Search Results (93)

Nanosurface energy transfer (NSET) has emerged as a pivotal mechanism in nanobiophotonics, facilitating the development of highly sensitive biosensors with extended dynamic ranges. Unlike conventional Förster resonance energy transfer, NSET exhibits an inverse fourth-power dependence on distance, enabling quantitative measurements over distances up to 40 nm. This review comprehensively explores the fundamental principles governing NSET, with particular emphasis on non-radiative coupling between fluorescent donors and metallic nanostructures such as gold nanoparticles. Additionally, the applications of these probes are surveyed across various bioanalytical domains, including nucleic acid assays, immunoassays, real-time intracellular monitoring, and various biomolecule detection. Additionally, the evolving integration of NSET, plasmonics, and nanophotonic architectures is discussed, focusing on emerging trends and the trajectory for developing next-generation, multiplexed, and point-of-care diagnostic platforms. Current challenges and prospective pathways for translating these advanced sensing systems into clinical and field-deployable solutions are also considered. Full article

Thanks to both endogenous and exogenous antioxidants (AOs), the antioxidant defense system ensures redox homeostasis, which is crucial for protecting the body from oxidative stress and maintaining overall health. The food industry also exploits the antioxidant properties to prevent or delay the oxidation of other molecules during processing and storage. There are many classical methods for assessing antioxidant capacity/activity, which are based on mechanisms such as hydrogen atom transfer (HAT), single electron transfer (SET), electron transfer with proton conjugation (HAT/SET mixed mode assays) or the chelation of selected transition metal ions (e.g., Fe²⁺ or Cu¹⁺). The antioxidant capacity (AOxC) index value can be expressed in terms of standard AOs (e.g., Trolox or ascorbic acid) equivalents, enabling different products to be compared. However, there is currently no standardized method for measuring AOxC. Nanoparticle sensors offer a new approach to assessing antioxidant status and can be used to analyze environmental samples, plant extracts, foodstuffs, dietary supplements and clinical samples. This review summarizes the available information on nanoparticle sensors as tools for assessing antioxidant status. Particular attention has been paid to nanoparticles (with a size of less than 100 nm), including silver (AgNPs), gold (AuNPs), cerium oxide (CeONPs) and other metal oxide nanoparticles, as well as nanozymes. Nanozymes belong to an advanced class of nanomaterials that mimic natural enzymes due to their catalytic properties and constitute a novel signal transduction strategy in colorimetric and absorption sensors based on the localized surface plasmon resonance (LSPR) band. Other potential AOxC sensors include quantum dots (QDs, <10 nm), which are particularly useful for the sensitive detection of specific antioxidants (e.g., GSH, AA and baicalein) and can achieve very good limits of detection (LOD). QDs and metallic nanoparticles (MNPs) operate on different principles to evaluate AOxC. MNPs rely on optical changes resulting from LSPR, which are monitored as changes in color or absorbance during synthesis, growth or aggregation. QDs, on the other hand, primarily utilize changes in fluorescence. This review aims to demonstrate that, thanks to its simplicity, speed, small sample volumes and relatively inexpensive instrumentation, nanoparticle-based AOxC assessment is a useful alternative to classical approaches and can be tailored to the desired aim and analytes. Full article

A rapid, colorimetric sensor for histamine detection is presented using citrate-stabilized gold nanoparticles enhanced with Cu²⁺ coordination. The sensing mechanism involves dual recognition: protonated histamine first adsorbs electrostatically onto AuNP surfaces at pH 5.5, followed by Cu²⁺-mediated coordination between imidazole rings that induces interparticle coupling, resulting in a characteristic shift of the localized surface plasmon resonance from 520 to 620 nm. The optical response, measured as the absorbance ratio A₆₂₀/A₅₂₀, exhibits excellent linearity over the range of 1.25–10 μM with a detection limit of 0.95 μM and total assay time under 30 min. The dual-recognition mechanism provides high selectivity for histamine over structural analogs, including L-histidine, imidazole, and L-lysine. The metal ion-mediated colorimetric approach described here achieves sub-micromolar sensitivity in simple buffer solutions, which is comparable to the histamine level used in in vitro cell assays and food-related studies. Thus, the present system is best viewed as a mechanistic model that can inform the design of future biosensing and analytical methods, rather than as a fully optimized sensor for direct clinical measurements in complex biofluids. Full article

The study of the conformational stability of protein layers at the interface between gold surfaces and lipid membranes is crucial for determining the biological activity of these systems and understanding their interactions. The surfaces differ significantly in hardness: gold is a rigid substrate, while the POPC/POPS liposome layer is highly flexible. A quartz crystal microbalance with dissipation (QCM-D) monitoring method and multi-parametric surface plasmon resonance (MP-SPR) were used to determine the adsorption efficiency of lysozymes, the level of layer hydration, and changes occurring within the secondary structure and the thickness of the formed protein layer. In both methods, lysozyme adsorption on the gold surface was more effective at pH 4.0 than at pH 7.4. The lysozyme adsorption efficiency on the surface of the lipid layer was the same for both measurement conditions. In contrast, the affinity of lysozyme molecules to the lipid surface was higher than that of the gold surface. The composition of the secondary structure of lysozymes was monitored using the FT-IR method. Deconvolution of the Amide I band confirms the existence of different mechanisms underlying lysozyme molecule immobilization depending on the type of adsorption surface. Along with the change in the surface, there is a transition from the dominance of electrostatic to hydrophobic interactions, which significantly affects the structure of the interphase layer. High content of random structures on the lipid surface is evident, while, in the case of the gold surface, there is a decrease in random structures and the presence of antiparallel β-sheets. Interaction with the surface induces the transition of amyloidogenic domains of the protein to conformations, which are particularly susceptible to aggregation, consequently leading to oligomerization. Full article

Drug-resistant Mycobacterium tuberculosis (Mtb) remains a major global health challenge, prompting the need for new therapeutics targeting essential bacterial proteins. The caseinolytic protein C1 (ClpC1) is a promising drug target, and accurate measurement of its ATPase activity is critical for understanding drug mechanisms. We optimized a sensitive luminescence-based ATPase assay and evaluated ClpC1 constructs with various tag positions and truncations. N-terminal tagging significantly impaired enzymatic activity, whereas C-terminal tagging had no effect; truncated domains showed reduced activity compared to native full-length (FL) ClpC1. Using the native FL-ClpC1, we assessed ecumicin (ECU) and five analogs via ATPase activity and surface plasmon resonance (SPR), using rufomycin (RUF) and cyclomarin A (CYMA) as controls. RUF and CYMA bound tightly (K_D = 0.006–0.023 µM) and inhibited Mtb growth (MIC₉₀ = 0.02–0.094 µM) but modestly stimulated ATPase activity (≤2-fold). In contrast, ECU and its analogs strongly enhanced ATPase activity (4–9-fold) despite slightly weaker binding (K_D = 0.042–0.80 µM) and growth inhibition (MIC₉₀ = 0.19 µM). The partial correlation among AC₅₀, K_D, and MIC values highlights the complementary value of enzymatic, biophysical, and cellular assays. Our assay platform enables mechanistic characterization of ClpC1-targeting compounds and supports rational antitubercular drug development. Full article

Single-molecule detection (SMD) has reformed analytical science by enabling the direct observation of individual molecular events, thus overcoming the limitations of ensemble-averaged measurements. This review presents a comprehensive analysis of the principles, devices, and emerging materials that have shaped the current landscape of SMD. We explore a wide range of sensing mechanisms, including surface plasmon resonance, mechanochemical transduction, transistor-based sensing, optical microfiber platforms, fluorescence-based techniques, Raman scattering, and recognition tunneling, which offer distinct advantages in terms of label-free operation, ultrasensitivity, and real-time responsiveness. Each technique is critically examined through representative case studies, revealing how innovations in device architecture and signal amplification strategies have collectively pushed the detection limits into the femtomolar to attomolar range. Beyond the sensing principles, this review highlights the transformative role of advanced nanomaterials such as graphene, carbon nanotubes, quantum dots, MnO₂ nanosheets, upconversion nanocrystals, and magnetic nanoparticles. These materials enable new transduction pathways and augment the signal strength, specificity, and integration into compact and wearable biosensing platforms. We also detail the multifaceted applications of SMD across biomedical diagnostics, environmental monitoring, food safety, neuroscience, materials science, and quantum technologies, underscoring its relevance to global health, safety, and sustainability. Despite significant progress, the field faces several critical challenges, including signal reproducibility, biocompatibility, fabrication scalability, and data interpretation complexity. To address these barriers, we propose future research directions involving multimodal transduction, AI-assisted signal analytics, surface passivation techniques, and modular system design for field-deployable diagnostics. By providing a cross-disciplinary synthesis of device physics, materials science, and real-world applications, this review offers a comprehensive roadmap for the next generation of SMD technologies, poised to impact both fundamental research and translational healthcare. Full article

A comparison of two synthesis methods for depositing Au nanoparticles onto TiO₂ was performed: (1) impregnation with HAuCl₄ followed by thermal treatment in argon, and (2) magnetron sputtering from a Au disc. The obtained materials were used for acetaldehyde decomposition in a high temperature reaction chamber and ch aracterised by UV-Vis/DR, XPS, XRD, SEM, and photoluminescence measurements. The process was carried out using an air/acetaldehyde gas flow under UV or UV-Vis LED irradiation. The mechanism of acetaldehyde decomposition and conversion was elaborated by in situ FTIR measurements of the photocatalyst surface during the reaction. Simultaneously, concentration of acetaldehyde in the outlet gas was monitored using gas chromatography. All the Au/TiO₂ samples showed absorption in the visible region, with a maximum around 550 nm. The plasmonic effect of Au nanoparticles was observed under UV-Vis light irradiation, especially at elevated temperatures such as 100 °C, for Au/TiO₂ prepared by the magnetron sputtering method. This resulted in a significant increase in the conversion of acetaldehyde at the beginning, followed by gradual decrease over time. The collected FTIR spectra indicated that, under UV-Vis light, acetaldehyde was strongly adsorbed onto Au/TiO₂ surface and formed crotonaldehyde or aldol. Under UV, acetaldehyde was mainly adsorbed in the form of acetate species. The plasmonic effect of Au nanoparticles increased the adsorption of acetaldehyde molecules onto TiO₂ surface, while reducing their decomposition rate. The increased temperature of the process enhanced the decomposition of the acetaldehyde. Full article

This study investigates the effects of substrate flexibility and metal deposition methods on piezoelectric-enhanced Surface-Enhanced Raman Scattering (SERS) in metal-deposited ZnO nanorod (NR) nanocomposites (NCPs). ZnO NRs were grown on both rigid (ITO–glass) and flexible (ITO-PET) substrates, followed by gold (Au) deposition by pulsed-laser-induced photolysis (PLIP) or silver (Ag) deposition by thermal evaporation. Structural analysis revealed that ZnO NRs on flexible substrates exhibited smaller diameters (60–80 nm vs. 80–100 nm on glass), a higher density, and diverse orientations that enhanced piezoelectric responsiveness. Optical characterization showed distinct localized surface plasmon resonance (LSPR) peaks at 420 nm for Ag and 525 nm for Au systems. SERS measurements demonstrated that Ag-ZnO NCPs achieved superior detection limits (10⁻⁹ M R6G) with enhancement factors of 10⁸–10⁹, while Au-ZnO NCPs reached 10⁻⁸ M detection limits. Mechanical bending of flexible substrates induced dramatic signal enhancement (50–100-fold for Au-ZnO/PET and 2–3-fold for Ag-ZnO/PET), directly confirming piezoelectric enhancement mechanisms. This work establishes quantitative structure–property relationships in piezoelectric-enhanced SERS and provides design principles for high-performance flexible sensors. Full article

The detection of Fe²⁺ in environmental water sources is critical due to its biological relevance and potential toxicity at elevated levels. Herein, we report a plasmon-driven catalytic sensing nanoplatform based on p-aminothiophenol (pATP)-functionalized silver nanoparticles (AgNPs) for the selective and sensitive detection of Fe²⁺. The nanoplatform exploits the inhibition of the plasmon-driven catalytic conversion of pATP to 4,4-dimercaptoazobenzene (DMAB), monitored via surface-enhanced Raman scattering (SERS) spectroscopy. The catalytic efficiency was quantified by the intensity ratio between the formed DMAB-specific Raman band and the common aromatic ring vibration band of pATP and DMAB. This ratio decreased proportionally with increasing Fe²⁺ concentration over a range of 100 µM to 1.5 mM, with a calculated limit of detection of 39.7 µM. High selectivity was demonstrated against common metal ions, and excellent recovery rates (96.6–99.4%) were obtained in real water samples. Mechanistic insights, supported by chronopotentiometric measurements under light irradiation, revealed a competitive oxidation pathway in which Fe²⁺ preferentially consumes plasmon-generated hot holes over pATP. This mechanism clarifies the observed catalytic inhibition and supports the design of redox-responsive SERS sensors. The platform offers a rapid, low-cost, and portable solution for Fe²⁺ monitoring and holds promise for broader applications in detecting other redox-active analytes in complex environmental matrices. Full article

This paper presents a carbon monoxide (CO) detection mechanism achieved through further improvement of the sensing antenna based on hybrid spoof localized surface plasmons (SLSPs) and cavity resonance. Unlike conventional approaches relying on chemical reactions or photoelectric effects, the all-metal configuration detects dielectric variations through microwave-regime resonance frequency shifts, enabling CO/air differentiation with theoretically enhanced robustness and environmental adaptability. The designed system achieves measured figures of merit (FoMs) of 183.2 RIU⁻¹, resolving gases with dielectric contrast below 0.1%. Experimental validation successfully discriminated CO (ε_r = 1.00262) from air (ε_r = 1.00054) under standard atmospheric pressure at 18 °C. Full article

This study presents a comprehensive numerical and experimental investigation of electric field enhancement in inverted-pyramidal gold (Au) array substrates, focusing on variable inter-pyramidal spacing for surface-enhanced Raman scattering (SERS) applications. We conducted a series of finite element method (FEM) simulations to model the spatial distribution of electromagnetic fields within plasmonic metasurfaces under 780 nm laser excitation. The results show that reducing the spacing between inverted pyramidal structures from 10 μm to 3.2 μm significantly increases the electric field intensity at both the tip and edge regions of the inverted-pyramidal Au structure, with maximum fields reaching 6.75 × 10⁷ V/m. Experimental SERS measurements utilizing 4-mercaptobenzoic acid as a Raman reporter support the simulation findings, indicating enhanced signal intensity in closely spaced configurations. These results confirm that geometric field concentration and plasmonic coupling are the dominant mechanisms responsible for SERS enhancement in these systems. This work provides a strategic framework for optimizing the geometry of plasmonic substrates to improve the sensitivity and reliability of SERS-based sensing platforms. Full article

Ultraviolet (UV) photodetectors play a crucial role in various applications, ranging from environmental monitoring to biomedical diagnostics. This paper presents the fabrication and characterization of a high-performance UV photodetector using hexagonal boron nitride (hBN) decorated with gold nanoparticles (AuNPs). The hBN flakes were mechanically exfoliated onto SiO₂ substrates, and AuNPs were formed via thermal evaporation, resulting in the creation of a plasmonically active surface that enhanced light absorption and carrier dynamics. Raman spectroscopy, transmission electron microscopy, and electrical measurements were performed to comprehensively analyze the device structure and performance. The photodetector exhibited significantly improved photocurrent and responsivity under UV-B (306 nm) and UV-C (254 nm) illumination, with the responsivity reaching an increase of nearly two orders of magnitude compared to that of the pristine hBN device. These improvements are attributed to the synergistic effects of the wide bandgap of hBN and the localized surface plasmon resonance of the AuNPs. These findings demonstrate the potential of AuNP-decorated hBN for advanced UV photodetection applications and provide a pathway toward more efficient and miniaturized optoelectronic devices. Full article

This paper outlines the design and fabrication of a portable optomechatronic system based on the theta-2theta configuration, which explores various optical characterization techniques for transparent materials and dielectric thin films. These techniques include Brewster angle and Abelès-Brewster angle measurements, critical angle measurements, and the surface plasmon resonance technique. The system consists of a mechanical assembly of rotating stages, a semiconductor laser, a photodiode connected to a data acquisition card, and a user interface for controlling the stepper motor rotation stages. Utilizing a BK7 substrate, the motorized stage achieved a resolution of 0.010. The Brewster angle measured was 56.550, with a refractive index (n) of 1.5137. The relative error obtained was Δn/n = 3.82 × 10⁻⁴, with a sensitivity of 164.27 RIU/degree and an accuracy of 0.37/degree. Furthermore, the discrepancies between theoretical and experimental refractive indices for different prisms at 639 nm ranged from ±7 × 10⁻⁴ to ±73 × 10⁻⁴. After testing various samples, the system demonstrated its capability to perform fast, precise, and non-invasive measurements. Its portability allows for use in diverse environments and applications. Full article

The dynamic interplay between a multimeric phosphoprotein (P) and polymeric nucleoprotein (N) in complex with the viral RNA is at the heart of the functioning of the RNA-synthesizing machine of negative-sense RNA viruses of the order Mononegavirales. P multimerization and N phosphorylation are often cited as key factors in regulating these interactions, but a detailed understanding of the molecular mechanisms is not yet available. Working with recombinant rabies virus (RABV) N and P proteins and using mainly surface plasmon resonance, we measured the binding interactions of full-length P dimers and of two monomeric fragments of either circular or linear N-RNA complexes, and we analyzed the equilibrium binding isotherms using different models. We found that RABV P binds with nanomolar affinity to both circular and linear N-RNA complexes and that the dimerization of P protein enhances the binding affinity by 15–30-fold as compared to the monomeric fragments, but less than expected for a bivalent ligand, in which the binding domains are connected by a flexible linker. We also showed that the phosphorylation of N at Ser389 creates high-affinity sites on the polymeric N-RNA complex that enhance the binding affinity of P by a factor of about 360. Full article

Laser nanostructuring of thin films with ultrashort laser pulses is widely used for nanofabrication across various fields. A crucial parameter for optimizing and understanding the processes underlying laser processing is the absorbed laser fluence, which is essential for all damage phenomena such as melting, ablation, spallation, and delamination. While threshold fluences have been extensively studied for single compound thin films, advancements in ultrafast acoustics, magneto-acoustics, and acousto-magneto-plasmonics necessitate understanding the laser nanofabrication processes for functional multilayer films. In this work, we investigated the thickness dependence of ablation and delamination thresholds in Ni/Au bilayers by varying the thickness of the Ni layer. The results were compared with experimental data on Ni thin films. Additionally, we performed femtosecond time-resolved pump-probe measurements of transient reflectivity in Ni to determine the heat penetration depth and evaluate the melting threshold. Delamination thresholds for Ni films were found to exceed the surface melting threshold suggesting the thermal mechanism in a liquid phase. Damage thresholds for Ni/Au bilayers were found to be significantly lower than those for Ni and fingerprint the non-thermal mechanism without Ni melting, which we attribute to the much weaker mechanical adhesion at the Au/glass interface. This finding suggests the potential of femtosecond laser delamination for nondestructive, energy-efficient nanostructuring, enabling the creation of high-quality acoustic resonators and other functional nanostructures for applications in nanosciences. Full article