Nm In Diameter Research Articles

Does the ionic distribution in the electrical double layer modify second harmonic scattering?

Surface-specific nonlinear optical techniques are ideally suited to investigate the complex structure of aqueous interfaces. For colloidal particles dispersed in aqueous solutions, interfacial properties can be retrieved with angle-resolved second harmonic scattering (AR-SHS). The mathematical framework of AR-SHS does not require a priori knowledge on the electrostatic distribution in the first few nanometers close to the interface, therefore allowing us to formulate a molecular-level description of the electrical double layer (EDL) based on the experimental data. However, farther away from the interface, an analytical form of the electrostatic potential decay is necessary to account for the distance dependence of the surface electrostatic field propagating into the solution. This requirement is especially important at low ionic strengths, where the electrostatic field is not efficiently screened by counterions. Here, we examine to what extent the analytical form of the electrostatic potential decay impacts the AR-SHS data analysis. We analyze the effect of different functions on the scattering form factors, on the integrated AR-SHS signal intensity, and on the surface parameters extracted from fitting the AR-SHS data. We find that the trends of the surface parameters remain similar regardless of the chosen function, demonstrating the robustness of our approach to establish a molecular-level picture of the EDL. At ionic strengths <10-4M for 100-nm diameter particles, a functional form that physically represents counterions packed more densely in the vicinity of the surface than in the case of the Poisson-Boltzmann distribution has the largest impact, resulting in an overestimation of the obtained surface potential.

Synthesis and characterization of Ag@Ni co-axial nanocables and their fluorescent and catalytic properties

Abstract We report here a convenient, rapid one-pot synthesis of new metal–metal core–shell nanocomposites comprising silver nanowires (AgNWs) coated with nickel. The resulting AgNWs and nickel-coated silver nanocables average 60–80 nm in diameter were prepared by the polyol synthetic route. This method employed ethylene glycol as a reducing agent and polyvinylpyrrolidone as a capping agent. These nanomaterials are designated as AgNWs (0.1 M) and Ag@Ni (0.2 M), Ag@Ni (0.3 M), Ag@Ni (0.4 M), and Ag@Ni (0.5 M) nanocables based on the nickel content and were characterized by scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), UV–Visible (UV–Vis) spectroscopy, and photoluminescence (PL) spectroscopy. The morphology of each nanowire and nanocable was clarified using SEM, while EDX quantified the presence of Ni. XRD patterns confirmed the face-centered cubic structure of the nanomaterials. The Debye–Scherrer formula was applied to establish different characteristics such as crystallite size and lattice constant. Surface plasmon resonance was measured using UV−Vis spectroscopy and fluorescence of each product was determined by PL spectroscopy, respectively. Both the AgNWs and Ag@Ni nanocables catalyze the reduction of p-nitrophenol to p-aminophenol by sodium borohydride.

PH- and Photoresponsive Liquid Plasticine.

Liquid marbles (LMs) can be prepared by adsorption of hydrophobic particles at the air-liquid interface of a water droplet. LMs have been studied for their application as microreaction vessels. However, their opaqueness poses challenges for internal observation. Liquid plasticines (LPs), akin to LMs, can be prepared by the adsorption of hydrophobic particles with a diameter of 50 nm or less, at the air-liquid interface of a water droplet. Unlike LMs, LPs are transparent, allowing for internal observation, thus presenting promising applications as reactors and culture vessels on a microliter scale. In this study, the surface of silica particles, approximately 20 nm in diameter, was rendered hydrophobic to prepare hydrophobic silica particles (SD0). A small amount of poly(2-(diisopropylamino)ethyl methacrylate) (PDPA) was then grafted onto the surface of SD0, yielding SD1. SD0 particles exhibited consistent hydrophobicity irrespective of the environmental pH atmosphere. Under acidic conditions, SD1 became hydrophilic due to the protonation of pendant tertiary amines in the grafted PDPA chains. However, SD1 alone was unsuitable for LP preparation due to its high surface wettability regardless of atmospheric pH, attributable to the presence of PDPA-grafted chains. Therefore, to prepare pH-responsive LP, SD1 and SD0 were mixed (SD1/SD0 = 3/7). Upon exposure to HCl gas, these LPs ruptured, with the leaked water from the LPs being absorbed by adjacent paper. Moreover, clear LPs, prepared using an aqueous solution containing a water-soluble photoacid generator (PAG), disintegrated upon exposure to light as PAG generated acid, leading to LP breakdown. In summary, pH-responsive LPs, capable of disintegration under acidic conditions and upon light irradiation, were successfully prepared in this study.

Comparative transcriptomics revealed neurodevelopmental impairments and ferroptosis induced by extremely small iron oxide nanoparticles

Iron oxide nanoparticles are a type of nanomaterial composed of iron oxide (Fe3O4 or Fe2O3) and have a wide range of applications in magnetic resonance imaging. Compared to iron oxide nanoparticles, extremely small iron oxide nanoparticles (ESIONPs) (∼3 nm in diameter) can improve the imaging performance due to a smaller size. However, there are currently no reports on the potential toxic effects of ESIONPs on the human body. In this study, we applied ESIONPs to a zebrafish model and performed weighted gene co-expression network analysis (WGCNA) on differentially expressed genes (DEGs) in zebrafish embryos of 48 hpf, 72 hpf, 96 hpf, and 120 hpf using RNA-seq technology. The key hub genes related to neurotoxicity and ferroptosis were identified, and further experiments also demonstrated that ESIONPs impaired the neuronal and muscle development of zebrafish, and induced ferroptosis, leading to oxidative stress, cell apoptosis, and inflammatory response. Here, for the first time, we analyzed the potential toxic effects of ESIONPs through WGCNA. Our studies indicate that ESIONPs might have neurotoxicity and could induce ferroptosis, while abnormal accumulation of iron ions might increase the risk of early degenerative neurological diseases.

Cutting nanodisks in graphene down to 20 nm in diameter

A direct focused He+ beam direct machining is presented to fabricate solid-state nano-disk at the surface of a graphene multilayer micro-flake deposited on an Au/Ti/sapphire surface. At irradiation doses larger than 5.0 × 1017 ions cm−2 and with a beam size well below 1 nm, graphene disks down to 20 nm in diameter have been machined with for nano-disk down to 50 nm in diameter, a central hole for preparing the positioning of a rotation axle. The local heat generated by this irradiation is inducing a partial graphene amorphization and deformation, leading to a complete graphene nano-disk vaporization at doses larger than 5 × 1018 ions cm−2. A dry transfer printing technique followed by a graphene surface cleaning was used to transfer the nano-disks from its initial surface to a fresh and clean surface. Tapping mode atomic force micrograph have been recorded to follow the vaporization as a function of the He+ dose to confirm the graphene solid-state nano-disk fabrication limit to about 20 nm with this process.

Identification and molecular characterization of two novel viruses from Allamanda cathartica in China.

Allamanda cathartica is an ornamental medicinal plant that grows widely in the tropics. In the present study, two novel viruses, Allamanda chlorotic virus A (AlCVA) and Allamanda chlorotic virus B (AlCVB), were identified in an A. cathartica plant with interveinal chlorosis by ribosomal RNA-depleted total-RNA sequencing. Phylogenetic analysis and sequence comparisons confirmed that AlCVA and AlCVB belong to the families Closteroviridae and Betaflexiviridae, respectively. Long, flexuous, filamentous virus particles approximately 12 nm in diameter and 784-2291 nm in length were observed using transmission electron microscopy. A specific RT-PCR assay was used to demonstrate a consistent association of viral infection with symptoms.

Kinetic study of adsorption and photocatalytic degradation of methylene blue dye using TiO2 nanoparticles with activated carbon

Abstract Activated carbon (AC) exhibits limited adsorption capacity for pollutants. Conversely, titanium dioxide (TiO2) demonstrates excellent photocatalytic performance, making it a popular choice for pollutant removal. This study investigates the removal of methylene blue (MB) dye from wastewater using AC, TiO2@AC-2, and TiO2@AC-10 samples via adsorption and photocatalysis. The Energy Dispersive analysis of X-rays (EDAX) has confirmed the presence of Ti, C and O in the prepared samples without any impurities. All the diffraction peaks in X-ray diffractograms indicated the presence of pure anatase TiO2 (tetragonal phase) with no evidence of any other phase. Fourier transform infrared spectroscopy (FTIR) analysis identified a peak around 545 cm⁻¹ in the TiO2@AC-2 sample, indicative of O-Ti-O stretching vibrations. This peak shifted to 602 cm⁻¹ in the TiO2@AC-10 sample. Raman spectroscopy confirmed the presence of carbon (D and G bands) at 1310-1347 cm⁻¹ and 1582-1597 cm⁻¹. Additionally, characteristic Raman active bands for anatase TiO2 were observed at 154 cm⁻¹ (Eg), 204 cm⁻¹ (Eg), 398 cm⁻¹ (B1g), 508 cm⁻¹ (A1g), and 628 cm⁻¹ (Eg). N2 adsorption-desorption isotherms revealed a mesoporous structure for all samples (AC, TiO2@AC-2, and TiO2@AC-10) with hysteresis loops, indicating pores ranging from 2 nm to 50 nm in diameter. Reflectance spectra of TiO2@AC-2 and TiO2@AC-10 displayed absorption edges at 368 nm and 385 nm, respectively, corresponding to a direct band gap of approximately 3.22 eV. Subsequently, these prepared samples were effectively employed for the removal of methylene blue (MB) dye from wastewater utilizing both adsorption and photocatalysis method. Under dark conditions, 20 mg/L doses of TiO2@AC-2 and TiO2@AC-10 resulted in 60% and 36% dye adsorption within 60 minutes respectively. In the presence of UV radiation, the degradation of dye was observed to be 74% and 95% by TiO2@AC-2 and TiO2@AC-10 respectively. This observation indicates that TiO2 nanoparticles along with AC leads to enhanced photocatalytic activity. The Langmuir-Hinshelwood model reveals lower rate constants for AC compared to the composite samples. This is likely because AC lacks inherent catalytic activity, requiring UV light to trigger adsorption. Conversely, TiO2@AC-10 exhibits the highest rate constants (K1 = 24.25 × 10-3 min⁻¹ and K2 = 82.71 × 10-3 min⁻¹), aligning with its higher TiO2 content confirmed by EDAX analysis. This suggests a significantly faster photocatalytic rate and superior degradation efficiency, even at a low sample concentration (20 mg/L).

Self-assembly of the porphyrin monomer on the surface of Fe/graphene material: a novel sensing material for the detection of chloramphenicol antibiotic in aqueous solution.

Currently, electrochemical sensors are in the process of being developed and widely used in various fields, and new materials are being explored to enhance the precision and selectivity of the sensors.The Fe/graphene nanoparticles were synthesized utilizing a green approach, wherein leaf extract was employed as the reducing agent. The resulting materials underwent comprehensive characterization utilizing a range of contemporary techniques, including scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and Raman spectroscopy. The findings of the study revealed that the nanocomposites of Fe/graphene/porphyrin comprised zero-valent iron nanoparticles, exhibiting an average particle size ranging from 15 to 60 nm. These nanoparticles were seen to be evenly dispersed across the graphene sheets. The presence of nanostructure porphyrin nanofibers, measuring 20 nm in diameter, was also shown to exhibit strong integration with the surface of the Fe/graphene nanomaterials. The electrochemical properties of the Fe/graphene/porphyrin nanocomposite were also investigated, demonstrating that the prepared material could be effectively employed as a sensing electrode in the electrochemical sensor for detecting Chloramphenicol (CAP) through CV, EIS, and DPV techniques using a three-electrode electrochemical system. Under optimal conditions, Fe/graphene/porphyrin exhibited a high current response when detecting CAPs.

Selected ice nanoparticle accelerator hypervelocity impact mass spectrometer (SELINA-HIMS): features and impacts of charged particles.

The selected ice nanoparticle accelerator, SELINA, was used to prepare beams of single ice particles with positive or negative charge. Positively charged particles were prepared from deionized water and 0.05-0.2 molar solutions of sodium chloride in water, and negatively charged ice particles were generated from water without salt. Depending on the electrospray source configuration, the measured particles vary from 50 to 1000 nm in diameter. The kinetic energy per charge for all particles was set to 200 eV by the collisional equilibration in quadrupoles, which resulted in primary velocities up to 600 m/s for the lowest m/z particles. The electrospray ionization and thus particle formation from SELINA become less efficient with increasing salt concentration, resulting in a lower detected particle frequency and size. Good instrument operation is achievable for concentrations below 0.2 M. After we have verified and characterized positively and negatively charged ice particles, we have combined SELINA with a target and time-of-flight spectrometer for a 'proof-of-principle' post acceleration of 120 nm particles towards hypervelocity (v ~ 3000 m/s) and detection of fragments from the particle impact (SELINA-HIMS). General conditions are discussed for the acceleration of particles between 50 and 1000 nm to velocities well above 3000 m/s with SELINA-HIMS instrument. This article is part of the theme issue 'Dust in the Solar System and beyond'.

Polystyrene Plastic Particles Result in Adverse Outcomes for Hyalella azteca When Exposed at Elevated Temperatures

Micro- and nano-plastics are pervasive pollutants in global ecosystems, yet their interactions with aquatic wildlife and abiotic factors are poorly understood. These particles are recognized to cause subtle detrimental effects, underscoring the necessity for sensitive endpoints in ecotoxicological exposure studies. We investigated the effects of particle uptake, size, and temperature on Hyalella azteca. Organisms were exposed to blue fluorescent polystyrene beads (500 nm and 1000 nm in diameter) at 0.43 mg/L for 96 h at temperatures mirroring climate predictions (21 °C, 24 °C, 27 °C). Besides survival and growth, particle uptake, visualized via confocal microscopy, and swimming behavior were analyzed. Mortality rates increased at 27 °C, and particle presence and temperature affected organism growth. Particle treatments influenced various behaviors (thigmotaxis, cruising, movement, acceleration, meander, zone alternation, and turn angle), with hypoactivity observed with 1000 nm particles and hypo- as well as hyper-activity responses with 500 nm particles. Particle uptake quantities were variable and increased with temperature in 500 nm treatments, but no migration beyond the gut was observed. Particle size correlated with uptake, and relationships with behavior were evident. Elevated temperatures exacerbated particle effects, highlighting the urgency of addressing plastic pollution in light of climate change for aquatic organism welfare and ecosystem health.

Long-Chain Lipids Facilitate Insertion of Large Nanoparticles into Membranes of Small Unilamellar Vesicles.

Insertion of hydrophobic nanoparticles into phospholipid bilayers is limited to small particles that can incorporate into a hydrophobic membrane core between two lipid leaflets. Incorporation of nanoparticles above this size limit requires the development of challenging surface engineering methodologies. In principle, increasing the long-chain lipid component in the lipid mixture should facilitate incorporation of larger nanoparticles. Here, we explore the effect of incorporating very long phospholipids (C24:1) into small unilamellar vesicles on the membrane insertion efficiency of hydrophobic nanoparticles that are 5-11 nm in diameter. To this end, we improve an existing vesicle preparation protocol and utilized cryogenic electron microscopy imaging to examine the mode of interaction and evaluate the insertion efficiency of membrane-inserted nanoparticles. We also perform classical coarse-grained molecular dynamics simulations to identify changes in lipid membrane structural properties that may increase insertion efficiency. Our results indicate that long-chain lipids increase the insertion efficiency by preferentially accumulating near membrane-inserted nanoparticles to reduce the thermodynamically unfavorable disruption of the membrane.

Structural colour in the brown algal genus Sporochnus (Sporochnales, Phaeophyceae)

ABSTRACT The colour produced by an object’s microstructure rather than by pigments is generally called structural colour. Various macroalgae have some mechanisms of structural colouration. The presence of structural colour in the brown algae is well known in the Dictyotales and Fucales but has recently been reported in the Sporochnales where Sporochnus dotyi has structures in the terminal assimilatory filaments (trichothallic hairs) that produce a pronounced green iridescence. Based on observations by light microscopy, the structural colour of this species was caused by iridescent bodies, 10–15 µm in diameter, within the cells of assimilatory filaments. In contrast, another Sporochnus species known as S. radiciformis in Japan (S. radiciformis auct. japon.) also contains iridescent bodies of 6–10 µm diameter in the assimilatory filaments, but no significant structural colour was observed. In epi-illumination observations using red, green and blue LED light sources, iridescent bodies of S. dotyi showed stronger reflection of green compared with red and blue, whereas the reflections were similar among those colours in S. radiciformis. Transmission electron microscopy (TEM) using a rapid freezing method revealed that homogeneous globules 130–160 nm in diameter were tightly packed inside the iridescent bodies of S. dotyi, whereas the sizes of the globules were markedly irregular in iridescent bodies of S. radiciformis. Therefore, we conclude that the structural colouration of S. dotyi is caused by the interference and diffraction of incident light caused by the crystal lattice-like structure of tightly packed and regularly arranged globules of homogeneous size in the iridescent bodies, which is similar to the mechanism causing iridescence in opal. A similar opal-like structure of iridescent bodies causing structural colouration was recently reported in Ericaria selaginoides, but that of S. dotyi lacked the dynamic shift of the globules shown in E. selaginoides that resulted in a change of the wavelength of reflected light.

Preparation of silymarin-loaded zein polysaccharide core–shell nanostructures and evaluation of their biological potentials

Abstract Silymarin-loaded zein polysaccharide core–shell nanoparticles (SZPCS-NPs) were synthesized where sodium alginate and pectin offer stability and controlled release qualities to zein, a maize protein, having excellent biocompatibility. The present study is an attempt to develop zein–silymarin polysaccharide core–shell nanostructures to enhance water solubility, thereby improving bioavailability and producing enhanced biological responses in living systems. SZPCS-NPs were prepared using pH-induced antisolvent precipitation method. Five different types of SZPCS-NPs were synthesized using different combinations of sodium alginate and pectin, namely P100–A00 (non-uniform size ranging from 20 to 100 nm), P70–A30 (spherical and uniform size measuring approximately 80 nm in diameter), P50–A50, P30–A70, and P00–A100 exhibited irregular shapes with the presence of some triangular and oval structures and non-uniform size ranging from 20 to 100 nm. The SZPCS-NPs P70–A30 possessed the best results in terms of shape, size, and other characterization studies. Furthermore, the SZPCS-NPs possessed a percent drug loading of 72.5% and entrapment efficiency of 51.7%, respectively. The resulting SZPCS-NPs exhibited an excellent relative bioavailability percentage of 97.4% in comparison to commercial silymarin, having 58.1%, and crude silymarin, having 46.97% bioavailability percentage, correspondingly. In addition, SZPCS-NPs possessed an almost two folds’ increase in antioxidant activity in comparison to crude and commercially available silymarin. Similarly, SZPCS-NPs also showed better stabilization in hepatic biomarker enzymes and possessed better hepatoprotective activity for a period of 6 weeks, in contrast to commercial and crude silymarin formulations.

Long-term polystyrene nanoparticles exposure reduces electroretinal responses and exacerbates retinal degeneration induced by light exposure

The impact of plastic pollution on living organisms have gained significant research attention. However, the effects of nanoplastics (NPs) on retina remain unclear. This study aimed to investigate the effect of long-term polystyrene nanoparticles (PS-NPs) exposure on mouse retina. Eight weeks old C57BL/6J mice were exposed to PS-NPs at the diameter of 100nm and concentration of 10mg/L in drinking water for 3 months. PS-NPs were able to penetrate the blood-retina barrier, accumulated at retinal tissue, caused increased oxidative stress level and reduced scotopic electroretinal responses without remarkable structural damage. PS-NPs exposure caused cytotoxicity and reactive oxygen species accumulation in cultured photoreceptor cell. PS-NPs exposure increased oxidative stress level in retinal pigment epithelial (RPE) cells, leading to changes of gene and protein expression indicative of compromised phagocytic activity and cell junction formation. Long-term PS-NPs exposure also aggravated light-induced photoreceptor cell degeneration and retinal inflammation. The transcriptomic profile of PS-NPs-exposed, light-challenged retinal tissue shared similar features with those of age-related macular degeneration (AMD) patients in the activation of complement-mediated phagocytic and proinflammatory responses. Collectively, these findings demonstrated the oxidative stress- and inflammation-mediated detrimental effect of PS-NPs on retinal function, suggested that long-term PS-NPs exposure could be an environmental risk factor contributing to retinal degeneration.

Staphylococcus Aureus Membrane Vesicles Kill Tumor Cells Through a Caspase-1-Dependent Pyroptosis Pathway.

Nanosized outer membrane vesicles (OMVs) from Gram-negative bacteria have attracted increasing interest because of their antitumor activity. However, the antitumor effects of MVs isolated from Gram-positive bacteria have rarely been investigated. MVs of Staphylococcus aureus USA300 were prepared and their antitumor efficacy was evaluated using tumor-bearing mouse models. A gene knock-in assay was performed to generate luciferase Antares2-MVs for bioluminescent detection. Cell counting kit-8 and lactic dehydrogenase release assays were used to detect the toxicity of the MVs against tumor cells in vitro. Active caspase-1 and gasdermin D (GSDMD) levels were determined using Western blot, and the tumor inhibition ability of MVs was determined in B16F10 cells treated with a caspase-1 inhibitor. The vesicular particles of S. aureus USA300 MVs were 55.23 ± 8.17 nm in diameter, and 5 μg of MVs remarkably inhibited the growth of B16F10 melanoma in C57BL/6 mice and CT26 colon adenocarcinoma in BALB/c mice. The bioluminescent signals correlated well with the concentrations of the engineered Antares2-MVs (R2 = 0.999), and the sensitivity for bioluminescence imaging was 4 × 10-3 μg. Antares2-MVs can directly target tumor tissues in vivo, and 20 μg/mL Antares2-MVs considerably reduced the growth of B16F10 and CT26 tumor cells, but not non-carcinomatous bEnd.3 cells. MV treatment substantially increased the level of active caspase-1, which processes GSDMD to trigger pyroptosis in tumor cells. Blocking caspase-1 activation with VX-765 significantly protected tumor cells from MV killing in vitro and in vivo. S. aureus MVs can kill tumor cells by activating the pyroptosis pathway, and the induction of pyroptosis in tumor cells is a promising strategy for cancer treatment.

Sb-doped tin oxide nanonets for improved conductivity in transparent conductive coatings

In light of the three primary challenges faced by transparent conductive coatings, namely poor conductivity, elevated the active substance content, and insufficient visible light transmittance, net-like conductive agents due to the unique morphology and structure have been developed to address these concerns simultaneously. A straightforward synthesis of antimony-doped tin oxide (ATO) nanonets was accomplished through a simple two-step coprecipitation and hydrothermal methods. Firstly, an antimony-doped stannic hydroxide hydrogel precursor was generated through coprecipitation. Secondly, by adjusting the pH value in the hydrothermal reaction, ATO nanocrystals network were obtained without the need for additional materials. The synthesized ATO, with a net-like morphology, comprises particles of approximately 3-5 nm in diameter. Throughout the reaction, ammonium hydroxide, used as a pH regulator, played a vital role as a reducing agent in forming ATO nanonets without the need for further post-treatment. Moreover, net-like ATO compounded with SiO2 transparent conductive coatings exhibited exceptional transparent conductive properties, with a visible-light transmittance of approximately 84.7% at the wavelength of 550 nm and a square resistance of 0.5 kΩ/sq upon spin-coating deposition on glass. This remarkable performance can be attributed to the generation of a continuous conductive network. In comparison to granular ATO, the network structure ATO nanocrystal showcases a significant improvement in resistivity, demonstrating its exemplary transparent conductivity. The approach for the preparation of ATO nanonets was simple and easy to scale up to provide an enormous potential and broad prospect for the application of net-like ATO in transparent conductive coating.

Simultaneous Detection of Carbon Quantum Dots as Tracers for Interwell Connectivity Evaluation in a Pattern with Two Injection Wells.

This study aimed to develop and implement a nanotechnology-based alternative to traditional tracers used in the oil and gas industry for assessing interwell connectivity. A simple and rapid hydrothermal protocol for synthesizing carbon quantum dots (CQDs) using agroindustry waste was implemented. Three commercial CQDs were employed (CQDblue, CQDgreen, and CQDred); the fourth was synthesized from orange peel (CQDop). The CQDs from waste and other commercials with spherical morphology, nanometric sizes less than 11 nm in diameter, and surface roughness less than 3.1 nm were used. These tracers demonstrated high colloidal stability with a negative zeta potential, containing carbonyl-type chemical groups and unsaturations in aromatic structures that influenced their optical behavior. All materials presented high colloidal stability with negative values of charge z potential between -17.8 and -49.1. Additionally, individual quantification of these tracers is feasible even in scenarios where multiple CQDs are present in the effluent with a maximum percentage of interference of 15.5% for CQDop in the presence of the other three nanotracers. The CQDs were injected into the field once the technology was insured under laboratory conditions. Monitoring the effluents allowed the determination of connectivity for five first-line producer wells. This study enables the application of CQDs in the industry, particularly in fields where the arrangement of injector and producer wells is intricate, requiring the use of multiple tracers for a comprehensive description of the system.

A new strategy for the treatment of middle ear infection using ciprofloxacin/amoxicillin-loaded ethyl cellulose/polyhydroxybutyrate nanofibers

A middle ear infection occurs due to the presence of several microorganisms behind the eardrum (tympanic membrane) and is very challenging to treat due to its unique location and requires a well-designed treatment. If not treated properly, the infection can result in severe symptoms and unavoidable side effects. In this study, excellent biocompatible ethyl cellulose (EC) and biodegradable polyhydroxybutyrate (PHB) biopolymer were used to fabricate drug-loaded nanofiber scaffolds using an electrospinning technique to overcome antibiotic overdose and insufficient efficacy of drug release during treatment. PHB polymer was produced from Halomonas sp., and the purity of PHB was found to around be 90 %. Additionally, ciprofloxacin (CIP) and amoxicillin (AMX) are highly preferable since both drugs are highly effective against gram-negative and gram-positive bacteria to treat several infections. Obtained smooth nanofibers were between 116.24 and 171.82 nm in diameter and the addition of PHB polymer and antibiotics improved the morphology of the nanofiber scaffolds. Thermal properties of the nanofiber scaffolds were tested and the highest Tg temperature resulted at 229 °C. The mechanical properties of the scaffolds were tested, and the highest tensile strength resulted in 4.65 ± 6.33 MPa. Also, drug-loaded scaffolds were treated against the most common microorganisms that cause the infection, such as S.aureus, E.coli, and P.aeruginosa, and resulted in inhibition zones between 10 and 21 mm. MTT assay was performed by culturing human adipose-derived mesenchymal stem cells (hAD MSCs) on the scaffolds. The morphology of the hAD MSCs' attachment was tested with SEM analysis and hAD MSCs were able to attach, spread, and live on each scaffold even on the day of 7. The cumulative drug release kinetics of CIP and AMX from drug-loaded scaffolds were analysed in phosphate-buffered saline (pH: 7.4) within different time intervals of up to 14 days using a UV spectrophotometer. Furthermore, the drug release showed that the First-Order and Korsmeyer-Peppas models were the most suitable kinetic models. Animal testing was performed on SD rats, matrix and collagen deposition occurred on days 5 and 10, which were observed using Hematoxylin-eosin and Masson's trichrome staining. At the highest drug concentration, a better repair effect was observed. Results were promising and showed potential for novel treatment.

Deterministic Single-Row-Droplet Catalyst Formation for Uniform Growth Integration of High-Density Silicon Nanowires.

Planar silicon nanowires (SiNWs), grown by using low temperature catalytic approaches, are excellent 1D channel materials for developing high-performance logics and sensors. However, a deterministic position and size control of the metallic catalyst droplets, that lead to the growth of SiNWs, remains still a significant challenge for reliable device integration. In this work, we present a convenient but powerful edge-trimming catalyst formation strategy, which can help to produce a rather uniform single-row of indium (In) catalyst droplets of Dcat = 67 ± 5 nm in diameter, with an exact one-droplet-on-one-step arrangement. This approach marks a significant achievement in self-assembled catalyst formation and offers a foundation to attain a reliable and scalable growth of density SiNW channels, via an in-plane solid-liquid-solid (IPSLS) mechanism, with a uniform diameter down to Dnw = 35 ± 4 nm, and do not rely on high-precision lithography techniques. Prototype SiNW-based field effect transistors (FETs) are also fabricated, with a high Ion/Ioff current ratio and small subthreshold swing of >107 and 262 mV·dec-1, respectively, indicating a reliable new routine to integrate a wide range of SiNW-based logic, sensor, and display applications.

Bone marrow mesenchymal stem cell-derived extracellular vesicles promote corneal epithelial repair and suppress apoptosis via modulation of Caspase-3 in vitro.

Corneal injuries are the major cause of blindness and visual impairment. Available treatments are limited by their efficacy and side effects. Mesenchymal stem cell-derived extracellular vesicles are presumed as functional equivalents and potential candidates for cell-free therapy. This study reports isolation and characterization of extracellular vesicles from human bone marrow mesenchymal stem cells and evaluates their role in mediating epithelial repair and apoptosis in cultured corneal epithelial cells through scratch assay, PCR, immunofluorescence, and flow cytometry in vitro. The isolated extracellular vesicles were spherical, < 150 nm in diameter, and characterized as CD9+, CD63+, CD81+, TSG101+, and Calnexin-. Further, these vesicles promoted corneal epithelial repair by enhancing proliferation and suppressed apoptosis by regulating the expression of BAD, P53, BCL-2, and cleaved CASPASE-3. Thus, our results suggest that BM-MSC-EVs might have the potential to be used for the treatment of injury-induced corneal epithelial defects. Clinical translation of this work would require further investigations.