ACS Applied Materials & Interfaces
·
2024
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IF 8.3
Ruya Wang,Weidong Zhang,Weiqiang Liang,Xiao Wang,Lili Li,Zhenhua Wang,Miaomiao Li,Jun Li,Chunxia Ma
Quinolone residues resulting from body metabolism and waste discharge pose a significant threat to the ecological environment and to human health. Therefore, it is essential to monitor quinolone residues in the environment. Herein, an efficient and sensitive matrix-assisted laser desorption/ionization mass spectrometry (MALDI/MS) method was devised by using a novel molecularly imprinted heterojunction (MIP-TNs@GCNs) as the matrix. Molecularly imprinted titanium dioxide nanosheets (MIP-TNs) and graphene-like carbon nitrides (GCNs) were associated at the heterojunction interface, allowing for the specific, rapid, and high-throughput ionization of quinolones. The mechanism of MIP-TNs@GCNs was clarified using their adsorption properties and laser desorption/ionization capability. The prepared oxygen-vacancy-rich MIP-TNs@GCNs heterojunction exhibited higher light absorption and ionization efficiencies than TNs and GCNs. The good linearity (in the quinolone concentration range of 0.5–50 pg/μL, R2 > 0.99), low limit of detection (0.1 pg/μL), good reproducibility (n = 8, relative standard deviation [RSD] < 15%), and high salt and protein resistance for quinolones in groundwater samples were achieved using the established MIP-TNs@GCNs–MALDI/MS method. Moreover, the spatial distributions of endogenous compounds (e.g., amino acids, organic acids, and flavonoids) and xenobiotic quinolones from Rhizoma Phragmitis and Rhizoma Nelumbinis were visualized using the MIP-TNs@GCNs film as the MALDI/MS imaging matrix. Because of its superior advantages, the MIP-TNs@GCNs–MALDI/MS method is promising for the analysis and imaging of quinolones and small molecules.
研究领域:
分析化学
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环境科学
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质谱学
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材料科学
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产品关联
DOI
PubMed
高影响因子
Journal of Materials Chemistry B
·
2021
·Vol. 9
·期 20
·4249-4256
·
IF 6.331
Mingmei Shen,Yuanyuan Wang,Xianwen Kan
Thrombin plays an essential role in blood coagulation and some physiological and pathological processes. The convenient, rapid, sensitive, and specific detection of thrombin is of great significance in clinical research and diagnosis. Herein, surface molecularly imprinted polymer (MIP) was modified on aptamer-functionalized Fe3O4 nanoparticles (MIP–aptamer–Fe3O4 NP) for thrombin colorimetric assay by taking advantage of the peroxidase-like activity of Fe3O4 NP. With the adsorption of thrombin into imprinted cavities, the exposed surface area of Fe3O4 NP decreased, causing a decrease in its peroxidase-like activity toward 3,3′,5,5′-tetramethylbenzidine (TMB) in the presence of H2O2. On the other hand, the reductive amino acids on the thrombin surface also impeded the oxidation of TMB. Both phenomena caused the light blue color of the sensing solution. Thus, a specifically sensitive colorimetric approach for the visual detection of thrombin was proposed with a linear range and limit of detection of 108.1 pmol L−1–2.7 × 10−5 mol L−1 and 27.8 pmol L−1, respectively. Moreover, due to the double recognition elements of MIP and aptamer, the prepared MIP–aptamer–Fe3O4 NP showed higher selectivity to thrombin than that based on only one recognition element. It is worth noting that no special property (e.g. electrochemical or fluorescence activity) of the template was required in this work. Thus, more template molecules can be easily, selectively, and sensitively detected based on the proposed MIP–aptamer–mimic enzyme colorimetric sensing strategy.
研究领域:
生物化学
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纳米技术
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临床诊断
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分析化学
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产品关联
DOI
PubMed
高影响因子
ANALYTICA CHIMICA ACTA
·
2022
·
IF 6.911
Tianrun Zhang,Xiuwei Xuan,Mingji Li,Cuiping Li,Penghai Li,Hongji Li
Molecularly imprinted polymer (MIP) membranes prepared in situ present several advantages: they maintain the original morphology, adhere strongly to the collector, and exhibit a controllable structure. In this study, a Ni-polyacrylamide (PAM)-MIP matrix was fabricated in situ on glassy carbon via the one-step electro-polymerization of AM monomers in the presence of Ni and template molecules. Ni 2+ ions were introduced as oxidants to promote AM polymerization and bulking agents to fabricate a three-dimensional porous PAM-MIP matrix. The Ni-PAM-based MIP sensor exhibited a quantitative dual response toward dopamine (DA) and adenine (Ade) in the pH range of 5.0–9.0. The linear concentration range changed depending on the pH environment, and the concentrations of DA and Ade ranged from 0.6 to 200 μM and from 0.4 to 300 μM, respectively. The ranges of detection limits (S/N = 3) were 0.12–0.37 μM for DA and 0.15–0.36 μM for Ade. In addition, the dual-MIP sensor exhibited high reliability in the detection of DA and Ade in human serum owing to its excellent anti-interference ability and long-term stability. The technique developed in this study is expected to facilitate the construction of multi-target response electrochemical biosensors and the reliable determination of small molecules with high selectivity and stability.
研究领域:
分析化学
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生物传感器
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材料科学
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电化学
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生物分析化学
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产品关联
DOI
PubMed
高影响因子
Journal of Food Measurement and Characterization
·
2023
·Vol. 17
·期 6
·5972-5979
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IF 3.4
Zhao Shujun,Liu Wei,Song Dapeng
The detection of the herbicide propachlor in environmental and food samples is critical due to its potential toxic effects. In this study, a sensitive and selective electrochemical sensor based on a molecularly imprinted polymer (MIP), polyethyleneimine-treated multi-walled carbon nanotubes (PEI-MWCNTs), and gold nanoparticles (AuNPs) was developed for propachlor detection. The PEI-MWCNTs enhanced the conductivity of the sensor, while AuNPs promoted electron transfer during the detection process, resulting in a lower detection limit (78 nM) and a wider linear range (0.5 µM to 70 µM) compared to traditional sensors. Furthermore, the sensor exhibited high selectivity against other herbicides, with interference suppression percentages above 92% for common contaminants. The performance of the sensor was further improved by integrating an XGBoost machine learning algorithm for data analysis, which improved the predictive accuracy of propachlor concentration. Reproducibility tests on three independently prepared sensors showed a relative standard deviation (RSD) below 5%. This innovative approach presents a significant advancement in the field of propachlor detection, providing an effective tool for environmental monitoring and food safety.
研究领域:
分析化学
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环境科学
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食品科学
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机器学习
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Yan Huang,Daixin Ye,Jing Yang,Huan Lu,Li Li,Yaping Ding
Herein, based on the dual-signal strategy, an electrochemical sensor with molecularly imprinted polymer (MIP) was designed for the analysis of p-Hydroxyacetophenone (p-HAP) for the first time. The sensor was fabricated by modifying the electrode with NiFe prussian blue analogue (NiFe-PBA) and followed by SnS 2 , obtaining the dual-signal from [Fe(CN) 6 ] 3−/4− at 0.20 V and NiFe-PBA at 0.52 V. In the electropolymerization of the MIP film, o-phenylenediamine was used as functional monomer and p-HAP acted as template molecule. After the adsorption of p-HAP, the two above oxidation peak currents decreased simultaneously compared with the elution, achieving the dual-signal analysis. Under the optimal conditions, the sensor exhibited a wide linear range of 10 −13 M to 10 −7 M and a low detection limit of 3.52 × 10 −14 M (3σ). Moreover, it was successfully applied to the p-HAP detection in human serum and environment water samples with satisfactory recovery.
研究领域:
分析化学
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电化学
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环境科学
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材料科学
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DOI
高影响因子
BIOSENSORS & BIOELECTRONICS
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2015
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IF 6.409
Hui Jiang,Donglei Jiang,Jingdong Shao,Xiulan Sun
We have developed a novel and economical electrochemical sensor to measure Gram-negative bacterial quorum signaling molecules (AHLs) using magnetic nanoparticles and molecularly imprinted polymer (MIP) technology. Magnetic molecularly imprinted polymers (MMIPs) capable of selectively absorbing AHLs were successfully synthesized by surface polymerization. The particles were deposited onto a magnetic carbon paste electrode (MGCE) surface, and characterized by electrochemical measurements. Differential Pulse Voltammetry (DPV) was utilized to record the oxidative current signal that is characteristic of AHL. The detection limit of this assay was determined to be 8×10 −10 mol L −1 with a linear detection range of 2.5×10 −9 mol L −1 to 1.0×10 −7 mol L −1 . This Fe 3 O 4 @SiO 2 -MIP-based electrochemical sensor is a valuable new tool that allows quantitative measurement of Gram-negative bacterial quorum signaling molecules. It has potential applications in the fields of clinical diagnosis or food analysis with real-time detection capability, high specificity, excellent reproducibility, and good stability.
研究领域:
分析化学
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生物传感器
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微生物学
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材料科学
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电化学
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产品关联
DOI
PubMed
高影响因子
Journal of Water Process Engineering
·
2025
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IF 6.7
Leikai Ye,Fangyan Chen,Yubin Tang,Wenqian Sun,Yanhua Song
At present, the rapid, sensitive, and highly selective detection of trace organic contaminants is a research spot in the field of environment. Herein, a novel fluorescent nanoprobe N, S-CDs@MIP based on N/S co-doped carbon quantum dots (CDs) coupled with amoxicillin molecularly imprinted polymer was synthesized. The fluorescent property of N, S-CDs@MIP and fluorescence quenching level of amoxicillin to N, S-CDs@MIP was explored. Furthermore, the fluorescence analysis method based on N, S-CDs@MIP probe for quantitatively detecting amoxicillin was established. The synthesized N, S-CDs@MIP has a maximum fluorescence emission wavelength of 440 nm and a significantly selective fluorescence response toward amoxicillin with a large imprinting factor of 4.07. For the developed fluorescence analysis method, the detection limit, the linear range of the standard curve, and relative standard deviation (RSD) were obtained as 1.17 ng/mL, 5.8–200 ng/mL, and <3 %, respectively. The real environmental water samples were measured with a high accuracy with the recovery of 83.6 % ~ 104.7 % and RSD of 2.3 % ~ 5.1 %. Compared to the HPLC-UV, HPLC-MS, and the fluorescence detection method based on CDs or doped CDs, the established fluorescence detection method exhibits high selectivity, wide linear range, and low detection limit. It is greatly promising in the quick detection of trace amoxicillin.
研究领域:
环境科学
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分析化学
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产品关联
DOI
高影响因子
REACTIVE & FUNCTIONAL POLYMERS
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2024
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IF 4.5
Jiongfeng Sun,Yi Hong,Guofu Qiao
The synthesis and processing of most polymer adhesives rely on energy-inefficient and environmentally burdensome manufacturing approaches. In this paper, a novel synthesis strategy, UV-initiated frontal polymerization (FP) for the fast synthesis of high-strength, self-propagating epoxy adhesives at room temperature, was presented, in which the self-propagating rate reached 71.4 mm min −1 . CuCl 2 was used as a catalyst to decrease the onset temperature of polymerization and ensure sufficient polymerization on the surface of the material to be bonded. Mild steel, glass, ceramic, wood, PMAA, and concrete were successfully bonded within several minutes at room temperature. In the same material system, the adhesive strength with the FP curing approach was greater than that of thermal curing, and the former had a better pore structure , as determined by MIP analysis. This paper provides a promising idea for the in-situ fast synthesis of high-strength epoxy adhesives at room temperature.
研究领域:
材料科学
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高分子化学
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粘接技术
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产品关联
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2021
·
IF 6.901
Cuizhu Ye,Xingguang Chen,Dong Zhang,Junjun Xu,Huiting Xi,Tiantian Wu,Danwen Deng,Chunhong Xiong,Jinsheng Zhang,Ganhui Huang
Coated with polypyrrole (Ppy)-based molecularly imprinted polymer (MIP), 3D CoFe-metal organic frameworks (CoFe-MOFs) with gold nanoparticles (AuNPs) was developed for electrochemical trace detection of norfloxacin (NOR). On one hand, the trace detection of NOR was realized with MIP/CoFe-MOFs/AuNPs/Glassy carbon electrode (GCE). The effective surface area of the imprinted cavities capable of identifying NOR on MIP/CoFe-MOFs/AuNPs/GCE increased to 0.1058 cm 2 after 3D CoFe-MOFs/AuNPs was modified, which indicates that CoFe-MOFs/AuNPs could generate more imprinted cavities, thus contributing to a lower limit of detection (LOD) of 0.131 pmol L −1 (S/N = 3) with a wider linear range (5–100, 100–1000 and 1000–6000 pmol L −1 ). On the other hand, the recognition reaction to NOR by MIP/CoFe-MOFs/AuNPs/GCE is an irreversible electrochemical oxidation reaction involving an electron and a proton, controlled by a mixed adsorption-diffusion mechanism. Rapid and precise detection of NOR in prescription (norfloxacin capsules with the specification of 0.1 g) and pure milk with the recovery rates between 97.04 and 110.2% and the relative standard deviations (RSD) were less than 5.7%. The measured results by MIP/CoFe-MOFs/AuNPs/GCE were close to the commercial norfloxacin enzyme-linked immunosorbent assay (ELISA) kit, demonstrates its high potential to NOR trace detection in environmental and animal foods.
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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环境科学
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食品科学
✓ 已验证
产品关联
DOI
高影响因子
TALANTA
·
2024
·
IF 5.6
Heng Zhang,Bin Luo,Ke Liu,Cheng Wang,Peichen Hou,Chunjiang Zhao,Aixue Li
Palmitic acid (PA) is a kind of saturated high fatty acid, which is involved in physiological safety and food quality. A surface molecularly imprinted polymer (MIP) electrochemical sensor was prepared on MXene surface using dopamine (DA) as functional monomer. The electrode was modified with gold nanoparticles (AuNPs), ferrocene-graphene oxide-multiwalled carbon nanotubes (Fc-GO-MWCNT) composite to enhance the electroactive area and conductivity. The sensor was characterized by scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS), electrochemical impedance spectroscopy (EIS) and Differential pulse voltammetry (DPV), respectively. The parameters concerning this assay and various regeneration conditions have been carefully studied. The sensor can detect PA in the range of 1 nM-1 mM (R 2 = 0.995), the limit of detection (LOD) is 0.48 nM (S/N = 3), and the limit of quantification (LOQ) is 1.61 nM. The artificial neural network (ANN) model in machine learning is further used to analyze the data collected by the sensor. The results show that the back propagation (BP) neural network in ANN is more suitable for the intelligent analysis of PA. The practicality of the sensor was confirmed by detecting PA in pork samples. This is the first MIP-based electrochemical sensor for PA, and it has great potential in practical applications.
研究领域:
分析化学
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电化学
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机器学习
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食品科学
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材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Biosensors-Basel
·
2024
·Vol. 14
·期 3
·121
·
IF 4.9
Chuanxiang Zhang,Song Li,Lingxiao Tang,Shuo Li,Changchun Hu,Dan Zhang,Long Chao,Xueying Liu,Yimin Tan,Yan Deng
Development of an efficient technique for accurate and sensitive dibutyl phthalate (DBP) determination is crucial for food safety and environment protection. An ultrasensitive molecularly imprinted polymers (MIP) voltammetric sensor was herein engineered for the specific determination of DBP using poly-l-lysine/poly(3,4-ethylenedioxythiophene)/porous graphene nanocomposite (PLL/PEDOT−PG) and poly(o-phenylenediamine)-imprinted film as a label-free and sensing platform. Fabrication of PEDOT−PG nanocomposites was achieved through a simple liquid–liquid interfacial polymerization. Subsequently, poly-l-lysine (PLL) functionalization was employed to enhance the dispersibility and stability of the prepared PEDOT−PG, as well as promote its adhesion on the sensor surface. In the presence of DBP, the imprinted poly(o-phenylenediamine) film was formed on the surface of PLL/PEDOT−PG. Investigation of the physical properties and electrochemical behavior of the MIP/PLL/PEDOT−PG indicates that the incorporation of PG into PEDOT, with PLL uniformly wrapping its surface, significantly enhanced conductivity, carrier mobility, stability, and provided a larger surface area for specific recognition sites. Under optimal experimental conditions, the electrochemical response exhibited a linear relationship with a logarithm of DBP concentration within the range of 1 fM to 5 µM, with the detection limit as low as 0.88 fM. The method demonstrated exceptional stability and repeatability and has been successfully applied to quantify DBP in plastic packaging materials.
研究领域:
分析化学
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材料科学
·
环境科学
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食品科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
TALANTA
·
2017
·
IF 4.162
Le Sheng,Yulong Jin,Yonghuan He,Yanyan Huang,Liushui Yan,Rui Zhao
Superparamagnetic core-shell molecularly imprinted polymer nanoparticles (MIPs) were prepared via surface initiated reversible-addition fragmentation chain transfer (si-RAFT) polymerization for the selective recognition of 2,4-dichlorophenoxyacetic acid (2,4-D) in real samples. The construction of uniform core-shell structure with a 50 nm MIP layer was successfully accomplished, which favored mass transfer and resulted in fast recognition kinetics. The static equilibrium experiments revealed the satisfied adsorption capacity and imprinting efficiency of Fe 3 O 4 @MIP. Moreover, the Fe 3 O 4 @MIP exhibited high selectivity and affinity towards 2,4-D over structural analogues. The prepared Fe 3 O 4 @MIP nanoparticles were used for the selective enrichment of 2,4-D in tap water and Chinese cabbage samples. Combined with RP-HPLC, the recoveries of 2,4-D were calculated from 93.1% to 103.3% with RSD of 1.7–5.4% (n = 3) in Chinese cabbage samples. This work provides a versatile approach for fabricating well-constructed core-shell MIP nanoparticles for rapid enrichment and highly selective separation of target molecules in real samples.
研究领域:
分析化学
·
环境科学
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材料科学
·
纳米技术
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）