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A label-free, flexible, and disposable aptasensor was designed for the rapid on-site detection of vancomycin (VAN) levels. The electrochemical sensor was based on lab-printed carbon electrodes (C-PE) enriched with cauliflower-shaped gold nanostructures (AuNSs), on which VAN-specific aptamers were immobilized as biorecognition elements and short-chain thiols as blocking agents. The AuNSs, characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM), enhanced the electrochemical properties of the platform and the aptamer immobilization active sites. The developed disposable aptasensor allowed label-free detection of VAN via electrochemical impedance spectroscopy (EIS) across a wide range of concentrations (50–1000 nM), with a limit of detection (LOD) of 1.721 nM. The aptasensor presented good selectivity against some commonly found interferences in human serum and milk and was successfully applied to the analysis of these samples. Graphical Abstract

Electrocatalytic CO₂ reduction is a promising way to provide renewable energy from gaseous CO₂. The development of nanostructures improves energy efficiency and selectivity for value-added chemicals, but complex nanostructures limit the CO₂ conversion rates due to poor mass transport during vigorous electrolysis. Herein, we propose a three-dimensional (3D) hierarchically porous Au comprising interconnected macroporous channels (200–300 nm) and nanopores (∼10 nm) fabricated via proximity-field nanopatterning. The interconnected macropores and nanopores enable efficient mass transport and large active areas, respectively. The roles of each pore network are investigated using reliable 3D nanostructures possessing controlled pore distribution and size. The hierarchical nanostructured electrodes show a high CO selectivity of 85.8% at a low overpotential of 0.264 V and efficient mass activity that is maximum 3.96 times higher than that of dealloyed nanoporous Au. Hence, the systematic model study shows the proposed hierarchical nanostructures have important value in increasing the efficiency of expensive Au.

Plasmonic optical tweezers and thermophoresis are promising tools for nanomaterial manipulation. When a gold nanostructure is irradiated with laser light, an electric field around the nanostructure is enhanced because of the localized surface plasmon resonance, which increases the optical radiation pressure applied to the nanomaterials. In addition, a temperature gradient is also generated by the photothermal conversion, and thermophoretic force is then generated. This study numerically evaluated the electric and temperature fields induced by the localized surface plasmon resonance between two gold nanostructures. Here, we focused on the effect of the gap width between nanostructures on the optical radiation pressure and thermophoretic force. The simulation results show that the electric field is locally enhanced according to the gap width, but the effect on the temperature rise due to the photothermal heating is small. This fact suggests that the gap effect between the nanostructures is particularly dominant in nanomanipulation using optical force, whereas it has little effect in nanomanipulation using thermophoresis.

Nanotechnology is a rapidly growing area of research in part due to its integration into many biomedical applications. Within nanotechnology, gold and silver nanostructures are some of the most heavily utilized nanomaterial due to their unique optical, photothermal, and facile surface chemical properties. In this review, common colloid synthesis methods and biofunctionalization strategies of gold and silver nanostructures are highlighted. Their unique properties are also discussed in terms of their use in biodiagnostic, imaging, therapeutic, and drug delivery applications. Furthermore, relevant clinical applications utilizing gold and silver nanostructures are also presented. We also provide a table with reviews covering related topics.

In this study, dense gold-assembled SiO2 nanostructure (SiO2@Au) was successfully developed using the Au seed-mediated growth. First, SiO2 (150 nm) was prepared, modified by amino groups, and incubated by gold nanoparticles (ca. 3 nm Au metal nanoparticles (NPs)) to immobilize Au NPs to SiO2 surface. Then, Au NPs were grown on the prepared SiO2@Au seed by reducing chloroauric acid (HAuCl4) by ascorbic acid (AA) in the presence of polyvinylpyrrolidone (PVP). The presence of bigger (ca. 20 nm) Au NPs on the SiO2 surface was confirmed by transmittance electronic microscopy (TEM) images, color changes to dark blue, and UV-vis spectra broadening in the range of 450 to 750 nm. The SiO2@Au nanostructure showed several advantages compared to the hydrofluoric acid (HF)-treated SiO2@Au, such as easy separation, surface modification stability by 11-mercaptopundecanoic acid (R-COOH), 11-mercapto-1-undecanol (R-OH), and 1-undecanethiol (R-CH3), and a better peroxidase-like catalysis activity for 5,5′-Tetramethylbenzidine (TMB) and hydrogen peroxide (H2O2) reaction. The catalytic activity of SiO2@Au was two times better than that of HF-treated SiO2@Au. When SiO2@Au nanostructure was used as a surface enhanced Raman scattering (SERS) substrate, the signal of 4-aminophenol (4-ATP) on the surface of SiO2@Au was also stronger than that of HF-treated SiO2@Au. This study provides a potential method for nanoparticle preparation which can be replaced for Au NPs in further research and development.

Nanotheranostics, which combines optical multiplexed disease detection with therapeutic monitoring in a single modality, has the potential to propel the field of nanomedicine toward genuine personalized medicine. Currently employed mainstream modalities using gold nanoparticles (AuNPs) in diagnosis and treatment are limited by a lack of specificity and potential issues associated with systemic toxicity. Light‐mediated nanotheranostics offers a relatively non‐invasive alternative for cancer diagnosis and treatment by using AuNPs of specific shapes and sizes that absorb near infrared (NIR) light, inducing plasmon resonance for enhanced tumor detection and generating localized heat for tumor ablation. Over the last decade, significant progress has been made in the field of nanotheranostics, however the main biological and translational barriers to nanotheranostics leading to a new paradigm in anti‐cancer nanomedicine stem from the molecular complexities of cancer and an incomplete mechanistic understanding of utilization of Au‐NPs in living systems. This work provides a comprehensive overview on the biological, physical and translational barriers facing the development of nanotheranostics. It will also summarise the recent advances in engineering specific AuNPs, their unique characteristics and, importantly, tunability to achieve the desired optical/photothermal properties. Nanotheranostics, which combines optical multiplexed disease detection with therapeutic monitoring in a single modality, has the potential to propel the field of nanomedicine toward genuine personalized medicine. A comprehensive overview of the recent advances in engineering gold nanoconstructs for nanotheranostics is provided. Their unique characteristics, required tunability to achieve the desired optical/photothermal properties and potential translational barriers faced are discussed.

In order to investigate structure-property relationships, the catalytic properties of gold nanoparticles were evaluated in the reduction of 4-nitrophenol by NaBH4. Using catalyst suspensions with identical amounts of gold, the following key results were obtained: first, the nanostars showed increased activity as compared to spherical gold nanoparticles; second, larger gold nanostars showed higher activity, likely because of the abundance of flat/spiky features on these particles, which show high metal utilization; third, treatment of the nanostar colloid with cucurbit[7]uril can be used to balance catalyst stability and activity; fourth, as expected from the decreasing surface atom fraction, the specific activity of the spherical nanoparticles decreased with increasing particle size.

In this work, we report a new approach for detecting SARS-CoV-2 RBD protein (RBD) using the surface-enhanced Raman spectroscopy (SERS) technique. The optical enhancement was obtained thanks to the preparation of nanostructured Ag/Au substrates. Fabricated Au/Ag nanostructures were used in the SERS experiment for RBD protein detection. SERS substrates show higher capabilities and sensitivity to detect RBD protein in a short time (3 s) and with very low power. We were able to push the detection limit of proteins to a single protein detection level of 1 pM. The latter is equivalent to 1 fM as a detection limit of viruses. Additionally, we have shown that the SERS technique was useful to figure out the presence of RBD protein on antibody functionalized substrates. In this case, the SERS detection was based on protein-antibody recognition, which led to shifts in the Raman peaks and allowed signal discrimination between RBD and other targets such as Bovine serum albumin (BSA) protein. A perfect agreement between a 3D simulated model based on finite element method and experiment was reported confirming the SERS frequency shift potential for trace proteins detection. Our results could open the way to develop a new prototype based on SERS sensitivity and selectivity for rapid detection at a very low concentration of virus and even at a single protein level.

The presence of excess L-amino acid in the Murchison meteorite, circular polarization effect in the genesis of stars and existence of chirality in interstellar molecules contribute to the origin of life on earth. Chiral-sensitive techniques have been employed to untangle the secret of the symmetries of the universe, designing of effective secure drugs and investigation of chiral biomolecules. The relationship between light and chiral molecules was employed to probe and explore such molecules using spectroscopy techniques. The mutual interaction between electromagnetic spectrum and chirality of matter give rise to distinct optical response, which advances vital information contents in chiroptical spectroscopy. Chiral plasmonic gold nanoparticle exhibits distinctive circular dichroism peaks in broad wavelength range thereby crossing the limits of its characterization. The emergence of strong optical activity of gold nanosystem is related to its high polarizability, resulting in plasmonic and excitonic effects on incident photons. Inspired by the development of advanced chiral plasmonic nanomaterials and exploring its properties, this review gives an overview of various chiral gold nanostructures and the mechanism behind its chiroptical properties. Finally, we highlight the application of different chiral gold nanomaterials in the field of catalysis and medical applications with special emphasis to biosensing and biodetection. Graphical abstract

This study presents a novel electrochemical immunosensor designed for the highly sensitive detection of vascular endothelial growth factor (VEGF). The sensor utilizes gold nanostructures grown on fluorine-doped tin oxide (FTO) electrodes through a polyethylene glycol (PEG)-mediated electrochemical process. Fabrication involves a two-step immobilization strategy, combining physical vapor deposition (PVD) of a gold thin film with thermal annealing. The nanostructured electrode is subsequently modified electrochemically via PEG mediation, followed by antibody functionalization to enhance binding specificity. PEG-mediated control over nanostructure growth yields irregular short nanorods and leaf-like dendrites, significantly enhancing sensor performance. Extensive electrochemical analyses, including cyclic voltammetry and impedance spectroscopy, confirm improved sensitivity and stability. The optimized immunosensor achieves an ultralow detection limit of 6 fg/mL (corresponding to ~ 9500 VEGF molecules in 60 µL, and a broad linear detection range of 10 fg/mL to 10⁵ fg/mL, with excellent reproducibility. Given VEGF’s pivotal role in angiogenesis and tumor progression, this ultrasensitive platform offers a promising tool for early cancer diagnostics.