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FOOD AND AGRICULTURAL IMMUNOLOGY · 2019 · IF 2.398

Development of a sandwich ELISA and immunochromatographic strip for the detection of shrimp tropomyosin

Lu Zeng,Shanshan Song,Qiankun Zheng,Pengjie Luo,Xiaoling Wu,Hua Kuang

Shrimp tropomyosin is one of the most important causes of shellfish allergy. The objective of this study was to develop a highly sensitive and specific immunoassay for the detection of shrimp tropomyosin in food. Ten monoclonal antibodies against shrimp tropomyosin were obtained by fusion and cell screening. We found two optimum monoclonal antibodies (mAbs); mAb 2 was used as the capture antibody, and HRP-labelled mAb 3 was used as the detection antibody. Using this pair of mAbs, a sandwich enzyme-linked immunosorbent assay (ELISA) was developed with the limit of detection (LOD) of 0.45 ng/mL. Cross-reactivity with other food allergens using this method was found to be negligible. An immunochromatographic assay strip was also developed for the rapid detection of shrimp tropomyosin with the LOD of 0.5 ng/mL. The results demonstrated that our developmental methods represent a useful tool for the detection of shrimp tropomyosin in food.

CAS / MDL: 9000-70-8 9003-99-0
研究领域: 免疫学 · 食品安全 · 生物技术
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ANALYTICA CHIMICA ACTA · 2017 · IF 4.95

Enhancement of visual chiral sensing via an anion-binding approach: Novel ionic liquids as the chiral selectors

Datong Wu,Qiuhong Yin,Pengfei Cai,Xiaoyong Zhao,Yuanjiang Pan

Novel task-specific ionic liquids derived from (S)-phenyl amino acid were prepared as a chiral sensor for the first time. It was found that the ionic liquids exhibited different chiral visual responses to the enantiomers . When (S)-tryptophan was treated with the sensor and Cu(II) in water, the clear solution would change to a sapphire suspension. Differently, another enantiomer could not produce the precipitate. Furthermore, the enantiomers could generate different colors in DMSO under the same conditions. The substantial difference contributes to the easy discrimination with visual determination. Four racemates were successfully tested with this strategy. The precipitation was isolated in the range of 90–94% yields after complete formation of the coordinative bonds, which could be as a simple way for enantioseparation. The responsive mechanism of the sensor was studied by NMR spectroscopy , FTIR and SEM . UV-vis spectrophotometer was used to monitor the colorimetric signal of the racemate with different e.e. values.

研究领域: 分析化学 · 有机化学 · 超分子化学 · 药物化学 · 化学生物学 · 材料科学 · 分子识别
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JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS · 2010 ·Vol. 52 ·期 4 ·615-619 · IF 2.453

On-line molecular imprinted solid-phase extraction flow-injection fluorescence sensor for determination of florfenicol in animal tissues

Shenguang Ge,Mei Yan,Xiaoliang Cheng,Congcong Zhang,Jinghua Yu,Peini Zhao,Weiqiang Gao

A simple and convenient on-line molecular imprinted solid-phase extraction flow-injection fluorescence sensor was developed in this study. Florfenicol (FF)-imprinted polymer was prepared by self-assembly with acrylamide (AM) as functional monomer and ethylene glycol dimethacrylate (EGDMA) as cross-linker. The binding characteristics of the imprinted polymer to florfenicol were evaluated by equilibrium binding experiments, and the morphology of the imprinted polymer was studied by scanning electron microscope (SEM). Fluorescence intensity of 3-p-nitrylphenyl-5-(2′-sulfonophenylazo) rhodanine (4NRASP) and bovine serum albumin (BSA) was inhibited by FF. Under optimum conditions the intensity of fluorescence shows a linear relationship with the concentration of FF over the range of 1.2   ×   10 −6 to 2.6   ×   10 −5   g   mL −1 with a regression equation of Δ I   =   23.54   +   17.86 c ( c 10 −6   g   mL −1 ) ( r   =   0.9965, n   =   6). The low detection limit of FF was found to be 3.4   ×   10 −7   g   mL −1 according to 11 parallel determinations for the blank solution. The relative standard deviation for the determination of 2.0   ×   10 −6   g   mL −1 FF solution was 3.5% ( n   =   11). This proposed sensor could be satisfactorily applied to the determination of FF in liver and meat samples.

研究领域: 分析化学 · 药物残留检测 · 食品安全 · 分子识别 · 环境监测 · 兽药代谢
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RSC Advances · 2015 ·Vol. 5 ·期 123 ·101982-101988 · IF 3.84

Highly effective chemosensor of a luminescent silica@lanthanide complex@MOF heterostructured composite for metal ion sensing

Chang Liu,Bing Yan

Heterostructured chemosensors have excellent chemical stability, low contamination and excellent recyclability, and are regarded as a promising new generation of sensors with critical properties related to their sensing sensitivity and selectivity. Our preparation strategy for a heterostructured sensor is to construct it using a luminescent lanthanide complex and metal organic framework (MOF). A heterogeneous sensor is systematically produced using EuTTA and ZIF-8 to cover silica, and thin particles are obtained with small size and uniform morphology. Then, the particles were used as a highly selective and sensitive sensor to detect Cu2+ in aqueous solution. Eventually, we find that the well-structured silica@EuTTA@ZIF-8 microspheres have a good fluorescence stability, low detection limit and broad linear range in aqueous environments. These excellent properties make it a potential chemosensor for sensing of Cu2+ in environmental or biological solution systems.

研究领域: 分析化学 · 环境监测 · 生物传感 · 材料科学 · 无机化学 · 纳米技术
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ANALYTICA CHIMICA ACTA · 2019 · IF 5.256

An efficient thin-walled Pd/polypyrrole hybrid nanotube biocatalyst for sensitive detection of ascorbic acid

Mengxiao Zhong,Maoqiang Chi,Yun Zhu,Ce Wang,Xiaofeng Lu

Controllable fabrication of novel and uniform noble metal nanoparticles on a specific support with a superior catalytic or electrocatalytic performance is of significantly importance for practical applications. In this report, we demonstrated an effective way to fabricate uniform thin-walled Pd/polypyrrole (PPy) hollow nanotubes . The prepared Pd/PPy hybrid nanotubes exhibited an excellent peroxidase-like activity to oxidize a typical peroxidase substrate such as 3,3′,5,5′-tetramethylbenzidine in comparison with traditional Pd/C and Pd black catalysts. The outstanding catalytic activity of the Pd/PPy hybrid nanotubes for peroxidase mimicking could be resulting from their unique hollow characteristic and an interfacial effect between PPy and Pd components. Based on the favorable catalytic property of the Pd/PPy hybrid nanotubes, a convenient and rapid colorimetric way to sensitively determine ascorbic acid has been presented. The detection limit was around 0.062 μM and an excellent selectivity was also achieved. The developed detection system in this study could be extended to the fields of bioscience and biotechnology with promising prospects.

研究领域: 生物化学 · 材料科学 · 分析化学
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SENSORS AND ACTUATORS B-CHEMICAL · 2019 · IF 6.393

A modified sensitive ELISA based on dual catalysis of Pd@Pt porous nanoparticles and horseradish peroxidase

Weiguo Wang,Rongkai Du,Changzhi Dong,Jinwu Yan,Lei Zhang

A sensitive enzyme-linked immunosorbent assay (ELISA) has been developed based on the dual catalysis of dendritic Pd-Pt porous nanoparticles and horseradish peroxidase (HRP). The Pd-Pt porous nanoparticles, for the first time, were used to immobilize HRP. As a proof-of-concept demonstration, HRP functioned Pd-Pt porous nanoparticles were applied in hCG detection with a detection limit of 0.07 IU L −1 . The linear intervals is 0.1–6.4 IU L -1 . The Pd-Pt-HRP possesses a better sensitivity than the traditional BA-ELISA. Furthermore, the precision and reproducibility and selectivity were assessed to be eligible for the hCG monitoring.

研究领域: 生物化学 · 医学诊断 · 纳米技术
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ANALYTICA CHIMICA ACTA · 2014 · IF 4.517

Highly sensitive and selective sensing platform based on π–π interaction between tricyclic aromatic hydrocarbons with thionine–graphene composite

Shan Liu,Maochao Wei,Xiangli Zheng,Shuai Xu,Changli Zhou

We are just beginning to exploit the fascinating potential of thionine , called electrochemical probe that can selectively recognize specific polycyclic aromatic hydrocarbons (PAHs), as tools for the detection of tricyclic aromatic hydrocarbons phenanthrene (PHE) and anthracene (ANT). A novel electrochemical sensing platform by modification of electroactive thionine functionalized graphene onto glass carbon electrode (Th/GRs/GCE) surface was constructed. The immobilized thionine showed a remarkable stability, which may benefit from the π–π stacking force with graphene. Under optimum conditions, the proposed electrochemical sensor exhibited high sensitivity and low detection limit for detecting PHE and ANT. The total amount of PHE and ANT could be quantified in a wide range of 10   pM–0.1   μM with a good linearity ( R 2   =   0.9979) and a low detection limit of 0.1   pM ( S / N   =   3). Compounds which possess one or two benzene rings or PAHs with more than three rings, such as benzene, naphthalene (NAP), benzo[a]pyrene (BaP) and pyrene (PYR) show little interference on the detection. Consequently, a simple and sensitive electrochemical method was proposed for the determination of PHE and ANT, which was used to determine PHE and ANT in waste water samples. The electrochemical method provides a general tool that complements the commonly used spectroscopic methods and immune method for the detection of PAHs.

研究领域: 分析化学 · 环境监测 · 电化学传感器 · 分子识别 · 污染物检测
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International Journal of Electrochemical Science · 2023 ·Vol. 11 ·期 12 ·9868-9880 · IF 1.5

Simultaneous Determination of m-Trihydroxybenzene and p-Nitrophenol at Glassy Carbon Electrode Modified with Graphene Oxide

Hongying Li,Xueliang Wang,Tao Wang,Zhaoxia Wang,Wei Zhao

A modified electrode was fabricated by casting graphene oxide (GO) suspension onto the surface of active glassy carbon electrode (GCE), and it can significantly enhanced the oxidation peak currents of m-trihydroxybenzene (m-THB) and p-nitrophenol (p-NP). Based on this, a sensitive analytical method towards their simultaneous determination was established. Many influencing factors such as the type of electrolyte, acidity, scan rates and concentrations were explored. Under the optimal experimental conditions, the oxidation peak currents of m-THB and p-NP were linearly increased with their concentrations ranging from 9 to 100 μM, with the detection limits both of 1 μM. Comparing with other reported methods, this sensor showed wider linear range and lower detection limit. In addition, the proposed method was successfully used to analysis of real environmental water samples with satisfactory recoveries, which verified the practicability of the sensor.

研究领域: 分析化学 · 环境科学 · 电化学 · 传感器技术 · 污染物检测
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MICROCHIMICA ACTA · 2010 ·Vol. 171 ·期 3 ·385-392 · IF 2.648

Amperometric nitrite biosensor based on a gold electrode modified with cytochrome c on Nafion and Cu-Mg-Al layered double hydroxides

Yin Huanshun,Zhou Yunlei,Liu Tao,Cui Lin,Ai Shiyun,Qiu Yanyan,Zhu Lusheng

An amperometric biosensor for nitrite was prepared by immobilizing cytochrome c (Cyt c) on a gold electrode that was modified with Nafion and a Cu-Mg-Al layered double hydroxide (Cu-LDH). The Cu-LDH was characterized by Fourier transform infrared spectroscopy and powder X-ray diffraction. The UV-visible spectrum suggests that Cyt c retains its native conformation in the modified film. The direct electrochemical investigation indicated that the composite film represents a good platform for the immobilization of Cyt c as well as an excellent promoter for the electron transfer between Cyt c and the gold electrode. Moreover, the biosensor showed a remarkable bioelectrocatalytic activity for the oxidation of nitrite with a linear range from 0.75 to 123 μM. The detection limit is 2 × 10 −7  M (S/ N  = 3). The biosensor was successfully applied to the determination of nitrite in food samples.

研究领域: 生物分析化学 · 电化学传感 · 食品分析 · 生物传感器 · 分子诊断
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International Journal of Electrochemical Science · 2023 ·Vol. 13 ·期 2 ·1423-1440 · IF 1.5

A Novel Indium Doped Bismuth Nanofilm for Simultaneous Stripping Determination of Zn(II), Cd(II) and Pb(II) in River Water

Ruizhuo Ouyang,Lina Xu,Haifeng Wen,Penghui Cao,Pengpeng Jia,Tian Lei,Xia Zhou,Mei Tie,Xiaolei Fu,Yuefeng Zhao,Haizhou Chang,Yuqing Miao

A novel indium doped bismuth hybrid nanofilm was prepared on a glassy carbon electrode (Bi@In/GCE) and successfully used for the simultaneous measurements of aqueous zinc (Zn(II)), cadmium (Cd(II)) and lead (Pb(II)). The Bi@In hybrid nanofilm was greatly improved in the ability of electron transfer, surface morphology as well as hydrophilicity over single Bi or In film, and exhibited well-defined and separate peaks for Zn(II), Cd(II) and Pb(II) by square wave stripping voltammetry. Analytical characteristics of the developed Bi@In/GCE were explored by comparing with single Bi and In film modified electrodes with calibration curves, which exhibited the most preferable electrochemical behaviors toward three metals as predicted. The synergistic effect of Bi and In mainly contributed to the enhanced electrochemical activity of the new electrode. In the concentration range of 0-120 µg L -1 , a good linear relationship was achieved between the peak current and the metal concentration with correlation coefficient higher than 0.995. The detection limits were calculated to be 0.52, 0.15 and 0.67 µg L -1 for Zn(II), Cd(II) and Pb(II) (S/N=3), respectively. The analysis of river sample with Bi@In/GCE was performed with satisfactory recoveries higher than 98%, suggesting that the new method is promising as a simple, sensitive and efficient approach to detect the heavy metals in water samples.

研究领域: 分析化学 · 环境监测 · 电化学传感 · 纳米材料 · 水污染检测
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MICROCHIMICA ACTA · 2011 ·Vol. 174 ·期 1 ·41-46 · IF 2.578

Enhanced conductivity of a glassy carbon electrode modified with a graphene-doped film of layered double hydroxides for selectively sensing of dopamine

Wang Yinling,Peng Wei,Liu Lin,Tang Min,Gao Feng,Li Maoguo

A strategy is presented for doping graphene into layered double hydroxide films (LDHs) as a means of improving charge transport of the LDH film in a modified glassy carbon electrode. This result in an enhanced electrocatalytic current for dopamine (DA) and a good separation of the potentials of DA, uric acid and ascorbic acid. Under selected conditions, the square wave voltammetric response of the electrode to DA is linear in the concentration range from 1.0 to 199 μM even in the presence of 0.1 mM ascorbic acid, and the detection limit is 0.3 μM at a signal-to-noise ratio of 3. The method was applied to the determination of DA in pharmaceutical injections with satisfactory results. A strategy is presented for doping graphene into layered double hydroxide films (LDHs) as a means of improving charge transport of the LDH film in a modified glassy carbon electrode. This result in an enhanced electrocatalytic current for dopamine (DA) and the square wave voltammetric response of the electrode to DA is linear in the concentration range from 1.0 to 199 μM with the detection limit of 0.3 μM. The method was applied to the determination of DA in pharmaceutical injections with satisfactory results.

研究领域: 分析化学 · 电化学 · 生物传感器 · 纳米材料 · 药物分析 · 神经化学
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MICROWAVE AND OPTICAL TECHNOLOGY LETTERS · 2023 ·Vol. 65 ·期 5 ·1433-1438 · IF 1.5

Component identification of subsurface food additives by spatially offset Raman spectroscopy

Qiu-Shi Liu,Ming-Jiang Ma,Chong Lv,Guo-Qing Yang,Yan-Lei Yang,Jia-Hao Wang,Zhi-Xing Gao,Hong-Yu He,Xiao-Hua Zhang,Yuan-Peng Li,Bao-Zhen Zhao

Spatially offset Raman spectroscopy (SORS) is an important branch derived from conventional Raman spectroscopy. It has the characteristics to realize the concealed component identification covered by opaque and translucent media nondestructively and rapidly. This technology gradually plays an important role in basic and applied research of numerous areas. This paper focuses on the SORS potential application in food quality and safety inspection, and a SORS detection system has been setup. The ingredients of various concealed food additives have been identified by SORS and the optimum offset distance for detection has been obtained. Meanwhile, the identification effectiveness of the system for low-concentration additives in real foods has also been evaluated.

研究领域: 分析化学 · 食品科学 · 光谱学 · 食品安全 · 质量控制
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