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Estazolam (EST) is a common sedative-hypnotic drug with a risk of abuse. Therefore, rapid on-site detection of EST is necessary to control the abuse of EST. In this paper, a fast, simple, and sensitive method is demonstrated for the detection of EST in both water and beverages, using surface-enhanced Raman spectroscopy (SERS) techniques. Au@Ag core-shell nanoparticles (NPs) assembled on the filter paper as a SERS substrate exhibit good applicability and practicality. At the same time, density functional theory (DFT) is used to assign the vibration mode of the EST molecules, which can be used as a guide for subsequent experiments. The lowest detectable concentration of EST in aqueous solution can be as low as 5 mg/L, and signal uniformity is excellent (RSD = 5.56%, RSD = 4.35%). In addition, EST components artificially added to orange juice and pomegranate juice can be effectively detected by simple pretreatment with a minimum detection concentration as low as 10 mg/L. Therefore, this study found that the use of Au@Ag core-shell nanoparticles paper-based SERS substrate provides a quick and easy method for the detection of illegally added drugs in beverages.
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http://dx.doi.org/10.2116/analsci.19P361 | DOI Listing |
Mikrochim Acta
August 2025
Key Laboratory of the Evaluation and Monitoring of Southwest Land Resources, Ministry of Education, College of Chemistry and Material Science, Sichuan Normal University, Chengdu, 610068, Sichuan, China.
A Au@Ag core-shell nanoparticles (NPs)-based digital image colorimetric method, coupled with headspace single-drop microextraction technique (HS-SDME), was developed for the sensitive speciation of sulfite and sulfide. The entire experiment was conducted in a compact headspace bottle with Au@Ag NPs as droplets that selectively reacted with HS to generate a brown product, prior to the readout of RGB values through a smartphone, thus to conduct the accurate qualitative and quantitative determination. In this way, the speciation differentiation of sulfite and sulfide was achieved by controlling their respective conditions of vapor generation.
View Article and Find Full Text PDFChemistry
August 2025
Instituto de Investigaciones Fisicoquímicas, Teóricas y Aplicadas, Universidad Nacional de La Plata - CONICET, Diagonal 113 y 64 S/N, La Plata, Buenos Aires, 1900, Argentina.
This work demonstrates a spontaneous synthesis of ∼8.0, ∼7.0, and ∼3.
View Article and Find Full Text PDFLangmuir
September 2025
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560012, India.
Digestive ripening has emerged as an outstanding solution-based methodology to obtain colloidal bimetallic nanomaterials with excellent control over their size and composition. Solvated metal atom dispersion (SMAD) in conjunction with digestive ripening has been used as a synthetic protocol to derive colloidal gold-silver nanoalloys. A comprehensive study has been carried out to elucidate the mechanistic pathways through which nanoalloying of gold and silver takes place via digestive ripening.
View Article and Find Full Text PDFACS Sens
August 2025
Department of Laboratory Medicine, Xiamen Key Laboratory of Genetic Testing, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen 361005, PR China.
The quantitative and ultrasensitive detection of amyloid-beta peptides Aβ in blood is considered as a powerful strategy for early screening of Alzheimer's disease (AD). In this study, combining dual-aptamer recognition and magnetic-induced enrichment, a background-free surface-enhanced Raman scattering (SERS) platform had been developed for efficient Aβ detection. Au@Ag-4-ethynylaniline@Au nanoparticles (Au@Ag-4-EA@Au NPs) had been designed and modified on aptamer2 of Aβ to form Au@Ag@4-EA@Au-Apt2 (SERS probe).
View Article and Find Full Text PDFMikrochim Acta
July 2025
Department of Nanobiotechnology and Biomimetics School of Life Science Engineering College of Interdisciplinary Science and Technology, University of Tehran, P. O. Box: 14395-1561, Tehran, Iran.
A non-invasive, enzyme-based colorimetric biosensor was developed for urea detection in saliva, utilizing a growth-based method with Au@Ag core-shell nanostructures, including CTAB-coated gold nanoparticles (AuNPs) and CTAB-coated gold nanorods with short (SAuNRs) and high (HAuNRs) aspect ratios. The biosensing mechanism relies on urease-mediated hydrolysis of urea, which raises the pH and enhances the reduction capability of ascorbic acid, leading to the formation of a silver shell on the gold nanostructures, causing colorimetric changes correlated to urea concentration. A machine-learning comparative analysis was also performed to assess how the nanostructure morphology of AuNPs, SAuNRs, and HAuNRs affects sensor performance.
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