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Biomass valorization is essential, particularly in emerging countries. Here, hydrochar from arabica coffee straw was functionalized with a triazole group (HD-TRz) for use as a support of palladium nanoparticles (PdNPs-HD-TRz) applied in the Ullmann coupling reaction for the first time. It provided remarkably excellent selectivities, conversions at a temperature as low as 45 °C and catalyst recyclability, surpassing previous literature performances. Hydrochar was obtained by one-pot reaction via hydrothermal synthesis, using NaOH solution as activating agent and functionalized with a 1,3-triazole group by CuAAC "click" reaction. The PdNPs were prepared via reduction of hydrochar-bound Pd(II) using NaBH 4 . Hydrochar functionalization was monitored by infrared spectroscopy, and X-ray diffraction (XRD) allowed to observe carbon and palladium planes in hydrochar and PdNPs HD-TRz structures. The PdNPs presented a spherical shape with 2.1 ± 0.1 nm size, homogeneously distributed in the carbon coverslips. The HD-TRz-supported PdNPs were used as a catalyst in the Ullmann reaction of iodobenzene, using ethanol as solvent with 100% of conversion and 91% selectivity at 45 °C. The material was reused, presenting 100% of conversion and selectivities of 92, 84 and 73% for the 1st, 2nd and 3rd cycle, respectively. The scope of the reaction was expanded to other molecules showing the potential of this and other triazole-hydrochar-supported nanocatalysts., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Electron transfer plays a major role in chemical reactions and processes, and this is particularly true of catalysis by nanomaterials. The advent of metal nanoparticle (NP) catalysts, recently including atomically precise nanoclusters (NCs) as parts of nanocatalyst devices has brought increased control of the relationship between NP and NC structures and their catalytic functions. Consequently, the molecular definition of these new nanocatalysts has allowed a better understanding and management of various kinds of electron transfer involved in the catalytic processes. This Minireview brings a chemist's view of several major aspects of electron-transfer functions concerning NPs and NCs in catalytic processes. Particular focus concerns the role of NPs and NCs as electron reservoirs and light-induced antenna in catalytic processes from H 2 generation to more complex reactions and sustainable energy production., (© 2021 Wiley-VCH GmbH.)

In this study, mycosynthesized zinc oxide nanoparticles (ZnONPs) are fabricated via Pleurotus sajor-caju mushroom extract, and their potential medical and environmental applications are demonstrated. The biosynthesized ZnONPs were assessed for their antibacterial, anticancer, and biodecolorization potential efficiency. They were also characterized and morphologically analyzed by UV-visible spectroscopy, XRD, FT-IR, FE-SEM, EDX, HR-TEM, Zeta potential, and GC-MS analysis. The UV visible spectrum analysis of synthesized ZnONPs analyzed outcome 354 nm was the SPR peak that the nanoparticles displayed. The characteristic Zn-O bond was indicated by a strong peak in the FT-IR study at 432.05 cm -1 . Based on XRD analysis, P. sajor-caju mediated ZnONPs were crystalline nature, with an average nano particle size of 14.21 nm and a polydispersity directory of 0.29. The nanoparticles exhibit modest constancy, as shown by their zeta potential value of - 33.2 mV. The presence of oxygen and zinc was verified by EDX analysis. The ZnONPs were found to be spherical in shape and crystalline nature structure, with smooth surface morphology and a mean particle size of 10 nm using HR-TEM and SAED analysis. The significant antibacterial activity against S. aureus (6.2 ± 0.1), S. mutans (5.4 ± 0.4), and B. subtilis (5.2 ± 0.1 mm) was demonstrated by the synthesized ZnONPs made using mushroom extract. It was discovered that when the concentration of mushroom extract was increased together with synthesized ZnONPs, the bactericidal activity increased considerably. A higher concentration of ZnONPs demonstrated superior antibacterial activity across the ZnONPs ratio tests. The in vitro cytotoxicity assay showed that ZnONPs, even at low doses, had a substantial number of cytotoxic effects on liver cancer cells (LC 50 values 47.42 µg/mL). The effectiveness test revealed that acid blue 129 was degraded. The best decolorization of acid blue 129 at 72.57% after 3 h of soaking serves as evidence for the theory that myco-synthesized ZnONPs by P. sajor-caju mushroom can function as catalysts in reducing the dye. The mycosynthesized ZnONPs from P. sajor-caju extract, and its potential for antibacterial, anticancer, and decolorization are in this investigation. The mycosynthesized ZnONPs suggest a novel use for nanoparticles in the creation of environmental and medicinal products., (© 2024. The Author(s), under exclusive licence to Springer Nature B.V.)

Dopamine (DA) is a potent neuromodulator in the brain that affects a wide range of motivated behaviors. Abnormal concentration of DA is related to a variety of diseases. Hence, it is imperative to establish a rapid and precise method for quantifying DA. In this work, we integrate orange-yellow emissive carbon dots (CDs) with target-induced silver deposition on gold nanoparticles (Au NPs), forming gold/silver core-shell nanoparticles (Au@Ag NPs), to construct a fluorometric and colorimetric dual-signal sensor for sensitive detection of DA. Au NPs and silver ions (Ag + ) have minimal effect on the fluorescence of CDs. DA can reduce the silver ions to Ag(0) on the surface of the Au NPs to form a silver shell, resulting in the blue-shift of the absorbance peak from 520 to 416 nm, which overlaps with the excitation spectrum of CDs. As a result, the system color turns from pink to orange-yellow, and the fluorescence of CDs is quenched due to the strong inner filter effect. The linear range of the colorimetry is 0.5-18 μM with a limit of detection (LOD) of 0.41 μM, while the linear range for the fluorometry method is 0.5-14 μM with a LOD of 0.021 μM. This method demonstrates notable advantages including a low detection limit, rapid response time, and straightforward operation in practical samples, showing great potential in biomedical analysis., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.)

In the current study, silver nanoparticles (AgNPs) incorporated Polyamide 66 (PA66) nanofiber mat as a photocatalyst which was prepared using electrospinning technique for degradation of methyl orange (MO). Considering the lack of reported studies on the influence of the ultrasonication on the size and stability of AgNPs, the purpose of the study was to produce a small size of AgNPs and compare it with the continuous stirring method. It is reasonable to report that the advantage of ultrasonication is to generate relatively smaller AgNPs (u-AgNPs) compared to fabrication by continuous stirring method (s-AgNPs). Helichrysum arenarium (HA) extract was used as a reducing agent as well as a capping agent in green synthesis of AgNPs. AgNPs were characterized by UV-visible spectrophotometry, Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and transmission electron microscope (TEM). PA66/u-AgNs nanofibers were then successfully electrospun and characterized by using scanning electron microscope (SEM), FT-IR, thermal gravimetric analysis (TGA), and water contact angle measurement (WCA). Fabricated PA66-based nanofiber mat with smooth surface and uniform diameters (330-340 nm) was used as a catalyst in MO degradation. PA66/u-AgNP nanofibers were also evaluated for antibacterial performance and showed significant inhibition against Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa bacteria. According to these findings, it is expected that the fabricated novel PA66/u-AgNP nanofibers can be announced as a promising potent and applied to the wastewater applications., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Gold nanoclusters (AuNCs) are a class of novel luminescent nanomaterials that exhibit unique properties of ultra-small size, featuring strong anti-photo-bleaching ability, substantial Stokes shift, good biocompatibility, and low toxicity. Various biomolecules have been developed as templates or ligands to protect AuNCs with enhanced stability and luminescent properties for biomedical applications. In this review, the synthesis of AuNCs based on biomolecules including amino acids, peptides, proteins and DNA are summarized. Owing to the advantages of biomolecule-protected AuNCs, they have been employed extensively for diverse applications. The biological applications, particularly in bioimaging, biosensing, disease therapy and biocatalysis have been described in detail herein. Finally, current challenges and future potential prospects of bio-templated AuNCs in biological research are briefly discussed., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.)

Pharmaceutical, food packing, cosmetics, agriculture, energy storage devices widely utilize metal and metal oxide nanoparticles prepared via different physical and chemical methods. It resulted in the release of several dangerous compounds and solvents as the nanoparticles were being formed. Currently, Researchers interested in preparing nanoparticles (NPs) via biological approach due to their unique physiochemical properties which took part in reducing the environmental risks. However, a number of microbial species are causing dangerous illnesses and are a threat to the entire planet. The metal and metal oxide nanoparticles played a significant role in the identification and elimination of microbes when prepared using natural extract. Its biological performance is thus also becoming exponentially more apparent than it was using in conventional techniques. Despite the fact that they hurt germs, their small size and well-defined shape encourage surface contact with them. The generation of Reactive Oxygen Species (ROS), weakens the bacterial cell membrane by allowing internal cellular components to seep out. The bacterium dies as a result of this. Numerous studies on different nanoparticles and their antibacterial efficacy against various diseases are still accessible. The main objective of the biogenic research on the synthesis of key metals and metal oxides (such as gold, silver, titanium dioxide, nickel oxide, and zinc oxide) using various plant extracts is reviewed in this study along with the process of nanoparticle formation and the importance of phytochemicals found in the plant extract., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

A highly sensitive colorimetric method (glycan-based nano(e)zyme) was developed for sensitive and rapid detection of the SARS-CoV-2 virus based on N-acetyl neuraminic acid (sialic acid)-functionalized gold nanoparticles (SA-Au NZs). A number of techniques were used to characterize the prepared nanomaterials including XRD, FT-IR, UV-vis, DLS, and TEM. DLS analysis indicates an average hydrodynamic size of 34 nm, whereas TEM analysis indicates an average particle size of 15.78 nm. This observation confirms that water interacts with nanoparticle surfaces, resulting in a large hydrodynamic diameter. The peroxidase-like activity of SA-Au NZs was examined with SARS-CoV-2 and influenza viruses (influenza A (H1N1), influenza A (H3N2), and influenza B). UV-visible spectroscopy was used to monitor and record the results, as well as naked eye detection (photographs). SA-Au NZs exhibit a change in color from light red to purple when SARS-CoV-2 is present, and they exhibit a redshift in their spectrum. N-acetyl neuraminic acid interacts with SARS-CoV-2 spike glycoprotein, confirming its ability to bind glycans. As a result, SA-Au NZs can detect COVID-19 with sensitivity and specificity of over 95% and 98%, respectively. This method was approved by testing saliva samples from 533 suspected individuals at Ghaem Hospital of Mashhad, Mashhad, Iran. Sensitivity and specificity were calculated by comparing the results with the definitive results. The positive results were accompanied by a color change from bright red to purple within five minutes. Statistical analysis was performed based on variables such as age, gender, smoking, diabetes, hypertension, and lung involvement. In clinical trials, it was demonstrated that this method can be used to diagnose SARS-CoV-2 in a variety of places, such as medical centers, hospitals, airports, universities, and schools., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)

Fabrication and development of nanoscale materials with tunable structural and functional properties require a dynamic arrangement of nanoparticles on architectural templates. The function of nanoparticles not only depends on the property of the nanoparticles but also on their spatial orientations. Proteins with self-assembling properties which can be genetically engineered to varying architectural designs for scaffolds can be used to develop different orientations of nanoparticles in three dimensions. Here, we report the use of naturally self-assembling bacterial micro-compartment shell protein (PduA) assemblies in 2D and its single-point mutant variant (PduA[K26A]) in 3D architectures for the reduction and fabrication of gold nanoparticles. Interestingly, the different spatial organization of gold nanoparticles resulted in a smaller size in the 3D architect scaffold. Here, we observed a two-fold increase in catalytic activity and six-fold higher affinity toward TMB (3,3',5,5'-tetramethylbenzidine) substrate as a measure of higher peroxidase activity (nanozymatic) in the case of PduA[K26A] 3D scaffold. This approach demonstrates that the hierarchical organization of scaffold enables the fine-tuning of nanoparticle properties, thus paving the way toward the design of new nanoscale materials., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)

Microbial synthesis of gold nanoparticles (AuNPs), which are used in various forms with different properties in medicine, as a renewable bioresource has become increasingly important in recent years. In this study, statistical optimization of stable and monodispersed AuNPs synthesis was performed using a cell-free fermentation broth of Streptomyces sp. M137-2 and AuNPs were characterized, and their cytotoxicity was determined. The three factors determined as pH, gold salt (HAuCl 4 ) concentration, and incubation time, which are effective in the extracellular synthesis of biogenic AuNPs, were optimized by Central Composite Design (CCD) and then UV-Vis Spectroscopy, Dynamic Light Scattering (DLS), X-Ray Diffraction (XRD), Scanning Electron Microscope (SEM), Scanning Transmission Electron Microscope (STEM), size distribution, Fourier-Transform Infrared (FT-IR) Spectroscopy, X-Ray Photoelectron Spectrophotometer (XPS) and stability analyzes of AuNPs were carried out. Optimum values of the factors were determined as pH 8, 10 - 3  M HAuCl 4 , and 72 h incubation using Response Surface Methodology (RSM). Almost spherical AuNPs with 20-25 nm protein corona on the surface, 40-50 nm in size, monodisperse, and highly stable form were synthesized. Biogenic AuNPs were confirmed from characteristic diffraction peaks in the XRD pattern, UV-vis peak centred at 541 nm. The FT-IR results confirmed the role of Streptomyces sp. M137-2 metabolites in the reduction and stabilization of AuNPs. The cytotoxicity results also showed that AuNPs obtained using Streptomyces sp. can be used safely in medicine. This is the first report to perform statistical optimization of size-dependent biogenic AuNPs synthesis using a microorganism., (© 2023. The Author(s), under exclusive licence to Springer Nature B.V.)

In the present research work, a highly recyclable catalyst of Ag-based agarose (HRC-Ag/Agar) hydrogel was successfully fabricated through a simple and efficient in situ reduction method without the aid of additional surface active agent. The interaction between the rich hydroxyl functional (-OH) groups in agarose and Ag can effectively control the growth and dispersion of Ag nanoparticles (NPs) in the HRC-Ag/Agar hydrogel and keep Ag NPs free from chemical contamination, which also guarantees the reusability of HRC-Ag/Agar hydrogel as catalysts. HRC-Ag/Agar hydrogel without freeze drying and calcination was investigated for their potential applications as highly active/recyclable catalysts in reducing aromatic organic pollutants (p-nitrophenol (4-NP), methylene blue (MB) and rhodamine B (RhB)) by KBH 4 . The optimal HRC-Ag/Agar-1.9 hydrogel can complete the catalytic reduction of 4-NP within 11 min. Moreover, HRC-Ag/Agar-1.9 hydrogel achieves the high conversion rate (> 99%) through ten catalytic runs. Similarly, HRC-Ag/Agar-1.9 hydrogel was able to achieve a reduction efficiency of RhB at 98% within 17 min and that of MB at 95% within 40 min. The advantages of simple synthetic procedure, no secondary pollution, strong stability and easily separated make the HRC-Ag/Agar hydrogel have great potential prospect for environmental applications., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Fe 3 O 4 /Au/porous Au nanohybrids being bi-functional nanoparticles with magnetic properties and high porosity, were synthesized and used for drug delivery. To achieve this purpose, after Fe 3 O 4 nanoparticles synthesis, a gold layer coats them to increase their stability. Then, to improve the loading capacity of Fe 3 O 4 /Au nanoparticles, a shell of porous gold was synthesized on the Fe 3 O 4 /Au surface by creating an Ag-Au nanohybrid layer on Fe 3 O 4 /Au and dissolving the metallic silver atoms in HNO 3 (0.01 M). The DLS results show that the synthesized nanohybrid has an average size of 68.0 ± 7.7 nm and a zeta potential of - 28.1 ± 0.2 mV. Finally, doxorubicin (DOX), as a pharmaceutical agent, was loaded onto the Fe 3 O 4 /Au/porous Au nanohybrids. The prepared nano-drug enhanced the therapeutic efficacy of DOX on MCF-7 cancer cells compared to the free DOX. These results confirmed a 1.5 times improvement in the antitumor activity of DOX-loaded Fe 3 O 4 /Au/porous Au nanohybrids., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)

Recently, nanozymes based on polymer-stabilized gold nanoparticles (AuNPs) have attracted more and more attention on account of their polymer-ligands' multiple functionalization sites. However, the contribution of polymer hydrogen bonding to the catalytic activity of AuNPs has received little attention. This study designed and fabricated poly(N-2-hydroxypropylmethacrylamide)-capped AuNPs (PHPAM@AuNPs) using a hydroxyl-rich polymer as the ligand. The PHPAM@AuNPs exhibited good peroxidase-mimicking activity capable of efficiently oxidizing 3,3'5,5'-tetramethylbenzidine (TMB) with H 2 O 2 . The effect of PHPAM hydrogen bonding on the catalytic activity of PHPAM@AuNPs was investigated. Under peroxidase-mimicking catalysis, homocysteine introduced a notable reduction in oxidation, allowing the creation of a colorimetric method for homocysteine detection with high selectivity and sensitivity. The ultraviolet-visible absorption intensity of oxidized TMB showed a strong linear relationship with homocysteine concentration in the range of 3.0-20.0 μM (R 2  = 0.998), with a limit of detection of 0.4 μM. The proposed colorimetric protocol was used to monitor homocysteine in rat serum following intraperitoneal injection. This work provides a new way to refine AuNP-based nanozymes by relying on polymer-ligand hydrogen bonding. It has strong application potential in the analysis of endogenous molecules in real samples., (© 2022. Springer-Verlag GmbH Germany, part of Springer Nature.)

Sensitive determination of ofloxacin (OFL) is very essential for human health and environmental protection. Here, a novel composite of gold nanoparticles(nAu)@MXene(Ti 3 C 2 T x )/poly-p-aminobenzene sulfonic acid (PABSA) was fabricated on the surface of glassy carbon electrode (GCE) and used to sensitively determine OFL. The results of experiments showed that the obtained nAu@Ti 3 C 2 T x /PABSA/GCE electrode could be used as an electrochemical sensor to directly detect ofloxacin (OFL) by differential pulse voltammetry (DPV). Under the optimal conditions, the proposed electrode displayed a broader linear range and a lower detection limit (LOD) for OFL determination when it was compared to those similar sensors. The linear range was from 5.0 × 10 -8 to 5.0 × 10 -4  mol/L and the LOD was 3.7 × 10 -8  mol/L (S/N = 3). The nAu@Ti 3 C 2 T x /PABSA/GCE electrode also showed good selectivity, repeatability, and reproducibility. Finally, the proposed electrode was used to detect OFL in commercial samples by the standard addition method. The obtained recovery was from 97.3% and 105.7% showing its potential applications in actual sample analysis., (© 2022. Springer-Verlag GmbH Germany, part of Springer Nature.)

Advances in nanotechnology and medical science have spurred the development of engineered nanomaterials and nanoparticles with particular focus on their applications in biomedicine. In particular, gold nanoparticles (AuNPs) have been the focus of great interest, due to their exquisite intrinsic properties, such as ease of synthesis and surface functionalization, tunable size and shape, lack of acute toxicity and favorable optical, electronic, and physicochemical features, which possess great value for application in biodetection and diagnostics purposes, including molecular sensing, photoimaging, and application under the form of portable and simple biosensors (e.g., lateral flow immunoassays that have been extensively exploited during the current COVID-19 pandemic). We shall discuss the main properties of AuNPs, their synthesis and conjugation to biorecognition moieties, and the current trends in sensing and detection in biomedicine and diagnostics. This article is categorized under: Diagnostic Tools > Biosensing Diagnostic Tools > In Vitro Nanoparticle-Based Sensing Diagnostic Tools > In Vivo Nanodiagnostics and Imaging., (© 2022 Wiley Periodicals LLC.)

Nanotechnology is an emerging and expanding technology worldwide. The manipulation of materials on a nanometric scale generates new products with unique properties called nanomaterials. Due to its significant expansion, nanotechnology has been applied in several fields of study, including developing materials for biomedical applications, i.e., nanomedicine. The use of nanomaterials, including nanoparticles, in nanomedicine, is promising and has been associated with pharmacokinetics, bioavailability, and therapeutic advantages. In this regard, it is worth mentioning the Gold Nanoparticles (AuNPs). AuNPs' biomedical application is extensively investigated due to their high biocompatibility, simple preparation, catalytic, and redox properties. Experimental studies have pointed out critical therapeutic actions related to AuNPs in different pathophysiological contexts, mainly due to their anti-inflammatory and antioxidant effects. Thus, in this review, we will discuss the main experimental findings related to the therapeutic properties of AuNPs in metabolic, neurodegenerative diseases, and ultimately brain dysfunctions related to metabolic diseases., (© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

Background: Triple-negative breast cancer (TNBC) is the most aggressive type of breast cancer with enhanced metastasis and poor survival. Though chemotherapy, radiotherapy, photothermal therapy (PTT), photodynamic therapy (PDT), and gene delivery are used to treat TNBC, various side effects limit these therapeutics against TNBC. In this review article, we have focused on the mechanism of action of gold nanoparticles (AuNPs) to enhance the efficacy of therapeutics with targeted delivery on TNBC cells., Methods: Research data were accumulated from PubMed, Scopus, Web of Science, and Google Scholar using searching criteria "gold nanoparticles and triple-negative breast cancer" and "gold nanoparticles and cancer". Though we reviewed many old papers, the most cited papers were from the last ten years., Results: Various studies indicate that AuNPs can enhance bioavailability, site-specific drug delivery, and efficacy of chemotherapy, radiotherapy, PTT, and PDT as well as modulate gene expression. The role of AuNPs in the modulation of TNBC therapeutics through the inhibition of cell proliferation, progression, and metastasis has been proved in vitro and in vivo studies. As these mechanistic actions of AuNPs are most desirable to develop drugs with enhanced therapeutic efficacy against TNBC, it might be a promising approach to apply AuNPs for TNBC therapeutics., Conclusion: This article reviewed the mechanism of action of AuNPs and their application in the enhancement of therapeutics against TNBC. Much more attention is required for studying the role of AuNPs in developing them either as a single or synergistic anticancer agent against TNBC., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

Due to being low cost and eco-friendly, biological nanomaterial synthesis and development have made broad spectral progress. This study aimed to optimize the phytomediated synthesis of catalytically active, antibacterial palladium nanoparticles (PdNPs) for adsorption-based removal of ethidium bromide (EtBr) from an aqueous solution. Optimization of synthesis demonstrated that a precursor to extract ratio of 4:1, pH 3, and incubation at 80 °C for 60 min were the optimum conditions that led to the synthesis of negatively charged, highly stable, polycrystalline, spherical, and monodispersed PdNPs of 5-10 nm. When tested as catalysts, PdNPs successfully catalyzed Suzuki-Miyaura cross-coupling between aryl halides and arylboronic acids resulting in the synthesis of 4-acetylbiphenyl. Furthermore, the antibacterial activity test demonstrated that biogenic PdNPs were most effective and potent against Staphylococcus aureus and Proteus vulgaris followed by Escherichia coli, Bacillus subtilis, and Bacillus cereus. In addition, PdNPs were found as an excellent adsorbent for adsorption of EtBr from water as the adsorption reaction obeyed pseudo-second-order kinetics with a linear regression coefficient (R 2  > 0.995). The adsorption reaction fitted well with the Freundlich and Temkin isotherm models, indicating multi-layer adsorption. Estimating thermodynamic parameters resulted in a positive value of ΔH 0 and ΔG 0 , demonstrating adsorption was non-spontaneous and endothermic., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Metal nanoparticles (NPs) exhibit several unique physicochemical properties, including redox activity, surface plasmon resonance, ability to quench fluorescence, biocompatibility, or a high surface-to-volume ratio. They are being increasingly used in analysis and preconcentration of thiol containing compounds, because they are able to spontaneously form a stable Au/Ag/Cu-S dative bond. They thus find wide application in environmental and particularly in medical science, especially in the analysis of biological thiols, the endogenous compounds that play a significant role in many biological systems. In this review article, we provide an overview of various types of NPs that have been applied in analysis and preconcentration of biological thiols, mainly in human biological fluids. We first discuss shortly the types of NPs and their synthesis, properties, and their ability to interact with thiol compounds. Then we outline the sample preconcentration and analysis methods that were used for this purpose with special emphasis on optical, electrochemical, and separation techniques., (© 2022 Wiley-VCH GmbH.)

The presence of humic acid compounds in water resources, as one of the precursors of Trihalomethanes and Holoacetic acids, causes health problems for many communities. The aim of this research study was to investigate the photocatalytic degradation efficiency of humic acid using MnFe 2 O 4 @TiO 2 nanoparticles which produced by green synthesis method. The synthesis of metal nanoparticles using plant extracts and the study of their catalytic performance is a relatively new topic. Many chemical techniques have been proposed for the synthesis of MnFe 2 O 4 @TiO 2 nanoparticles, but green synthesis has received much attention due to its availability, simplicity, and non-toxicity. The properties of synthesized nanoparticles were determined by SEM, FT-IR, XRD, EDS, and DLS analysis. The results of the study showed that under optimal experimental conditions (pH = 3, nanocomposite dose = 0.03 g/L, humic acid initial concentration = 2 mg/L, and contact time = 20 min), it is possible to achieve maximum degradation of humic acid. Therefore; MnFe 2 O 4 @TiO 2 nanoparticles have high efficiency for removing of humic acid from aqueous solutions under UV light., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Wild-type microorganisms have become tolerant to higher antibiotic and antimicrobial agent concentrations due to the global increase in antibiotic consumption. Green-synthesized nanoparticles (NPs) have been proposed as potential antimicrobial agents to overcome the problem. This research prepared cadmium nanoparticles (Cd NPs) using Artemisia persica extract. To clarify the biological behavior of Cd NPs and Cd (NO 3 ) 2 , cytotoxicity, antibacterial, anti-biofilm, and biocompatible experiments were performed. Since Cd toxicity is associated with liver, kidney damage, and other deficits, HepG2 and HUVEC cell lines were employed as the in vitro cytotoxicity models. Cd NPs had a lower cytotoxic effect than Cd (NO 3 ) 2 against both HepG2 and HUVEC cells. The Cd NPs exhibited no hemolysis activity. The antibacterial and anti-biofilm studies were conducted using gram-positive Staphylococcus aureus and gram-negative Proteus mirabilis and Pseudomonas aeruginosa with the ability to form severe adherent biofilms. The antibacterial activity of Cd NPs against clinically isolated S. aureus, P. mirabilis, and P. aeruginosa was above 2560 µg mL - 1 . The Cd NPs (640 µg mL - 1 ) decreased the biofilm formation of S. aureus, P. mirabilis, and P. aeruginosa by 24.6%, 31.6%, and 26.4%, respectively.Moreover, adding Cd NPs (100 µg/disc) to antibiotic discs increased the antibacterial activity of vancomycin, gentamicin, tetracycline, streptomycin, meropenem, and kanamycin against Methicillin-resistant S. aureus, significantly. Due to the emergence of resistant microorganisms, Cd NPs can be used as an exciting material to counterattack global health problems. Further research is needed to clarify the molecular mechanisms underlying Cd NPs' pharmacological and toxicological effects., (© 2022. The Author(s), under exclusive licence to Springer Nature B.V.)

Long-term and continuous monitoring of the microRNA (miRNA) expression in living cells is essential in biomedical research, but it is currently limited by fast consumption and easy digestion of probes in the intracellular environment. Herein, we report polydopamine-modified gold nanoparticles (AuNPs@PDA) as protective and efficient nanocarriers for DNA hairpin probes (hpDNA), achieving long-term monitoring (48 h) of the miRNA (let-7a) levels in living cells after drug treatments. This method enabled excellent sensitivity and high selectivity toward let-7a with a limit of detection of 0.51 nM (n = 3) and a linear range from 1 to 100 nM. More importantly, AuNPs@PDA can not only efficiently improve the loading of hpDNA on each nanoparticle, but also effectively protect hpDNA from hydrolysis in the cell microenvironment, finally realizing the continuous monitoring of let-7a in living cells for 48 h. This simple method would be of great significance for drug screening and precision medicine., (© 2022. Springer-Verlag GmbH Germany, part of Springer Nature.)

Nanoparticles plays a key role in the development of novel antibacterial substances against various pathogenic microorganisms. These nanoparticles due to their smaller size could be very effective as they can improve the antibacterial activity through lysis of bacterial cell wall. In the present research work, ZnO, MgO, NiO, AlO nanoparticles, and MgNiO, and AlZnO composite oxides were synthesized by green method from Ocimum basilicum leaves extract. The nanoparticles formed were evaluated using FTIR, XRD, EDX, and SEM to confirm the formation of NPs and to determine the morphology, elemental composition, shape and size, composition, and nature of bonds present in the NPs. Further, the NPs were tested for their antibacterial activity. In particular, ZnO NPs showed a good inhibitory effect against Pseudomonas aeruginosa with 20 mm zone of inhibition. Hence, the process reported herein could be optimized for large-scale preparation of NPs. RESEARCH HIGHLIGHTS: Green synthesis of ZnO, MgO, NiO, AlO nanoparticles, and MgNiO, and AlZnO composite oxides using Ocimum basilicum leaves extract NPs were characterized by various established characterization techniques like FTIR, XRD, EDX, and SEM. NPs showed antibacterial activity which was investigated by agar well diffusion method against Bacillus cereus, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Staphylococcus aureus. The method proved to be very simple, cost-efficient, and convenient., (© 2022 Wiley Periodicals LLC.)

In this research, a novel synthesis of CaO nanoparticles via a green, environmentally, and economical method is developed. Crataegus pontica C.Koch leaves extract was used as a green reducing and stabilizing agent to synthesize the calcium oxide nanoplates ranging from 40 to 65 nm. The synthesized CaO NPs are characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), transmission electron microscopy (TEM), and Fourier transform infrared (FT-IR) spectroscopy. The CaO NPs were evaluated successfully for photocatalytic degradation of methylene blue (MB) dye with 98.99% degradation efficiency under sunlight by a simple technique. The recoverability and reusability of the CaO photocatalyst were considered under the optimized reaction conditions, which are showed high chemical stability after at least five runs., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In this experimental study, we aimed to evaluate the antibacterial and anti-biofilm effects of photodynamic therapy with a photosensitizer in conjunction with Gold nanoparticles against Streptococcus mutans as an important cariogenic bacterial agent. This experimental in vitro study evaluated the antibacterial and anti-biofilm effect of five groups as followed against S. mutans: methylene blue (MB), Gold nanoparticles (AuNPs), methylene blue conjugated with Gold nanoparticles (MB-AuNPs), MB mediated photodynamic therapy (MB mediated PDT) and methylene blue conjugated with Gold nanoparticles mediated photodynamic therapy (MB-AuNPs mediated PDT). InGaAlP laser (Azor-2 K) with 25 mW total output, 660 nm wavelength and laser probe cross-section of 0.78 cm 2 was used for methylene blue activation. Total dose of 19.23 J/cm 2 for 10 min was irradiated to each group. Minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and colony forming unit (CFU) were determined. Bacterial biofilm formation inhibition was assessed by crystal violet staining (The microtiter plate biofilm assay). The viability of S. mutans cells was assessed by MTT assay. MB mediated PDT and MB-AuNP mediated PDT were the most effective method for S. mutans biofilm inhibition (P < 0.05). MB alone, MB-AuNP alone and MB mediated PDT and MB-AuNP mediated PDT had the same effect against the planktonic phase of S. mutans (P > 0.05). Also they had similar pattern for bacterial growth inhibition and bactericidal effect (P > 0.05). Gold nano particle mediated photodynamic therapy represented antibacterial and antibiofilm activity against S. mutans; but this modality was not more effective than routine PDT., (© 2021. The Author(s), under exclusive licence to Springer-Verlag London Ltd., part of Springer Nature.)

Gold nanoparticles (GNPs) are well-documented for their size and surface chemistry-dependent electronic and optical properties that are extensively utilized to develop highly sensitive immunoassays. GNP-based immuno-polymerase chain reaction (immuno-PCR) is especially interesting due to the facile loading of biomolecules on the surface of GNP probes and has been utilized to develop analyte-specific assays. In this study, the role of size and surface chemistry of GNPs is explored in detail to develop a highly sensitive and reproducible immuno-PCR assay for specific detection of biotinylated analytes. Our results indicate that smaller-sized gold nanoparticles outperform the larger ones in terms of their sensitivity in immuno-PCR assay and show superior loading of proteins and oligonucleotides on the surface of nanoparticles. Furthermore, the role of different macromolecular stabilizers (such as polyethylene glycol (PEG), bovine serum albumin (BSA), and PEGylated BSA) was compared to optimize the loading of biomolecules and to improve the signal-to-noise ratio of GNP probes. mPEG-BSA-functionalized GNP probes of 15 nm were found to be highly sensitive at low concentrations of analytes and significantly (~ 30 fold) improve the limit of detection of analytes in comparison with ELISA assay., (© 2022. Springer-Verlag GmbH Germany, part of Springer Nature.)

In this paper, novel synergetic PtNP@Co 3 O 4 hollow nanopolyhedrals with peroxidase-like activities are designed and prepared, which can be used as electrochemical and colorimetric signal labels for the enzyme-free dual-channel homogeneous sensing of prostate-specific antigen. When prostate-specific antigens are present, the aptamer-modified PtNP@Co 3 O 4 hollow nanopolyhedrals and magnetic beads form sandwich structures, which have excellent peroxidase-like activities, because of the synergetic effect of PtNP@Co 3 O 4 hollow nanopolyhedrals. The sandwich structures can be separated from the mixture by the magnetic effect of the magnetic beads and catalyze the redox reactions between H 2 O 2 and TMB, generating quantitative electrochemical and colorimetric responses in homogeneous solution simultaneously. Under the optimized conditions, the linear range of both electrochemical (0.01 to 10 ng/ml) and colorimetric (0.01-15 ng/ml) channels can satisfy the demand of prostate-specific antigen detection in clinic (4 ng/ml), and the electrochemical and colorimetric channels have a low detection limit of 0.0079 ng/ml and 0.01 ng/ml respectively without using natural enzymes. The strategy by using synergetic PtNP@Co 3 O 4 hollow nanopolyhedrals as signal probes provides a promising scheme for developing simple, rapid, reliable, and ultrasensitive dual-channel homogeneous biosensors, which has a great potential as a powerful tool in prostate cancer diagnosis., (© 2021. Springer-Verlag GmbH Germany, part of Springer Nature.)

Immunotherapy of tumors has become a research hotspot. Tumor-associated macrophages (TAMs) are the most abundant interstitial cells in a tumor's microenvironment. As the concentration of the prepared nanoparticles increased, so their cytotoxicity of intensified. Under photothermal conditions, mAb-CD163/Au inhibited tumor invasion by killing M2 macrophages in vitro. After exposure to near-infrared (NIR) laser, mAb-CD163/Au inhibited tumor growth in vivo. The gold nanoparticles were modified to target M2 macrophages. Under NIR laser irradiation, mAb-CD163/Au achieved antitumor effects by killing M2 macrophages in vitro and in vivo., (© 2021. The Author(s), under exclusive licence to Springer-Verlag London Ltd. part of Springer Nature.)

This study presents the development of a sustainable production process of environmentally benign silver nanoparticles (AgNPs) from aqueous root extract of Rhodiola imbricata (RI) and Withania somnifera (WS) for mitigating environmental pollution and investigating their potential applications in agriculture and biomedical industry. RIWS-AgNPs were characterized using several analytical techniques (UV-Vis, DLS, HR-TEM, SAED, EDX and FTIR). The antioxidant and anticancer activity of RIWS-AgNPs were estimated by DPPH and MTT assay, respectively. UV-Vis and DLS analysis indicated that equal ratio of RIWS-extract and silver nitrate (1:1) is optimum for green synthesis of well-dispersed AgNPs (λ max : 430 nm, polydispersity index: 0.179, zeta potential: - 17.9 ± 4.14). HR-TEM and SAED analysis confirmed the formation of spherical and crystalline RIWS-AgNPs (37-42 nm). FTIR analysis demonstrated that the phenolic compounds are probably involved in stabilization of RIWS-AgNPs. RIWS-AgNPs showed effective catalytic degradation of hazardous environmental pollutant (4-nitrophenol). RIWS-AgNPs treatment significantly increased the growth and photosynthetic pigments of Hordeum vulgare in a size- and dose-dependent manner (germination (77%), chlorophyll a (12.62 ± 0.07 μg/ml) and total carotenoids (7.05 ± 0.04 μg/ml)). The DPPH assay demonstrated that RIWS-AgNPs exert concentration-dependent potent antioxidant activity (IC 50 : 12.30 μg/ml, EC 50 : 0.104 mg/ml, ARP: 959.45). Moreover, RIWS-AgNPs also confer strong cytotoxic activity against HepG2 cancer cell line in dose-dependent manner (cell viability: 9.51 ± 1.55%). Overall, the present study for the first time demonstrated a green technology for the synthesis of stable RIWS-AgNPs and their potential applications in biomedical and agriculture industry as phytostimulatory, antioxidant and anticancer agent. Moreover, RIWS-AgNPs could potentially be used as a green alternative for environmental remediation., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

An Au-based nanozyme composite (AuNPs/Cu,I) was constructed by using Cu,I-doped carbon dots (Cu,I-CDs) as the reducing agent as well as the nanozyme. Notably, AuNPs/Cu,I nanozyme not only possessed the intrinsic activity of mimicking enzymes of superoxide dismutase, peroxidase, and catalase at different conditions but was also employed as surface-enhanced Raman spectroscopy (SERS) enhancer. The combination of Cu,I-CDs and AuNPs promoted the electron transferability, leading to increased peroxidase-like activity and superoxide-like activity. Compared to the individual Cu,I-CDs and AuNPs nanozyme, the AuNPs/Cu,I composite demonstrated promising peroxidase-like activity by transferring electrons instead of generating OH. Interestingly, the multienzyme-like activity of AuNPs/Cu,I nanozyme could be finely tuned by changing the composition of Cu 0 /Cu + and Au. The tert-butyl hydroquinone (TBHQ) as the substrate could be catalyzed with AuNPs/Cu,I nanozyme to produce red substances, resulting in a significant Raman enhancement effect at the same time, showing good linear range from 0.11 to 10 mg L -1 . Overall, the current investigation provides a flexible and controllable way to design multifunctional nanozymes along with the Raman enhancement strategy based on the catalysis of nanozyme., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)

This study presents a promising approach for the one-pot generation of the biotin-derived gold nanoparticles (GNPs@biotin). We report a direct method for the reduction of tetrachloroauric acid with biotin and generation of the labels due to nets formed via biotin-streptavidin interactions. The synthesized GNPs@biotin have a characteristic plasmon maximum, excellent colloidal stability, and streptavidin coupling efficiency. The size of the GNPs@biotin:streptavidin nets and the efficiency of interaction with specific antibodies can be easily customized by the component concentrations and time of their interaction. Moreover, the proposed labels require no additional reagents or manipulations for the synthesis, separation, or purification. The developed labels were applied for the detection of the model antigen of C-reactive protein (CRP) as a major inflammation biomarker. The assembling labels demonstrated a competitive advantage limit of CRP detection (LOD) of 1.2 ng/mL and a limit of quantification (LOQ) of 3.9 ng/mL in human plasma comparable to classical immunoassays. Moreover, the proposed approach is universal and can be potentially applied for the quantitative determination of other biomarkers in a variety of immunoassays in a combination with specific biotinylated antibodies., (© 2021. Springer-Verlag GmbH Germany, part of Springer Nature.)

Metal nanoparticles have been widely used for catalysis because of its excellent catalytic activity and selectivity. Green and sustainable supports play a quite important role in the enhancement of the efficiency and recyclability of metal nanoparticles. Here, a cellulose/β-cyclodextrin hydrogel is applied to support tannic acid-encapsulated metal (such as Ag, Au, Pd and Cu) nanoparticles to generate nanocomposite hydrogels for catalysis. TEM analysis indicates that these metal nanoparticles have the average diameters of 6.5 nm for Au nanoparticles, 7.0 nm for Ag nanoparticles, 5.0 nm for Pd nanoparticles and 4.0 nm for Cu nanoparticles, respectively. The catalytic activities of the as-prepared metal nanocomposite hydrogels are estimated in a series of chemical reactions in the aqueous system. The recyclability, applicability and generality of these nanocomposite hydrogels are also well investigated. The nanocomposite hydrogels can be reused for at least 10 times in the 4-nitrophenol reduction, 8 times for Suzuki–Miyaura coupling reaction and 6 times for click reaction, respectively. Furthermore, good yields are obtained in the catalytic process. This study gives a green and sustainable strategy to support metal nanoparticles with good catalytic activity and recyclability. [ABSTRACT FROM AUTHOR]

Nanoparticle synthesis under environmentally friendly conditions has been conducted utilizing natural resources in order to reduce the reliance on hazardous chemicals. For example, the utilization of microbial synthesis has enabled the production of nanoparticles that exhibit biocompatibility, stability, and safety. Microorganisms facilitate the growth of crystals while preventing aggregation. They serve as both reducing agents and capping agents by offering enzymes, peptides, poly(amino acids), polyhydroxyalkanoate, and polysaccharides. In this review, we present an overview of nanoparticle synthesis based on microorganisms including bacteria, fungi, algae, and actinobacteria, encompassing metals such as gold (Au), silver (Ag), platinum (Pt), palladium (Pd), copper (Cu), titanium dioxide ((TiO2), zinc oxide (ZnO), iron oxide (Fe2O3), and selenium (Se). The nanoparticles typically vary in size from 1 to 100 nm and exhibit various shapes including spherical, rod-shaped, triangular, cubic, and hexagonal shapes. Additionally, this review discusses the mechanisms behind the synthesis of metal nanoparticles by microorganisms, whether they occur intracellularly or extracellularly. [ABSTRACT FROM AUTHOR]

The versatility of aza- and oxa-heterocyclic compounds has garnered significant attention in recent times. A large number of currently approved pharmaceutical products include nitrogen- and oxygen-containing heterocycles. Recent nanotechnological developments have propelled an upsurge in the applications of nanocatalysis for heterocyclic synthesis. Metal nanoparticles (MNPs) have emerged as promising catalysts for the synthesis of aza- and oxa-heterocycles owing to their unique physicochemical properties. Various MNPs including gold, silver, nickel and palladium have been evaluated for their catalytic activities in different reaction types, including cyclisation, coupling, hydrogenation and oxidative transformations. The MNPs have exhibited remarkable catalytic efficiency when utilised under optimal conditions. These catalysts have showcased high reusability and recyclability, yielding satisfactory amounts of the desired heterocyclic compound. The present work provides a detailed overview of recent advances in the area of MNP-assisted synthetic construction of aza- and oxa-heterocycles, published during the previous calendar year, 2022. The review serves as a valuable resource and also paves the way for future investigations in the development of novel catalytic strategies for heterocycle synthesis. 1 Introduction 2 Nanocatalysis 3 Aza- and Oxa-Heterocycle Synthesis Catalysed by MNPs 3.1 AuNPs 3.2 CuNPs 3.3 CoNPs 3.4 FeNPs 3.5 NiNPs 3.6 PdNPs 3.7 PtNPs 3.8 SiNPs 3.9 ZnNPs 3.10 Bimetallic NPs 3.11 Other MNPs 4 Summary and Outlook [ABSTRACT FROM AUTHOR]

Gold nanoparticles (AuNPs) have been synthesized directly inside liposomes using honey as a reducing agent. The obtained aggregates, named Cassyopea® Gold due to the method used for their preparation, show remarkable properties as reactors and carriers of the investigated AuNPs. A mean size of about 150 nm and negative surface charge of -46 mV were measured for Cassyopea® Gold through dynamic light scattering and zeta potential measurements, respectively. The formation of the investigated gold nanoparticles into Cassyopea® liposomes was spectroscopically confirmed by the presence of their typical absorption band at 516 nm. The catalytic activity of the combined liposome–AuNP nanocomposites was tested via the thermal cis–trans isomerization of resonance-activated 4-methoxyazobenzene (MeO-AB). The kinetic rate constants (kobs) determined at 25 °C in the AuNP aqueous solution and in the Cassyopea® Gold samples were one thousand times higher than the values obtained when performing MeO-AB cis–trans conversion in the presence of pure Cassyopea®. The results reported herein are unprecedented and point to the high versatility of Cassyopea® as a reactor and carrier of metal nanoparticles in chemical, biological, and technological applications. [ABSTRACT FROM AUTHOR]

The process of noble metal nanoparticle synthesis is complex and consists of at least two steps: slow nucleation and fast autocatalytic growth. The kinetics of these two processes depends on the reductant "power" and the addition of stabilizers, as well as other factors (e.g., temperature, pH, ionic strength). Knowing these parameters, it is possible to synthesize materials with appropriate physicochemical properties, which can be simply adjusted by the type of the used metal, particle morphology and surface property. This, in turn, affects the possibility of their applications in various areas of life, including medicine, catalysis, engineering, fuel cells, etc. However, in some cases, the standard route, i.e., the chemical reduction of a metal precursor carried out in the batch reactor, is not sufficient due to problems with temperature control, properties of reagents, unstable or dangerous intermediates and products, etc. Therefore, in this review, we focused on an alternative approach to their chemical synthesis provided by microreactor systems. The use of microreactors for the synthesis of noble metal nanomaterials (e.g., Ag, Au, Pt, Pd), obtained by chemical reduction, is analyzed, taking into account investigations carried out in recent years. A particular emphasis is placed on the processes in which the use of microreactors removed the limitations associated with synthesis in a batch reactor. Moreover, the opportunities and challenges related to the synthesis of noble nanomaterials in the microreactor system are underlined. This review discusses the advantages as well as the problems of nanoparticle synthesis in microreactors. [ABSTRACT FROM AUTHOR]

This study investigates the significant impact of metal–support interactions on catalytic reaction mechanisms at the interface of oxide-supported metal nanoparticles. The distinct and contrasting effects of SiO2 and TiO2 supports on reaction dynamics using NaBD4 were studied and focused on the relative yields of [HD]/[H2] and [D2]/[H2]. The findings show a consistent increase in HD yields with rising [BD4−] concentrations. Notably, the sequence of HD yield enhancement follows the order of TiO2-Au0-NPs < Au0-NPs < SiO2-Au0-NPs. Conversely, the rate of H2 evolution during BH4- hydrolysis exhibits an inverse trend, with TiO2-Au0-NPs outperforming the others, followed by Au0-NPs and SiO2-Au0-NPs, demonstrating the opposing effects exerted by the TiO2 and SiO2 supports on the catalytic processes. Further, the catalytic reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) confirms the catalytic mechanism, with TiO2-Au0-NPs demonstrating superior activity. The catalytic activity observed aligns with the order of TiO2-Au0-NPs > Au0-NPs > SiO2-Au0-NPs, suggesting that SiO2 donates electrons to Au0-NPs, while TiO2 withdraws them. It is of interest to note that two very different processes, that clearly proceed via different mechanisms, are affected similarly by the supports. This study reveals that the choice of support material influences catalytic activity, impacting overall yield and efficiency. These findings underscore the importance of selecting appropriate support materials for tailored catalytic outcomes. [ABSTRACT FROM AUTHOR]

This review presents a brief discussion on the numerous synthetic techniques used to prepare metal nanoparticles supported on various two-dimensional (2D) materials. Special emphasis has been given to graphene and other 2D analogues such as g-C3N4, h-BN, MoS2, WS2 etc. supported metal nanoparticles. In addition to these, this review outlines the applications of the developed metal nanoparticles–2D composite materials for catalytic coupling reactions, which have recently emerged as a promising strategy in carbon–heteroatom or carbon–carbon bond formation. The effect of size and morphology of metal nanoparticles–2D composite materials on their catalytic performance toward different coupling reactions such as Suzuki, Heck, Sonogashira, etc. have been discussed in detail. [ABSTRACT FROM AUTHOR]

The reaction of glycerol with CO2 to produce glycerol carbonate was performed successfully in the presence of gold nanoparticles (AuNPs) supported by a metal–organic framework (MOF) constructed from mixed carboxylate (terephthalic acid and 1,3,5-benzenetricarboxylic acid). The most efficient were two AuNPs@MOF catalysts prepared from pre-synthesized MOF impregnated with Au3+ salt and subsequently reduced to AuNPs using H2 (catalyst 4%Au(H2)@MOF1) or reduced with NaBH4 (catalyst 4%Au@PEI-MOF1). Compared to existing catalysts, AuNPs@MOFs require simple preparation and operate under mild and sustainable conditions, i.e., a much lower temperature and the lowest CO2 overpressure ever reported, with MgCO3 having been found to be the optimal dehydrating agent. Although the yield of the process is still not competitive with previously developed systems, the most promising advantage is the highest TOF (78 h−1) ever reported for this reaction. The optimal parameters observed for AuNPs were also tested on AgNPs and CuNPs with promising results, suggesting their great potential for industrial application. The catalysts were characterized by XRD, TEM, SEM-EDS, ICP-MS, XPS, and porosity measurements, confirming that AuNPs are present in low concentration, uniformly distributed, and confined to the cavities of the MOF. [ABSTRACT FROM AUTHOR]

The branched structures of dendronized polymers can provide good steric stabilization for metal nanoparticle catalysts. In this work, an amphiphilic dendronized copolymer containing hydrophilic branched triethylene glycol moieties and hydrophobic branched ferrocenyl moieties is designed and prepared by one-pot ring-opening metathesis polymerization, and is used as the stabilizer for metal (Au, Ag and Pd) nanoparticles. These metal nanoparticles (Au nanoparticles: 3.5 ± 3.0 nm; Ag nanoparticles: 7.2 ± 4.0 nm; Pd nanoparticles: 2.5 ± 1.0 nm) are found to be highly active in both the 4-nitrophenol reduction and Suzuki–Miyaura reactions. In the 4-nitrophenol reduction, Pd nanoparticles have the highest catalytic ability (TOF: 2060 h−1). In addition, Pd nanoparticles are also an efficient catalyst for Suzuki–Miyaura reactions (TOF: 1980 h−1) and possess good applicability for diverse substrates. The amphiphilic dendronized copolymer will open a new door for the development of efficient metal nanoparticle catalysts. [ABSTRACT FROM AUTHOR]

Fine-tuned interaction between reacting molecules and metal surface is of great importance in heterogeneous catalysis for the design of highly selective processes. Conventional strategies based on adjusting the intrinsic catalyst properties such as particle size, metal-support interaction and morphology suffer from complicated and time-consuming synthetic procedures. Recently, the modification of metal nanoparticles with non-metallic promoters has been demonstrated as an effective tool to regulate the interfacial environment of metallic catalysis. Herein, we will give an overview of recent progress in this area. A general analysis will be proposed about the electronic, steric effects and new functionalities imposed by non-metallic promoters of metal catalysts. The potential for the selectivity enhancement of the promoted metal catalysts in various industrially important reactions is discussed. [ABSTRACT FROM AUTHOR]

Owing to their remarkable properties, gold nanoparticles are applied in diverse fields, including catalysis, electronics, energy conversion and sensors. However, for catalytic applications of colloidal gold nanoparticles, the trade-off between their reactivity and stability is a significant concern. Here we report a universal approach for preparing stable and reactive colloidal small (~3 nm) gold nanoparticles by using multi-dentate polyoxometalates as protecting agents in non-polar solvents. These nanoparticles exhibit exceptional stability even under conditions of high concentration, long-term storage, heating and addition of bases. Moreover, they display excellent catalytic performance in various oxidation reactions of organic substrates using molecular oxygen as the sole oxidant. Our findings highlight the ability of inorganic multi-dentate ligands with structural stability and robust steric and electronic effects to confer stability and reactivity upon gold nanoparticles. This approach can be extended to prepare metal nanoparticles other than gold, enabling the design of novel nanomaterials with promising applications. For catalytic nanoparticles there is often a trade-off between stability and activity. Here the authors report a route to ultra-stable and catalytically active colloidal small (~3 nm) gold nanoparticles using multi-dentate polyoxometalates as protecting agents in nonpolar solvents. [ABSTRACT FROM AUTHOR]

Antimicrobial resistance (AMR) has become an alarming threat to the successful treatment of rapidly growing bacterial infections due to the abuse and misuse of antibiotics. Traditional antibiotics bear many limitations, including restricted bioavailability, inadequate penetration and the emergence of antimicrobial-resistant microorganisms. Recent advances in nanotechnology for the introduction of nanoparticles with fascinating physicochemical characteristics have been predicted as an innovative means of defence against antimicrobial-resistant diseases. The use of nanoparticles provides several benefits, including improved tissue targeting, better solubility, improved stability, enhanced epithelial permeability and causes minimal side effects. However, except for gold nanoparticles (AuNPs), the biological safety of the majority of metal nanoparticles remains a serious problem. AuNPs appear to be promising for drug delivery and medicinal applications because of their minimal toxicity, biocompatibility, functional flexibility, chemical stability and versatile biological activities, such as their antiviral, antifungal, anti-inflammatory and antimicrobial properties. Hence, we are focusing on the gold nanoparticles possessing antimicrobial activity in this article. This review will cover recent strategies in the preparation of gold nanoparticles, with special emphasis placed on antibiotics-coated AuNPs with enhanced antimicrobial properties and how they fight against disease-causing bacteria and eradicate biofilms, along with their activities and physicochemical properties. [ABSTRACT FROM AUTHOR]

Developing green fibrous materials with uniformly distributed metal nanoparticles for highly efficient and recyclable catalysis remains a major challenge. Herein, we developed a simple, effective, and green method to immobilize gold nanoparticles (AuNPs) on polydopamine (PDA)-functionalized silk fibers (SFs) for efficient catalytic reduction of 4-nitrophenol (4-NP). The density and size of AuNPs on the PDA-coated SFs can be tuned by adjusting precursor concentration and synthesis duration, respectively. The AuNPs-PDA-SFs catalysts prepared under optimized conditions could catalyze the reduction of 4-NP, 4-nitroaniline (4-NA), and 4-amino-3-nitrophenol (4-A-3-NP) at the apparent rate constants of 0.087, 0.091, and 0.063 min−1, respectively. After six rounds of flow-through reduction of 4-NP, the AuNPs-PDA-SFs could maintain a 4-NP conversion rate greater than 92%, indicating their superior reusability and consistent catalytic activity. Due to the protein properties of SFs, the AuNPs-PDA-SFs can be degraded by enzymes and alkali solutions. This work may provide new insights for designing advanced fiber-supported recyclable catalysts with high catalytic performance and reusability in wastewater treatment. [ABSTRACT FROM AUTHOR]

The requirement of green, sustainable, and prudent chemical procedures is one of the bottlenecks in synthetic organic chemistry. Nanostructured materials have the promise to fill the gap between homogeneous and heterogeneous catalysis and can offer benefits without compromising the selectivity in forming the desired products. Advancement of sustainable and green chemical processes under environmental benign conditions is one of the immense interests in modern organic chemistry. Significantly, the hydrogenation of nitroarenes is one of the most important useful catalytic processes in the fine and bulk chemical industry. The most recent advancement of catalysts with supported metal nanoparticles has prompted their enormous accomplishments in the course of the most recent years, provoking their noteworthy applications as "standard" catalysts. Currently, this topic has gotten a lot of consideration. However, despite the fact that support materials have a great diversity in the catalysts for the reactions and modifications, a systematic rationalization of the field is lacking. In this review, we cover and categorize the recent progress in support materials tuning strategies to enhance catalytic performance for the hydrogenation of nitroarenes. Also, importance of support materials in the heterogeneous catalytic hydrogenation of nitroarenes is discussed. [ABSTRACT FROM AUTHOR]

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The work considers the preparation in an undivided cell of Pd–Cu and Pd–Au bimetallic nanoparticles (NPs) by methylviologen (MV2+)-mediated electrochemical reduction of equimolar amounts of Cu(II), Pd(II), and Au(I) in the presence of poly(N-vinylpyrrolidone) (PVP) and nanocellulose (NC) under controlled potential of the generating MV•+ cation radical in aqueous medium at room temperature. Electrosyntheses are performed by sequential or joint reduction of metal ions by passing a theoretical charge. When Pd(II) ions are added to CuNPs, as well as when Au(I) ions are added to PdNPs, a galvanic replacement process is observed, namely oxidation of Cu0 by Pd(II) and Pd0 Au(I) ions. The results of the complete reduction are nanocomposites of mainly spherical MNPs, dispersed in the solution bulk and stabilized by PVP on the surface of the NC. In the sequential synthesis of CuNPs and then PdNPs, the nanocomposite is represented as Cu2O nanoroses coated with fine PdNPs. Pd nanocomposites with Cu2O or Au are represented mainly by spherical particles with size of 4–50 nm depending on the production method. X-ray powder diffraction (XRPD) data of the nanocomposites confirm the formation of a mixture of PdNPs (0.8–10 nm) with large gold crystallites (up to 24 nm), as well as the oxidation of CuNPs to cuprite (Cu2O). The size of the metal crystallites and copper oxide varies in the range from 0.8 to 24 nm. In the test reaction of p‑nitrophenol reduction with sodium borohydride in aqueous medium, all of the tested nanocomposites show time-increasing catalytic activity. When Cu is added to Pd, the catalytic reduction reaction is maintained, while the addition of Au to Pd decreases the catalytic activity of PdNPs by an order of magnitude. [ABSTRACT FROM AUTHOR]

Metal nanoparticles (NPs) have garnered considerable attention, due to their unique physicochemical properties, that render them promising candidates for various applications in medicine and industry. This article offers a comprehensive overview of the most recent advancements in the manufacturing, characterization, and biomedical utilization of metal NPs, with a primary focus on silver and gold NPs. Their potential as effective anticancer, anti-inflammatory, and antimicrobial agents, drug delivery systems, and imaging agents in the diagnosis and treatment of a variety of disorders is reviewed. Moreover, their translation to therapeutic settings, and the issue of their inclusion in clinical trials, are assessed in light of over 30 clinical investigations that concentrate on administering either silver or gold NPs in conditions ranging from nosocomial infections to different types of cancers. This paper aims not only to examine the biocompatibility of nanomaterials but also to emphasize potential challenges that may limit their safe integration into healthcare practices. More than 100 nanomedicines are currently on the market, which justifies ongoing study into the use of nanomaterials in medicine. Overall, the present review aims to highlight the potential of silver and gold NPs as innovative and effective therapeutics in the field of biomedicine, citing some of their most relevant current applications. [ABSTRACT FROM AUTHOR]

Uniform-size, non-native oxide-passivated metallic aluminum nanoparticles (Al NPs) have desirable properties for fuel applications, battery components, plasmonics, and hydrogen catalysis. Nonthermal plasma-assisted synthesis of Al NPs was previously achieved with an inductively coupled plasma (ICP) reactor, but the low production rate and limited tunability of particle size were key barriers to the applications of this material. This work focuses on the application of capacitively coupled plasma (CCP) to achieve improved control over Al NP size and a ten-fold increase in yield. In contrast with many other materials, where NP size is controlled via the gas residence time in the reactor, the Al NP size appeared to depend on the power input to the CCP system. The results indicate that the CCP reactor assembly, with a hydrogen-rich argon/hydrogen plasma, was able to produce Al NPs with diameters that were tunable between 8 and 21 nm at a rate up ∼ 100 mg h−1. X-ray diffraction indicates that a hydrogen-rich environment results in crystalline metal Al particles. The improved synthesis control of the CCP system compared to the ICP system is interpreted in terms of the CCP's lower plasma density, as determined by double Langmuir probe measurements, leading to reduced NP heating in the CCP that is more amenable to NP nucleation and growth. [ABSTRACT FROM AUTHOR]

This document is an editorial from the journal Processes, titled "Advances in Supported Nanoparticle Catalysts." It highlights a collection of research papers that showcase the forefront of innovation in developing and utilizing supported nanoparticle catalysts. The research papers cover various topics such as the efficient removal of anionic dyes from water, the synthesis of metal nanoparticles for environmentally benign processes, the fabrication of superhydrophobic carbon nanomaterials, and the enhancement of polymer nanoparticles for immunoanalysis applications. The document emphasizes the importance of understanding supported nanoparticle systems for optimizing photocatalytic processes and tailoring catalysts for diverse catalytic reactions. [Extracted from the article]