Search Results (466)

Shigella is a foodborne bacterial pathogen with a low infectious dose and significant public health impact. Culture-based and molecular techniques provide reliable identification but are time-consuming. Nanoparticle-based biosensors offer sensitive, selective, and compact alternatives. Recent advances in nanoparticle-based biosensors for Shigella spp. (S. flexneri, S. sonnei, S. dysenteriae, and S. boydii) detection have been reviewed in terms of signal amplification, biorecognition, biological targets, sensor types, and performance in real food matrices. Detection strategies rely on gene-level and whole-cell recognition. Targeting virulence genes, invasion plasmid antigen H (ipaH), provides stable genus-level identification, whereas whole-cell recognition facilitates rapid detection without extensive sample preparation. Optical biosensors, including fluorescence-based methods, surface-enhanced Raman spectroscopy (SERS), and localized surface plasmon resonance (LSPR), achieve low detection limits with strong tolerance to complex food matrices. Electrochemical biosensors offer operational simplicity, portability, and suitability for food screening. Lateral flow and hybrid systems provide rapid detection through simplified assay formats and visual readout, with performance influenced by the balance between speed and sensitivity. Validation in real food matrices shows acceptable recoveries, minimal cross-reactivity, and agreement with reference methods. This overview provides a design-oriented framework for nanoparticle-based biosensor selection in food safety by integrating nanomaterial function, biosensor design, and performance characteristics. Full article

Metal phthalocyanines (MPcs) possess outstanding thermal stability and versatile optical, catalytic, and semiconducting properties. Here, the effects of central metal ions, peripheral substituents, and substitution positions on the vibrational properties of MPcs were systematically investigated using Raman spectroscopy. The characteristic Raman band near 1530 cm⁻¹ exhibits systematic shifts with changing metal centers (NiPc > CoPc > CuPc > ZnPc), reflecting differences in metal-ligand interactions and electronic structure. Peripheral substituents and their positions further influence the Raman response through electronic effects, vibrational coupling, and resonance enhancement. In particular, four-substituted MPcs show greater Raman shifts than their three-substituted counterparts. The results reveal clear correlations between molecular structure and Raman characteristics, providing a useful framework for understanding and designing functional phthalocyanine-based materials. Full article

Alzheimer’s disease (AD) is the most common neurodegenerative disorder worldwide. Early diagnosis of AD is crucial for delaying disease progression and improving patients’ quality of life. Blood biomarkers, particularly amyloid-beta (Aβ) and Tau proteins along with their phosphorylated isoforms, show advantages such as convenient sampling, minimal invasiveness, and excellent repeatability. However, the extremely low concentrations of AD biomarkers in blood impose stringent requirements on the sensitivity, specificity, and anti-interference capability of detection methods. Optical methods provide promising analytical platforms to address these challenges in view of their intrinsic merits of high sensitivity and selectivity; rapid response; and potential for miniaturization. This review systematically summarizes the latest advances in optical methods for the detection of the two core AD blood biomarkers (Aβ and Tau), covering techniques such as colorimetry, fluorescence, chemiluminescence, surface plasmon resonance (SPR), and surface-enhanced Raman scattering (SERS). The sensing principles, design strategies, and analytical performances of these methods are discussed, with special emphasis on different signal amplification strategies. In addition, several challenges and future prospects are provided with a primary focus on single-molecule detection, insufficient sensitivity and stability, lack of validation with large clinical cohorts, and absence of standardization. This review aims to provide researchers with guidance for the rational development of high-performance optical methods to achieve early diagnosis of AD. Full article

Plasmonic biosensing technologies have emerged as powerful analytical tools for sensitive and label-free characterisation of biomolecular interactions and complex samples. The increasing demand for comprehensive molecular profiling has accelerated the development of multiplexing strategies that enable simultaneous analysis of multiple analytes and molecular interactions. This Feature Paper examines multiplexing through the complementary spatial, spectral, and temporal dimensions of multiplexing, together with their hybrid combinations and associated analytical trade-offs. Compared with other optical biosensing approaches, including interferometric, photonic, and fluorescence-based sensing platforms, plasmonic biosensors remain attractive owing to their combination of label-free detection, real-time interaction monitoring, sensitive interfacial analysis, and compatibility with multiplexed assay formats. This Feature Paper critically discusses current multiplexing strategies, focusing primarily on surface plasmon resonance (SPR), imaging SPR (SPRi), localised SPR (LSPR), surface-enhanced Raman scattering (SERS), and related nanoplasmonic biosensing approaches, together with recent advances in surface biofunctionalisation, antifouling interfaces, and molecular recognition strategies. Representative applications in biomedical diagnostics and non-clinical settings are highlighted, with examples such as liquid biopsy, glycoprofiling, extracellular vesicle profiling, and food and environmental analysis, alongside key challenges in reproducibility, standardisation, data interpretation, and clinical translation. In addition, selected non-plasmonic optical biosensing technologies are briefly discussed to position plasmonic biosensing within the broader landscape of multiplexed optical biosensing. This Feature Paper argues that the future of multiplexed plasmonic biosensing will depend less on further improvements in sensor performance than on robust, standardised analytical systems. Full article

This study investigated twelve gem-quality color-change fluorite specimens exhibiting a purple–blue gradient from Nova Era, Brazil, using colorimetry, Raman spectroscopy, UV-Vis spectroscopy, photoluminescence spectroscopy, EDXRF, and DiamondView imaging to explore the relationship between color depth and coloration mechanism. Raman spectroscopy further revealed enhanced defect-related peaks in dark samples, indicating cumulative irradiation-induced lattice damage. EDXRF analysis revealed that the radioactive element Th was detected exclusively in dark samples, with the darkest specimen reaching 0.184 wt.% Th, confirming that long-term Th-induced irradiation is the primary driver of color deepening. In UV-Vis spectra, the ~583 nm plasmon resonance absorption band of calcium colloids progressively red-shifted and broadened with increasing color depth, indicating elevated colloid concentrations and enhanced aggregation that directly intensify body color. DiamondView fluorescence weakened with deepening color, attributed to the quenching effect of calcium colloids. Photoluminescence spectra showed that the Eu²⁺ emission peak intensified in dark samples, while the broad 700–900 nm emission band systematically blue-shifted, reflecting differential responses of luminescence centers to radiation damage. This study provides non-destructive spectroscopic criteria for the fluorite color-change mechanism without relying on micro-area compositional analysis, establishing an analytical paradigm linking color gradients with spectral characteristics. Full article

In our prior research (2022), a Fe₃O₄@PDA@Au@GO composite was reported as a surface-enhanced Raman scattering (SERS) substrate for phenanthrene detection, with a detection limit of 10⁻⁷ g/L. The current study is a mechanistic follow-up investigation, which aims to explore the enhancement and enrichment mechanisms of the same substrate. By integrating density functional theory (DFT) calculations, adsorption experiments, and spectroscopic analyses (Raman, FTIR, XPS) before and after adsorption, the surface enhancement mechanism of the Fe₃O₄-PDA-Au-GO composite substrate is investigated. Our findings suggest that Fe₃O₄ enables efficient magnetic separation. The polydopamine (PDA) modification layer appears to enhance the uniformity and stability of the substrate surface, which is beneficial for uniform loading of Au nanoparticles (Au NPs). Graphene oxide (GO) and PDA are found to contribute to the effective enrichment of phenanthrene. Au NPs (mostly in the metallic Au⁰ state) may provide electromagnetic enhancement through localized surface plasmon resonance, and may also contribute to chemical enhancement through possible interactions with phenanthrene. Overall, the stepwise comparison presented in this study is consistent with the proposed roles of Au and GO in enhancing the SERS performance, which collectively improve the detection sensitivity. Full article

The persistent accumulation of tetracycline (TC) antibiotics in aquatic environments poses severe ecological and public health risks, necessitating the development of multifunctional platforms capable of simultaneous detection and degradation. Herein, we report magnetically recoverable plasmonic Fe₃O₄/Cu₂O-Ag nanocomposites (NCs) that integrate visible-light-driven photocatalysis with ultrasensitive surface-enhanced Raman scattering (SERS) detection. Hierarchical flower-like Fe₃O₄ nanocrystals were employed as magnetic supports, followed by in situ growth of Cu₂O nanocrystals and controlled deposition of Ag nanocrystals. The optimized composite (FCA-2) exhibited enhanced visible-light absorption (E_g = 1.86 eV), suppressed electron–hole recombination, and improved photocurrent response, which were attributed to Schottky barrier formation at the Cu₂O-Ag interface and localized surface plasmon resonance (LSPR) effects. Under simulated solar irradiation, FCA-2 NCs achieved 91.79% degradation of TC within 60 min, following pseudo-first-order kinetics (k = 20.37 × 10⁻³ min⁻¹). Finite-difference time-domain (FDTD) simulations revealed that optimal Ag loading maximized plasmonic “hot spot” density, thereby enhancing electromagnetic field intensity and SERS performance. The FCA-2 substrate enabled ultrasensitive TC detection with a limit of detection of as low as 10⁻¹⁰ M. Moreover, the superparamagnetic Fe₃O₄ core allowed for rapid magnetic separation and sustained performance over multiple SERS–photocatalysis cycles, with negligible signal attenuation after 30 days. This work presents a rational strategy for constructing plasmonic magnetic NCs that synergistically couple photocatalytic remediation, ultrasensitive sensing, and magnetic recyclability, offering significant potential for integrated environmental monitoring and sustainable water treatment applications. Full article

Surface-enhanced Raman spectroscopy (SERS) has emerged as a transformative tool in biomedical diagnostics, offering a highly sensitive and non-invasive method for detecting molecular biomarkers at exceptionally low concentrations. This approach takes advantage of the plasmonic characteristics of customized metallic nanostructures that produce intense localized electromagnetic fields via localized surface plasmon resonance and facilitate electron transfer reactions that notoriously enhance the intrinsically weak Raman scattering signals of molecular entities which reside on or next to their surfaces. SERS-based assays have shown remarkable potential in detecting cancer biomarkers, circulating tumor DNA (ctDNA), and proteins at early stages, enabling timely and targeted intervention. Additionally, the combination of SERS with AI-driven data analysis has facilitated real-time diagnostics, enhancing the precision and efficiency of point-of-care testing. Despite its promising capabilities, challenges such as substrate fouling, signal degradation, and the need for better biocompatibility remain. Nevertheless, ongoing research in substrate development, coupled with advances in AI, positions SERS as a leading technology for future diagnostic tools. This paper explores the current state of SERS in biomedical applications, highlighting its potential to revolutionize diagnostics and personalized medicine while addressing the existing limitations and future research directions. Full article

We demonstrate a mechanism-oriented Surface-Enhanced Raman Scattering (SERS) platform based on a hybrid structure integrating monolayer molybdenum disulfide (MoS₂) and gold nanospheres (AuNSs) on an optical microfiber (MF). The microfiber serves as a whispering-gallery-mode (WGM) microcavity. Monolayer MoS₂, grown directly on the microfiber surface via chemical vapor deposition (CVD), provides a chemically active interface for molecular adsorption and charge-transfer-related chemical enhancement. Subsequently deposited AuNSs couple with the microfiber-supported WGM, leading to the formation of hybrid photonic–plasmonic modes. This coupling results in a narrowed scattering resonance and a localized electromagnetic hotspot near the AuNS–microfiber interface. The combined contribution of electromagnetic enhancement from the microfiber–AuNS hybrid cavity and chemical enhancement from the MoS₂ layer produces discernible Raman enhancement for Rhodamine 6G (R6G) molecules under proof-of-concept measurement conditions. This work provides a useful platform for studying SERS enhancement mediated by hybrid photonic–plasmonic modes and offers guidance for the future development of optimized fiber-based SERS sensors. Full article

The development of cost-effective and resource-rich materials is crucial for the practical application of microwave absorbers. This study demonstrates the successful fabrication of core-shell Fe and TiC nanoparticles encapsulated within carbon shells using the arc discharge method. The samples are designated as Fe3Ti1 and Fe1Ti3, where the numbers indicate the Fe-to-Ti mass ratio in the precursor (e.g., Fe1Ti3 = 1:3 by mass). In the arc discharge synthesis mechanism, the mass ratio of Fe to Ti in the raw material was adjusted from 3:1 to 1:3 to optimize the Fe/TiC/C interfaces under a CH₄ forming gas atmosphere. TEM analysis reveals spherical and polyhedral nanoparticles with diameters of 30–50 nm and a uniform carbon shell thickness of 3–4 nm. Raman spectroscopy shows that the Fe1Ti3 sample has a higher defect density (I_D/I_G = 1.13) compared to Fe3Ti1 (0.87), indicating a more disordered carbon structure. Magnetic measurements yield saturation magnetization values of 87 emu/g for Fe3Ti1 and 50 emu/g for Fe1Ti3, with coercivities of 190.72 Oe and 203.65 Oe, respectively. When composited with paraffin at 50 wt% loading, the Fe1Ti3 sample exhibits superior microwave absorption performance, achieving a minimum reflection loss (RL) of −25.22 dB at 8.23 GHz and an effective absorption bandwidth (RL ≤ −10 dB) of 4 GHz (6.5–10.5 GHz) at a thickness of 2.5 mm. This enhanced performance is attributed to the synergistic effect of multiple loss mechanisms, including conduction loss within the three-dimensional core-shell architecture, interfacial polarization at the heterojunctions between the core and the carbon shell, and magnetic loss induced by ferromagnetic behavior associated with defects in both the shell and carbon atomic layers. The magnetic loss in the (Fe/TiC)@C nanocomposites primarily arises from the natural resonance (at ~6.5 GHz) and exchange resonance (at ~12 GHz) of the Fe cores. The dielectric loss is primarily attributed to dipole, interfacial, and space charge polarization from TiC and the carbon shell, as well as multiple scattering effects between nanoparticles. Furthermore, far-field radar cross-section simulations substantiate that the Fe/TiC@C nanocomposite demonstrates excellent radar wave attenuation capability. Further, first principles simulations reveal that introducing Fe at the C/TiC interface induces strong charge redistribution and orbital hybridization, transforming a localized dielectric interface into a highly conductive and electronically coupled C/Fe/TiC system. This interfacial modulation enhances both dielectric loss (via charge transport and polarization) and magnetic loss (via Fe-induced magnetic interactions), thereby enabling optimized dielectric-magnetic synergy for broadband microwave absorption in (Fe/TiC)@C nanocomposites. Full article

Background/Objectives: Andrographolide (ADG) is a plant-derived compound with promising anticancer properties, but its medical use is limited due to poor water solubility and low bioavailability. This study proposes developing a gold-based nanocomposite drug delivery system, using a simplified synthesis method, to improve ADG’s hydrophilicity and enhance its delivery efficiency. Methods: A one-step method was used to synthesize gold nanocomposites with carbon quantum dots (CBQDs) and doped CBQDs acting as reducing and stabilizing agents. These nanocomposites were then conjugated with ADG and thoroughly characterized using multiple structural and spectroscopic techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–Vis), transmission electron microscopy (TEM), Raman spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy. Hydrophilicity enhancement was evaluated using NMR-based log P measurements. Biological assessment involved cell viability assays and confocal microscopy studies in PC3 prostate cancer cells, along with the morphological evaluation of human red blood cells. Results: XRD confirmed the formation of crystalline, face-centered cubic gold nanoparticles, while spectroscopic analyses verified successful nanocomposite formation and ADG conjugation. NMR results showed enhanced hydrophilicity of ADG. Biological tests demonstrated that the nanocomposites were compatible with cells. Conclusions: This study presents a straightforward strategy for synthesizing gold-based nanocomposites that enhance the hydrophilicity and delivery potential of andrographolide, supporting their applicability as nanocarrier platforms for anticancer drug delivery. Full article

Noble metal nanostructures based on localized surface plasmon resonance (LSPR) can induce metal-enhanced fluorescence (MEF) and surface-enhanced Raman scattering (SERS), significantly improving trace detection sensitivity for biomedical and chemical analysis. While self-assembly of noble metal nanoparticles offers simplicity and low equipment dependence, achieving large-area, uniform, and controllable nanostructures remains challenging. In this study, angle-dependent dip coating (ADDC) technology was employed to achieve efficient, controllable self-assembly of silver nanoparticles (AgNPs) on glass slides, establishing a fabrication process for MEF/SERS dual-functional substrates. A stable AgNPs-anhydrous ethanol suspension was prepared and extracted from an inclined substrate reservoir using a microfluidic syringe pump, enabling large-area uniform nanostructure assembly. Systematic investigation revealed that substrate inclination angle provides better morphology and fluorescence enhancement control than withdrawal flow rate. The silver nanostructured surface fabricated under a withdrawal flow rate of 16 mL/h and a substrate inclination angle of 30° exhibited a Cy3 detection limit as low as ${10}^{-1}$ nM, with an enhancement factor ranging from 19.14 to 28.66, as well as an R6G SERS detection limit of ${10}^{-10}$ M with an enhancement factor of 4.07 × ${10}^8$. This study confirms that ADDC technology enables simple, efficient, large-area uniform AgNPs self-assembly for superior dual-function enhancement substrates, offering a cost-effective and efficient strategy for highly sensitive trace detection. Full article

Bilirubin is an important biomarker, where a small unbound fraction dissociated from albumin can cross the blood–brain barrier and induce neurotoxicity, such as kernicterus, at low nanomolar levels. Accurate detection of this low-level fraction remains challenging. Surface-enhanced Raman spectroscopy (SERS) enables label-free molecular detection; however, variations in the local refractive index (RI) at plasmonic hotspots can detune the resonance from the excitation wavelength, leading to signal fluctuations and limited quantitative reliability. Here, we present a multi-resonant nanolaminate SERS substrate designed to achieve RI-insensitive and robust signal enhancement. The vertically stacked metal–insulator–metal architecture provides broadband spectral overlap with both excitation and Raman scattering under dielectric loading, maintaining consistent enhancement across varying RI conditions. We demonstrate label-free bilirubin detection with a highly linear response over 10⁻⁹ to 10⁻⁴ M, achieving an R² value of 0.99. Compared with previously reported bilirubin SERS substrates relying mainly on single-resonant plasmonic enhancement, this RI-insensitive design offers improved quantitative reliability under dielectric environmental changes. These results highlight the importance of RI-insensitive SERS design for reliable quantification and provide a general strategy for robust SERS-based biosensing. Full article

Biosensors have evolved significantly since their invention in the mid-twentieth century. From a simple electrochemical device to the current inclusion of AI, these sophisticated tools are capable of label-free, real-time multiplex detection. To make these sensing systems even more powerful, the incorporation of DNA origami has allowed this technology to become extremely precise, recognisable, and programmable to a range of molecules. This paper systematically summarises the incorporation of DNA origami with biosensors such as fluorescence, surface-enhanced Raman spectroscopy (SERS), surface plasmon resonance (SPR), and electrochemical sensors as well as approaches that are used to design DNA origami nanostructures. These tools allow a range of targets to be detected, ranging from small molecules to larger biological species. Collectively, these studies demonstrate that DNA origami-based biosensors provide high sensitivity; precise spatial control; and rapid, modular detection capabilities. Furthermore, their versatility enables applications across a diverse range of sectors. However, key challenges including limited reproducibility, structural instability, photobleaching, and non-specific binding continue to hinder their widespread adoption. This review proposes future directions aimed at overcoming key limitations, including enhancing biocompatibility and structural stability, to support the development of more advanced and clinical point-of-care-applicable biosensors. Full article

Noble metal nanostructures provide versatile platforms for light manipulation through localized surface plasmon resonances (LSPRs). Among them, triangular silver nanoplates (AgNPTs) exhibit strong field-enhancement and spectral tunability, yet assembling them reproducibly on solids is challenging. We report a two-step functionalization strategy for constructing ordered AgNPT dimers on silica substrates, combining 3-aminopropyltriethoxysilane (APTES) anchoring with 1,4-butanedithiol bridging. AFM reveals face-to-face dimers with well-defined sub-nanometer gaps. Large-area AFM statistics collected over multiple regions (N = 80 nanoplates per condition) confirm reproducible and selective vertical dimerization. Extinction spectroscopy reveals sequential dielectric and coupling effects: thiol adsorption red-shifts the main resonance from 700 to 780 nm because of increased local refractive index and near-field damping, whereas dimerization partially restores it to ≈750 nm, consistent with plasmon hybridization within rigid ∼0.7 nm molecular gaps, where nonclassical moderation may occur but classical hybridization fully explains the observed shifts. Concomitantly, the extinction intensity doubles, following an exponential growth toward saturation during assembly. Surface-enhanced Raman scattering (SERS) measurements using 4-mercaptobenzoic acid (4-MBA) confirm a fourfold increase in the SERS enhancement factor from monolayer to bilayer, consistent with near-field coupling and hotspot formation at interplate junctions. Quantitative plasmon sensitivity analysis yields comparable results between experiments and finite-difference-time-domain simulations, confirming that the observed spectral shifts arise from near-field coupling and dielectric modulation rather than ensemble effects. This reproducible methodology enables precise tuning of NPT orientation, spacing, and optical response, providing a robust platform for enhanced sensing, SERS, and nanophotonic device engineering. Full article