FOOD CHEMISTRY
·
2023
·
IF 8.8
Huilin Li,Jingying Yang,Ran Han,Yueyao Wang,Xintong Han,Shuo Wang,Mingfei Pan
Rapid, sensitive, specific and stable detection of mycotoxin in food remains an extremely crucial issue. Herein, a magnetic-fluorescent immunosensing platform for the detection of zearalenone (ZEN) was proposed. The platform utilized Au nanoparticles (AuNPs) heterogeneous fluorescent metal–organic framework (MIL-53(Al)@AuNPs) labeled with ZEN-bovine serum albumin (ZEN-BSA) as signal probe and ZEN mono-antibodies coupled with magnetic NPs (MNPs-mAbs) as capture probe. Specifically, the heterogenization of AuNPs on the MIL-53(Al) surface improved its biocompatibility, and facilitated the loading of ZEN-BSA conjugates. The MNPs-mAbs could rapidly capture the target ZEN, simplify the immunoassay process and further improve the detection efficiency. The established competitive magnetic-fluorescent immunosensing platform had a wider linear response to ZEN in the range of 0.001–100 ng/mL with a lower limit of detection (LOD) at 0.0035 ng/mL, and could finish the whole detection process within 20 min, showing great potential for rapid and sensitive detection of food contaminants.
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高影响因子
TALANTA
·
2020
·
IF 5.339
Yuhuan Wang,Zhixing Zeng,Jianyu Qiao,Shuqing Dong,Qing Liang,Shijun Shao
An ultrasensitive and high-performance electrochemical nitrite sensing platform based on gold nanoparticles deposited on poly (dimethyl diallyl ammonium chloride)-decorated MXene (Ti 3 C 2 T x ) (AuNPs/Ti 3 C 2 T x -PDDA) was constructed. AuNPs/Ti 3 C 2 T x -PDDA on the surface of electrode displayed synergetic catalytic effect for oxidizing NO 2 ‾ originating from especially catalytic activity of AuNPs, large area and excellent conductivity of Ti 3 C 2 T x , as well as electrostatic interaction of PDDA. The amperometry technique was employed for quantitative determination of nitrite, in which the AuNPs/Ti 3 C 2 T x -PDDA/GCE sensing platform showed outstanding linear relationship in 0.1–2490 μM and 2490–13490 μM for nitrite, meanwhile the detection limit of 0.059 μM. Besides, the prepared sensor possessed high sensitivity of 250 μA mM −1 cm −2 yet excellent selectivity, stability and reproducibility. Furthermore, this platform also exhibited satisfactory feasibility of nitrite sensing in running water and ham sausage sample. This work would broaden a facile approach to construct high sensitivity electrochemical sensing platform via two-dimension materials and its nanocomposites.
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JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
·
2020
·
IF 3.209
Xu Hun,Xiaohui Kong
Alzheimer’s disease is a worldwide health problem and it has attracted extensive attention. Tau protein is an important biomarker in the pathogenesis of Alzheimer’s disease. Herein, we devise a in situ enzyme catalysis generating electron donor photoelectrochemical (PEC) biosensor for Tau-381 protein. Tau-381 protein aptamer is immobilized onto the surface of AuNPs/MoSe 2 nanosheets modified electrode. In the presence of Tau-381 protein, an aptamer-protein duplex is formed. Meanwhile, the Tau-381 antibody and the protein G/AP (protein G labeled with alkaline phosphatase) are captured with the affinity interaction between Tau-381 protein and Tau-381 antibody, Tau-381 antibody and protein G/AP. The electron donor, ascorbic acid, is in situ produced by the catalyzing of ascorbic acid 2-phosphate in the PEC detection solution. As a result, low blank noise and strong photocurrent response are engendered. The photocurrent response is related to the concentration of Tau-381 protein. The detection range of Tau-381 protein is from 0.5 fM to 1.0 nM with detection limit of 0.3 fM. This in situ generating electron donor PEC biosensor can detect various targets by simply alternating antibody, antigen, or aptamer commercially. Thus, this work represents a simple and general sensing protocol.
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高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2020
·Vol. 55
·期 16
·7029-7038
·
IF 3.553
Li Jingwen,Wang Wen,Xie Chengbei,Jia Qin,Yan Changchun,Yao Yue,Fang Zheng,Duan Lingfeng,Cheng Jie,Qu Lulu,Han Caiqin
2,3,7,8-Tetrachlorodibenzo- p -dioxin (TCDD) is a highly toxic persistent organic pollutant (POP) that can remain present in the environment for a long time. Prolonged exposure to TCDD may bring about a wide variety of deleterious health effects to humans. Based on these circumstances, a rapid and facile surface-enhanced Raman scattering (SERS) method with gold nanoparticle-modified silver nanorod (AuNP@AgNR) substrates was developed for detection of 2,3,7,8-TCDD. Compared with SERS-active gold nanoparticles and silver nanorod substrate, the prepared AuNP@AgNR substrate showed an outstanding SERS performance with an enhancement factor of up to 2.4 × 10 8 . Furthermore, using AuNP@AgNR as a SERS substrate, we achieved the highly sensitive detection of 2,3,7,8-TCDD, and a density functional theory calculation was 6 to assign the characteristic peaks of 2,3,7,8-TCDD. The reliable linear range was determined to be 10 ng mL −1 to 10 μg mL −1 , with the limit of detection and the limit of quantitation as low as 7.1 and 8.2 ng mL −1 , respectively. By this method, the recovery rates of 2,3,7,8-TCDD spiked in the river samples were 82.3–97.4% with a relative standard deviation between 1.9 and 8.4%. These results show that the AuNP@AgNR substrate can be used for highly sensitive detection of 2,3,7,8-TCDD and has potential applications in the detection of other POPs.
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ANALYTICAL CHEMISTRY
·
2020
·
IF 6.785
Danli Hu,Hongfeng Liang,Xinyang Wang,Fang Luo,Bin Qiu,Zhenyu Lin,Jian Wang
A gold nanoparticle (AuNPs)/gallium nitride (GaN) Schottky junction was fabricated by growing AuNPs in situ on the surface of GaN and then etched by H2O2 to appropriate diameter. The photogenerated electrons of GaN can be captured and transferred by the AuNPs to increase the migration efficiency, and the electron–hole pairs were separated, which results in the enhancement of the photoelectric performance of the system. The Fermi energy level of AuNPs and the charge transfer efficiency of the AuNPs/GaN can be adjusted by controlling the size of the AuNPs. Then the AuNPs/GaN Schottky photoelectrode had been applied to develop a novel photoelectrochemical (PEC) aptasensor for the epithelial ovarian cancer marker-CA125 detection. The DNA aptamer of CA125 was modified on the surface of the AuNPs via Au–S bonds. The aptamer can bind with the target with high selectivity, and the photoelectron transfer process of the system can be blocked by the protein, which results in the decrease of the photocurrent of the system. The ratio of photocurrent before and after incubation with CA125 (I1/I0) has a linear with the concentration of CA125 in the range of 1–100 U/mL with a detection limit of 0.3 U/mL. The standard addition recovery rates were between 86.01% and 90.09%. This method showed good sensitivity, selectivity, and reliability in detecting CA125 in serum.
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JOURNAL OF ELECTRONIC MATERIALS
·
2019
·Vol. 48
·期 12
·7960-7969
·
IF 1.676
Huang Yanyan,Wu Zunyi,Zhao Guangying,Dou Wenchao
In this study, we used gold nanoparticles (AuNPs) modified screen-printed carbon electrodes (SPCE) with a large area working electrode for the detection of Escherichia coli O157:H7 ( E. coli O157:H7) in a direct method by antigen–antibody specificity binding. We compared four SPCE with different working electrode diameters (2 mm, 2.5 mm, 3 mm and 3.5 mm) to choose the optimum one. After electrodepositing chloroauric acid (HAuCl 4 ) on SPCE, a working electrode diameter of 3.5 mm SPCE show the maximum signal. Cyclic voltammetry and electrochemical impedance spectroscopy were used to characterize the electrochemical sensor. With the combination of large area working electrode and the great property of AuNPs, this immunoassay plays an ideal detection range from 1.19 × 10 3 CFU mL −1 to 1.19 × 10 9 CFU mL −1 and the limit of detection is 5.94 × 10 2 CFU mL −1 (equivalent to 3.5 CFU) at a signal-to-noise ratio of 3. The immunoassay showed the acceptable specificity, reproducibility, and stability for detection of E. coli O157:H7. These results indicate that this immunoassay has a promising application in the food safety industry.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2019
·
IF 2.931
Yingying Qi,Jiahuan He,Fu-Rong Xiu,Xuan Yu,Yifan Li,Yongwei Lu,Xiang Gao,Zhiqi Song,Baoxin Li
Heparin is a glycosaminoglycan with the highest negative charge density of any known biological molecule. Herein, this highly negative charge structure of heparin and the charge effect from positively-charged AuNPs for luminol chemiluminescence (CL) reaction were combined to build a facile and sensitive CL strategy for detection of heparin. The highly negative charge structure of heparin molecules (four negatively-charged side groups per repeat unit) and the effective signal amplification of charge effect from positively-charged AuNPs make this analysis to display high sensitivity for heparin detection, and the detection limit is as low as 0.06 ng/mL. It is about two orders of magnitude lower than the previously reported colorimetric assay and far lower than the current analysis methods. The established CL strategy is to use the electrostatic interaction between heparin and signal probe (positively-charged AuNPs). Since polyanionic heparin has the highest negative charge in biological system, this CL sensing shows high selectivity for the detection of heparin, and hyaluronic acid (HA), an analogue of heparin, cannot cause interference. This CL sensing succeeded in detecting heparin in human serum samples. Besides, polycationic protamine, heparin antidote, can respond to the system's CL signals through its strong interactions with heparin, thus indirectly detecting protamine. For protamine in serum samples, the detection result was basically consistent with Coomassie brilliant blue assay.
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Journal of Materials Chemistry B
·
2013
·Vol. 1
·期 11
·1607-1613
·
IF 0
Zhongde Mu,Xiangwei Zhao,Zhuoying Xie,Yuanjin Zhao,Qifeng Zhong,Ling Bo,Zhongze Gu
Recently, surface enhanced Raman spectroscopy (SERS) has been widely studied for chemical and biological sensing. SERS substrates combined with photonic architectures have attracted more and more attention. Photonic architectures in butterfly wings are too complicated to fabricate with either “top-down” or “bottom-up” approaches. Herein, we developed a simple, reproducible, inexpensive and green method to fabricate SERS substrates from different butterfly wings where the component chitosan/chitin was utilized as in situ reducer to synthesize gold nanoparticles in natural 3D photonic architectures. The SERS performances of three butterfly wings are compared. And the results show that a SERS substrate based on M. menelaus is better than the other three substrates, which could detect 10−9 M 4-ATP and has the lowest RSD and moderate SNR. In situ synthesis of AuNPs in butterfly wings with photonic architectures paves the way for fabricating multiple SERS substrates based on natural materials.
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Analytical Methods
·
2017
·Vol. 9
·期 42
·6032-6037
·
IF 1.9
Bo Ling,Yuanhui Ma,Hongqi Chen,Lun Wang
A new aptamer-based surface plasmon resonance (SPR) system has been designed to detect Hg2+ that utilizes near-infrared (NIR)-to-NIR gold nanoparticle coated NaYF4:Yb,Tm,Gd up-conversion nanoparticles (AuNPs@NaYF4:Yb,Tm,Gd UCNPs) as probes. The AuNPs@NaYF4:Yb,Tm,Gd UCNPs were prepared and excited by near-infrared light (980 nm) which emitted at a near-infrared wavelength (808 nm) using an inexpensive infrared continuous wave laser diode. The AuNPs@NaYF4:Yb,Tm,Gd UCNPs were conjugated with Hg2+ aptamers. In the presence of Hg2+, the AuNPs@NaYF4:Yb,Tm,Gd UCNPs were brought into close proximity because of the formation of T–Hg2+–T base pairs. Then the luminescence enhanced because of the plasmon resonance effects. Based on this, a new SPR system was developed for the detection of Hg2+ that had high sensitivity and selectivity in the NIR region. This method was successfully applied to detect Hg2+ concentration in real samples.
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Nanomaterials
·
2017
·Vol. 7
·期 10
·317
·
IF 3.553
Rong Guo,Tifeng Jiao,Ruirui Xing,Yan Chen,Wanchun Guo,Jingxin Zhou,Lexin Zhang,Qiuming Peng
Gold nanoparticles (AuNPs) have attracted widespread attention for their excellent catalytic activity, as well as their unusual physical and chemical properties. The main challenges come from the agglomeration and time-consuming separation of gold nanoparticles, which have greatly baffled the development and application in liquid phase selective reduction. To solve these problems, we propose the preparation of polyvinyl alcohol(PVA)/poly(acrylic acid)(PAA)/Fe3O4nanocomposites with loaded AuNPs. The obtained PVA/PAA/Fe3O4composite membrane by electrospinning demonstrated high structural stability, a large specific surface area, and more active sites, which is conducive to promoting good dispersion of AuNPs on membrane surfaces. The subsequently prepared PVA/PAA/Fe3O4@AuNPs nanocomposites exhibited satisfactory nanostructures, robust thermal stability, and a favorable magnetic response for recycling. In addition, the PVA/PAA/Fe3O4@AuNPs nanocomposites showed a remarkable catalytic capacity in the catalytic reduction of p-nitrophenol and 2-nitroaniline solutions. In addition, the regeneration studies toward p-nitrophenol for different consecutive cycles demonstrate that the as-prepared PVA/PAA/Fe3O4@AuNPs nanocomposites have outstanding stability and recycling in catalytic reduction.Keywords:Au nanoparticles;composite materials;catalytic reduction;electrospinning;p-nitrophenol
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BIOELECTROCHEMISTRY
·
2024
·
IF 4.8
Zhikai Wang,Yunpeng Li,Zhuanzhuan Shi,Xiaohai Wang,Chunxian Guo,Chang Ming Li,Xiaoshuai Wu
The main challenges (sluggish electron transfer , low energy density) hinder the future application of enzymatic biofuel cells (EBFCs), which urgent to take effective measures to solve these issues. In this work, a composite of Au nanoparticles decorated graphdiyne (AuNPs@GDY) is fabricated and employed as the carrier of enzyme (G6PDH), and a mechanism based on π-π interaction of electron transfer is proposed to understand bioelectrocatalysis processes. The results show that the AuNPs@GDY composite exhibits the highest current density among the three materials (GDY, AuNPs, and AuNPs@GDY), which is 3.4 times higher than that of GDY and 2.5 times higher than that of AuNPs. Furthermore, the results reveal that the AuNPs could increase the loading of enzymes and provide more active site for reaction, while GDY provides highly π-conjugated structure and unique sp/sp 2 -hybridized linkages interface. This work provides new insights to explore a theoretical basis for the development of more efficient bioelectrocatalytic systems.
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MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Zhi Luo,Jing Li,Shenglan Hu,Lingling Zheng,Lixin Xu,Biyang Deng
In this study, Ru(bpy) 3 2+ and oxalate (C 2 O 4 2− ) in Ru@Zn-MOF generated self-enhanced electrochemiluminescence (ECL). The self-enhanced ECL composite exhibited a short electron transfer distance and minimal energy loss, which ensured the high and stable luminescence efficiency of Ru@Zn-MOF. A MnO 2 @AuNPs nanocomposite was introduced into Ru@Zn-MOF via antigen–antibody interactions in the presence of squamous cell carcinoma antigen (SCCA). This significantly quenched the ECL signal due to the combined effect of the dual quenchers, MnO 2 NFs and AuNPs. A highly efficient ECL-RET immunosensor was constructed for the sensitive detection of SCCA in the linear range of 1 fg/mL to 100 ng/mL, with a limit of detection of 0.26 fg/mL (S/N = 3). This immunosensor has broad clinical applications for the quantitative detection of biomarkers.
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