spectra region up to 550 nm. Furthermore, the fluorescent intensity is greatly increased due to the sonication of bulk S-g-C3N4 into quantum dots. As a result, S-g-C3N4 quantum dots not only show a blue cell imaging, but have a bright green color. Therefore, S-g-C3N4 quantum dot is a promising candidate for bioimaging benefiting from the efficient fluorescent property, good biocompatibility, and low toxicity.
关键词： Doped carbon nitride,Fluorescent property,In vitro cytotoxicity,Quantum dots,Bioimaging
更新于2025-11-14 17:04:02
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Development of a fluorescence immunoassay for highly sensitive detection of amantadine using the nanoassembly of carbon dots and MnO2 nanosheets as the signal probe
摘要： Fluorescence immunoassays are rapid, convenient and cost-effective for the sensitive quantitation of chemical contaminants in foodstuff. In this study, a competitive fluorescence ELISA was developed for the sensitive detection of amantadine (AMD) based on the alkaline phosphatase (ALP)-triggered fluorescence "turn-on" signals. As a fluorescence substrate, carbon dots (CDs) were adsorbed onto the surface of the MnO2 nanosheets (NSs) and formed a nanoassembly of p-CDs@MnO2 NSs which results in the fluorescence quench of CDs. The ALP labelled on antibody could catalyze the hydrolysis of the 2-phospho-L-ascorbic acid into ascorbic acid. The latter could then reduce and decompose the MnO2 NSs, which was accompanied by the release of CDs from the surface of MnO2 NSs and led to the fluorescence recovery of CDs. The change of the fluorescence intensity is related to the concentration of AMD in solution and thus could be applied to detect AMD in an ALP-based ELISA system. The fluorescent ELISA showed a linear detection for AMD in the range of 0.048 ng mL?1 to 1.1 ng mL?1 with a detection limit (LOD) of 0.035 ng mL?1. The novel fluorescent ELISA shows potential for the highly sensitive detection of AMD and other analytes in food analysis.
关键词： manganese dioxide nanosheets,carbon dots,fluorescent immunoassay,amantadine
更新于2025-11-14 17:04:02
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Bifunctional gold nanoclusters enable ratiometric fluorescence nanosensing of hydrogen peroxide and glucose
摘要： The accurate quantification of hydrogen peroxide (H2O2) and glucose is essential significance in clinical diagnosis. Herein a selective and sensitive ratiometric fluorescent nanosensor was developed for the determination of H2O2 and glucose by integrating peroxidase–like catalytic and fluorescent bifunctional properties of glutathione protected gold nanoclusters (GSH–AuNCs). The GSH–AuNCs exhibit inherent peroxidase–like activity and accelerate the decomposition of H2O2 into hydroxyl radicals. The produced hydroxyl radicals oxidize terephthalic acid (TA), a typical non–fluorescent substrate of peroxidase, to a highly fluorescent product hydroxyterephthalate (TAOH). Upon excitation with single–wavelength at 315 nm, dual–emission fluorescence peaks were recorded at 430 and 600 nm simultaneously. The fluorescence signal of TAOH at 430 nm continuously increased with increasing the concentration of H2O2 while the fluorescence signal of GSH–AuNCs at 600 nm remained unchangeable. Based upon on these facts, a ratiometric fluorescent nanosensor was fabricated for H2O2 assay with TAOH as response unit and GSH–AuNCs as reference, respectively. By converting glucose into H2O2 with catalytic oxidation of glucose oxidase (GOx), this nanosensor was further exploited for glucose assay. Under the optimum conditions, the detection limits of 10 nmol/L H2O2 and 20 nmol/L glucose were acquired. The relative standard deviations were less than 5% for both H2O2 and glucose (5.0 μmol/L solution, n = 11). The practicability of the nanosensor was verified by the determination of glucose in human serum samples. This nanosensor can be easily expanded as a general platform for the detection of other substances involving H2O2 produced or consumed.
关键词： Intrinsic peroxidase-like activity,Fluorescent gold nanoclusters,Hydrogen peroxide,Glucose,Ratiometric fluorescence,Nanosensor
更新于2025-11-14 17:03:37