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Solid–lipid nanoparticles and nanostructured lipid carriers are delivery systems for the delivery of drugs and other bioactives used in diagnosis, therapy, and treatment procedures. These nanocarriers may enhance the solubility and permeability of drugs, increase their bioavailability, and extend the residence time in the body, combining low toxicity with a targeted delivery. Nanostructured lipid carriers are the second generation of lipid nanoparticles differing from solid lipid nanoparticles in their composition matrix. The use of a liquid lipid together with a solid lipid in nanostructured lipid carrier allows it to load a higher amount of drug, enhance drug release properties, and increase its stability. Therefore, a direct comparison between solid lipid nanoparticles and nanostructured lipid carriers is needed. This review aims to describe solid lipid nanoparticles and nanostructured lipid carriers as drug delivery systems, comparing both, while systematically elucidating their production methodologies, physicochemical characterization, and in vitro and in vivo performance. In addition, the toxicity concerns of these systems are focused on.

The nanomaterial industry generates gigantic quantities of metal-based nanomaterials for various technological and biomedical applications; however, concomitantly, it places a massive burden on the environment by utilizing toxic chemicals for the production process and leaving hazardous waste materials behind. Moreover, the employed, often unpleasant chemicals can affect the biocompatibility of the generated particles and severely restrict their application possibilities. On these grounds, green synthetic approaches have emerged, offering eco-friendly, sustainable, nature-derived alternative production methods, thus attenuating the ecological footprint of the nanomaterial industry. In the last decade, a plethora of biological materials has been tested to probe their suitability for nanomaterial synthesis. Although most of these approaches were successful, a large body of evidence indicates that the green material or entity used for the production would substantially define the physical and chemical properties and as a consequence, the biological activities of the obtained nanomaterials. The present review provides a comprehensive collection of the most recent green methodologies, surveys the major nanoparticle characterization techniques and screens the effects triggered by the obtained nanomaterials in various living systems to give an impression on the biomedical potential of green synthesized silver and gold nanoparticles.

Magnesium oxide nanoparticles (MgO-NPs) were synthesized using the fungal strain Aspergillus terreus S1 to overcome the disadvantages of chemical and physical methods. The factors affecting the biosynthesis process were optimized as follows: concentration of Mg(NO3)2·6H2O precursor (3 mM), contact time (36 min), pH (8), and incubation temperature (35 °C). The characterization of biosynthesized MgO-NPs was accomplished using UV-vis spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy—energy dispersive X-ray (SEM-EDX), X-ray diffraction (XRD), and dynamic light scattering (DLS). Data confirmed the successful formation of crystallographic, spherical, well-dispersed MgO-NPs with a size range of 8.0–38.0 nm at a maximum surface plasmon resonance of 280 nm. The biological activities of biosynthesized MgO-NPs including antimicrobial activity, biotreatment of tanning effluent, and chromium ion removal were investigated. The highest growth inhibition of pathogenic Staphylococcus aureus, Bacillus subtilis, Pseudomonas aeruginosa, Escherichia coli, and Candida albicans was achieved at 200 μg mL–1 of MgO-NPs. The biosynthesized MgO-NPs exhibited high efficacy to decolorize the tanning effluent (96.8 ± 1.7% after 150 min at 1.0 µg mL–1) and greatly decrease chemical parameters including total suspended solids (TSS), total dissolved solids (TDS), biological oxygen demand (BOD), chemical oxygen demand (COD), and conductivity with percentages of 98.04, 98.3, 89.1, 97.2, and 97.7%, respectively. Further, the biosynthesized MgO-NPs showed a strong potential to remove chromium ions from the tanning effluent, from 835.3 mg L–1 to 21.0 mg L–1, with a removal percentage of 97.5%.

Industrial dye contamination in wastewater poses significant environmental challenges, necessitating the development of efficient photocatalysts for degradation. In this work, we investigate the In doping effect in the photocatalytic activity of zinc oxide (ZnO) nanoparticles for effective RhB degradation. Indium-doped ZnO nanoparticles were synthesized via sol–gel method and x-ray diffraction (XRD) analysis revealed a wurtzite hexagonal structure, with the crystallite size being varying from 65 nm to 53 nm with the introduction of In content. XPS measurements on the 3% In-doped ZnO sample revealed distinct core level spectra for In 3d, Zn 2p, and O 1s regions, confirming the presence of indium, zinc, and oxygen. Brunauer–Emmett–Teller (BET) analysis revealed increased surface area and pore size, with specific surface areas escalating from 0.9 m²/g for pure ZnO to 10.1 m²/g for 3% indium-doped ZnO. Photocatalytic experiments exhibited significant RhB degradation, with degradation efficiencies reaching 93% for 3% indium-doped ZnO under visible light irradiation due to the effect of the presence of In, which causing light absorption enhancement, narrow the band gap and improve charge carrier separation. These findings underscore the potential of indium-doped ZnO nanoparticles as efficient and sustainable photocatalysts for wastewater treatment, offering a promising avenue to address environmental challenges associated with industrial dye-contaminated effluents. Graphical Abstract Highlights Sol–gel synthesis of Indium-doped ZnO offers a scalable method for effective photocatalysts in wastewater treatment. Achieved 93% Rhodamine B degradation with Indium-doped ZnO nanoparticles under visible light. XRD analysis showed a reduction in crystallite size from 65 nm (pure ZnO) to 53 nm (3% In-doped ZnO). BET surface area increased from 0.9 m²/g (pure ZnO) to 10.1 m²/g (3% In-doped ZnO). UV-Vis spectroscopy indicated a reduced band gap in Indium doped ZnO (3.19 eV). TGA analysis highlighted improved thermal stability in Indium doped ZnO nanoparticles.

The detection and characterization of soluble metal nanoparticles in plant tissues are an analytical challenge, though a scientific necessity for regulating nano-enabled agrichemicals. The efficacy of two extraction methods to prepare plant samples for analysis by single particle ICP-MS, an analytical method enabling both size determination and quantification of nanoparticles (NP), was assessed. A standard enzyme-based extraction was compared to a newly developed methanol-based approach. Au, CuO, and ZnO NPs were extracted from three different plant leaf materials (lettuce, corn, and kale) selected for their agricultural relevance and differing characteristics. The enzyme-based approach was found to be unsuitable because of changes in the recovered NP size distribution of CuO NP. The MeOH-based extraction allowed reproducible extraction of the particle size distribution (PSD) without major alteration caused by the extraction. The type of leaf tissue did not significantly affect the recovered PSD. Total metal losses during the extraction process were largely due to the filtration step prior to analysis by spICP-MS, though this did not significantly affect PSD recovery. The methanol extraction worked with the three different NPs and plants tested and is suitable for studying the fate of labile metal-based nano-enabled agrichemicals.

Manufacturers of nanoparticle-based products rely on detailed information about critical process parameters, such as particle size and size distributions, concentration, and material composition, which directly reflect the quality of the final product. These process parameters are often obtained using offline characterization techniques that cannot provide the temporal resolution to detect dynamic changes in particle ensembles during a production process. To overcome this deficiency, we have recently introduced Optofluidic Force Induction ( of2 i) for optical real-time counting with single particle sensitivity and high throughput. In this paper, we apply of2 i to highly polydisperse and multi modal particle systems, where we also monitor evolutionary processes over large time scales. For oil-in-water emulsions we detect in real time the transition between high-pressure homogenization states. For silicon carbide nanoparticles, we exploit the dynamic of2 i measurement capabilities to introduce a novel process feedback parameter based on the dissociation of particle agglomerates. Our results demonstrate that of2 i provides a versatile workbench for process feedback in a wide range of applications. Graphical abstract

The functionalization of textiles with nanomaterials through green synthesis offers a promising pathway for sustainable material innovation. This study explores the in situ green synthesis of silver nanoparticles (AgNPs) onto cotton fabrics using Solanum tuberosum (potato) peel extract as a natural reducing and stabilizing agent. The synthesis conditions were optimized by varying silver nitrate concentration, extract volume, temperature, pH, and reaction time, after which the optimized protocol was applied for fabric treatment. The presence and distribution of AgNPs were confirmed through UV-Visible spectroscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy and dynamic light scattering. The treated fabrics demonstrated strong and durable antibacterial performance, with inhibition zones of 23 ± 0.02 against Escherichia coli and 16 ± 0.01 against Staphylococcus aureus. Notably, antibacterial activity was retained even after 20 washing cycles, demonstrating the durability of the treatment. Mechanical testing revealed a 32.25% increase in tensile strength and a corresponding 10.47% reduction in elongation at break compared to untreated fabrics, suggesting improved durability with moderate stiffness. Air permeability decreased by 8.8%, correlating with the rougher surface morphology observed in Scanning Electron Microscopy images. Thermal analysis showed a decrease in thermal stability relative to untreated cotton, highlighting the influence of AgNPs on degradation behavior. Overall, this work demonstrates that potato peel waste, an abundant and underutilized biomass, can be used as a sustainable source for the green synthesis of AgNP-functionalized textiles. The approach provides a cost-effective and environmentally friendly strategy for developing multifunctional fabrics, while supporting circular economy goals in textile engineering.

Abstract Bovine serum albumin (BSA) nanoparticles have attracted a lot of interest as biocompatible and biodegradable carriers for a range of pharmacological and biological uses. BSA nanoparticles have several advantages over other types of nanoparticles, including their ability to increase the stability and solubility of encapsulated drugs, their non-toxicity, and their ease of surface modification. Cancer treatment, immunological modulation, enzyme immobilization, controlled release systems, bioimaging, and theranostics are some of its potential applications. This protocol offers a detailed and accessible methodology for the synthesis, drug encapsulation, and characterization of albumin nanoparticles, with particular emphasis on reproducibility and adaptability. The synthesis uses the desolvation process and crosslinking with the compound glutaraldehyde for stability. The crosslinking ratio, pH, and BSA content are important factors that can be adjusted to control size, surface charge, and dispersity. The methods used for characterization are described in detail, including dynamic light scattering for particle size and zeta potential, transmission and scanning electron microscopy for morphology, Fourier-transform infrared spectroscopy, and nanoparticle tracking analysis for stability assessment. The stability of the nanoparticles was evaluated under physiologically relevant ionic and pH conditions by dispersing them in phosphate-buffered saline, providing insight into their colloidal behavior in a simulated physiological environment. This technique facilitates the design of functionalized BSA nanoparticles for certain biomedical and therapeutic applications by acting as a fundamental reference for researchers. This work promotes innovation in nanoparticle-based technology and advances the field by standardizing preparation and characterization techniques.

Silver nanoparticles (AgNPs) are one of the most produced nanoproducts due to their unique biocide properties. The natural organic matter has an important impact on nanoparticle’s dispersion as it may alter their fate and transport, as well as their bioavailability and toxicity. Therefore, this study aimed to evaluate the mitigatory effect of humic acids (HAs) on AgNP toxicity. For this purpose, we carried out an ex vivo exposure of gill of Piaractus mesopotamicus fish to 100 μg L −1 of AgNPs or AgNO 3 , alone and in combination with 10 mg L −1 of HAs. In parallel, a complete AgNP characterization in the media, including the presence of HAs, was provided, and the Ag + release was measured. We analyzed Ag bioaccumulation, antioxidant enzymes activities, lipid peroxidation, antioxidant capacity against peroxyl radicals, and reduced glutathione levels in fish tissue. Our results indicated the Ag + release from AgNPs decreased 28% when the HAs were present in the media. The Ag accumulation in gill tissue exposed to AgNPs alone was higher than the AgNO 3 exposure, and sixfold higher than the treatment with the HA addition. Moreover, after both Ag forms, the catalase enzyme augmented its activity. However, those responses were mitigated when the HAs were present in the media. Then, our results suggested the mitigation by HAs under the exposure to both Ag forms, providing valuable information about the fate and behavior of this emergent pollutant.

Background The constant increase of the use of nanomaterials in consumer products is making increasingly urgent that standardized and reliable in vitro test methods for toxicity screening be made available to the scientific community. For this purpose, the determination of the cellular dose, i.e. the amount of nanomaterials effectively in contact with the cells is fundamental for a trustworthy determination of nanomaterial dose responses. This has often been overlooked in the literature making it difficult to undertake a comparison of datasets from different studies. Characterization of the mechanisms involved in nanomaterial transport and the determination of the cellular dose is essential for the development of predictive numerical models and reliable in vitro screening methods. Results This work aims to relate key physico-chemical properties of gold nanoparticles (NPs) to the kinetics of their deposition on the cellular monolayer. Firstly, an extensive characterization of NPs in complete culture cell medium was performed to determine the diameter and the apparent mass density of the formed NP-serum protein complexes. Subsequently, the kinetics of deposition were studied by UV -vis absorbance measurements in the presence or absence of cells. The fraction of NPs deposited on the cellular layer was found to be highly dependent on NP size and apparent density because these two parameters influence the NP transport. The NP deposition occurred in two phases: phase 1, which consists of cellular uptake driven by the NP-cell affinity, and phase 2 consisting mainly of NP deposition onto the cellular membrane. Conclusion The fraction of deposited NPs is very different from the initial concentration applied in the in vitro assay, and is highly dependent of the size and density of the NPs, on the associated transport rate and on the exposure duration. This study shows that an accurate characterization is needed and suitable experimental conditions such as initial concentration of NPs and liquid height in the wells has to be considered since they strongly influence the cellular dose and the nature of interactions of NPs with the cells.