- 标题
- 摘要
- 关键词
- 实验方案
- 产品
-
Preparation of Ag-AgVO3/g-C3N4 composite photo-catalyst and degradation characteristics of antibiotics
摘要： The degradation of tetracycline by silver vanadate (AgVO3), graphite-like carbon nitride (g-C3N4) and their composites was studied by visible light photocatalysis. Their structures and morphologies were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Their degradation intermediates were analyzed by GC-MS. Nanorod silver vanadate was synthesized by hydrothermal method. The results show that the gap between nanorods is reduced by adding spinning carbon nitride, and the photocatalytic performance of the composite is stronger than that of single material. The reaction rate constants of Ag-AgVO3/g-C3N4 composites were 0.0298 min-1, 2.4 and 2.0 times that of g-C3N4 (K=0.0125 min-1) and AgVO3 (K=0.0152 min-1), respectively. At 120 minutes, the degradation rate of the composites reached 83.6%. The degradation of tetracycline was confirmed by GC-MS, and a possible degradation process was proposed.
关键词： Photo-catalysis,Carbon nitride,Antibiotics,Visible light,Silver vanadate
更新于2025-11-21 10:59:37
-
A “turn-on” fluorometric assay for kanamycin detection by using silver nanoclusters and surface plasmon enhanced energy transfer
摘要： A rapid method is described for the determination of the antibiotic kanamycin. It integrates a kanamycin-binding aptamer and surface plasmon enhanced energy transfer (SPEET) between DNA-templated silver nanoclusters (AgNCs) and gold nanoparticles (AuNPs). The AgNCs and AuNPs were selected as energy donor and energy acceptor, respectively. The aptamer was designed to regulate the energy transfer between AgNCs and AuNPs. The aptamer was adsorbed on the AuNPs. Upon addition of kanamycin, the aptamer-kanamycin complex is formed, and this results in the aggregation of the AuNPs in high salt concentration, the formation of a blue coloration, and in the suppression of the SPEET process. The fluorescence of the AgNCs (with excitation/emission peaks at 560/600 nm) is quenched by the aptamer protected AuNPs in absence of kanamycin. The fluorescence on addition of kanamycin increases linearly in the 5 to 50 nM concentration range, with a lower detection limit of 1.0 nM (at S/N = 3). The assay can be performed within 30 min. It was successfully applied to the determination of kanamycin in spiked milk samples, and recoveries ranged between 90.2 and 95.4%. Conceivably, the strategy has a wide potential for screening by simply changing the aptamer.
关键词： Ag NCs,Milk analysis,Antibiotics detection,Au NPs,Food safety,Aptasensor
更新于2025-11-19 16:46:39
-
Enzyme-free fluorometric assay for chloramphenicol based on double stirring bar-assisted dual signal amplification
摘要： An enzyme-free fluorometric assay is described that accomplishes dual signal amplification by making use of a two stirring bars. Two Y-shaped DNA probes were designed and placed on the bars. When the target (with chloramphenicol as model analyte) is added, it triggers target recycling and simultaneously catalyzes hairpin assembly (CHA). A large fraction of DNA primers is released by the analyte from the bar to the supernatant and open hairpins with G-quadruplex DNA sequence. The G-quadruplex can specifically bind thioflavin T (ThT) to emit fluorescence (with excitation/emission maxima at 445 and 485 nm) for quantification of chloramphenicol. An enzyme is not needed. ThT is added to the system as a fluorescent DNA probe. All this strongly reduces the cost for sensor construction and usage. The dual signal amplification steps occur simultaneously which reduces the detection time. The assay was successfully employed to the determination of CAP in spiked milk and fish samples within 60 min and with a 16 pM limit of detection (at S/N = 3).
关键词： Food safety,Antibiotics detection,Thioflavin T,Catalyzed hairpin assembly,Target recycling
更新于2025-11-19 16:46:39
-
Zero background and triple-signal amplified fluorescence aptasensor for antibiotics detection in foods
摘要： It's important to eliminate matrix interference for accurate detecting antibiotic residues in complex food samples. In this study, we designed a zero-backgrounded fluorescence aptasensor to achieve on-site detection of antibiotic residues, with chloramphenicol (CAP) as representative analyte. Moreover, a three stir-bars assisted target recycling system (TSBTR) was designed to achieve triple signal amplification and increase the sensitivity. The bars included one magnetic stir-bar modified with two kinds of long DNA chains, and two gold stir-bars modified with Y shape-duplex DNA probes respectively. In the presence of CAP, the target could recurrently react with the probes on the bars and replace a large amount of long DNA chains into supernatant. After then, the bars were taken out and SYBR green dye was added to the solution. The dye can specifically intercalate into the duplex structures of DNA chains to emit fluorescence while not emitting a signal in its free state. Under the optimized experimental conditions, a wide linear response range of 5 orders of magnitude from 0.001 ng mL?1 to 10 ng mL?1 was achieved with a detection limit of 0.033 pg mL?1 CAP. The assay was successfully employed to detect CAP in food samples (milk & fish) with consistent results with ELISA's. High selectivity and sensitivity were attributed to the zero background signal and triple signal-amplification strategy. Moreover, the detection time can be shortened to 40 min due to that three signal amplified process can occur simultaneously. The fluorescent aptasensor was also label- and enzyme-free. All these ensure the platform to be rapid, cost-effective, easily-used, and is especially appropriate for detection antibiotics in food safety.
关键词： Three stir-bars assisted target recycling,Triple signal amplification,Zero background signal,Fluorescence aptasensor,Antibiotics
更新于2025-11-19 16:46:39
-
Impact of doped metals on urea-derived g-C3N4 for photocatalytic degradation of antibiotics: Structure, photoactivity and degradation mechanisms
摘要： Metal doping is an appealing modification strategy of graphitic carbon nitride (g-C3N4) to improve its photocatalytic activity. The interactions of g-C3N4 precursors with metals, however, has often been underappreciated, which can induce great impacts on g-C3N4 formation and properties. Herein, the impacts of metals (Na, K, Ca, Mg) on the morphology, structure, and photoactivity of urea-derived g-C3N4 were investigated. Our TEM and XPS results confirmed that the interactions of doped metals with urea precursors lead to the incorporation of O atoms from urea molecules into the framework of g-C3N4. Due to the synergistic effects of the metals and structural O atoms, doped g-C3N4 performed an elevated photodegradation of antibiotics under the visible light irradiation, which was attributed to the enhanced light-harvesting and reduced charge recombination. In addition, the doped metals presented uneven regulation on the band structures and morphology of g-C3N4. As a result, both superoxide and hydroxyl radicals were generated by g-CN-Na and g-CN-K, whereas, only superoxide radicals were involved in g-CN, g-CN-Ca and g-CN-Mg. Consequently, diversified photodegradation mechanisms for enrofloxacin (ENR) were observed that the g-CN, g-CN-Ca and g-CN-Mg reaction systems mainly attacked the piperazine moiety of ENR while g-CN-Na and g-CN-K provided additional photodegradation pathway by attacking quinolone core of ENR. The present work could provide new insights into further understanding of doping chemistry with g-C3N4.
关键词： Metal doping,Photocatalytic degradation of antibiotics,g-C3N4,Visible light photocatalysis
更新于2025-11-14 15:24:45
-
Efficient visible light driven degradation of sulfamethazine and tetracycline by salicylic acid modified polymeric carbon nitride via charge transfer
摘要： Photocatalysis has been widely studied as a promising technique for removal of organic pollutants in wastewater. A modified carbon nitride has been designed for this purpose. In this study, a facile method to synthesize distorted carbon nitride by simply copolymerizing urea and salicylic acid (SA) has been explored. The incorporation of SA induced the structure change from planar structure to distorted curls structure. Compared to pristine CN, the CN-SA shows wide light absorption, which is attributed to the n → π* transition at the nitrogen atoms with lone pair electrons of heptazine units. The photoelectrode of CN-SA exhibited higher photocurrent and lower charge resistance than that of pristine CN electrode, indicating that the photogenerated charge carriers of CN-SA are more efficiently separated. As a result, the optimal CN-SA shows 2-fold enhancement in degradation of tetracycline (TC) as compared to pristine CN. Furthermore, we found that the degradation rate of sulfamethazine (SMZ) was 0.0823 min?1 using the CN-SA photocatalyst, which is three times higher than that of pristine CN (0.0293 min?1). In addition, the CN-SA shows good stability without structural change or loss of photocatalytic performance after four cycles. According to the radical species trapping experiments and electron spin resonance analyses, ?O2? and h+ were the main active species involved in the degradation of organic pollutants. The developed strategy provides a novel approach to design the tunable band structure of organic semiconductor materials for various applications.
关键词： Salicylic acid,Photocatalysis degradation,Carbon nitride,Charge separation,Antibiotics
更新于2025-11-14 14:48:53
-
Fabrication of high efficiency visible light Z-scheme heterostructure photocatalyst g-C3N4/Fe0(1%)/TiO2 and degradation of rhodamine B and antibiotics
摘要： We have prepared and studied a novel low cost catalyst of g-C3N4/Fe0(1%)/TiO2, using a simple process involving the formation of zero valence iron by chemical reduction. This ternary catalyst g-C3N4/Fe0(1%)/TiO2 was characterized using XRD (X-Ray diffraction), UV–vis spectrum, EDS (Energy Dispersive spectrum) and TEM (transmission electron microscopy), it demonstrated high-visible-light activity in a wide range of pH condition, it can photo-catalytically degraded Rhodamine B (RhB), Tetracycline (TC), and Berberine hydrogen chloride (BH) (～98% in 90 min) under visible light. The high activity arises from the increased harvest of more visible light and the improved separation of photo-excited electrons and holes via Z-scheme and heterojunctions mechanism. Also, the time required to remove 100% RhB, TC, and 96% BH can be shortened from 90 min to 60 min by introducing 3.18 mM Na2SO3 to this photocatalysis system that assisted the generation of reactive oxidizing species and pollutant degradation. The results showed promising application prospect for this developed catalyst and the tested photocatalysis pollutant degradation system.
关键词： Antibiotics,z-scheme heterostructure,Rhodamine B,g-C3N4/Fe0(1%)/TiO2 photocatalyst,Visible-light
更新于2025-09-23 15:23:52
-
Enhanced removal of antibiotics from secondary wastewater effluents by novel UV/pre-magnetized Fe0/H2O2 process
摘要： Antibiotics have been frequently detected in the aquatic environment and are of emerging concern due to their adverse effect and potential of inducing antibiotic resistance. In this study, we developed an UV/pre-magnetized Fe0/H2O2 process (UV/pre-Fe0/H2O2) valid for neutral pH conditions, which could remove sulfamethazine (SMT) completely within only 30 min and enhance 1.8 times of SMT removal. Meanwhile, this process demonstrated outstanding mineralization capability with the TOC removal of 92.1%, while for UV/H2O2 and UV/Fe0/H2O2 system it was 53.9% and 72.1%, respectively. Better synergetic effect between UV irradiation and pre-Fe0/H2O2 system was observed, and the value of synergetic factor was 6.3 in the presence of both ions and humic acid, which was much higher than that in deionized water (4.4), humic acid (5.5) and ions (1.5). Moreover, the process could efficiently remove various antibiotics (800 μg L-1 oxytetracycline (OTC); 800 μg L-1 tetracycline (TC); 400 μg L-1 sulfadiazine (SD) and 400 μg L-1 SMT) in the secondary wastewater effluent. After optimization of Fe0 and H2O2 dosage, these antibiotics could be removed within 10 min (kapp (103) = 288.6 min-1) with a very low treatment cost of 0.1 USD m-3, and the EE/O value was only 1.22 kWh m-3. Compared with O3, UV/Fe2+/PDS, VUV/UV/Fe2+ and other US-based processes, the degradation rates by this process could enhance as high as 22.3 folds while the treatment cost or EE/O value could reduce greatly. Therefore, UV/pre-Fe0/H2O2 process is promising and cost-effective for the treatment of antibiotics in secondary wastewater effluents.
关键词： secondary wastewater effluents,synergetic effect,cost-effective,UV/pre-Fe0/H2O2 process,antibiotics
更新于2025-09-23 15:23:52
-
Magnetite-Supported Gold Nanostars for the Uptake and SERS Detection of Tetracycline
摘要： Magnetite nanoparticles (MNPs) decorated with gold nanostars (AuNSs) have been prepared by using a seed growth method without the addition of surfactants or colloidal stabilizers. The hybrid nanomaterials were investigated as adsorbents for the uptake of tetracycline (TC) from aqueous solutions and subsequent detection using surface-enhanced Raman scattering (SERS). Several parameters were investigated in order to optimize the performance of these hybrid platforms on the uptake and SERS detection of TC, including variable pH values and the effect of contact time on the removal of TC. The spatial distribution of TC and AuNS on the hybrid composites was accomplished by coupling SERS analysis with Raman imaging studies, allowing also for the determination of the detection limit for TC when dissolved in ultrapure water (10 nM) and in more complex aqueous matrices (1 μM). Attempts were also made to investigate the adsorption modes of the TC molecules at the surface of the metal NPs by taking into account the enhancement of the Raman bands in these different matrices.
关键词： SERS,antibiotics,magnetite nanoparticles,Au nanostars,water pollutants
更新于2025-09-23 15:23:52
-
A Signal-On Fluorosensor Based on Quench-Release Principle for Sensitive Detection of Antibiotic Rapamycin
摘要： An antibiotic rapamycin is one of the most commonly used immunosuppressive drugs, and also implicated for its anti-cancer activity. Hence, the determination of its blood level after organ transplantation or tumor treatment is of great concern in medicine. Although there are several rapamycin detection methods, many of them have limited sensitivity, and/or need complicated procedures and long assay time. As a novel fluorescent biosensor for rapamycin, here we propose “Q’-body”, which works on the fluorescence quench-release principle inspired by the antibody-based quenchbody (Q-body) technology. We constructed rapamycin Q’-bodies by linking the two interacting domains FKBP12 and FRB, whose association is triggered by rapamycin. The fusion proteins were each incorporated position-specifically with one of fluorescence dyes ATTO520, tetramethylrhodamine, or ATTO590 using a cell-free translation system. As a result, rapid rapamycin dose-dependent fluorescence increase derived of Q’-bodies was observed, especially for those with ATTO520 with a lowest detection limit of 0.65 nM, which indicates its utility as a novel fluorescent biosensor for rapamycin.
关键词： rapamycin,fluorescent biosensor,fluorescence quenching,photoinduced electron transfer,antibiotics
更新于2025-09-23 15:22:29