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Polyoxometalates (POMs) are metal-oxygen clusters composed of {MO6} octahedra that have attracted considerable attention due to their remarkable antiviral, antibacterial and antitumor activities. Despite their potential, the molecular mechanisms underlying their cellular toxicity remain poorly understood. This study investigates how Anderson-Evans type polyoxotungstates (POTs) and polyoxomolybdates (POMos) interact with biological membranes by examining their effects on the zeta (ζ) – potential of the lipid bilayer and the size of small unilamellar liposomes of different phospholipid compositions. POTs affected the ζ-potential of neutral (1,2-dioleoyl-sn-glycero-3-phosphocholine, DOPC) and slightly negatively charged (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine; DOPC:DOPE) membranes in the order [MnW6O24]8– > [Ni(OH)6W6O18]4– > [TeW6O24]6–. The addition of negatively charged cardiolipin (CL) to DOPC reduced the interaction of POTs with the membrane. An opposite effect was observed for POMos, which changed the ζ-potential of neutral and slightly negatively charged membranes in the order [Al(OH)6Mo6O18]3– > [Cr(OH)6Mo6O18]3– >> [Ni(OH)6Mo6O18]4–. The addition of POMos increased the size of the liposomes in reverse order. The binding of [Al(OH)6Mo6O18]3– to the PE-containing phospholipid membranes and the effect of ionic strength on the interaction of [Cr(OH)6Mo6O18]3– with DOPC:CL liposomes could be inhibited by potassium fluoride (KF). Interestingly, KF did not inhibit the interaction of other POMos with membranes as indicated by ζ-potential measurements. These results suggest that the interaction of Anderson-Evans type POMs with phospholipid membranes is influenced more by their addenda and central ions than by their total charge. By unravelling the structure-activity relationships for the different POMs, we contribute to the design of biologically active POMs for therapeutic use.

Electrokinetic measurements to determine the electrical properties (zeta potential) of membrane surfaces have become increasingly popular in the toolbox of characterization techniques. However, it has been established in the literature that parasitic phenomena such as electrokinetic leakage can hamper data interpretation, leading to not only quantitative but also qualitative errors in membrane zeta potential determination. To date, the only method for highlighting and accounting for electrokinetic leakage is limited to flat-sheet membranes. In this letter, we propose an alternative method that is much less time-consuming and applicable to all membrane geometries. This method is based on the determination of the electrokinetic index, which we define as the ratio of the apparent zeta potentials determined from single measurements of the streaming current and streaming potential coefficients. We show that variation in the electrokinetic index reflects modifications occurring within the membrane matrix (in addition to surface properties alteration). The chemical degradation of polyethersulfone (PES)-based flat-sheet and hollow-fiber membranes is used as a proof of concept, but the proposed approach is readily transposable to other problems of practical interest, such as e.g. membrane fouling. This work also paves the way for the development of a new type of electrokinetic sensors for on-line monitoring of membrane operations.

The continuous deepening of coal-seam extraction has sharply increased both gas pressure and content. The use of viscoelastic surfactant fracturing fluids (VESFFs) has been demonstrated to effectively improve coal-seam permeability and mitigate the occurrence of gas disasters. After injection into coal, VESFFs interact with the coal and affect its surface characteristics. In this study, to characterize changes in zeta potential, oxygen-containing functional groups, and the microcrystalline structure of hard and soft coal surfaces under the influence of VESFFs with different formulations, zeta potential measurements and Fourier-transform infrared and Raman spectroscopies were performed. The VESFFs enhanced the electrostatic repulsion between the pore wall and coal particles, which is favorable for the removal of coal particles from hard and soft coal surfaces. The combination of cationic with zwitterionic viscoelastic surfactants (VESs) in the VESFFs exposed more hydrophilic functional groups on the surfaces of hard and soft coal, increasing wettability and affecting nanometer pores. A VESFF based on anionic and zwitterionic VESs as the primary agents could enhance the extension of the aromatic layer (La) of the aromatic crystal nuclei and reduce the interlayer spacing (d002) of hard and soft coal, thereby increasing the volume of micropores. This research offers theoretical guidance for optimizing the primary components of VESFFs and elucidates the mechanism through which VESFFs act on nanopores in coal from a microscopic perspective.

1,2-propylene glycol and its 50-50 w/w mixture with water were used to prepare heat transfer fluids based on amino-functionalized silica. On top of pH-neutral dispersions (no reagents added except for the solvent and the particles), dispersions acidified with acetic acid and with HCl were used to enhance the positive electric charge of silica particles. The colloidal particles had a positive zeta potential >40 mV and showed apparent particle radii of 70 nm, and these properties remained unchanged on heating up to 80 °C for up to 28 days.

Surface fluorination with pure F2 gas can easily make the surface on PP (polypropylene) hydrophobic, and it causes limited dyeability, as reported in a previous paper. In this study, to produce a more hydrophilic surface, surface fluorination of PP was performed at 25 °C, total gas pressure of 13.3 kPa, and reaction time of 1 h using F2 and O2 mixtures with different proportions of F2 gas. The surface roughness of the fluorinated PP samples was about 1.5 times higher than that of the untreated sample (5 nm). Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy (XPS) results showed that the PP-derived bonds (-C-C- and -CHx) decreased because they were converted into polar groups (-C–O, -CHF-, and -CFx), which increased the surface electronegativity of the PP. The variation in the F2 gas proportion in the gas mixture significantly affected the hydrophilicity and surface composition of the PP. At F2 gas proportions of 2 gas proportions of >90%, the PP surface became hydrophobic owing to increased numbers of hydrophobic -CF3 bonds. Thus, enhanced PP dyeing can be controlled based on the composition of the F2 and O2 gas mixture.

Polyvinylidene fluoride (PVDF) membranes were coated with TiO2 and TiO2-Ag to enhance their efficiency for oil-in-water emulsion separation. The photocatalytic activities of the two modified membranes and their filtration performances were compared in detail. The significantly enhanced photocatalytic activity of the TiO2-Ag composite was proved using a methyl orange (MO) solution (c = 10−5 M) and a crude oil emulsion (c = 50 mg·L−1). The TiO2-Ag-coated membrane reduced the MO concentration by 87%, whereas the TiO2-modified membrane reached only a 46% decomposition. The photocatalytic reduction in the chemical oxygen demand of the emulsion was also ~50% higher using the TiO2-Ag-coated membrane compared to that of the TiO2-coated membrane. The photoluminescence measurements demonstrated a reduced electron/hole recombination, achieved by the Ag nanoparticle addition (TiO2-Ag), which also explained the enhanced photocatalytic activity. A significant improvement in the oil separation performance with the TiO2-Ag-coated membrane was also demonstrated: a substantial increase in the flux and flux recovery ratio (up to 92.4%) was achieved, together with a notable reduction in the flux decay ratio and the irreversible filtration resistance. Furthermore, the purification efficiency was also enhanced (achieving 98.5% and 99.9% COD and turbidity reductions, respectively). Contact angle, zeta potential, scanning electron microscopy (SEM), and atomic force microscopy (AFM) measurements were carried out to explain the results. SEM and AFM images revealed that on the TiO2-Ag-coated membrane, a less aggregated, more continuous, homogeneous, and smoother nanolayer was formed due to the ~50% more negative zeta potential of the TiO2-Ag nanocomposite compared to that of the TiO2. In summary, via Ag addition, a sufficiently hydrophilic, beneficially negatively charged, and homogeneous TiO2-Ag-coated PVDF membrane surface was achieved, which resulted in the presented advantageous filtration properties beyond the photocatalytic activity enhancement.

Introduction: The current understanding of the biological impacts of a static magnetic field (SMF) is restricted to the direct interactions of the magnetic field with biological membranes. The electrokinetic (zeta) potential is an electrochemical property of erythrocyte surfaces which was negatively charged in physiological media after SMF exposure (0.1‒2.0 T).Methods: The novel data about electrokinetic parameters of the erythrocytes is determined by microelectrophoresis after SMF-exposure in norm and heterozygous β-thalassemia. The methods of light scattering, lipid peroxidation, fluorescence microscopy are used.Results: The electrokinetic potential of erythrocytes in norm is increased after SMF intensities due to enhanced negatively exposed charges on the outer surface of the membrane accompanied by an increase in light scattering where changes in cell morphology are observed. Conversely, a decrease in the zeta potential of β-thalassemia erythrocytes upon SMF-treatment was determined because of the reduction in the surface electrical charge of the membranes, where a significant decrease in light scattering at 1.5 T and 2.0 T was recorded. Exposure to SMF (0.5–2.0 T) was associated with an increase in the malondialdehyde content in erythrocytes. Biophysical studies regarding the influence of SMF on the electrostatic free energy of cells shows an increase in negative values in healthy erythrocytes, which corresponds to the implementation of a spontaneous process. This is also the process in β-thalassemia cells after SMF exposure with lower negative values of free electrostatic energy than erythrocytes in norm.Discussion: The effect of static magnetic field (SMF 0.1–2.0 T) on the electrokinetic and morphological characteristics of erythrocytes in norm and β-thalassemia is determined and correlated with the increase/reduction in surface charge and shrinkage/swelling of the cells, respectively. Lipid peroxidation of healthy and β-thalassemia erythrocytes caused an enhancement of lipid peroxidation because of the higher concentrations of TBARS products in cellular suspension. SMF (0.1‒2.0 T) altered the spontaneous chemical processes with negative values of electrostatic free energy of erythrocytes in norm and β-thalassemia accompanied by a lower FITC-Concanavalin A binding affinity to membrane receptors (SMF 2.0 T). The electrokinetic properties of human erythrocytes in norm and β-thalassemia upon SMF treatment and their interrelationship with the structural-functional state of the membrane were reported. The presented work would have future fundamental applications in biomedicine.

Electrical stimulation (ES) and its effects on biological systems is an area of research in regenerative medicine. The focus here is on the mechanism of action of ES on cell membrane-related components. A short alternating current (AC) stimulation (10 min) was applied on suspended human MG-63 osteoblasts via a commercially available multi-channel system (IonOptix). The pulsed ES with 1 V or 5 V and frequencies of 20 Hz on cells was performed immediately after cell seeding. The in vitro investigations were conducted by microscopy, flow cytometry, and particle analysis via a Litesizer within 24 h. The short-time ES with the parameter 1 V and 20 Hz was beneficial for the process of cell attachment, which could be related to an enhanced deposition of fibronectin on the glass bottom from the protein-containing medium (10% FBS). The MG-63 cells’ spherical coat hyaluronan remained constant and did not contribute to this AC-triggered adhesion. In this context, the cells’ zeta potential also did not play a role. The membrane potential analyzed via DiBAC4(3) was unchanged. Only the aquaporin channel AQP 8 in the cell membrane was significantly enhanced. Suspended cells in an AC electric field were activated during their settlement, and the fibronectin adsorption on the bottom contributed to this effect but not the membrane-related components.

The incorporation of additional functional groups such as bismuth nanoparticles (Bi NPs) into magnetite nanoparticles (Fe3O4 NPs) is critical for their properties modification, stabilization, and multi-functionalization in biomedical applications. In this work, ultrasound has rapidly modified iron oxide (Fe3O4) NPs via incorporating their surface through coating with Bi NPs, creating unique Fe3O4@Bi composite NPs. The Fe3O4@Bi nanocomposites were synthesized and statistically optimized using an ultrasonic probe and response surface methodology (RSM). A face-centered central composite design (FCCD) investigated the effect of preparation settings on the stability, size, and size distribution of the nanocomposite. Based on the numerical desirability function, the optimized preparation parameters that influenced the responses were determined to be 40 ml, 5 ml, and 12 min for Bi concentration, sodium borohydride (SBH) concentration, and sonication time, respectively. It was found that the sonication time was the most influential factor in determining the responses. The predicted values for the zeta potential, hydrodynamic size, and polydispersity index (PDI) at the highest desirability solution (100%) were −45 mV, 122 nm, and 0.257, while their experimental values at the optimal preparation conditions were −47.1 mV, 125 nm, and 0.281, respectively. Dynamic light scattering (DLS) result shows that the ultrasound efficiently stabilized and functionalized Fe3O4NPs following modification to Fe3O4@Bi NPs, improved the zeta potential value from –33.5 to −47.1 mV, but increased the hydrodynamic size from 98 to 125 nm. Energy dispersive spectroscopy (EDX) validated the elemental compositions and Fourier transform infrared spectroscopy (FTIR) confirmed the presence of Sumac (Rhus coriaria) compounds in the composition of the nanocomposites. The stability and biocompatibility of Fe3O4@Bi NPs were improved by using the extract solution of the Sumac edible plant. Other physicochemical results revealed that Fe3O4NPs and Fe3O4@Bi NPs were crystalline, semi-spherical, and monodisperse with average particle sizes of 11.7 nm and 19.5 nm, while their saturation magnetization (Ms) values were found to be 132.33 emu/g and 92.192 emu/g, respectively. In vitro cytotoxicity of Fe3O4@Bi NPs on the HEK-293 cells was dose- and time-dependent. Based on our findings, the sonochemical approach efficiently produced (and RSM accurately optimized) an extremely stable, homogeneous, and biocompatible Fe3O4@Bi NPs with multifunctional potential for various biomedical applications.

Protein crystallization plays a crucial role in the food and pharmaceutical industries, enhancing product quality and efficiency by improving purity and controlled particle characteristics. This study focused on the crystallization of the versatile protein papain, extracted from papaya. Antisolvent crystallization was performed. This method is cost-effective and is a simple and energy-efficient approach. Beyond protein crystal production, the antisolvent crystallization process serves as a method for encapsulating active pharmaceutical ingredients (APIs). The study investigated organic solvents like ethanol, acetone, and acetonitrile as potential antisolvents. Additionally, the impact of variables such as the solvent-to-antisolvent (S:AS) volume ratio and papain concentration on particle size, particle size distribution, zeta potential, crystallization yield, and residual activity of papain crystals were examined. Ethanol emerged as the optimal antisolvent, reducing the solubility of papain and preserving papain’s crystalline structure with minimal activity loss. Optimal conditions were identified at a 1:4 S:AS volume ratio and a papain concentration of 30 mg/mL, resulting in nanosized spherical crystals with a high yield and preserved activity. This research underscored the crucial role of thoughtful parameter selection in antisolvent crystallization to achieve specific particle characteristics while maintaining the functionality of the crystallized substance.

The zeta potential of soils is an electric potential in the double-layer interface and is a physical property exhibited by any particle related to electrochemical attractive forces. On the other hand, the chemical aging phenomenon is seen as the chief mechanism of the aging of sands due to the dissolution and precipitation of minerals, resulting in the development of the cementation of particles in granular mediums. The present investigation focuses on determining whether granular materials can generate cementation due to electrokinetic forces, and if the zeta potential could be related as a measure of the potential of chemical aging. X-ray fluorescence and diffraction tests were performed to characterize four representative fractions of one kind of sand, and zeta potential studies were carried out to determine the electrical potential on the mineral surfaces of each one. Zeta potential analysis showed both dependence on the mineralogical content and the variation in the pH of the colloidal solution fluid because the increase in OH- ion concentrations increases the thickness of the diffuse double layer and the electrokinetic forces of attraction. Moreover, the zeta potential showed an increase in the thickness of the diffuse double layer, due to the electrokinetic forces, which can be associated with the development of cohesive forces with a dependence on the mineralogy of sands.

Self-assembly of colloidal nanoparticles is a promising approach for the fabrication of functional materials. Zeta potential strongly influences the self-assembly processes of nanoparticles. Light-induced zeta potential manipulation provides spatiotemporal resolution. However, current studies on photo-controllable zeta potential are based on ultraviolet (UV) light. In comparison with UV light, visible light is better suited to control the zeta potential of colloidal nanoparticles. In the present study, we applied visible light-responsive ruthenium (Ru) complexes, grafted onto the surface of silica nanoparticles (Ru-SNPs), to control their assembly. The Ru complexes were photoresponsive. Irradiation of Ru-SNPs induced the release of Ru complexes from the nanoparticle surface. The released Ru caused a decrease in the zeta potential of colloidal Ru-SNPs that further changed the assembly behavior and led to the aggregation of Ru-SNPs.

The article presents a comparative study of the surface properties of silica and alumina nanoparticles synthesized by various methods. Using the IR spectroscopy we demonstrated that the synthesis method affect the surface properties of nanoparticles while maintaining the phase composition of the material. The article demonstrates the relationship between the types of surface sites, their strength, and the interaction of nanoparticles with the dispersed medium. In particular, a significant difference was observed in the strength of the active sites for all samples, which was reflected in the rheology of nanofluids based on epoxy resin. This demonstrates the importance of accurate descriptions of the surface properties of nanoparticles, as they determine their interaction with other materials. The article also considers the possibility to evaluate the intensity of the particle-medium interaction based on the fractal dimension. Our study showed that it varies significantly depending on the synthesis method. The article discussed the possibility to determine the intensity of the particle-medium interaction using the values of the nanoparticle’s zeta potential and the interfacial layer

Green nanotechnology has emerged as a viable option for the production of nanoparticles. The purpose of the current investigation was to synthesize silver nanoparticles (AgNPs) using Eucalyptus camaldulensis and Terminalia arjuna extracts, as well as their combinations, as green reducing and capping agents. The parameters (concentration of silver nitrate solution and plant extract, time, pH, and temperature) were optimized for maximal yields, regulated size, and stability of silver nanoparticles. The ultraviolet–visible spectrophotometer (UV-Vis) and the surface plasmon resonance band (SPR) were used to validate the synthesis of AgNPs. The size, shape, and stability of nanoparticles were assessed using a zeta analyzer and a scanning electron microscope (SEM). The biomolecules responsible for the reduction of silver ion (Ag+) and the stability of silver nanoparticles generated with the plant extracts were identified using Fourier-transform infrared spectroscopy (FTIR). The agar-well diffusion method was used to test the antimicrobial activity of biosynthesized nanoparticles against Bacillus subtilis, Staphylococcus aureus, Pasteurella multocida, and Escherichia coli. When 1 mM of silver nitrate (AgNO3) was added to plant extracts and incubated for 60 min at 75°C in a neutral medium, maximum nanoparticles were produced. Biosynthesized silver nanoparticles were stable, spherical, and monodispersed according to zeta potential and scanning electron microscopy. Silver nanoparticles synthesized with combination 2 and T. arjuna showed the highest zone of inhibition (16 mm) against B. subtilis while combination 3 showed the largest zone of inhibition against S. aureus (17 ± 0.8). It was concluded that greenly produced silver nanoparticles showed good antibacterial activity while causing negligible cytotoxicity.

Biocompatible gold nanoparticles (AuNPs) are used in wound healing due to their radical scavenging activity. They shorten wound healing time by, for example, improving re-epithelialization and promoting the formation of new connective tissue. Another approach that promotes wound healing through cell proliferation while inhibiting bacterial growth is an acidic microenvironment, which can be achieved with acid-forming buffers. Accordingly, a combination of these two approaches appears promising and is the focus of the present study. Here, 18 nm and 56 nm gold NP (Au) were prepared with Turkevich reduction synthesis using design-of-experiments methodology, and the influence of pH and ionic strength on their behaviour was investigated. The citrate buffer had a pronounced effect on the stability of AuNPs due to the more complex intermolecular interactions, which was also confirmed by the changes in optical properties. In contrast, AuNPs dispersed in lactate and phosphate buffer were stable at therapeutically relevant ionic strength, regardless of their size. Simulation of the local pH distribution near the particle surface also showed a steep pH gradient for particles smaller than 100 nm. This suggests that the healing potential is further enhanced by a more acidic environment at the particle surface, making this strategy a promising approach.

We present a simple synthetic route to submicron-sized both potassium- and sodium-based geopolymer nanoaggregates whose nanostructure is suitable for applications in polymer composites. The new synthetic method is based on the chemical mechanism of geopolymer formation in which the extent of cross-liking of geopolymer primary particles is dependent of the alkali concentration and the relative amount of water in the precursor mixture. The products exhibited ∼50–60 nm-sized primary particles along with ∼15–20 nm-sized smaller particles. The external surface areas of the products were high, up to 231 m2/g, especially for the sodium-based geopolymer. The primary particles are fused together to form aciniform nanoaggregates with average size of about 400 nm and mesopore volume up to about 0.59 cm3/g. The zeta potential of the nanoaggregates was below ‒ 40 mV in the pH range of 5.7–12, demonstrating that the particles are stable in this pH region and do not undergo aggregation and/or agglomeration. All these characteristics make the new material favorable in application of the material in nanofiller application.

The paper presents the results of a comprehensive study of the electrokinetic properties of non-aqueous suspensions of the Al2O3–Al nanopowder obtained by the method of electric explosion of wires (EEW) with 0.3 wt.% of metallic aluminum in its composition. The dependence of zeta potential on the concentration of the Al2O3–Al suspension is revealed. The nature of long-term changes in zeta potential and pH in suspensions is established. Appearance of bubbles in the deposited coatings due to the interaction of metallic aluminum particles with the liquid suspension medium during electrochemical reactions on the electrodes is defined as the main feature of the electrophoretic deposition (EPD) process in the Al2O3–Al suspensions. The influence of the suspension preparation method on the deposited coatings’ morphology is demonstrated.

In this work, the electrokinetic properties of alkali and oxidatively modified jute fabrics were studied. In contrast to the control fabric, chemically modified jute fabrics had a small positive zeta potential in the basic pH range, which could be attributed to the presence of sodium cations (originating from the undertaken chemical modifications) on their surfaces. At lower pH values, the samples modified under milder alkali and oxidative conditions had about 2.2–3.5 times lower zeta potential since the protonation process led to the formation of a higher positive charge in the electrochemical double layer, causing higher adsorption of Cl- (originating from the electrolyte). On the other hand, more intensive chemical modifications increased the zeta potential at lower pH values due to the increased amount of carboxyl groups and the ability of the fibres for water retention and hence swelling. The isoelectric point of the fabrics, having lower zeta potentials than that of the control fabric, was shifted towards higher pH values, indicating to a lower contribution of surface acidic groups of the fabrics. In the case of extensive oxidation conditions (60 and 90 min), the isoelectric point was shifted toward lower pH values because of lignin removal and the mentioned higher availability of newly formed carboxyl groups.

Nanoparticles have gained significance in modern science due to their unique characteristics and diverse applications in various fields. Zeta potential is critical in assessing the stability of nanofluids and colloidal systems but measuring it can be time-consuming and challenging. The current research proposes the use of cutting-edge machine learning techniques, including multiple regression analyses (MRAs), support vector machines (SVM), and artificial neural networks (ANNs), to simulate the zeta potential of silica nanofluids and colloidal systems, while accounting for affecting parameters such as nanoparticle size, concentration, pH, temperature, brine salinity, monovalent ion type, and the presence of sand, limestone, or nano-sized fine particles. Zeta potential data from different literature sources were used to develop and train the models using machine learning techniques. Performance indicators were employed to evaluate the models’ predictive capabilities. The correlation coefficient (r) for the ANN, SVM, and MRA models was found to be 0.982, 0.997, and 0.68, respectively. The mean absolute percentage error for the ANN model was 5%, whereas, for the MRA and SVM models, it was greater than 25%. ANN models were more accurate than SVM and MRA models at predicting zeta potential, and the trained ANN model achieved an accuracy of over 97% in zeta potential predictions. ANN models are more accurate and faster at predicting zeta potential than conventional methods. The model developed in this research is the first ever to predict the zeta potential of silica nanofluids, dispersed kaolinite, sand–brine system, and coal dispersions considering several influencing parameters. This approach eliminates the need for time-consuming experimentation and provides a highly accurate and rapid prediction method with broad applications across different fields.

Currently, highly luminescent colloidal upconversion nanoparticles (UCNPs) have expanded an increasing interest of researchers because of their facilitating lability in the biomedical/clinical field. In this study, NaYF4:Yb,Er UCNPs are prepared by eco-friendly metal complexation-based thermal decomposition method at a lower temperature in aqueous media. The phase structure, crystallinity, phase purity, morphology, colloidal dispersibility, surface structure, surface charge, and optical and luminescent properties were evaluated carefully by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), energy dispersive x-ray analysis (EDX), Thermogravimetric analysis (TGA), zeta potential, Fourier transform infrared (FTIR), UV/visible and photoluminescent spectroscopic techniques. XRD pattern shows a pure single-phase cubic structure with an average grain size of 30–35 nm. TEM and SEM micrographs exhibited irregularly shaped spherical morphologies, porous surface structures highly aggregated UCNPs with the narrow-size distribution. Positive zeta potential has shown value signifying high absorption in the visible region which indicates particle's good colloidal stability in aqueous media. Under NIR-laser light excitation, the UCNPs emit strong UC emission transitions in the visible region. A broad infrared absorption peak of hydroxyl groups (–OH) in FTIR spectrum and mass loss at a lower temperature in TGA verified the surface functionality of UCNPs, with high colloidal stability, and excellent biocompatibility in aqueous media. In terms of their surface characteristics and high luminescent properties, the NaYF4:Yb,Er UCNPs could be interestingly applied in tagging of biomolecules, drug delivery, proteins labeling, and therapeutic and thermostats applications.

Solid Lipid Nanoparticles (SLN) have been prepared by high-pressure homogenization and optimized in order to protect ferulic acid from Ferula assa-foetida L. extract. The influence of lipid and surfactant concentration on the mean particle size (Z-Ave), polydispersity index (PDI), and zeta potential (ZP) of SLN was analyzed. In addition, other parameters for the preparation of ferulic acid-loaded nanoparticles, such as extract concentration and variable parameters for the synthesis method used (e.g., pressure), were adjusted to obtain the smallest particle size and polydispersity index, as well as the highest value for zeta potential, which are characteristic of the stable SLN. The established formulation obtained from the optimized synthesis was composed of 6.0 wt.% of the lipid phase and 1.5 wt.% of surfactant, giving stable SLN with Z-Ave, PDI, and ZP values of 163.00 ± 1.06 nm, 0.16 ± 0.01, and −41.97 ± 0.47 mV, respectively. The loading of ferulic acid from Ferula assa-foetida L. extract within the SLN resulted in particles with a mean size of 155.3 ± 1.1 nm, polydispersity index of 0.16 ± 0.01, zeta potential of −38.00 ± 1.12 mV, and encapsulation efficiency of 27%, the latter being quantified on the basis of RP-HPLC analysis. Our findings highlight the added value of SLN as a delivery system for phenolic phytochemical compounds extracted from Ferula assa-foetida L.

Dispersing particles in a liquid phase is significant for producing various functional nano/bio applications. The wet-jet milling method has been gaining attention as an attractive dispersing method in the preparation of soft material suspensions. This is because the main driving force of dispersion by the wet-jet milling method is the shear force, which is weaker than that it is in the ultrasonication dispersing method. In the wet-jet milling method, the pressure of the narrow channel which the liquid is passes through and the number of passes are used as the control parameters for dispersing the particles. However, the values of the pressure depend on the size (diameter and length) of the narrow channel, thus, it is not a commonly used dispersing parameter in dispersing by wet-jet milling to set the dispersing condition by various wet-jet milling instruments. In addition, wet-jet milling users must optimize the dispersing conditions such as the pressure and number of passes in the narrow channel, therefore, a simple prediction/optimization method of the dispersing size by the wet-jet milling method is desired. In this study, we established a novel colloidal dispersing concept, the dispersing energy input based on a calorimetric idea, for particle suspension preparation using the wet-jet milling method. The dispersing energy input by wet-jet milling was quantitatively calculated under various conditions during the dispersing by wet-jet milling, and then, the dispersing size of the particles was easily predicted/optimized. We demonstrated the usability of the concept by preparing aqueous suspensions of calcium carbonate (CaCO3) particles with various surfactants using the wet-jet milling method. Based on the established concept, in a case study on dispersing CaCO3, we found that changes in the micelle sizes of the surfactants played a role in wet-jet milling. The novel idea of the representation of energy input makes it possible to estimate the appropriate condition of the dispersing process by wet-jet milling to control the size of particles.

To cope with the problem that the setting time and hardening time of high-belite sulphoaluminate cement (HBCSA) is too fast and not easily controlled, three common retarders, citric acid (CA), β-cyclodextrin (β-CD), and borax (B), were selected and compounded with polycarboxylate superplasticizer (PCE). Based on the cement slurry fluidity, fluidity loss, setting time, and mechanical properties of cement mortar, combined with X-ray diffraction (XRD), scanning electron microscopy (SEM), and Zeta potential tests, the interaction and mechanism of different retarders and high-belite sulphoaluminate cement were studied. The results show that β-CD and CA can significantly delay the hydration process of HBCSA cement, effectively improve the fluidity loss, and make the dispersion more stable, but the strength of cement mortar decreases, which is not conducive to the development of strength. However, the addition of B has no obvious retarding effect on the HBCSA cement, and the dispersibility of the cement paste decreases. In microscopic tests, XRD and SEM tests verified that the combination of retarder and PCE had a certain inhibitory effect on the early hydration of HBCSA, and the zeta potential indicated that the addition of retarder would interact with PCE to improve the fluidity loss of HBCSA. In addition, when the retarders CA and B were, respectively, compounded with β-CD, the two would have a synergistic effect. The retardation effect is more obvious, and the time interval between the initial and final setting is shorter, which is more controllable. The initial fluidity is also improved under the auxiliary plasticization of cement paste by β-CD.

Structural and colloidal stability of proteins at different surfaces and interfaces is of great importance in many fields including medical, pharmaceutical, or material science. Due to their flexibility, proteins tend to respond to their environmental conditions and can undergo structural and conformational changes. For instance, alterations in physiological factors such as temperature, ions concentration, or pH as well as the adsorption to an interface can initiate protein aggregation. Therefore, at different surfaces and interfaces the characterization of the structural and colloidal stability of proteins, which is mainly influenced by their electrostatic and hydrophobic interactions, is of fundamental importance. In this study, we utilized sum frequency generation (SFG) spectroscopy to assess the role of solution pH on the polarity and magnitude of the electric field within the hydration shell of selected model proteins adsorbed to a hydrophobic surface. We used polystyrene (PS) as a model hydrophobic surface and determined the isoelectric point (IEP) of four structurally different model proteins. Comparing the measured IEP of proteins at the PS/solution or air/solution interface with that determined in the bulk solution via zeta potential measurement, we found significant similarities between the IEP of surface adsorbed proteins and those in the bulk aqueous phase. The pH dependence behavior of proteins was correlated to their amino acid composition and degree of hydrophobicity.

The electrophoretic deposition (EPD) of coatings and bulk compacts in a wide range of thicknesses (from 23 to 1800 μm) from stable suspensions of a magnesium-doped aluminum oxide nanopowder with subsequent sintering of samples into dense ceramics was studied. The initial nanopowder was obtained by the method of electric explosion of an Al-Mg alloy wire with a Mg content of 1.3 wt. %. The study of the dispersion composition, kinetics of deaggregation under the ultrasonic treatment and zeta potential in the nanopowder-based suspensions was carried out. It was shown that a nearly linear increase in the deposited mass and thickness of EPD deposits occurred at a constant voltage of 20 V and an average deposition current of approximately 40 μA when the deposition time was varied from 1 to 180 min. Drying of the coatings with a thickness of less than 35 μm led to the formation of a net of small cracks, while drying of the bulk compacts with a thickness of more than 1 mm occurred without cracking. The ceramic bulk sample with a thickness of 1.2 mm and the density of 98.7% TD was successfully obtained by sintering at 1650 °C for 4 h. It was characterized by a dense grain structure with an average grain size of 5 μm and the presence of a small number of closed pores less than 1 μm in size. Sintering of ceramics was revealed to be accompanied by the formation of a MgAl2O4 crystalline spinel phase, localized mainly at grain boundaries.

Ultrafine bubble (UFB) is a bubble with a diameter of less than 1 μm. Little attention has been paid to the defoaming and removal of UFBs. This study proposes a method to destabilize UFBs by using indirect ultrasonic irradiation. Besides, the destabilization mechanism of UFB was investigated. The ultrasonic frequency was 1.6 MHz and the dissipated power was 30 W. UFB dispersions were prepared using two different types of bubble generators: pressurized dissolution method and swirling liquid flow method. The effects of ultrasonic irradiation on the stability of UFBs were evaluated by particle tracking analysis (PTA) and electrophoretic zeta potential measurement. Results showed that the indirect ultrasonic irradiation for 30 min reduced the number concentration of UFBs by 90% regardless of the generation method. This destabilization was attributed to a decrease in the magnitude of zeta potential of UFBs due to the changes in pH and electrical conductivity. These changes in the electrochemical properties were caused by the formation of nitric acid. To study the destabilization mechanism, the pH of the UFB dispersions were modified by titration; the chemical and mechanical effects of ultrasound were separately examined. It was found that not only the chemical effect caused by the formation of nitric acid but also the mechanical effect contributed to the destabilization of UFB. Feasibility studies were also performed for UFBs in an aqueous surfactant solution and UFBs in a solid particle dispersion. The proposed method selectively destabilized UFBs in the solutions.

Mesoporous Silica Nanoparticles (MSNs) have received increasing attention in biomedical applications due to their tuneable pore size, surface area, size, surface chemistry, and thermal stability. The biocompatibility of MSNs, although generally believed to be satisfactory, is unclear. Physicochemical properties of MSNs, such as diameter size, morphology, and surface charge, control their biological interactions and toxicity. Experimental conditions also play an essential role in influencing toxicological results. Therefore, the present study includes studies from the last five years to statistically analyse the effect of various physicochemical features on MSN-induced in-vitro cytotoxicity profiles. Due to non-normally distributed data and the presence of outliers, a Kruskal–Wallis H test was conducted on different physicochemical characteristics, including diameter sizes, zeta-potential measurements, and functionalisation of MSNs, based on the viability results, and statistical differences were obtained. Subsequently, pairwise comparisons were performed using Dunn’s procedure with a Bonferroni correction for multiple comparisons. Other experimental parameters, such as type of cell line used, cell viability measurement assay, and incubation time, were also explored and analysed for statistically significant results.

Nanoemulsions are colloidal systems with a wide spectrum of applications in several industrial fields. In this study, crude oil-in-water (O/W) nanoemulsions were formulated using different dosages of the anionic sodium dodecylbenzenesulfonate (SDBS) surfactant. The formulated nanoemulsions were characterized in terms of emulsion droplet size, zeta potential, and interfacial tension (IFT). Additionally, the rheological behavior, long-term stability, and on-demand breakdown of the nanoemulsions via a pH-responsive mechanism were evaluated. The obtained results revealed the formation of as low as 63.5 nm average droplet size with a narrow distribution (33–142 nm). Additionally, highly negative zeta potential (i.e., −62.2 mV) and reasonably low IFT (0.45 mN/m) were obtained at 4% SDBS. The flow-ability of the nanoemulsions was also investigated and the obtained results revealed an increase in the nanoemulsion viscosity with increasing the emulsifier content. Nonetheless, even at the highest SDBS dosage of 4%, the nanoemulsion viscosity at ambient conditions never exceeded 2.5 mPa·s. A significant reduction in viscosity was obtained with increasing the nanoemulsion temperature. The formulated nanoemulsions displayed extreme stability with no demulsification signs irrespective of the emulsifier dosage even after one-month shelf-life. Another interesting and, yet, surprising observation reported herein is the pH-induced demulsification despite SDBS not possessing a pH-responsive character. This behavior enabled the on-demand breakdown of the nanoemulsions by simply altering their pH via the addition of HCl or NaOH; a complete and quick oil separation can be achieved using this simple and cheap demulsification method. The obtained results reveal the potential utilization of the formulated nanoemulsions in oilfield-related applications such as enhanced oil recovery (EOR), well stimulation and remediation, well-bore cleaning, and formation fracturing.

This paper presents the experimental forced convective heat transfer coefficient (HTC) of nanorods (NRs) zinc oxide–ethylene glycol nanofluids (ZnO–EG NFs) in laminar flow. First, ZnO NRs were synthesized using a hydrothermal method that uses zinc acetate dihydrate [Zn(CH3COO)2·2H2O] as a precursor, sodium hydroxide as a reducing agent, and polyvinylpyrrolidone (PVP) as a surfactant. The hydrothermal reaction was performed at 170 °C for 6 h in a Teflon-lined stainless-steel tube autoclave. The sample’s X-ray diffraction (XRD) pattern confirmed the formation of the hexagonal wurtzite phase of ZnO, and transmission electron microscopy (TEM) analysis revealed the NRs of the products with an average aspect ratio (length/diameter) of 2.25. Then, 0.1, 0.2, and 0.3 vol% of ZnO–EG NFs were prepared by adding the required ZnO NRs to 100 mL of EG. After that, time-lapse sedimentation observation, zeta potential (ζ), and ultraviolet-visible (UV–vis) spectroscopy was used to assess the stability of the NFs. Furthermore, the viscosity (μ) and density (ρ) of NFs were measured experimentally as a function of vol% from ambient temperature to 60 °C. Finally, the HTC of NFs was evaluated utilizing a vertical shell and tube heat transfer apparatus and a computer-based data recorder to quantify the forced convective HTC of NFs in laminar flow at Reynolds numbers (Re) of 400, 500, and 600. The obtained results indicate that adding only small amounts of ZnO NRs to EG can significantly increase the HTC, encouraging industrial and other heat management applications.

To reveal the ion-exchange mechanism in the leaching process of weathered crust elution-deposited rare earth ores with different leaching agents, the effects of a variety of cations and anions at different concentrations on the leaching process were investigated, including Al3+, Fe3+, Ca2+, Mg2+, Na+, K+, NH4+ and Cl−, NO3-, and SO42-. Meanwhile, the relationships between different concentrations of cations and anions and leaching efficiency were investigated, as was the relationship between different concentrations of cations and anions and zeta potential. The effect of different ions on the swelling of clay minerals during leaching process was also investigated. The results shown that NH4+ was the most affected electrolyte cation in terms of rare earth leaching efficiency during the leaching process of weathered crust elution-deposited rare earth ore among three different cationic valence states, and the leaching efficiency was 86.93% at the optimal leaching concentration. The influence of the three anions on the leaching efficiency of rare earth was NO3->Cl->SO42-, and the leaching efficiency of rare earth were 83.21, 81.52, and 80.12% at the optimal leaching concentration, respectively. The NH4+ had the greatest effect on the zeta potential of weathered crust elution-deposited rare earth ore, and the zeta potential was −18.1 mV at the optimal leaching concentration. Additionally, the order of the effect of three anions on zeta potential was SO42->NO3->Cl-. Combined with the effect on the rare earth leaching process, anions and cations were considered separately, and NH4+ and Cl− were selected; the relationship between the rare earth leaching efficiency and zeta potential conforms to the follow equations: NH4+:Y = −0.48X2 – 13.51X – 1.58, R2 = 0.98133 and Cl−:Y= −1.22X2 – 17.64X + 23.29, R2 = 0.99010. It was also found in the swelling experiment of the weathered crust elution-deposited rare earth ore that the swelling ratio of clay minerals was the lowest when the cation and anion were NH4+ and Cl− and the swelling ratios were 1.874 and 2.015%, respectively.

Deep Eutectic Solvents (DESs) are emerging as a promising medium for many chemical processes. They can be used to observe specific properties required for nanomaterials' applications. Controlled CO2 adsorption requires disaggregation of carbon nanotubes into smaller bundles which can be accomplished by dispersing them in aqueous DES system. In this study, response surface methodology (RSM) was adopted to examine the impacts of three important factors on the dispersion of single walled carbon nanotubes (SWNTs) in Choline Chloride-Glycerol (ChCl-Gly) DES; (i) ChCl-Gly (mass% in water), (ii) sonication energy input (J/mL), and (iii) SWNTs' concentration (mg/L). The net negative surface charge of ChCl-Gly, a “green solvent,” provided superior dispersion of inherently negatively charged SWNTs in water via electrostatic repulsion. The impacts of the dispersion factors were quantified by the average aggregate diameter (nm) and polydispersity (polydispersity index, PDI) of SWNTs in aqueous-DES systems. Models were developed, experimentally verified, and statistically validated to map the impacts of these factors and to obtain optimized dispersions. The optimized dispersions, characterized by the small (

Silver nanoparticles having uniform size and shape, a diameter range of 10–50 nm, excellent stability, and high zeta potential are always desirable for many applications. The silver nanoparticles were synthesized by chemical reduction method using some reducing agents in a polyvinyl alcohol solution. This study aims at determining the effect of reducing agents on the chemical and physical properties of silver nanoparticles. Ascorbic acid, sodium borohydride, hydrazine, sodium citrate, and glucose were used as reducing agents. Surface Plasmon Resonance (SPR) absorbance, morphology, zeta potential, crystal system, and stability of the products were studied. The results showed that the chemical and physical properties of the colloidal Ag nanoparticles were dependent on the reducing agents. In general, the produced silver nanoparticles have an fcc crystal system with a unit cell of 4.0906–4.0992 Å. The SPR absorbance of the colloids has the peak in the range of 401–433 nm. We found that the colloid of silver nanoparticles prepared by using ascorbic acid has uniform spherical shape, the diameter of about 20 nm, and zeta potential of -10.4 mV. After being stored for one month, the SPR absorbance of the colloid decreased by only 5%. This type of colloidal Ag nanoparticles prepared by using ascorbic acid is expected to be used for chemical sensors, an antibacterial agent, and so on.

Here, we prepared water-soluble highly luminescent CdSe/ZnS quantum dots having different surface charge and examined how zeta potential of quantum dots affected their uptake by cancer cells. Water soluble quantum dots with varied zeta potential were prepared through encapsulation with amphiphilic polymer poly(maleic anhydride-alt-1-tetradecene) (PMAT) containing ziwitterions formed by spatially separated carboxyl and quaternary amino groups. Varying the ration of negatively charged carboxyl and positively charged quaternary amino-groups during chemical modification of PMAT we control the sign and magnitude of zeta potential of encapsulated quantum dots. Quantum dots having nearly equal amount of carboxyl and quaternary amino groups possess pH-controlled zeta potential which can vary from negative to positive value when pH changes from basic to acidic condition. Cellular uptake of encapsulated quantum dots has been found to be strongly dependent of their surface charge: positively charged quantum dots efficiently internalized by cells, while negatively charged adsorbed mostly at the cell membrane. Zwitterionic QDs do not demonstrate any charge-dependent cellular toxicity at least within few hours. Long-term incubation of cells stained with zwitterionic quantum dots results in the decrease of the fluorescence signal mainly due to the cell proliferation.

The mycelium-free supernatant (MFS) of a five-day-old culture medium of Fusarium oxysporum was used to synthesize gold nanoparticles (AuNPs). The experimental design of the study was to answer the question: can this production process of AuNPs be controllable like classical chemical or physical approaches? The process of producing AuNPs from 1 mM tetrachloroauric (III) acid trihydrate in MFS was monitored visually by color change at different pH values and quantified spectroscopically. The produced AuNPs were analyzed by transmission electron microscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The presence of capping agents was confirmed by Fourier transform infrared spectroscopy (FTIR). Two AuNP samples with acidic and alkaline pH were selected and adjusted with the pH gradient and analyzed. Finally, the size and zeta potential of all samples were determined. The results confirmed the presence of the proteins as capping agents on the surface of the AuNPs and confirmed the production of AuNPs at all pH values. All AuNP samples exhibited negative zeta potential, and this potential was higher at natural to alkaline pH values. The size distribution analysis showed that the size of AuNPs produced at alkaline pH was smaller than that at acidic pH. Since all samples had negative charge, we suspect that there were other molecules besides proteins that acted as capping agents on the surface of the AuNPs. We conclude that although the biological method of nanoparticle production is safe, green, and inexpensive, the ability to manipulate the nanoparticles to obtain both positive and negative charges is limited, curtailing their application in the medical field.

Despite the broad range of interest and possible applications, the controls on the electric surface charge and the zeta potential of gneiss at conditions relevant to naturally fractured systems remain unreported. There are no published zeta potential measurements conducted in such systems at equilibrium, hence, the effects of composition, concentration and pressure remain unknown. This study reports zeta potential values for the first time measured in a fractured Lewisian gneiss sample saturated with NaCl solutions of various concentrations, artificial seawater and artificial groundwater solutions under equilibrium conditions at confining pressures of 4 MPa and 7 MPa. The constituent minerals of the sample were identified using X-ray diffraction and linked to the concentration and composition dependence of the zeta potential. The results reported in this study demonstrate that the zeta potential remained negative for all tested solutions and concentrations. However, the values of the zeta potential of our Lewisian gneiss sample were found to be unique and dissimilar to pure minerals such as quartz, calcite, mica or feldspar. Moreover, the measured zeta potentials were smaller in magnitude in the experiments with artificial complex solutions compared with those measured with NaCl, thus suggesting that divalent ions (Ca2+, Mg2+ and SO42−) acted as potential determining ions. The zeta potential was also found to be independent of salinity in the NaCl experiments, which is unusual for most reported data. We also investigated the impact of fracture aperture on the electrokinetic response and found that surface electrical conductivity remained negligibly small across the range of the tested confining pressures. Our novel results are an essential first step for interpreting field self-potential (SP) signals and facilitate a way forward for characterization of water flow through fractured basement aquifers.

Phosphorus-containing heterocyclic cationic surfactants alkyldimethylphenylphospholium bromides with the alkyl chain length 14 to 18 carbon atoms were used for the stabilization of silver nanodispersions. Zeta potential of silver nanodispersions ranges from +35 to +70 mV, which indicates the formation of stable silver nanoparticles (AgNPs). Long-chain heptadecyl and octadecyl homologs of the surfactants series provided the most intensive stabilizing effect to AgNPs, resulting in high positive zeta potential values and smaller diameter of AgNPs in the range 50–60 nm. A comparison with non-heterocyclic alkyltrimethylphosphonium surfactants of the same alkyl chain length showed better stability and more positive zeta potential values for silver nanodispersions stabilized with heterocyclic phospholium surfactants. Investigations of biological activity of phospholium-capped AgNPs are represented by the studies of antimicrobial activity and cytotoxicity. While cytotoxicity results revealed an increased level of HepG2 cell growth inhibition as compared with the cytotoxicity level of silver-free surfactant solutions, no enhanced antimicrobial action of phospholium-capped AgNPs against microbial pathogens was observed. The comparison of cytotoxicity of AgNPs stabilized with various non-heterocyclic ammonium and phosphonium surfactants shows that AgNPs capped with heterocyclic alkyldimethylphenylphospholium and non-heterocyclic triphenyl-substituted phosphonium surfactants have the highest cytotoxicity among silver nanodispersions stabilized by the series of ammonium and phosphonium surfactants.

Laboratory scale filtration tests utilizing leachate were conducted to investigate fouling and filtration performance of nanofiltration membranes. The work presented in this study is conducted on real samples rather than model water. Physico-chemical analyses showed that the leachate contained a lot of organic substances, exceeding 20000 mg/L O2 expressed as chemical oxygen demand. Proper pre-treatment method must be chosen in order to reduce fouling index. Coagulation pre-treatment using poly-aluminium chloride was chosen. Two thin film polysulfone membranes were used, purchased by Osmonic Desal. The focus of this research is to assess the influence of the particle size and zeta-potential of the colloidal fraction in leachate on nanofiltration performance. The isoelectric point of both membranes was 4.7 and 4.3, respectively. The fouled membranes were negatively charged over the pH range with isoelectric point shifting to the left (lower pH) indicating the foulant material mainly not charged. It was confirmed by its zeta-potential, measured at -2 mV.

In recent times, plant-mediated synthesis of nanoparticles has garnered wide interest owing to its inherent features such as rapidity, simplicity, eco-friendliness and cheaper costs. For the first time, silver nanoparticles were successfully synthesized using Calliandra haematocephala leaf extract in the current investigation. The as-formed silver nanoparticles were characterized by UV–Vis spectrophotometer and the characteristic surface plasmon resonance peak was identified to be 414 nm. The morphology of the silver nanoparticles was characterized by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) was used to detect the presence of elemental silver. X-ray diffraction (XRD) was employed to ascertain the crystalline nature and purity of the silver nanoparticles which implied the presence of (111) and (220) lattice planes of the face centered cubic (fcc) structure of metallic silver. Fourier transform infrared spectroscopy (FTIR) was used to key out the specific functional groups responsible for the reduction of silver nitrate to form silver nanoparticles and the capping agents present in the leaf extract. The stability of the silver nanoparticles was analyzed by zeta potential measurements. A negative zeta potential value of −17.2 mV proved the stability of the silver nanoparticles. The antibacterial activity against Escherichia coli – pathogenic bacteria – and the capacity to detect hydrogen peroxide by the silver nanoparticles were demonstrated which would find applications in the development of new antibacterial drugs and new biosensors to detect the presence of hydrogen peroxide in various samples respectively.

A series of recent works have demonstrated the spontaneous Ag+ adsorption onto gold surfaces. However, a mechanistic understanding of the Ag+ interactions with gold has been controversial. Reported herein is a systematic study of the Ag+ binding to AuNPs using several in-situ and ex-situ measurement techniques. The time-resolved UV-vis measurements of the AuNP surface plasmonic resonance revealed that the silver adsorption proceeds through two parallel pseudo-first order processes with a time constant of 16(±2) and 1,000(±35) s, respectively. About 95% of the Ag+ adsorption proceeds through the fast adsorption process. The in-situ zeta potential data indicated that this fast Ag+ adsorption is driven primarily by the long-range electrostatic forces that lead to AuNP charge neutralization, while the time-dependent pH data shows that the slow Ag+ binding process involves proton-releasing reactions that must be driven by near-range interactions. These experimental data, together with the ex-situ XPS measurement indicates that adsorbed silver remains cationic, but not as a charged-neutral silver atom proposed by the anti-galvanic reaction mechanism. The surface-enhanced Raman activities of the Ag+-stained AuNPs are slightly higher than that for AuNPs, but significantly lower than that for the silver nanoparticles (AgNPs). The SERS feature of the ligands on the Ag+-stained AuNPs can differ from that on both AuNPs and AgNPs. Besides the new insights to formation mechanism, properties, and applications of the Ag+-stained AuNPs, the experimental methodology presented in this work can also be important for studying nanoparticle interfacial interactions.

A better understanding of their interaction with cell-based tissue is a fundamental prerequisite towards the safe production and application of engineered nanomaterials. Quantitative experimental data on the correlation between physicochemical characteristics and the interaction and transport of engineered nanomaterials across biological barriers, in particular, is still scarce, thus hampering the development of effective predictive non-testing strategies. Against this background, the presented study investigated the translocation of gold and silver nanoparticles across the gastrointestinal barrier along with related biological effects using an in vitro 3D-triple co-culture cell model. Standardized in vitro assays and quantitative polymerase chain reaction showed no significant influence of the applied nanoparticles on both cell viability and generation of reactive oxygen species. Transmission electron microscopy indicated an intact cell barrier during the translocation study. Single particle ICP-MS revealed a time-dependent increase of translocated nanoparticles independent of their size, shape, surface charge, and stability in cell culture medium. This quantitative data provided the experimental basis for the successful mathematical description of the nanoparticle transport kinetics using a non-linear mixed effects modeling approach. The results of this study may serve as a basis for the development of predictive tools for improved risk assessment of engineered nanomaterials in the future.

Although hollow mesoporous silica nanoparticles (HMSNs) have been intensively studied as nanocarriers, selecting the right HMSNs for specific drugs still remains challenging due to the enormous diversity in so far reported HMSNs and drugs. To this end, we herein made a comprehensive study on drug loading in HMSNs from the viewpoint of impacting factors and loading efficiency. Specifically, two types of HMSNs with negative and positive zeta potential were delicately constructed, and three categories of drugs were selected as delivery targets: highly hydrophobic and lipophobic (oily), hydrophobic, and hydrophilic. The results indicated that (i) oily drugs could be efficiently loaded into both of the two HMSNs, (ii) HMSNs were not good carriers for hydrophobic drugs, especially for planar drugs, (iii) HMSNs had high loading efficiency towards oppositely charged hydrophilic drugs, i.e., negatively charged HMSNs for cationic molecules and vice versa, (iv) entrapped drugs would alter zeta potential of drug-loaded HMSNs. This work may provide general guidelines about designing high-payload HMSNs by reference to the physicochemical property of drugs.