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Food Bioscience · 2026 · IF 6.2

A nanoengineered Au@Ag@PVP SERS solid-phase substrate empowered by machine learning for rapid and trace-level screening of pesticide residues in tea

Xifan Zhan,Xinying Wang,Md Mehedi Hassan,Fangling Jiang,Jiaying Xu,Yuan Zhang,Shanghua Li,Sha Zou,Hongfa Liu,Yi Xu,Quansheng Chen

Pesticide residues in tea pose significant health risks to consumers. This research focuses on developing a surface-enhanced Raman scattering (SERS) sensor using a solid-phase substrate made of Au@Ag@PVP nanoparticles (NPs), combined with machine learning chemometric techniques, for the rapid detection of trichlorfon, carbendazim, and clothianidin in tea. Au@Ag@PVP NPs were immobilized onto anodic aluminum oxide (AAO) filter membranes via vacuum filtration, yielding densely packed NPs that generate strong electromagnetic hot spots, thereby increasing SERS sensitivity. Raman spectra of tea infusions containing different concentrations of pesticides were acquired and analyzed using three machine-learning algorithms. Among these models, competitive adaptive reweighted sampling-partial least squares (CARS-PLS) demonstrated superior predictive performance, with Rc = 0.9950, Rp = 0.9942, and RPD = 9.2893 for trichlorfon; Rc = 0.9955, Rp = 0.9942, and RPD = 9.1010 for carbendazim; and Rc = 0.9981, Rp = 0.9957, and RPD = 9.7523 for clothianidin. This approach enables the rapid, quantitative detection of pesticide residues with minimal sample preparation and high sensitivity, representing a practical method for monitoring tea safety.

CAS / MDL: 10605-21-7 210880-92-5
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ACS Applied Materials & Interfaces · 2017 · IF 7.504

Small and Sharp Triangular Silver Nanoplates Synthesized Utilizing Tiny Triangular Nuclei and Their Excellent SERS Activity for Selective Detection of Thiram Residue in Soil

Chun-Hong Zhang,Jian Zhu,Jian-Jun Li,Jun-Wu Zhao

The great harm of thiram residue in soil to environment and human health is usually ignored. Due to the complexity of soil compositions, the detection of thiram residue in soil faces considerable difficulties. In this work, a highly sensitive and selective surface-enhanced Raman scattering (SERS) substrate based on the triangular silver nanoplates (TSNPs) with small size and sharp corners is developed and used for the detection of thiram residue in soil for the first time. These TSNPs are synthesized by replacing the conventional seeds in the seed-mediated chemical reduction route with the tiny and uniform triangular silver nuclei (TSN) which can provide more growing space for generating sharp corners during the growth of TSNPs. It is interesting that the TSNPs with the smaller size have the better SERS performance. The possible mechanism behind this phenomenon is explained by the electromagnetic enhancement theory. On the basis of the Raman activity of the smallest TSNPs, a SERS-active substrate is prepared for detecting the thiram residue in soil. The thiram solution detection shows that the limit of detection (LOD) of these smallest TSNPs is lower than other nanoparticles, such as nanospheres, nanocubes, etc. For sensing the thiram residue in soil, the addition of poly(sodium 4-styrenesulfonate) realizes the specific adsorption of thiram by TSNPs. This method exhibits a good linear response from 0.12 to 4.8 μg/g with a low LOD of 90 ng/g, which is better than conventional methods. This work shows the great potential of the small TSNPs as a novel SERS substrate and its broader applications in pesticides detection.

研究领域: 纳米技术 · 分析化学 · 环境科学 · 拉曼传感 · 农药残留检测
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2022 · IF 4.831

Lotus leaf mastoid inspired Ag micro/nanoarrays on PDMS film as flexible SERS sensor for in-situ analysis of pesticide residues on nonplanar surfaces

Zhengdong Zhu,Xiaoyi Shi,Yating Feng,Meng He,Cheng Ye,Hongyang Zhou,Maofeng Zhang,Wei Zhang,Jianhua Li,Changlong Jiang

Conventional surface-enhanced Raman scattering (SERS) molecular detection are based on hard and brittle substrate, which are not suitable for in-situ detection of analytes adsorbed on nonplanar surfaces. Here, we report a simple biomimetic synthesis method to fabricate lotus leaf mastoid structured AgNPs micro/nanoarrays as reliable SERS substrate. By ideal replicating mastoid structure of lotus leaf into a flexible and transparent PDMS film, followed by depositing plasmonic AgNPs, a powerful chemical sensor with high sensitivity and multiplex detecting capability is demonstrated. The employ of periodic mastoid structure array endows the sensor with high signal repeatability (RSD ∼ 8.6 %), solving the general repeatability problem of SERS substrates. In addition, the detailed designed flexible and transparent PDMS substrate is capable of identifying trace analytes on curved surfaces with excellent durability. In the proof-of-concept experiment, a limit of detection (LOD) of (10 −5 M to 10 −7 M) was achieved on a portable Raman device for three common pesticides residues (thiram, fonofos and triadophos) on dendrobium leaves and stem according to the molecular fingerprint, indicating its excellent in-situ detection capability. Further, the multiplex detection ability of the Ag/PDMS film is also demonstrated by analyzing the mixture of four typical analytes. Benefiting from its high signal uniformity, this flexible Ag/PDMS substrate also showed good quantitative detection capabilities.

CAS / MDL: 14431-43-7 78560-45-9
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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Fabrication of magnetic Au/Fe3O4/MIL-101(Cr) (AF-MIL) as sensitive surface-enhanced Raman spectroscopy (SERS) platform for trace detection of antibiotics residue

Qinchao Shao,Xiubin Zhang,Pei Liang,Qiang Chen,Xiaohua Qi,Mingqiang Zou

Fabrication of a magnetic substrate based on metal–organic frameworks (MOFs) with high sensitivity and stability for surface-enhanced Raman scattering (SERS) analysis were reported in this paper. MIL-101(Cr) nanoparticle prepared via a traditional hydrothermal reaction, which was combined with Fe 3 O 4 to synthesize the Fe 3 O 4 /MIL-101(Cr) composites. Then, the concentration of chloroauric acid and the time of reduction reaction were adjusted to acquire the optimal Au/Fe 3 O 4 /MIL-101(Cr) (AF-MIL) SERS substrate. The detection ability of the substrate can down to 10 -8 mol/L for Rhodamine 6G (R6G) as probe molecule, and the relative standard deviation (RSD) is only about 4.48 %, which indicates that it possesses wonderful SERS performance and uniformity. Finally, the as-synthesized substrate has been adopted to test the trace level sulfapyridine, with its desirable detection ability can down to 10 -6 mol/L. Such desirable SERS substrate with facile and effective operation holds great promise in the fast sensitive detection of the antibiotic residue and some other pollutants in environment.

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MOLECULES · 2022 ·Vol. 27 ·期 13 ·4019 · IF 4.927

Ultrasensitive and Specific Detection of Anticancer Drug 5-Fluorouracil in Blood Samples by a Surface-Enhanced Raman Scattering (SERS)-Based Lateral Flow Immunochromatographic Assay

Hanwen Liu,Ying Liu,Ting Zhou,Penghui Zhou,Jianguo Li,Anping Deng

5-Fluorouracil (5-FU) is an effective anticancer drug widely used in the world. To improve therapy efficiency and reduce side effects, it is very important to frequently detect the concentration of 5-FU in blood samples of patients. In this work, a new type of lateral flow immunochromatographic assay (LFIA) based on surface-enhanced Raman scattering (SERS) for ultrasensitive and specific detection of 5-FU in blood samples was developed. Au@Ag/Au nanoparticles (NPs) employing Au particles as the core and Ag/Au alloy as the shell were synthesized, characterized and used as the substrate in SERS-LFIA due to their high SERS enhancement and biocompatibility. The immunoprobe was made in the form of AuMBA@Ag/Au-Ab in which mercaptobenzoic acid (MBA, a common Raman active reporter) was embedded in the core–shell layer and the monoclonal antibody (mAb) against 5-FU was immobilized on the surface. The performance of SERS-LFIA was similar to that in colloidal gold based-LFIA, and the entire assay time was within 20 min. According to the color intensity on the testing (T) lines of LFIA strips visualized by eyes, the contents of 5-FU in the samples could be qualitatively or semi-quantitatively identified. Furthermore, by measuring the characteristic Raman intensities of MBA on T lines, quantitative detection of 5-FU in the samples were achieved. The IC50and limit of detection (LOD) of the LFIA for 5-FU were found to be 20.9 pg mL−1and 4.4 pg mL−1, respectively. There was no cross-reactivity (CR) of the LFIA with nine relative compounds, and the CR with cytosine, tegafur and carmofur were less than 4.5%. The recoveries of 5-FU from spiked blood samples were in the range of 78.6~86.4% with the relative standard deviation (RSD) of 2.69~4.42%. Five blood samples containing 5-FU collected from the Cancer Hospital were measured by SERS-LFIA, and the results were confirmed by LC-MS/MS. It was proven that the proposed method was able to simply and rapidly detect 5-FU in blood samples with high sensitivity, specificity, accuracy and precision.Keywords:surface-enhanced Raman scattering (SERS);lateral flow immunochromatographic assay (LFIA);5-fluorouracil (5-FU);anticancer drug;blood samples

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TALANTA · 2022 · IF 6.556

A SERS-Fluorescence dual-signal aptasensor for sensitive and robust determination of AFB1 in nut samples based on Apt-Cy5 and MNP@Ag-PEI

Haoyang He,Da-Wen Sun,Hongbin Pu,Zhihui Wu

Food aflatoxin B1 (AFB1) contamination greatly threatens human health and its sensitive determination is imperative. In this study, a surface-enhanced Raman scattering (SERS) and fluorescence dual-signal aptasensor was constructed for sensitive AFB1 detection in peanuts, walnuts, and almonds samples. Fluorescent dye cy5 was used as fluorophore and Raman reporter, while polyethyleneimine modified Ag coating magnetic nanoparticles (MNP@Ag-PEI) were utilized to absorb the cy5 modified aptamer (apt-cy5). Results indicated that linear ranges of 0.001–1000 ng/mL and 0.2–20,000 ng/mL with detection limits of 0.45 pg/mL and 0.135 ng/mL for the SERS and fluorescence methods were obtained, respectively, and AFB1 detection in the nut samples using the aptasensor achieved satisfactory recoveries of 95.2%–108.6% for SERS and 94.7%–109.7% for fluorescence. Compared with other mono signal detection, the established aptasensor facilely fused the merits of the two signals and improved the detection accuracy and flexibility.

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TALANTA · 2022 · IF 6.556

In-situ and amplification-free imaging of hERG ion channels at single-cell level using a unique core-molecule-shell-secondary antibody SERS nanoprobe

Wen-Shu Zhang,Xiao-Peng Liu,Shuai Yue,Ya-Ning Wang,Yue Wang,Zhang-Run Xu

Research on ion channels and their monoclonal antibodies plays a critical role in drug development and disease diagnosis. The current ion channel researches are often not conducted in the microenvironment for cells survival , which restricts the mechanism study of the links between the cell structure and the ion channel function. In this work, we synthesized gold core-4-mercaptobenzonitrile-sliver shell-goat anti-rabbit immunoglobulin G ( [email protected] @ [email protected] ) nanoparticles as surface-enhanced Raman scattering (SERS) nanoprobes for investigating the human ether-a-go-go related gene (hERG) potassium ion channel in cell membranes. This is the first attempt to study ion channels using SERS. Due to the unique core-molecule-shell structure and the silver shell of nanoprobes, strong and stable SERS signal was obtained. With the help of antibodies, the [email protected] @ [email protected] nanoprobes were captured by hERG antibodies and then bonded with hERG ion channels based on the sandwich immune response. The reporter molecule, 4-MBN, displayed a strong and sharp characteristic peak at 2233 cm - 1 in the Raman silent region. The intensity of this peak denoted the concentration of antibodies and the expression of ion channel proteins. We successfully applied this amplification-free method for in-situ imaging the distribution of the hERG ion channel on the transfected HEK293 cell surface at the single-cell level. This hERG ion channel profiling strategy promises a maneuverable tool for ion channel research.

CAS / MDL: 25952-53-8 68-04-2
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MICROCHEMICAL JOURNAL · 2021 · IF 4.821

In situ photochemical deposition of Ag nanoparticles on polyester fiber membranes as flexible SERS substrates for sensitive detection of sodium saccharin in soft drinks

Weiwei Zheng,Wentao Tian,Xiaojun Liu,Qingquan Zhang,Chenghua Zong,Jia-Ping Lai,Wenfeng Zhao

Flexible surface-enhanced Raman scattering (SERS) substrates, specifically paper-based SERS substrates, are generally employed in many practical applications. However, paper-based SERS substrate quantitation is still challenging because of the inferior uniformity originating from the irregular morphology of the paper. The present study synthesized Ag nanoparticles (NPs) via the in situ photochemical reduction of Ag + ions on a titanium dioxide (TiO 2 ) film at the polyester fiber membranes (PFMs) surface. This generated many “hot spots” that presented significant SERS activity with an enhancement factor of 2.1 × 10 9 . Sodium saccharin (SS) bonded to the Ag NPs surface via the carbonyl oxygen and ring nitrogen atoms. A SERS sensor with photochemically deposited Ag NPs was prepared for the sensitive and rapid detection of SS in soft drinks with a limit of detection of 0.3 mg/L. The recovery rate ranged from 93% to 103%, indicating that this method is reliable in actual sample detection with simple pretreatment steps and can be potentially applied for the on-site detection of food additives for food safety.

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ACS Omega · 2020 · IF 2.87

Label-Free Detecting of the Compaction and Decompaction of ctDNA Molecules Induced by Surfactants with SERS Based on a nanoPAA-ZnCl2-AuLs Solid Substrate

Bojuan Hao,Kaige Wang,Yukun Zhou,Chaofan Sui,Lei Wang,Ren Bai,Zhaojin Yang

DNA molecular compaction/decompaction is of great significance for the exploration of basic life processes, the research of biomedical and genetic engineering, and so forth. However, the detailed mechanism of DNA compaction/decompaction caused by surfactants remains an open and challenging problem that has not been fully solved so far. In this paper, a sort of novel solid substrate, nanoPAA-ZnCl2-AuLs, with good stability and high sensitivity, was prepared by a self-assembly method. Based on this substrate, the surface-enhanced Raman scattering (SERS) technology was employed to investigate characteristics of interactions between DNA molecules and surfactants at a single molecular level. SERS spectra of calf thymus DNA (ctDNA), cetyl trimethyl ammonium bromide (CTAB), and sodium dodecyl sulfate (SDS) with a concentration as low as 10–9 M, and SERS spectra of ctDNA–CTAB and ctDNA–CTAB–SDS composites were collected, respectively. The interactions between ctDNA and surfactants were analyzed by changes in SERS spectra, for example, disappearances and appearances of SERS bands and relative changes of peak intensity, in which CTAB resulted in the compaction of the DNA molecule while SDS induced the decompaction of the ctDNA–CTAB complex. Moreover, UV–visible spectrophotometry was employed to demonstrate the compaction/decompaction of ctDNA molecules caused by surfactants. The local binding modes of ctDNA molecules and surfactant molecules were expounded. This work will be helpful for understanding biological processes such as DNA compaction and recombination within nucleus or/and cells and for the development of gene therapy technologies.

CAS / MDL: 989-38-8
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SENSORS AND ACTUATORS B-CHEMICAL · 2023 · IF 8.4

Development of an ultrasensitive SERS aptasensor for determination of aflatoxin B1 by modifying magnetic beads with UiO-66-NH2 for enhanced signal probe capturing

Yumin Chen,Weiwei Cheng,Yuling Yang,Di Wu,Yan Zhang,Xiaozhi Tang

A versatile Surface-enhanced Raman Spectroscopy (SERS) aptasensor was fabricated for ultrasensitive and stable aflatoxin B1 (AFB1) detection using complementary DNA strands (cDNA) modified Fe 3 O 4 @UiO-66-NH 2 as capture probe and aptamer modified Au@ 4-MBA@AgNPs as signal probe . The surface of the Fe 3 O 4 beads was functionalized with UiO-66-NH 2 to improve the surface area and content of reactive amino groups for stable immobilization of cDNA and capture of more signal probes. Raman tag (4-mercaptobenzoic acid, 4-MBA) embedded Au@AgNPs nanoparticles (Au@4-MBA@AgNPs) was used as signal probes to achieve strong SERS intensity and protect the tag molecules from external interference. When no AFB1 existed, a strong SERS intensity of the signal probe was observed due to the DNA hybridization reaction between the capture and signal probe. While, the addition of AFB1 led to the dissociation of signal probes from the capture probes, leading to a decreased Raman intensity . As a result, a low limit of detection of 1.47 × 10 −7 ng/mL and wide linear range from 10 −6 to 10 2 ng/mL were obtained for determination of AFB1 based on the fabricated aptasensor. Moreover, an excellent selectivity and desirable recoveries from 94.3 % to 103.3 % in real maize samples were obtained, demonstrating the fabricated SERS aptasensor is promising in practical applications.

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Analytical Methods · 2023 ·Vol. 15 ·期 35 ·4582-4590 · IF 3.1

Casting liquid PDMS on self-assembled bilayer polystyrene nanospheres to prepare a SERS substrate with two layers of nanopits for detection of p-nitrophenol

Xiurui Ke,Jinran Chen,Lin Chang,Zhou Zhou,Wei Zhang

p-Nitrophenol (PNP) is widely used in pesticides, pharmaceuticals, and dyestuffs. It is vital to detect trace PNP in the environment, because it poses significant environmental hazards due to its high toxicity. In this paper, a new method was reported for preparing a SERS substrate with excellent SERS activity by combining self-assembly techniques and flexible materials. First, the three-dimensional (3D) polystyrene (PS) photonic crystal (PC) structural master was fabricated by stacking two layers of self-assembled PS nanospheres with different diameters. Polydimethylsiloxane (PDMS) with a complementary structure to the master was obtained by casting, curing and peeling off. Finally, the PDMS–Ag substrate was fabricated by sputtering a thin Ag layer on the PDMS structure. The enhancement factor (EF) of the PDMS–Ag substrate was calculated to be 2.90 × 109 by using 4-amino thiophenol (ATP) as the probe molecule, and the limit of detection (LOD) for ATP can reach 10−11 M. And the RSD of the SERS intensity for the peak at 1078 cm−1 on the PDMS–Ag substrates from batch to batch was within 2%, indicating the high reproducibility of the as-prepared substrate. The quantitative analysis of PNP was achieved with a LOD of 10−8 M. Therefore, the PDMS–Ag substrate exhibits high sensitivity and reproducibility, and it can detect PNP in trace amounts, with great potential for detecting other contaminants.

CAS / MDL: 151-21-3
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ACS Applied Materials & Interfaces · 2019 · IF 8.456

Growth of Spherical Gold Satellites on the Surface of Au@Ag@SiO2 Core–Shell Nanostructures Used for an Ultrasensitive SERS Immunoassay of Alpha-Fetoprotein

Ying Yang,Jian Zhu,Jing Zhao,Guo-Jun Weng,Jian-Jun Li,Jun-Wu Zhao

The identification and detection of cancer biomarkers in early stages is an important issue for the therapy of cancer. However, most methods are time-consuming and have limited sensing sensitivity and specificity. In this work, we prepared a novel plasmonic multilayered core–shell–satellite nanostructure (Au@Ag@SiO2–AuNP) consisting of a gold nanosphere with a silver coating core (Au@Ag), an ultrathin continuous silica (SiO2) shell, and a high coverage of gold nanosphere (AuNP) satellites. The Au@Ag core is a prominent surface enhanced Raman scattering (SERS) platform, and the thin SiO2 layer exhibits a long-range plasmon coupling between the Au@Ag core to the AuNP satellites, further leading to enhanced Raman scattering. Meanwhile, the outer AuNP satellites have a high biocompatibility and long-term stability. Combining the above advantages, the well-designed metallic nanoassemblies would be a promising candidate for SERS-based applications in biochemistry. For specific detection of alpha-fetoprotein (AFP), we utilized the SERS-active core–shell–satellite nanostructures modified with AFP antibody as immune probes and nitrocellulose membrane (NC) stabilized captured anti-AFP antibodies as solid substrate. To improve the detection performance, we further systematically optimized the parameters, including the silver coating thickness of the Au@Ag core and the density and size of the satellite AuNPs. Under the optimized conditions, AFP could be detected by the SERS-based sandwich immunoassay with an ultralow detection limit of 0.3 fg/mL, and the method exhibited a wide linear response from 1 fg/mL to 1 ng/mL. The limit of detection (LOD) was considerably lower than conventional methods in the literature. This work relies on the unique Au@Ag@SiO2–AuNP nanostructures as the immune probe develops a new outlook for the application of multilayered nanoassemblies and demonstrates the great potential in early tumor marker detection.

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