COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2024
·
IF 4.9
Rui Liu,Xin Zhang,Tianheng Wu,Rijia Liu,Wenyu Cui,Yuan Sun,Binqiao Ren
Developing efficient and sensitive techniques for detecting ofloxacin (OFL) residues is crucial for ensuring food safety and environmental protection. In this study, the electropolymerization method was utilized with polypyrrole (Ppy) as the functional monomer and OFL as the template to produce a molecularly imprinted composite material comprising silver (Ag) and graphitic carbon nitride (g-C 3 N 4 ) (MIP-Ag/g-C 3 N 4 /GCE) for the electrochemical detection of OFL. The electrochemical characterization was conducted using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Under the optimal conditions, the prepared sensor demonstrated decent sensitivity and selectivity using the differential pulse voltammetry (DPV) technique. The sensor demonstrated an optimal linear range of 10 −13 to 10 −11 mol L −1 , with a low limit of detection (LOD) of 8.842×10 −14 mol L −1 and a limit of quantification (LOQ) of 2.947×10 −13 mol L −1 , which can successfully detect OFL in milk and honey samples, showing a recovery range of 97.38–104.00 %, and 99.45–102.00 %, with relative standard deviations (RSD) below 2.82 % and 2.16 % (n=5), respectively. The sensor exhibited high selectivity, high stability, and decent reproducibility in OFL determination. This study offers valuable insights into the application of semiconductor-based electrochemical sensors, opening new possibilities for the field and contributing to the improvement of food safety and environmental protection.
研究领域:
分析化学
·
食品安全
·
环境科学
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DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2024
·
IF 4.9
Nana Tang,Aiting Chen,Yanping Wei,Shuting Shi,Chuanqin Zhou,Quanguo He,Jun Liu
Acyclovir (Acyclovir, ACV) is an antiviral drug which, despite its favorable safety profile, can have systemic adverse effects, following improper use. This study prepared a clay-like two-dimensional transition metal carbide Ti 3 C 2 by etching Ti 3 AlC 2 with LiF and HCl. Carboxylated multi walled carbon nanotubes (Carboxylated multi-walled carbon nanotubes , MWCNTs-COOH) were combined with Ti 3 C 2 using chitosan (Chitosan, CS) as solvent and ultrasonic treatment . The nanocomposite was then modified onto the surface of a glassy carbon electrode (Glassy carbon electrode, GCE) to develop an electrochemical sensor for the detection of ACV. The Ti 3 C 2 -CS-MWCNTs-COOH/GCE nanocomposite was characterized by X-ray diffractometry (X-ray diffractometry, XRD), scanning electron microscope (Scanning electron microscope,SEM), and cyclic voltammetry (Cyclic voltammetry,CV), as well as the electrochemical impedance method (Electrochemical impedance,EIS). The successful preparation of Ti 3 C 2 -CS-MWCNTs-COOH, and the good electrochemical performance of the electrode were verified. Linear scanning voltammetry (Linear scan voltammetry,LSV) was used to quantify the ACV. The linear range of the method is wider than other works (0.05 ∼ 20.0 and 20.0 ∼ 500.0 μM), with a low detection limit (0.088 μM). The sensor achieves sensitive detection of ACV and can be used for the analysis of ACV in pharmaceutical and urine dosage forms , with recoveries of 95.5∼97.6% and 95.6∼97.5%, respectively. For the first time, this sensor utilizes clay-like Ti 3 C 2 with a larger specific surface area in combination with MWCNTs-COOH for ACV detection, which exhibits excellent immunity to interference, repeatability, reproducibility, and stability. This method provides a rapid and sensitive method for the determination of ACV, and lays foundations for developing miniaturized field rapid test detectors.
研究领域:
药理学
·
分析化学
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产品关联
DOI
高影响因子
MATERIALS RESEARCH BULLETIN
·
2020
·
IF 4.019
Jun Liu,Lingling Sun,Guangli Li,Jue Hu,Quanguo He
In this study, spindle-like α-Fe 2 O 3 mesocrystals/reduced-graphene-oxide composites modified glassy carbon electrode (α-Fe 2 O 3 /rGO/GCE) is developed for ultrasensitive electrochemical detection of DA. Morphologies and crystal structures of this composite are characterized by SEM, TEM , XRD , Raman spectrum, and XPS , respectively. The electrochemical behavior of DA on these electrodes are investigated by CV and EIS . The electrochemical conditions are optimized systematically. As results, the oxidation current of DA on α-Fe 2 O 3 /rGO/GCE is 38.13-fold increase than that on bare GCE. It is ascribed to the high catalytic activity of α-Fe 2 O 3 mesocrystals and large electrochemical active area of rGO. Under the best voltammetric condition, wide linear detection range (from 1.0×10 −8 to 9.0×10 -4 mol/L) and low LOD of 3.26 nM (S/N=3) are obtained on the α-Fe 2 O 3 /rGO/GCE. Furthermore, this electrode is also used for DA detection in real human serums samples successfully. This α-Fe 2 O 3 /rGO/GCE provides a good example in design of other mesocrystals-based composite materials for electrochemical detection.
研究领域:
分析化学
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材料科学
·
生物医学工程
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产品关联
DOI
高影响因子
Journal of Pharmaceutical Analysis
·
2017
·
IF 0
Satar Tursynbolat,Yrysgul Bakytkarim,Jianzhi Huang,Lishi Wang
An ultrasensitive electrochemical sensor based on polydopamine/carboxylic multi-walled carbon nanotubes (MWCNTs−COOH) nanocomposites modified glassy carbon electrode (GCE) was presented in this work, which has been developed for highly selective and highly sensitive determination of an antimicrobial drug, metronidazole. The preparation of polydopamine/MWCNTs–COOH nanocomposites/GCE sensor is simple and possesses high reproducible, where polydopamine can be coated on the surface of MWCNTs–COOH via a simple electropolymerization process. Under optimized conditions, the proposed sensor showed ultrasensitive determination for metronidazole with a wide linear detection range from 5 to 5000 µmol/dm 3 and a low detection limit of 0.25 µmol/dm 3 (S/N = 3). Moreover, the proposed sensor has been successfully applied for the quantitative determination of metronidazole in real drug samples. This work may provide a novel and effective analytical platform for determination of metronidazole in application of real pharmaceutical and biological samples analysis.
研究领域:
分析化学
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电化学
·
纳米技术
·
药物分析
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产品关联
DOI
PubMed
MICROCHEMICAL JOURNAL
·
2023
·
IF 4.8
Li Feng,Xiaoyun Lin,Junhui Feng,Xiaoqin Min,Yongnian Ni
This study presents the preparation of a novel electrochemical non-enzymatic sensor for the detection of glucose in natural saliva based on a metal organic framework (MOF) derivative (Cu-MOF-C) and nickel nanoparticle (NiNP) composite modified glassy carbon electrodes (GCE). The morphology and structural evolution were thoroughly characterized using scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), ultraviolet and visible spectrum (UV) and Fourier transform infrared spectrum (FTIR). Moreover, the electrocatalytic activity of the NiNPs/Cu-MOF-C/GCE for glucose was investigated using cyclic voltammetry (CV) and the amperometric i-t technique. The NiNPs/Cu-MOF-C/GCE sensor exhibits a wide linear range of 0.3–1150 μM and low detection limit (DL) of 0.090 μM at a signal/noise ratio (S/N) of 3. The average recovery rate of this method is satisfactory between 97.3% and 108.4%. Furthermore, the sensor exhibited excellent repeatability, good stability and reproducibility for glucose detection. Compared with traditional invasive measurement, the detection of glucose in natural saliva can reduce the pain caused by continuous blood collection, which is an ideal method for patients requiring continuous monitoring of glucose.
研究领域:
分析化学
·
医学诊断
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产品关联
DOI
高影响因子
ANALYTICAL LETTERS
·
2023
·
IF 2
Dan Shao,Ge Guo,Zhaomei Wu,Tingting Li,Zhiyan Chen,Yajun Gao
The accurate and sensitive determination of tyrosine is of paramount value. In this work, we reported the synthesis and characterization of a new nanohybrid composed of silver nanoparticles and hollow carbon nanospheres (Ag/HMCS) for the amperometric sensing of tyrosine. The Ag/HMCS nanohybrid was used to modify electrodes and to fabricate an amperometric sensor for tyrosine at a working potential of 450 mV in aqueous 0.1 M phosphate buffer at pH 7.0. Under optimal conditions, the sensor determined tyrosine from 0.08 to 100 μM with a detection limit of 0.02 μM.
研究领域:
分析化学
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纳米技术
·
电化学
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产品关联
DOI
高影响因子
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2019
·Vol. 166
·期 6
·B498
·
IF 3.12
Xintong Geng,Jing Bao,Ting Huang,Xiaojing Wang,Changjun Hou,Jingzhou Hou,Mickey Samalo,Mei Yang,Danqun Huo
Guanine (G) and adenine (A) are two important components of nucleic acid and some small molecules in an organism. In this paper, we developed a new and convenient biosensor for the simultaneous determination of G and A based on overoxidized polypyrrole/multi- walled carbon nanotube and molybdenum disulfide modified glassy carbon electrode (PPyox/ MWNTs-MoS2/GCE). The composite material exhibited remarkable electro-catalytic properties toward the oxidation of G and A due to its large surface area and fast electron transfer. The oxidation peak positions of G and A were at 0.73 V and 1.03 V, respectively, which allowed simultaneous detection of the two substances in coexistence solution. The designed biosensor exhibited linear responses to G and A both in the ranges 5–30 μM and 30–120 μM, with detection limits (S/N = 3) of 1.6 μM (G) and 1.7 μM (A), respectively. Moreover, interferences from some coexisting electro-active species including inorganic ions, glucose, glycine and citric acid were nearly negligible. Further, the sensing strategy was successfully used for the detection of G and A in real samples with satisfactory results, indicating a potential application for the simultaneous electrochemical detection of G and A.
研究领域:
分析化学
·
生物化学
·
材料科学
·
电化学
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产品关联
DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Jing Zhang,Ye Yang,Yi-Ping Liu,Guo-Cong Liu,Xi Zhu,Xin-Yu Jiang,Jin-Gang Yu
Electrochemical sensors have been considered as one of the most important methods to determine amino acid (AA) enantiomers. An interesting and highly-efficient electrochemical sensor, gold nanoparticles/D-sorbitol modified glass carbon electrode (Au NPs/D-sorbitol/GCE), was developed for the chiral recognition of Tyrosine (Tyr) enantiomers. Au NPs/D-sorbitol/GCE sensor exhibited excellent chiral recognition efficiency for Tyr enantiomers (I L /I D = 1.99, ∆Ep = 36 mV) by square wave voltammetry (SWV). The possible recognition mechanism was also proposed by cyclic voltammetry (CV) at different scanning rates, wettability measurements, and density-functional theory (DFT) calculations. The smaller steric hindrance and more suitable molecular distance are beneficial to the selective formation of hydrogen bonds between L-Tyr and the chiral interface of the sensor. The energy difference caused by the formation of hydrogen bonds between the chiral interface and Tyr enantiomers can be expressed as different peak currents to achieve chiral recognition. The redox peak current of Tyr enantiomers at Au NPs/D-sorbitol/GCE showed good linear relationship with their concentration, and the limits of detection (LOD) were calculated to be 4.12 μM and 8.07 μM for L-Tyr and D-Tyr, respectively. Importantly, Au NPs/D-sorbitol/GCE can also predict the mass ratios of L-Tyr in the enantiomeric mixtures. In addition, the sensor has shown good anti-interference ability, high stability, and excellent reproducibility.
研究领域:
分析化学
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电化学
·
生物传感
·
手性分析
·
纳米材料
·
分子识别
·
氨基酸检测
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产品关联
DOI
高影响因子
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2019
·Vol. 166
·期 2
·B35
·
IF 3.12
Juanjuan Gao,Weiqing Zhu,Haiou Song,Shupeng Zhang
p-Phenylenediamine (PPD) and hydroquinone (HQ) are hair dye precursors for permanent dyeing and are used globally. We report a novel and economic approach for the selective and simultaneous detection of the cathodic peaks of PPD and HQ by using a bare glassy carbon electrode, compared with modified electrodes that are obtained by tedious or expensive functionalized and that failed to achieve a peak-to-peak separation of PPD and HQ. Linear relationships between the simultaneous cathodic peak current of PPD and HQ concentrations were obtained for 0.5–400 μM and 5–4,000 μM with detection limits (S/N = 3) of 0.163 and 0.353 μM, respectively. The glassy carbon electrode sensor was applied to determine PPD and HQ in Nanjing river water with a recovery for these two analogues of 98.7–103.9% and 98.0–102.4%, respectively.
研究领域:
分析化学
·
环境科学
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DOI
高影响因子
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
·
2011
·Vol. 11
·期 5
·4163-4166
·
IF 1.352
Zhao Dongbo,Tian Jingqi,Sheng Qifeng,Sun Xuping
An eletrodeposition of random arrays of Pt nanoparticles, supported on glassy carbon electrode (GCE), is reported. It has been shown that such arrays exhibited good catalytic activity with respect to methanol oxidation in an acidic medium and longer deposition time produced more Pt
nanoparticles on GCE leading to larger effective catalytic area and higher catalytic current. It was found that the process of methanol oxidation was controlled by the diffusion of methanol and the Pt nanoparticles formed stable film on GCE surface and also exhibited stable catalytic performance
towards methanol oxidation.
研究领域:
电化学
·
纳米材料
·
催化
·
能源材料
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DOI
高影响因子
Journal of Biomedical Nanotechnology
·
2018
·Vol. 14
·期 10
·1688-1694
·
IF 5.068
Lai Yuxuan,Deng Yan,Yang Gaojian,Li Song,Zhang Chuanxiang,Liu Xueying
A novel molecular imprinted polymer (MIP) electrochemical sensor was successfully fabricated for sensitive detection of carcinomaembryonic antigen (CEA). We used CEA as template, dopamine (DA) as imprinted monomers. Through controlling electropolymerization, a "PDA-CEA"complex was achieved.
After elution, the specific cavities adsorbed the target molecules. In addition, polythionine (PTh) and AuNPs were applied as the electrode modifying materials to enhance electron transfer rate and improve detection signal. Using differential pulse voltammetry (DPV) detection, the peak current
decreased with the increase in concentration of CEA, and the linear response range of the MIP sensor was from 0.001 ng/mL to 1000 ng/mL with the detection limit as low as 0.2589 pg/mL. The MIP sensor had a low sample consumption, good stability, and high sensitivity, and could become a new
promising method for the detection of CEA. Furthermore, this MIP sensor was demonstrated in testing CEA in human serum sample with satisfactory results.
研究领域:
分析化学
·
生物传感器
·
电化学
·
癌症诊断
✓ 已验证
产品关联
DOI
PubMed
高影响因子
MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Rui Liu,Bolin Wu,Rijia Liu,Xin Zhang,Yuan Sun,Jing Ma
The accurate and real-time detection of antibiotics in the complex mixtures remain a significant challenge in the clinical drug monitoring, the food safety and the environmental surveillance. In this study, we developed an innovative electrochemical sensor platform, i.e. Ag/ZIF-67/g-C 3 N 4 /GCE, combined with the assistance of machine learning for the detection of chloramphenicol (CHL) in the practice pharmaceutical and urine samples. The incorporation of machine learning into the sensor design represents a key advancement, enabling the intelligent analysis and the enhanced sensing performance. The Ag/ZIF-67/g-C 3 N 4 composite electrode exhibited remarkable electrochemical properties, including a broad linear detection range (0.01–250.00 μmol L −1 ) and an ultralow detection limit of 5.32 nmol L −1 . The sensor demonstrated excellent selectivity, reproducibility and stability, even in the complex sample matrices. For practical application, the developed sensor achieved high recovery rates (98.00–103.00 % in the pharmaceutical samples and 96.67–103.33 % in the urine samples) with the standard deviations below 2.56 % and 2.26 %, respectively. More importantly, the artificial neural network (ANN), specifically the backpropagation (BP) neural network, was applied to analyze the collected sensor data, successfully predicting and validating the CHL sensing efficiency. This study highlights the synergistic combination of the advanced materials and machine learning for the intelligent and the accurate detection of antibiotics, paving ways for the AI-powered electrochemical sensing platforms with potential applications in both health monitoring and real-world sample analysis.
研究领域:
分析化学
·
环境科学
·
生物医学工程
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产品关联
DOI
高影响因子