ANALYTICA CHIMICA ACTA
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2020
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IF 5.977
Yan Liu,Lianying Zhang,Qinge Li,Han Dai,Ting Xiang,Gangyi Yang,Ling Li
In this work, a colorimetric assay for visfatin detection is described. The mixed valence state Ce-MOF (MVCM) modified by platinum nanoparticles (Pt NPs) is used as a novel catalyst. MVCM exhibits excellent intrinsic peroxidase-like catalytic activity due to the spontaneous recycling of the Ce(III)/Ce(IV) system. Pt NPs serve not only as a carrier of the –NH 2 -modified single strand DNA (S1) but also as a synergistic catalyst of MVCM. The capture probe (S2) attached to the streptavidin-modified magnetic beads (Mag-SA) could combine with the aptamer to form the Mag-SA/S2/aptamer complex. When in the presence of the target visfatin, aptamer specifically combines with the visfatin, which induces the release of Mag-SA/S2 from the Mag-SA/S2/aptamer complex. At this time, the [email protected] /S1 complex connects with the released Mag-SA/S2, which quickly catalyzes the 3,3,3′,3′-tetramethylbenzidine (TMB), leading to a color change. Under optimal conditions, the absorbance increases linearly when the concentration ranges from 1 ng mL −1 to 100 ng mL −1 , and the detection limit is as low as 0.11 ng mL −1 . Furthermore, Mag-SA/S2 can be reused at least five times by using the uracil-DNA glycosylase (UDG) and an external magnetic field. The proposed method shows satisfying reproducibility, stability, specificity, and sensitivity, and it was successfully applied to detect visfatin in spiked human serum samples. Thus, it has great potential for clinical research, detection, and catalytic applications.
研究领域:
分析化学
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纳米技术
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生物传感器
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临床诊断
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产品关联
DOI
PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Baihe Sun,Guanghui Li,Yue Wu,Junwei Gai,Min Zhu,Weiwei Ji,Xiaoying Wang,Fenghua Zhang,Wanting Li,Jingjin Hu,Yuxin Lou,Gusheng Feng,Xijun Han,Jinwen Dong,Jiayuan Peng,Jiawei Pei,Yakun Wan,Yanfei Li,Linlin Ma
Apolipoprotein A1 (Apo-A1) is a well-recognized biomarker in tissues, closely associated with cardiovascular diseases such as atherosclerosis, coronary artery disease, and heart failure. However, existing methods for Apo-A1 determination are limited by costly equipment and intricate operational procedures. Given the distinct advantages of electrochemical immunosensors, including affordability and high sensitivity, along with the unique attributes of nanobodies (Nbs), such as enhanced specificity and better tissue permeability, we developed an electrochemical immunosensor for Apo-A1 detection utilizing Nb technology. In our study, Ce-MOF@AuNPs nanocomposites were synthesized by using ultrasonic methods and applied to modify a glassy carbon electrode. The Nb6, screened from an Apo-A1 immunized phage library, was immobilized onto the nanocomposite material, establishing a robust binding interaction with Apo-A1. The recorded peak current values demonstrated a logarithmic increase corresponding to Apo-A1 concentrations ranging from 1 to 100,000 pg/mL, with a detection limit of 36 fg/mL. Additionally, the developed immunosensors demonstrated high selectivity, good stability, and reproducibility. Our methodology was also effectively utilized for serum sample analysis, showing good performance in clinical assessments. This electrochemical immunosensor represents a promising tool for Apo-A1 detection, with significant potential for advancing cardiovascular disease diagnostics.
研究领域:
生物医学工程
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分析化学
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纳米技术
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心脏病学
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免疫学
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产品关联
DOI
PubMed
高影响因子
FOOD CONTROL
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2024
·
IF 5.6
Yiting Zhou,Jingming Zhou,Yankai Liu,Yumei Chen,Hongliang Liu,Xifang Zhu,Peiyang Ding,Chao Liang,Enping Liu,Sixuan Wu,Aiping Wang
A novel electrochemical immunosensor for the sensitive detection of monensin (MON) was developed. The sensor platform utilized anti-MON monoclonal antibodies and a nanocomposite (Ce-MOF@AgAuNPs), composed of cerium-based metal-organic frameworks decorated with silver-gold nanoparticles. The physicochemical properties of the Ce-MOF@AgAuNPs nanocomposite were investigated using transmission electron microscopy, energy dispersive X-ray, UV–Vis spectrophotometry, and fourier transform infrared techniques. The stepwise fabrication process and electrochemical performance of the immunosensor were investigated through electrochemical impedance spectroscopy and cyclic voltammetry. The sensor exhibited excellent analytical performance for MON detection, with a wide linear response range from 0.05 to 250 ng mL −1 and a low LOD of 0.008 ng mL −1 . Additionally, the immunosensor exhibited high accuracy, with recovery rates ranging from 97.4% to 103.2% in chicken liver and 96.0%–104.7% in milk. This developed immunosensor shows great potential for food safety applications, demonstrating high specificity, stability, and reproducibility in the detection of MON.
研究领域:
分析化学
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电化学
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食品安全
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纳米技术
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产品关联
DOI
高影响因子
TALANTA
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2024
·
IF 5.6
Yi Xiao,Pengcheng Huang,Fang-Ying Wu
α-Glucosidase, which directly involves in the metabolism of starch and glycogen and causes an increase in blood sugar level, is the major target enzyme for the precaution and therapy of type II diabetes. Based on the previous work, we adopted a post-synthetic modification method to encapsulate Tb 3+ into Ce-MOF nanozyme which owned mixed valence states. Tb@Ce-MOF displayed induced luminescence characteristic and exceptional oxidase-like activity that could oxidize colorless 3,3′,5,5′-tetramethylbenzidine (TMB) to blue ox-TMB. α-Glucosidase can hydrolyze the substrate l -ascorbic acid-2- O -α- d -glucopyranosyl (AAG) to generate ascorbic acid (AA), which could increase the Ce 3+ /Ce 4+ redox valence mode in Tb@Ce-MOF, leading to the inhibition of the allochroic reaction of TMB and the decreased absorption of ox-TMB at 652 nm. The energy transfer (EnT) process from Ce 3+ to Tb 3+ will enhance due to the increased Ce 3+ /Ce 4+ mode in Tb@Ce-MOF, which will result in an enhanced fluorescence signal of Tb@Ce-MOF at 550 nm. But the addition of inhibitor acarbose will inhibit the above process. We have constructed a dual-mode detection platform of α-glucosidase and its inhibitor via colorimetric and fluorometric method. The linear range of α-glucosidase were 0.01–0.5 U/mL (colorimetric mode) and 0.8–1.5 U/mL (fluorometric mode), respectively, with a detection limit as low as 0.0018 U/mL. Furthermore, our approach was also successfully employed to the analysis of α-glucosidase in serum samples.
研究领域:
分析化学
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生物化学
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材料科学
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糖尿病研究
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产品关联
DOI
PubMed
高影响因子
TALANTA
·
2023
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IF 6.1
Yilin Wang,Jia Chen,Chenxi Wang,Li Zhang,Yaqi Yang,Chao Chen,Yixi Xie,Pengcheng Zhao,Junjie Fei
As a common antioxidant and nutritional fortifier in food chemistry, rutin has positive therapeutic effects against novel coronaviruses. Here, Ce-doped poly(3,4-ethylenedioxythiophene) (Ce-PEDOT) nanocomposites derived through cerium-based metal-organic framework (Ce-MOF) as a sacrificial template have been synthesized and successfully applied to electrochemical sensors. Due to the outstanding electrical conductivity of PEDOT and the high catalytic activity of Ce, the nanocomposites were used for the detection of rutin. The Ce-PEDOT/GCE sensor detects rutin over a linear range of 0.02–9 μM with the limit of detection of 14.7 nM (S/N = 3). Satisfactory results were obtained in the determination of rutin in natural food samples (buckwheat tea and orange). Moreover, the redox mechanism and electrochemical reaction sites of rutin were investigated by the CV curves of scan rate and density functional theory. This work is the first to demonstrate the combined PEDOT and Ce-MOF-derived materials as an electrochemical sensor to detect rutin, thus opening a new window for the application of the material in detection.
研究领域:
分析化学
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电化学
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材料科学
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食品化学
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产品关联
DOI
PubMed
高影响因子
Separations
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2024
·Vol. 11
·期 5
·144
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IF 2.5
Xinbiao Mao,Mingyu Ou,Wenjun Zhao,Shuangting Yu,Hao Xu
Levofloxacin (LFX), which is difficult to degrade effectively due to its molecular stability, has become an problem that needs to be solved urgently. The advanced oxidation technology of persulfate has received increasing attention from researchers. In this study, a Ce-MOF derivative (Ce-MOF-T) was prepared by hydrothermal synthesis and calcination, which synergistically responded to electroactivation to generate sulfate radicals for the efficient degradation of LFX. It has been proven that electrical activation and the Ce-MOF derivatives work together to generate sulfate radicals and effectively degrade LFX. Ce-MOF-550-modified carbon cloth was used as the cathode and a platinum electrode as the anode, the concentration of LFX was 20 mg·L−1, the loading of Ce-MOF-550 was 15 mg, pH = 5, the concentration of sodium persulfate (PMS) was 0.3 g·L−1, the current density was 100 A·m−2, and the degradation rate was 82.05% after 1 h of reaction and 95% after 3 h of reaction. After five cycle tests, the degradation rate was still higher than 75.00%, indicating that the material had good stability. In addition, the degradation of LFX was consistent with a quasi-primary kinetic reaction with apparent rate constants of 2.26 × 10−2min−1.
研究领域:
环境科学
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化学工程
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材料科学
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水处理
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高级氧化过程
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产品关联
DOI
高影响因子
PROGRESS IN ORGANIC COATINGS
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2025
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IF 7.3
Xianliang Li,Yawei Shao,Zhihao Chen,Yanqiu Wang,Junyi Wang
In this study, a fluorescence and Fe 3+ ions-responsive cerium-based metal organic framework is decorated on phytic acid-glucose hydrothermal copolymer-coated montmorillonite (MMT@CP@Ce-MOF) nanocontainer, which was developed for Q235 carbon steel's corrosion protection and detection in solution, waterborne epoxy coatings (WEP), and solvent epoxy coatings (EP). In the solution phase, the corrosion detection ability of Q235 carbon steel was introduced, relying on the Fe 3+ ions-responsive characteristic of MMT@CP@Ce-MOF. In the coating phase, WEP and EP with good barrier effect, active anti-corrosion, self-detection, and good mechanical performance were fabricated by integrating MMT@CP@Ce-MOF nanocontainers. The EIS results indicated that 2D MMT@CP@Ce-MOF based composite coating showed better anti-corrosion performance (the |Z| f= 0.01Hz value of EP-MMT@CP@Ce-MOF and WEP-MMT@CP@Ce-MOF remained 1.33 × 10 9 Ω·cm 2 and 2.71 × 10 8 Ω·cm 2 , respectively, far higher than the bare coating) after 40 d immersion. At the same time, the Ce-MOF nanosensor could accurately reflect the occurrence of corrosion at the coating damage sites. Furthermore, high adhesion force (2–3 times higher than bare coating) and results of coating fracture surface showed that homogenously incorporated MMT@CP@Ce-MOF could improve the composite coating mechanical properties by chemical interaction with the epoxy polymer.
研究领域:
材料科学
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腐蚀工程
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纳米技术
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表面工程
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涂层技术
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传感器
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
Nanomaterials
·
2024
·Vol. 14
·期 16
·1352
·
IF 4.4
Teng Gao,Hongqi Chu,Shijie Wang,Zhenzi Li,Wei Zhou
Photocatalysis is the most promising green approach to solve antibiotic pollution in water, but the actual treatment effect is limited by photocatalytic activity. Herein, Bi and BiOCl were loaded onto the surface of Ce-MOF (metal–organic framework) using an electrostatic adsorption method, and a special ternary heterojunction of Ce/Bi/BiOCl was successfully prepared as a photocatalyst for the degradation of tetracycline (TC). FTIR demonstrated that the obtained photocatalyst contains functional groups such as -COOH belonging to Ce-MOF and characteristic crystal planes of Bi and BiOCl, indicating the successful construction of a ternary photocatalyst. The results of UV–vis absorption spectra confirm that the band gap of Ce/Bi/BiOCl heterojunction is reduced from 3.35 eV to 2.7 eV, resulting in an enhanced light absorption capability in the visible light region. The special ternary heterojunction constructed by Ce-MOF, Bi, and BiOCl could achieve a narrow band gap and reasonable band structure, thereby enhancing the separation of photogenerated charges. Consequently, the photocatalytic performance of the Ce/Bi/BiOCl ternary heterojunction was significantly enhanced compared to Ce-MOF, Bi, and BiOCl. Therefore, Ce/Bi/BiOCl can achieve a photocatalytic degradation rate of 97.7% within 20 min, which is much better than Bi (14.8%) and BiOCl (67.9%). This work successfully constructed MOF-based ternary photocatalysts and revealed the relationship between ternary heterojunctions and photocatalytic activity. This provides inspiration for constructing other heterogeneous catalysts for use in the field of photocatalysis.
研究领域:
环境科学
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材料科学
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产品关联
DOI
PubMed
高影响因子
Catalysts
·
2019
·Vol. 9
·期 8
·682
·
IF 3.444
Wenjie Sun,Xiaomin Li,Chao Sun,Zhen Huang,Hualong Xu,Wei Shen
Metal organic frameworks (MOFs) have recently been used as precursors of the catalysts for the combustion of volatile organic compounds (VOCs). In the present work, three kinds of CeO2catalysts were successfully synthesized from Ce-MOF-808, Ce-BTC, and Ce-UiO-66, with specific topological structures and coordinate environments. Catalysts with small particle size, stacking mode, and structural defects could be created by pyrolysis of Ce-MOFs, which affects the activity in the toluene combustion significantly. Raman spectra, XPS, and OSC studies were performed to reveal the formation of defect sites. The thermal redox properties were determined by H2-TPR. Catalytic activity tests were conducted on the toluene combustion, and CeO2-MOF-808 showed the best catalytic performance (T90 = 278 °C) due to its having the largest specific surface area, abundant active surface oxygen species, and low-temperature reducibility.Keywords:Ce-MOF;cerium oxide;catalytic combustion of toluene;environmental catalysis;pyrolysis process
研究领域:
材料科学
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环境科学
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催化化学
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产品关联
DOI
高影响因子
MICROCHEMICAL JOURNAL
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2025
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IF 5.1
Jiatong Li,Jie Li,Jiakang Hu,Yongxin Li,Hui Huang
The dual enzyme-like activities (phosphatase-like activity and laccase-like activity) of one nanozyme (Ce-MOF-808) were employed to develop a nanozyme cascade sensor for the facile and selective detection of profenofos. It was found that the nanozyme Ce-MOF-808 had phosphatase-like activity (V max = 0.31 μM/min and K m = 0.014 mM) and laccase-like activity (V max = 6.27 μM/min and K m = 0.033 mM). In the cascade sensor process, profenofos was first hydrolyzed by Ce-MOF-808. The P O bond was cleaved to produce 4-bromo-2-chlorophenol containing phenol through the phosphatase-like activity of nanozyme. The colorless product was efficiently oxidized because of the laccase-like activity of nanozyme, and then reacted with the color rendering agent 4-aminoantipyrine to produce the red quinone imine. The absorbance peak at 510 nm fitted a linear curve. The limit of detection (LOD) was determined to be 3.33 μg/mL in this method. The quantitative detection of profenofos was conducted on a variety of different real samples. Nanozymes could be stored at 4 ℃ for a long time and the detection method was simple and direct. The nanozyme cascade sensor was convenient and rapid for the detection of pesticides and had promising application prospects in the conventional rapid detection of pesticides in the field.
研究领域:
生物化学
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分析化学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
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2018
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IF 5.667
Jing Zhang,Xiaojian Xu,Lu Chen
This work constructed an ultrasensitive electrochemical bisphenol A (BPA) sensor using hierarchical Ce-metal-organic framework (Ce-MOF) modified with cetyltrimethylammonium bromide (CTAB) as a sensing platform. Ce-MOF had been successfully prepared and conveniently modified with a cationic surfactant (CTAB) via the electrostatic interaction. Ce-MOF and CTAB/Ce-MOF were characterized by scanning electron microscopy, X-ray diffraction, infrared spectrum, thermogravimetric analysis and zeta potentials analysis. CTAB/Ce-MOF suspension was dropped onto glassy carbon electrode (GCE) surface to fabricate CTAB/Ce-MOF/GCE. Combined with preconcentration of BPA of the long alkane chain in CTAB via hydrophobic interaction and electrocatalytic activity of Ce-MOF, the dual amplification made CTAB/Ce-MOF/GCE exhibit high electrochemical response toward the oxidation of BPA, and an electrochemical BPA sensor was constructed based on CTAB/Ce-MOF/GCE by differential pulse voltammetry. The designed BPA sensor had a wide linear range from 0.005 to 50 μmol L −1 and a low detection limit of 2.0 nmol L −1 (S/N = 3). The proposed sensor had excellent reproducibility, stability and anti-interference, and was successfully employed for BPA detection in real samples. This convenient and sensitive sensor proved to be a promising and reliable tool for detecting BPA in food and environmental pollution.
研究领域:
环境科学
·
分析化学
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产品关联
DOI
高影响因子
Molecular Catalysis
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2021
·
IF 5.062
Rui Tang,Niamat Ullah,Yajun Hui,Xin Li,Zhenhua Li
Carbon dioxide hydrogenation for value-added chemicals has been regarded as a promising way for CO 2 utilization. This paper describes the preparation of Ni/CeO 2 catalysts derived from Ce-MOF precursor by impregnation or one-pot method and their application in carbon dioxide methanation. Various techniques were employed to characterize the prepared catalysts, including N 2 adsorption–desorption, X-ray diffraction (XRD), Raman spectroscopy, field emission scanning electron microscopy (SEM), H 2 -temperature programmed reduction (H 2 -TPR), H 2 -temperature programmed desorption (H 2 -TPD) and CO 2 -temperature programmed desorption (CO 2 -TPD). The results showed that compared with commercial CeO 2 and CeO 2 prepared by precipitation, CeO 2 derived from Ce-MOF exhibited more oxygen vacancies and lower temperature reducibility, making it more beneficial for the adsorption and activation of CO 2 . Consequently, nickel supported on rod-shaped CeO 2 derived from Ce-MOF exhibited higher CO 2 conversion and methane selectivity at low temperatures. Furthermore, the Ni/CeO 2 −M-1 catalysts prepared by one-pot method showed superior activity since nickel could be partially incorporated into ceria lattice, leading to the formation of Ce 1-x Ni x O 2-y solid solutions and oxygen vacancies. The effect of nickel loading on the properties of the catalysts by one-pot method was also investigated, and the optimum Ni loading was 15 wt.% owing to the maximum number of oxygen vacancies being reached.
研究领域:
催化化学
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环境科学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）