ELECTROCHIMICA ACTA
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2022
·
IF 7.336
Weijie Fu,Kai Zhang,Xiaohua Zhang,Guorong Fan,Zongde Wang,Shangxing Chen,Yangping Wen,Peng Wang
Transition metal sulfide functionalized hierarchically porous carbons as colorimetric-electrochemical dual-mode nanozyme sensing platform for the visual qualitative colorimetric and quantitative electrochemical detection of dopamine (DA) are synthesized by hydrothermal method using Chinese fevervine herb rich in sulfur as the carbon source and sulfur source, and different transition metal chlorides as the metal sources. The introduction of FeCl 3 is more favorable to the generation of micropores, while the introduction of other transition metal chlorides is beneficial to the generation of mesopores and macropores. FeS 2 functionalized hierarchically porous carbon (FSPC) with large specific surface area shows better conductivity, more excellent electrocatalytic ability, and higher peroxidase-like and oxidase-like activities. The inhibitory colorimetric assay for DA designed by the oxidase-like properties of FSPC without the intervention of H 2 O 2 , making the reaction system more stable. FSPC displays excellent electrochemical responses for DA with about 50-fold peak current compared with bare electrode, and possesses a low detection limit of 0.015 μM (S/ N = 3) in a wide linear range of 0.05–1000 μM. This work will provide a new idea for the nanozyme sensing of DA with colorimetric-electrochemical dual-mode and a new possibility for application in clinical medicine.
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PREPARATIVE BIOCHEMISTRY & BIOTECHNOLOGY
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2022
·
IF 3.141
YuLiang Jiao,YuYing Zhu,ShuMin Zeng,ShuFang Wang,Jing Chen,XiangHong Zhou,GuiZhen Ma
A novel uricase producing marine bacterium Priestia flexa alkaAU was isolated and identified. The 16S rDNA and the uricase coding gene were sequenced, analyzed and submitted to GenBank. The uricase from Priestia flexa alkaAU (PFU) was purified, determined to be 58.87 kDa, and conjugated with carboxymethyl chitosan (CMCS) by ionic gelation. CMCS conjugation had no effect on the optimum pH of PFU but decreased the optimum temperature by 10 °C. CMCS conjugation increased the specific activity of PFU by 53% at the human body temperature (37 °C) and small intestine’s pH (pH 6.8). Uricase thermostabilizing ability of CMCS was significant in the range of 37–80 °C but not at lower temperatures. For improvement of the pH stability of PFU, CMCS was more effective at pHs 3–5 than pHs 6–11. CMCS increased the half-life of PFU against artificial intestinal fluid by 1.5 folds, which demonstrated the potential capability of CMCS–PFU for oral administration.
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FOOD CHEMISTRY
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2022
·
IF 9.231
Xun Zhou,Yongxiang Wu,Yao Jiang,Chen Li,Longping Xu,Peng Cui,Xinsong She
Integrated one–dimensional CuO–nanowire arrays/Cu–foam (CuO–NWAs/Cu–foam) nanostructure, which was fabricated by oxidation and calcination, has been newly utilized as non–enzymatic electrocatalytic electrode for exploring histamine level. Under optimal condition of pH at 13 and potential at 0.55 V ( vs Ag/Ag/Cl), the sensitivity of CuO–NWAs/Cu–foam electrode towards non–enzymatic electrochemical histamine determination presented as high as 12.94 mA mM −1 cm −2 , linear range spanned between 0.5 and 1046 μM, a detection limit (S/N = 3) was about 44 nM. The unprecedented causes of ultrahigh sensitivity were physically contributed to enhancing active surface area and declining charge transfer resistance. More crucially, the outstanding selectivity, stability and reproducibility facilitated its practical capacity on evaluating histamine levels in different–bacteria fermented mandarin fish, which triggered the potential feasibility for commercializing non–enzymatic electrochemical determination of histamine with high sensitivity, reliable precision and low expenditure.
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SENSORS AND ACTUATORS B-CHEMICAL
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2022
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IF 9.221
Qing Zhang,Shangshang Ma,Li Zhang,Hongyan Wang,Xin Zhuo,Guizhi Wang,Yanyun Shen,Keying Zhang,Shao Su
Microfluidic chip for sensing heavy metal ions has been strongly attended due to its merits, but still remains a large challenge from long analysis time derived from the preconcentration process of metal ions. Herein, a heated flow channel was manufactured by 3D printing combined with a filter paper to construct a microfluidic chip, the thermocapillary convection strategy was introduced to accelerate ions migration, allowing for rapidly recognizing metal ions. The MnO 2 nanosheets-Au nanostars (MnO 2 NSs-AuNSs) film was employed as modifier to fabricate a flexible screen printed electrode (SPE) for high-efficiency detecting metal ions based on thermocapillary convection accelerating accumulation method. To verify the proposed strategy, the detection of Cu 2+ was chosen as a model. The results revealed that the proposed strategy possessed a rapid detection to Cu 2+ , which greatly improved the detection efficiency (saved 400 s of preconcentration time) and achieved a detection limit down to 0.0270 ppb. Interestingly, the constructed method was successfully used to evaluate Cu 2+ concentration in sweat samples with satisfactory results. This proposed method maybe provide new insight to develop a novel approach to rapidly and sensitively detect metal ions, which possess huge utilization potentiality for safeguarding human health.
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MOLECULES
·
2022
·Vol. 27
·期 20
·6779
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IF 4.927
Zhaoshen Li,Xiaochun Deng,Xiaoping Hong,Shengfa Zhao
Compared with natural enzymes, nanozymes have the advantages of good catalytic performance, high stability, low cost, and can be used under extreme conditions. Preparation of highly active nanozymes through simple methods and their application in bioanalysis is highly desirable. In this work, a nanozyme based on dispersion of hemin by graphene quantum dot (GQD) is demonstrated, which enables colorimetric detection of glutathione (GSH). GQD was prepared by a one-step hydrothermal synthesis method. Hemin, the catalytic center of heme protein but with low solubility and easy aggregation that limits its catalytic activity, can be dispersed with GQD by simple sonication. The as-prepared Hemin/GQD nanocomplex had excellent peroxidase-like activity and can be applied as a nanozyme. In comparison with natural horseradish peroxidase (HRP), Hemin/GQD nanozyme exhibited a clearly reduced Michaelis–Menten constant (Km) when tetramethylbenzidine (TMB) was used as the substrate. With H2O2being the substrate, Hemin/GQD nanozyme exhibited a higher maximum reaction rate (Vmax) than HRP. The mechanisms underlying the nanozyme activity were investigated through a free radical trapping experiment. A colorimetric platform capable of sensitive detection of GSH was developed as the proof-of-concept demonstration. The linear detection range was from 1 μM to 50 μM with a low limit of detection of 200 nM (S/N = 3). Determination of GSH in serum samples was also achieved.Keywords:nanozyme;graphene quantum dot;hemin;peroxidase-like activity;colorimetric determination of glutathione
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Chemosensors
·
2022
·Vol. 10
·期 10
·407
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IF 4.229
Yaqin Chen,Xia Peng,Yonghai Song,Guangran Ma
An electrochemical sensor based on a molecularly imprinted polymer membrane (MIP) was developed. The electrochemical sensor was prepared by electropolymerization of o-phenylenediamine (O-PD) on the surface of glassy carbon electrode (GCE), modified by AuNPs@covalent organic framework (COF) microspheres with ascorbic acid (AA) as template molecule. First, ultrasmall polyvinylpyrrolidone (PVP)-coated AuNPs were prepared by a chemical reduction method. Then, 1,3,5-tri(p-formylphenyl)benzene (TFPB) and N-boc-1,4-phenylene diamine (NBPDA) underwent an ammonaldehyde condensation reaction on PVP-coated AuNPs to form AuNPs@COFTFPB-NBPDAmicrospheres. The porous spherical structure of AuNPs@ COFTFPB-NBPDAcould accelerate the mass transfer, enlarge the specific surface area, and enhance the catalytic activity of PVP-coated AuNPs. The electrochemical sensors, based on AuNPs@ COFTFPB-NBPDA/GCE and nMIPs/AuNPs@COFTFPB-NBPDA/GCE, were applied for the detection of AA, with a detection limit of 1.69 and 2.57 μM, as well as linear ranges of 5.07 to 60 mM and 7.81 to 60 mM. The nMIPs/AuNPs@COFTFPB-NBPDAsensor had satisfactory stability, selectivity, and reproducibility for AA detection.Keywords:covalent organic framework;ascorbic acid;molecularly imprinted polymer;electrochemical sensor
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ANALYTICA CHIMICA ACTA
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2022
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IF 6.911
Qinqin Yang,Xipeng Cui,Ying Qin,Tiantian Lei,Yu He,Gongwu Song
MXene-based nanozymes have increased research enthusiasm in the field of food safety and environment monitoring. Herein, the Cu NCs/Ti 3 C 2 NSs nanocomposites were prepared by modifying copper nanoclusters (Cu NCs) on the surface of Ti 3 C 2 nanosheets (NSs) with a simple two-step method. The Cu NCs/Ti 3 C 2 NSs nanocomposites had outstanding tetraenzyme mimic activities, i.e. peroxidase (POD)-mimics, catalase (CAT)-mimics, ascorbic acid oxidase (AAO)-mimics and superoxide dismutase (SOD)-mimics. Modification of Cu NCs on Ti 3 C 2 NSs can enhance tetraenzyme mimic activities because of the synergistic catalytic effect between Cu NCs and Ti 3 C 2 NSs. The catalytic mechanism and steady-state kinetics of Cu NCs/Ti 3 C 2 NSs were also investigated. Based on the POD-mimic activity of Cu NCs/Ti 3 C 2 NSs, a simple and rapid colorimetric method was established for the on-site detection of hypoxanthine (Hx), with the linear range of 5–200 μM and limit of detection (LOD) was 0.25 μM. The visible color change with the increase of Hx concentration can be recognized by a smartphone APP to transfer the red (R), green (G) and blue (B) value for the quantitative analysis of Hx, with the linear range of 10–200 μM, which provided a convenient method for the real-time detection of Hx. This work not only provides a significant route to fabricate nanocomposite with outstanding tetraenzyme mimic activities but also offers a low-cost and rapid method for monitoring the freshness of aquatic products.
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NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 47
·22849-22861
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IF 3.925
Wenyue Li,Xiaoyan Ma,Senyang Song,Bo Shao,Xiaoju Liu,Jiahe Chen
With the development of wearable diagnostic and therapeutic technology, numerous researchers have shown great interest in integrated bifunctional electrode materials with a supercapacitor and sensing performance. Herein, we report a hydrangea-like metal–organic framework (Ni/Co-DAP MOF) with porous organic polymer DAP, obtained through the Schiff-base reaction of 3,5-diaminobenzoic acid (DABA) and terephthalaldehyde (TPAL), as a ligand for a supercapacitor and a glucose sensor. Benefiting from the porous and conjugated structure of DAP, the Ni/Co-DAP MOF presents a high specific capacitance of 2200 F g−1 at a current density of 1 A g−1. The asymmetric supercapacitor (ASC) device Ni/Co-DAP MOF//AC ASC with the Ni/Co-DAP MOF as the positive electrode delivers an outstanding energy density of 100.11 W h kg−1 at a power density of 849.98 W kg−1 and exhibits an excellent capacitance retention of 94% after 5000 cycles. In addition, the Ni/Co-DAP MOF also demonstrates excellent glucose sensing performance, including a high sensitivity of 278 μA cm−2 mM−1 in the range of 1.67 μM–8.03 mM and a detection limit of 0.557 μM (S/N = 3). The excellent electrochemical performance of the Ni/Co-DAP MOF highlights the general relevance of our reasonable design with porous DAP as a ligand and expands its broad prospects for energy storage and electrochemical sensing.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2022
·Vol. 33
·期 30
·23566-23579
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IF 2.779
Guo Qiwen,Liu Siyuan,Men Xinpeng,Chen Zhe,Yao Lei,Wang Geming,Zhao Hongyang,Lin Zhidong,Wu Qian
In this paper, an ultra-sensitive glassy carbon electrode modified with β-cyclodextrin and graphene oxide (β-CD-GO/GCE) has been prepared for the detection of biomolecules [ascorbic acid (AA), dopamine (DA) and uric acid (UA)] in aqueous solution at μM level. The three biomolecules (AA, DA and UA) can be simultaneously detected by the modified electrodes, and the electrical signals corresponding to various biomolecules can be identified clearly in cyclic voltammetry and differential pulse voltammetry curves. The simultaneous detection limits of AA, DA, UA were 4.58, 1.56, 1.27 μM, respectively. This ultra-sensitivity should be attributed to the formation of host–guest complexes between β-CD and the biomolecules. Furthermore, the anti-interference experiments indicated the β-CD-GO/GCE exhibited satisfactory selective recognition performance.
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CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Junming Zhang,Yingyi Ma,Yuhang Han,Kaizheng Xu,Shun Yao,Lei Shi,Min Zhu
Restacking or aggregation inhibition of MXene nanosheets is crucial to the maintenance of their excellent electrochemical performance during use. In this study, a positively charged surfactant is inserted into the MXene nanolayers through a simple self-assembly process based on electrostatic interaction, producing a MXene/surfactant complex with enlarged interlayer spacing. Then 3D MXene-based porous structure could be prepared by the facile and low-cost breath figure method, in which MXene/surfactant complex is used as a casting material, therefore the inhibition of restacking or aggregation and increase of surface area at multiscale are realized in one system at the same time. Benefiting from the high conductivity of MXene and increased surface area of 3D porous structure that can provide massive active sites and facilitate the electrolyte infiltration and ion or electron access, enhanced electrochemical performance, for instance, electrochemical sensing of dopamine (DA) is shown. A low detection limit of 36.8 nM with excellent anti-interference, reproducibility, repeatability and long-term stability is realized. Good accuracy for DA detection in real biological samples is also confirmed by determining DA concentration in complex human urine samples. More importantly, porous structure such as pore size, uniformity, order and porosity can be adjusted through tuning the fabrication conditions, thereby regulating its electrochemical properties. This work not only provides a high-performance electrode for electrochemical sensing, but also offers a simple and practical strategy for the construction of 3D porous MXene film that holds great potential in electromagnetic interference shielding, supercapacitors and batteries.
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ANALYTICA CHIMICA ACTA
·
2022
·
IF 6.911
Jing Qian,Juan Yang,Yuanyuan Zhang,Ting Zeng,Qijin Wan,Nianjun Yang
Development of sensitive, selective, and facile electrochemical analytical approaches to monitor tryptophan in different samples is of high significance. For such approaches, efficient electrodes play the key role. Herein, a NiMn-layered double hydroxide (LDH)@poly- l -lysine (PLL) composite has been prepared through in-situ electro-polymerization and further utilized to monitor tryptophan in medicament and biological systems. The as-synthesized NiMn-LDH@PLL composite is highly stable and features a flower-like morphology. It is found that the electron transfer rate of NiMn-LDH@PLL is greatly improved due to the introduction of PLL. The existing Lewis acid—base interaction between LDH and PLL contributes to the increase of unsaturated metal sites and endows this heterojunction composite with high electrocatalytic activity . Especially, the NiMn-LDH (2:1)@PLL composite displays much improved electrochemical response toward tryptophan sensing. This is due to reasonable balance between the outstanding electrocatalytic ability of nickel and the conductivity improvement caused by manganese species. On the other hand, the coordination promotion between NiMn-LDH and PLL is also conducive to improve the sensitivity of electrochemical response. The fabricated sensor exhibits wide linear response in the concentration ranges of 0.1–40 μM and 40–130 μM for tryptophan detection, along with a low detection limit of 52.7 nM. It further displays a high anti-interference ability for tryptophan monitoring even in the presence of other coexistent amino acids and small-sized biological molecules. This study provides a new way to employ LDHs as brilliant sensing platform to ensemble electrochemical sensors for the monitoring of biomolecules.
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NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 47
·22778-22785
·
IF 3.925
Xiaozhi Li,Jutao Qiao,Dan Luo,Siyi Xu,Yuefeng Liu,Hao Liu
In this study, Ni nanoparticles were grown on a silver-coated nylon yarn (SCNY) surface by electrochemical deposition to prepare SCNY@Ni. The hierarchical Ni–Ag nanostructure promoted their synergistic effect, which enhanced the electrocatalytic behavior of glucose oxidation. The test result of SCNY@Ni showed its high sensitivity (115.26 μA mM−1 cm−2 and 67.37 μA mM−1 cm−2) with a wide linear response (from 2 μM to 1 mM and from 1 mM to 22 mM) of glucose con-centration range, a low detection limit (LOD) of 2 μM, fast response time (3 s), and good selectivity for glucose determination in the presence of sucrose (SU), aceta-mino phenol (AP), D-fructose (D-Fru), ascorbic acid (AA), dopamine (DA), hydro-quinone (HQ) and uric acid (UA) as potential interference species. Also, SCNY@Ni exhibited excellent stability, repeatability, reproducibility and flexibility. It has good prospects for large-scale production.
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