Transmission Electron Microscopy Micrographs Research Articles

Study of Pure and Mixed-Phase TiO2 Nanomaterials Synthesized via a Modified Solvothermal Method and Their Optical Properties

The modified-solvothermal method has been used to synthesize pure anatase and anatase-rutile mixed-phase TiO2 nanomaterials using titanium isopropoxide, sodium hydroxide, and triethylamine as primary sources with different calcination temperatures (500 °C and 700 °C). The effect of the precipitating agent, capping agent, and calcination temperatures on the properties, such as structural, morphological, and optical of the resultant nanomaterials has been investigated through several techniques including X-ray diffraction (XRD), Raman spectroscopy, Transmission electron microscopy (TEM), UV–Vis absorption spectroscopy, Scanning electron microscopy (SEM), selected area electron diffraction (SAED), and high-resolution transmission electron microscopy (HRTEM). XRD and Raman spectra confirmed the pure anatase and anatase-rutile mixed structures of the prepared nanomaterials at 500 °C and 700 °C. Furthermore, the Raman active modes confirmed the formation of TiO2. It is noticed that the crystallite size of the nanomaterials increased with increasing calcination temperature of the XRD pattern. The morphologies of the prepared samples were displayed using SEM and TEM micrographs, which are almost the same in shape (cubic and cubic rod mixed). The particle size increased with an increase in calcination temperature and was found to be between 10 and 20 nm, which is similar to the crystallite size. The lattice fringes (d) from HRTEM images are assigned to the XRD plane (101) and (110) plane of anatase and anatase-rutile TiO2, respectively. The SAED exhibited well crystalline nature and confirmed the polycrystalline nature of the prepared nanomaterials by the bright points and the ring patterns. The optical band gap decreased with an increase in temperature and the optical properties are affected by calcination temperature and triethylamine.

Accurate quantification of dislocation loops in complex functional alloys enabled by deep learning image analysis

In-depth statistics of individual defects observed during transmission electron microscopy (TEM) experiments are essential for the thorough characterization of materials. In this study, we aim to quantitatively characterize the population of dislocation loops in ion-irradiated CrFeMnNi alloys. To this end, we propose an efficient guideline to prepare TEM micrographs dataset for deep learning analysis, adapted for accurate characterization of microstructures produced by thousands of overlapping defects, a very common situation in TEM images, unfeasible by previous existing methods. To reduce human effort, we annotate only a few images and complement the database through a two-step process: initially, singular value decomposition to normalize image background, followed by a controlled data augmentation. The performed analysis provides precise quantitative information about the number of loops of different types, as well as their spatial distribution, their size, and the inter-object distances. These characteristics provide insights into the nucleation, mobility, and growth of dislocation loops, as well as the elastic anisotropy of the material. Our results emphasize how accurate analysis of complex microstructures can provide insights into the physical properties of materials and open up many perspectives for attaining quantitative information on materials properties based solely on their image analysis.

Utility of Microwave-Synthesized Silver Nano Particles as Spectrofluorimetric Sensors for the Determination of Nano Concentrations of Favipravir: Application to Dosage Forms and Spiked Human Plasma.

A simple and facile microwave-assisted method was developed for the synthesis of highly fluorescent silver-nanoparticles (Ag-NPs). The synthesis of silver-nanoparticles depends on a redox reaction between silver nitrate and ascorbic acid using chitosan as a stabilizing agent. The produced Ag-NPs were characterized using Zeta potential and transmission electron microscope micrograph where they are spherical in shape with smooth surface morphology and size of 26.81 ± 2.2nm. Favipiravir (FAV) was found to cause an obvious enhancement in the fluorescence of Ag-NPs; hence, they were used for its spectrofluorimetric estimation. The fluorescence intensity was measured at 430nm after excitation at 360nm. Under optimum conditions, a good linear relationship was accomplished between the FAV concentration and the fluorescence intensity in a range of (5.0-200.0) ng/mL with a limit of detection of 1.59 ng/mL. The method was successfully applied for the assay of the drug in its commercial tablets and spiked human plasma samples, and the results obtained were satisfactory.

Banana fruit (Musa sp.) DNA-magnetite nanoparticles: Synthesis, characterization, and biocompatibility assays on normal and cancerous cells.

Magnet-mediated gene therapy has gained considerable interest from researchers as a novel alternative for treating genetic disorders, particularly through the use of superparamagnetic iron oxide nanoparticles (NPs)-such as magnetite NPs (Fe3O4NPs)-as non-viral genetic vectors. Despite their commercial availability for specific genetic transfection, such as in microglia cell lines, many potential uses remain unexplored. Still, ethical concerns surrounding the use of human DNA often impede genetic research. Hence, this study examined DNA-coated Fe3O4NPs (DNA-Fe₃O₄NPs) as potential transfection vectors for human foreskin fibroblasts (HFFs) and A549 (lung cancer) cell lines, using banana (Musa sp.) as a low-cost, and bioethically unproblematic DNA source. Following coprecipitation synthesis, DNA-Fe₃O₄NP characterization revealed a ζ-potential of 40.65 ± 4.10 mV, indicating good colloidal stability in aqueous media, as well as a superparamagnetic regime, evidenced by the absence of hysteresis in their magnetization curves. Successful DNA coating on the NPs was confirmed through infrared spectra and surface analysis results, while magnetite content was verified via characteristic X-ray diffraction peaks. Transmission electron microscopy (TEM) determined the average size of the DNA-Fe3O4NPs to be 14.69 ± 5.22 nm. TEM micrographs also showed no morphological changes in the DNA-Fe3O4NPs over a 30-day period. Confocal microscopy of HFF and A549 lung cancer cell lines incubated with fluoresceinamine-labeled DNA-Fe3O4NPs demonstrated their internalization into both the cytoplasm and nucleus. Neither uncoated Fe3O4NPs nor DNA-Fe3O4NPs showed cytotoxicity to A549 lung cancer cells at 1-50 μg/mL and 25-100 μg/mL, respectively, after 24 h. HFFs also maintained viability at 1-10 μg/mL for both NP types. In conclusion, DNA-Fe3O4NPs were successfully internalized into cells and exhibited no cytotoxicity in both healthy and cancerous cells across a range of concentrations. These NPs, capable of binding to various types of DNA and RNA, hold promise for applications in gene therapy.

Characterization and antibacterial application of peppermint essential oil nanoemulsions in broiler

In order to mitigate the risk of antibiotic resistance in poultry, scientists nowadays consider plant secondary metabolites to be a major organic antibacterial substitute. This study aimed to characterize and investigate the in silico, in vitro, and in vivo antibacterial effects of peppermint essential oil (PEO) in the form of a nanoemulsion (NE), termed PEONE. Menthol as a major compound of PEO has been identified by gas chromatography and mass spectroscopy (GCMS) analysis as 32.3 %, while lower droplet size, polydispersity Index (PDI), and optimum zeta potential values depicted the stability of PEONE have been observed and validated by transmission electron microscopy (TEM) micrograph image. In silico antibacterial activity was studied by molecular docking of menthol and enrofloxacin with Topoisomerase IV protein (PDB: 1s16;) of Escherichia coli K12 MG1655 and this effect was validated by in vitro and in vivo analysis. In vitro analysis, sustained release of PEONE has been observed against Escherichia coli and Staphylococcus aureus. In this study for in vivo experiments (n = 90) day-old broiler chicks were distributed into 6 dietary treatments with 5 replicates of 3 birds per replication. Dietary treatments included 1) Negative control (basal diet), 2) Positive control (basal diet + 200 µl enrofloxacin), 3) 25 µl PEONE + basal diet, 4) 50 µl PEONE + basal diet, 5) 75 µl PEONE + basal diet, and 6) 100 µl PEONE + basal diet. Analyzed data by different statistical tools confirmed that PEONE significantly affected body weight gain (BWG) with an improved feed conversion ratio (FCR) compared to the control group. A significant increase in cecal Lactobacillus count and a decrease in total coliform was observed. Positive effects on physiological parameters, visceral organs, and meat quality characteristics have been observed. In conclusion, our experiments suggest that PEONE can be used in the broiler industry as a substitute for antibiotics to minimize bacterial resistance.

Evaluation of antioxidant, catalytic and antidiabetic activity of Phaseolus vulgaris (French green bean) mediated nickel oxide and copper doped nickel oxide bimetallic nanoparticles

In this study, nickel oxide nanoparticles (NPs) and copper doped NiO bimetallic nanoparticles (Cu@NiO BMNPs) were synthesized using Phaseolus vulgaris extracts as reducing and stabilizing agents by sol gel methods. The chemical and physical properties of synthesized NiO NPs and Cu@NiO BMNPs were confirmed by various techniques, like UV Visible spectrophotometer (UV–Vis), Fourier transform infrared spectroscopy (FTIR), Scanning Electron Microscope (SEM), Energy Dispersive X-ray (EDX), Transmission Electron Microscope (TEM) and X-ray diffraction (XRD) analysis. The optical properties of both NPs observed by UV–Vis analysis with well-defined peak and band gap value 3.2 eV & 2.62 eV. FTIR analysis confirmed the presence of functional group of NPs with fruits extract. The morphology of NPs was confirmed by SEM and TEM analysis as polygonal, rod and spherical shape. The elements present in NPs were confirmed by EDX analysis. The crystalline size calculated based on the XRD analysis was 49.78 nm and 53.66 nm for NiO and Cu@ NiO NPs respectively which were found to be slightly smaller than particle size determined from SEM and TEM micrograph. Antioxidant activity of NPs was examined using 2,2-Diphenyl-1-picrylhydrazyl (DPPH) scavenging radicals, Catalytic activities were screened by the degradation of Methylene blue (MB) and by the inhibition of alpha-amylase enzyme, antidiabetic activity of NPs were evaluated using acarbose as standard drug. The Cu@NiO BMNPs showed 77.60 % antioxidant, 76.98 % photocatalytic and 88.86 % antidiabetic activity, which were found to be more as compared to NiO NPs. The NiO and Cu@NiO BMNPs were synthesized for the first-time using P. vulgaris extracts. This study clearly showed that P. vulgaris extracts mediated mono- and bimetallic NPs were more stable and biocompatible than their respective bulk particles.

Synthesis and characterization of fluorescent carbon dots obtained from citrus x sinensis by an eco-friendly method

The synthesis and characterization of fluorescent carbon dots (CDs) obtained by an environmentally friendly method through carbonization, fragmentation and centrifugation of orange peel (citrus x sinensis) are reported. By thermogravimetry, 4 degradation regions associated with hemicellulose, lignin and organic matter were found. The SEM micrograph shows a rough surface morphology with flakes and granulation due to the carbonization process. X-ray diffraction (XRD) shows a hexagonal crystalline structure associated with graphitic carbon, which was confirmed by Raman scatterings, Raman spectroscopy that presented two main vibrational bands, D and G, associated with active defects in the graphitic carbon crystalline structure. The Transmission electron microscopy (TEM) micrograph showed CDs of size 33.65 ± 0.68n, and with High-Resolution TEM (HRTEM) an interplanar distance of 0.213 nm in the direction of the crystal planes (100) of graphitic carbon was obtained, which were confirmed by XRD and Raman spectroscopy. X-ray photoelectron spectroscopy revealed the relative atomic composition and identified the strongest photoelectron transitions of carbon, sp2 (286 eV) and sp3 (285 eV), in graphitic carbon. Ultraviolet–visible (UV–Vis) spectroscopy of the CDs obtained from fragmentation graphitic carbon showed a band at 205 nm associated with CC bonds π-π* of CC and n-π*, as well as two bands at 276 and 328 nm associated with bond transitions. The Fourier Transform Infrared (FTIR) spectrum showed bands associated with CHs bonds as well as CC, CN bonds of the CDs. Fluorescence spectroscopy showed three emission bands at 2.43, 2.54 and 2.87 eV. The CDs showed the emission of the characteristic blue colour.

An Advanced Surface Treatment Technique for Coating Three-Dimensional-Printed Polyamide 12 by Hydroxyapatite

Polymer 3D printing has is used in a wide range of applications in the medical field. Polyamide 12 (PA12) is a versatile synthetic polymer that has been used to reconstruct bony defects. Coating its surface with calcium phosphate compounds, such as hydroxyapatite (HA), could enhance its bonding with bone. The aim of this study was to coat 3D-printed polyamide 12 specimens with hydroxyapatite by a simple innovative surface treatment using light-cured resin cement. Polyamide 12 powder was printed by selective laser sintering to produce 80 disc-shaped specimens (15 mm diameter × 1.5 mm thickness). The specimens were divided randomly into two main groups: (1) control group (untreated), where the surface of the specimens was left without any modifications; (2) treated group, where the surface of the specimens was coated with hydroxyapatite by a new method using a light-cured dental cement. The coated specimens were characterised by both Fourier transform infrared spectroscopy (FTIR) and Transmission Electron Microscopy (TEM), (n = 10/test). The control and treated groups were further randomly subdivided into two subgroups according to the immersion in phosphate-buffered saline (PBS). The first subgroup was not immersed in PBS and was left as 3D-printed, while the second subgroup was immersed in PBS for 15 days (n = 10/subgroup). The surfaces of the control and treated specimens were examined using an environmental scanning electron microscope (SEM) and energy dispersive X-ray analysis (EDXA) before and after immersion in PBS. Following the standard American Society for Testing and Materials (ASTM D3359), a cross-cut adhesion test was performed. The results of the FTIR spectroscopy of the coated specimens were confirmed the HA bands. The TEM micrograph revealed agglomerated particles in the coat. The SEM micrographs of the control 3D-printed polyamide 12 specimens illustrated the sintered 3D-printed particles with minimal porosity. Their EDXA revealed the presence of carbon, nitrogen, and oxygen as atomic%: 52.1, 23.8, 24.1 respectively. After immersion in PBS, there were no major changes in the control specimens as detected by SEM and EDXA. The microstructure of the coated specimens showed deposited clusters of calcium and phosphorus on the surface, in addition to carbon, nitrogen, and oxygen, with atomic%: 9.5, 5.9, 7.2, 30.9, and 46.5, respectively. This coat was stable after immersion, as observed by SEM and EDXA. The coat adhesion test demonstrated a stable coat with just a few loose coating flakes (area removed <5%) on the surface of the HA-coated specimens. It could be concluded that the 3D-printed polyamide 12 could be coated with hydroxyapatite using light-cured resin cement.

Evaluating the biomedical potential of phytomediated silver doped zinc oxide nanoparticles derived from n-butanol fraction of Adiantum venustum D. Don

Cancer and bacterial antibiotic resistance are the first two pressing issues confronting the pharmaceutical industry today. With this in mind, the current goal of this research is to create eco-friendly, green synthesized nanostructures that have the potential to at least partially eliminate these issues. The research aims to synthesize ZnO (zinc oxide) and Ag-doped ZnO (silver doped zinc oxide) nanoparticles with two different concentrations (AgxZn1-xO) and variations in their biological potential. To the best of our knowledge, the n-butanol fraction of A. venustum is being used as a first attempt to synthesize Ag-doped ZnO nanoparticles that too with varying concentrations. The XRD (X-ray diffraction) technique endorses the materialization of wurtzite structure for zinc oxide (ZnO–B) and hexagonal wurtzite configuration for the silver-doped complexes (AgZnO–B1 and AgZnO–B2). The Scherrer formula was utilized to examine the average crystallite sizes of ZnO–B (29.21 nm), AgZnO–B1 (22.03 nm), and AgZnO–B2 (27.76 nm). Using transmission electron microscopy micrographs, the grain sizes of AgZnO–B1 (57.72 ± 1.84 nm), AgZnO–B2 (75.31 ± 2.03 nm), and ZnO–B (45.84 ± 0.57 nm) were measured. The XPS (X-ray Photoelectron Spectroscopy) revealed the Zn2+ and Ag + oxidation state of green synthesized nanoparticles. Additionally, the antioxidant, anti-inflammatory, antimicrobial and anticancer activities were assessed in relation to the n-butanol fraction of A. venustum and the synthesized nanomaterials. Of all the synthesized nanoparticles, AgZnO–B1 has proven to be a potent biomedical agent in all biological activities. AgZnO–B1 was found to have potential as an anti-inflammatory (IC50- EAA 33.63 ± 0.05 μg/mL; BSA 28.02 ± 0.80 μg/mL) and anticancer (IC50 85.27 μg/mL) agent in the study. Therefore, it should be underlined that nanoparticles have enormous biological efficacy and used in a range of therapeutic contexts.

Thermal-dependent luminescence in Er³⁺-doped BaHfO₃ and SrHfO₃ perovskites: Improve temperature sensing via Ba-Sr exchange

The luminescence process behavior stimulated by temperature changes is examined by using the theory of thermally coupled energy levels of erbium ion (Er3+) 2H11/2 and 4S3/2. The different mechanisms and environments are compared and elucidated in crystalline structures of BaHfO3 and SrHfO3 as a product of the atomic exchange of Ba2+ for Sr2+ respectively. The undoped and erbium-doped materials were synthesized by hydrothermal route, the erbium-doped materials were impurified with different Er3+ concentrations; 0.25, 0.5, 1, 3, and 5 at.%. X-ray diffraction (XRD) patterns of both materials present a cubic perovskite-type phase, with space group Pm-3m. High-resolution transmission electron microscopy (HRTEM) micrographs show for both materials the presence of nanocrystals with straight profiles and with an approximate size of 36 nm for BaHfO3 and 32 nm for SrHfO3. The room temperature photoluminescent emission spectra shows the highest luminescent intensity at 1 % Er3+ for both materials, showing different spectral characteristic shapes for each material, due to the different electrostatic forces produced by either Ba2+ or Sr2+ ions surrounding Er3+. Using the “Fluoresce Intensity Ratio” (FIR) technique, the temperature sensing properties of these materials were analyzed and compared from 290 to 330 K covering the well-known physiological range (298.15 K–318.15 K). Both materials, BaHfO3:1%Er3+ and SrHfO3:1%Er3+, show dependence to temperature changes, and the experimental energy gap (ΔE) was used to improve (or decrease) the temperature sensing properties. The theoretical ΔE, maximum relative sensitivity (SRMAX), and the resolution in temperature (δT) were obtained, for BaHfO3: 1 % Er3+ these values were: ΔE = 505.73 cm−1, SRMAX = 0.87 % K−1 at 288.5 K and δT = 0.02 K, while for SrHfO3: 1 % Er3+ the values were: ΔE = 649.21 cm−1, SRMAX = 1.12 % K−1 at 288.5 K and δT = 0.01 K.

Robust Ag-Co bimetallic nanoparticles: Dual role in catalytic and triboelectric performance

Bimetallic nanoparticles are of great significance in numerous areas due to their unique properties and diverse applications. In the present study, silver (Ag) and cobalt (Co) monometallic nanoparticles (MNPs) and AgCo bimetallic nanoparticles (BNPs), are synthesized using a simple wet chemical route. Various analytical techniques are adopted for the confirmation of the BNPs. Powder X-ray diffraction (PXRD) analysis revealed the formation of FCC-structure. Transmission Electron Microscopy (TEM) micrographs confirmed the bimetallic nature and Janus structure. The synthesized nanoparticles exhibit higher catalytic activity for degrading 4-nitrophenol dye. Recognizing the potential of metal nanoparticles to significantly boost the efficiency of triboelectric nanogenerators (TENG), the synthesized AgCo bimetallic nanoparticles are incorporated into polymer matrix to meticulously analyze the impact on the triboelectric performance. Interestingly, TENG with a higher composite quantity of 8 ml BNPs exhibited greater performance, generating an output voltage of about 270.52 V and a current of 5.24 µA. Hence, the procured synergistic BNPs show their promising avenue towards both water treatment and energy harvesting applications.

Sil1-deficient fibroblasts generate an aberrant extracellular matrix leading to tendon disorganisation in Marinesco-Sjögren syndrome

BackgroundMarinesco-Sjögren syndrome (MSS) is an autosomal recessive neuromuscular disorder that arises in early childhood and is characterized by congenital cataracts, myopathy associated with muscle weakness, and degeneration of Purkinje neurons leading to ataxia. About 60% of MSS patients have loss-of-function mutations in the SIL1 gene. Sil1 is an endoplasmic reticulum (ER) protein required for the release of ADP from the master chaperone Bip, which in turn will release the folded proteins. The expression of non-functional Sil1 leads to the accumulation of unfolded proteins in the ER and this triggers the unfolded protein response (UPR). A dysfunctional UPR could be a key element in the pathogenesis of MSS, although our knowledge of the molecular pathology of MSS is still incomplete.MethodsRNA-Seq transcriptomics was analysed using the String database and the Ingenuity Pathway Analysis platform. Fluorescence confocal microscopy was used to study the remodelling of the extracellular matrix (ECM). Transmission electron microscopy (TEM) was used to reveal the morphology of the ECM in vitro and in mouse tendon.ResultsOur transcriptomic analysis, performed on patient-derived fibroblasts, revealed 664 differentially expressed (DE) transcripts. Enrichment analysis of DE genes confirmed that the patient fibroblasts have a membrane trafficking issue. Furthermore, this analysis indicated that the extracellular space/ECM and the cell adhesion machinery, which together account for around 300 transcripts, could be affected in MSS. Functional assays showed that patient fibroblasts have a reduced capacity of ECM remodelling, reduced motility, and slower spreading during adhesion to Petri dishes. TEM micrographs of negative-stained ECM samples from these fibroblasts show differences of filaments in terms of morphology and size. Finally, structural analysis of the myotendinous junction of the soleus muscle and surrounding regions of the Achilles tendon revealed a disorganization of collagen fibres in the mouse model of MSS (woozy).ConclusionsECM alterations can affect the proper functioning of several organs, including those damaged in MSS such as the central nervous system, skeletal muscle, bone and lens. On this basis, we propose that aberrant ECM is a key pathological feature of MSS and may help explain most of its clinical manifestations.

Malachite green dye removal with aluminosilicate nanopowder from aluminum dross and silicomanganese slag

Malachite green is a persistent, bioaccumulative, mutagenic, carcinogenic, and teratogenic dye that poses significant risks in water sources, making its removal from water a critical necessity. This study aims to fabricate a sorbent comprising amorphous aluminosilicate nanopowder utilizing silicomanganese slag (SMS) and secondary aluminum dross (SAD) waste materials to remediate dye-contaminated water. The silica and alumina components of the SMS and SAD were extracted as sodium silicate and sodium aluminate leachates, respectively, through an effective hydrometallurgical conversion process. An empirical formula of Al2O3·2.3SiO2 was deduced from the X-ray fluorescence analysis of the synthesized material. The X-ray diffraction (XRD) pattern indicated the amorphous nature of the synthesized aluminosilicate, with no evidence of nanocrystals or ordered clusters observed via high-resolution transmission electron microscopy (TEM). Based on TEM micrographs, the aluminosilicate particles ranged in size from 20 to 80 nm. The synthesized aluminosilicate nanopowder was utilized to treat wastewater containing malachite green dye, demonstrating a remarkable dye removal efficiency of 97% after a 15-min contact time using 30 mg of adsorbent in a 30 mL dye solution at 200 rpm. The methodology proposed in this study could facilitate the production of amorphous aluminosilicate powder as a high-value product from industrial waste. Studies on its reusability demonstrated that it could remove over 90% of the dye after three cycles of use.

Ceria nanocatalyst-supported oxidative organic transformations of aromatic alcohols and p-nitrotoluene

Hydrothermally derived nanocubes of CeO2(10 nm) were explored as an efficient heterogeneous catalyst in the partial oxidation of aromatic alcohols to the corresponding aldehydes and aerobic oxidation ofp-nitrotoluene top-nitrobenzoic acid. The CeO2nanocatalyst was characterized by x-ray diffraction, transmission electron microscopy (TEM), energy dispersive spectroscopy, x-ray photoelectron spectroscopy, Brunauer-Emmett-Teller (BET) surface area analysis, Fourier transform infrared spectroscopy, thermal gravimetric analysis and ultraviolet-visible spectroscopy. TEM/high-resolution TEM micrographs reveal a morphology of mostly cubic nanostructures with exposed highly active {100} and {110} facets. The surface area of nanoceria was determined by BET analysis and found to be 33.8 m2g-1. To demonstrate the universality of the catalytic system, the selective oxidation of different substrates of benzylic alcohol and complete oxidation ofp-nitrotoluene was investigated under mild conditions. Absolute selectivity towards their respective aldehydes was found to be 99.50% (benzaldehyde), 90.18% (p-chlorobenzaldehyde), 99.71% (p-nitrobenzaldehyde), 98.10% (p-fluorobenzaldehyde), 94.66% (p-anisaldehyde) and 86.14% (cinnamaldehyde). Moreover, the catalytic oxidative transformation of nitrotoluene results in 100% conversion with 99.29% selectivity towards nitrobenzoic acid.

Phytomediated Copper Oxide Nanoparticles Derived from the Fronds of Adiantum venustum D.Don: Evaluation of their Biomedical Potential.

The green synthesis of copper oxide nanoparticles (CuO) mediated by crude ethanolic extract and the n-butanol fraction of Adiantum venustum represents a groundbreaking approach in nanotechnology, combining ecological sustainability with advanced functionality. This innovative method leverages the natural bioactive compounds present in A. venustum to produce CuO nanoparticles, which exhibit remarkable antioxidant, anti-inflammatory, antimicrobial, and anti-proliferative properties. The green synthesized nanoparticles were characterized using a variety of techniques, as XRD confirmed the crystalline nature of the CuO nanoparticles, with a crystallite size of 14.65nm for CuO-C and 18.73nm for CuO-B. The grain sizes of CuO-C (14.09 ± 0.17nm) and CuO-B (67.88 ± 2.08nm) were determined using transmission electron microscopy micrographs. Furthermore, the synthesized nanomaterial and the crude ethanolic extract, n-butanol fraction, were examined for their biological potentials namely antioxidant, anti-inflammatory, antimicrobial, and anti-proliferative activity against HeLa cancer cells. Among the synthesized nanomaterials, copper oxide nanoparticles synthesized by utilizing the n-butanol fraction have appeared as a potential biomedical agent. CuO-B has arisen as an antioxidant agent with IC50 values of 44.63 ± 0.49µg/mL, 48.49 ± 0.17µg/mL, and 35.39 ± 0.61µg/mL for DPPH, FRAP, and reducing power assay, respectively. Furthermore, the significant antibacterial potential of CuO-B against gram-positive (S. aureus MIC 46.88µg/mL) and gram-negative (K. pneumonia MIC 23.48µg/mL) bacterial strains cannot be neglected either. Along with this, the IC50 value (138.07µg/mL) of CuO-B against HeLa cells proved it to be a potential anticancerous agent. Hence, this novel approach emphasized that these synthesized nanoparticles have tremendous biological potential and can be applied to various fields of agriculture and biomedicine.

Basal Linear Deposit: Normal Physiological Ageing or a Defining Lesion of Age-Related Macular Degeneration?

Objective: To determine if basal linear deposit (BLinD) is a specific lesion of age-related macular degeneration (AMD). Methods: The cohort was selected from a clinically and histopathologically validated archive (Sarks Archive) and consisted of 10 normal eyes (age 55-80 years) without any macular basal laminar deposit (BLamD) (Sarks Group I) and 16 normal aged eyes (age 57-88 years) with patchy BLamD (Sarks Group II). Only eyes with in vivo fundus assessment and corresponding high-resolution transmission electron microscopy (TEM) micrographs of the macula were included. Semithin sections and fellow-eye paraffin sections were additionally examined. BLinD was defined as a diffuse layer of electron-lucent vesicles external to the retinal pigment epithelium (RPE) basement membrane by TEM and was graded as follows: (i) Grade 0, absence of a continuous layer; (ii) Grade 1, a continuous layer up to three times the thickness of the RPE basement membrane (0.9 µm); (iii) Grade 2, a continuous layer greater than 0.9 µm. Bruch's membrane (BrM) hyalinisation and RPE abnormalities were determined by light microscopic examination of corresponding semithin and paraffin sections. Results: BLinD was identified in both normal (30%) and normal aged (62.5%) eyes. BLinD was thicker in normal aged eyes (p = 0.045; 95% CI 0.04-3.4). BLinD thickness positively correlated with both the degree of BrM hyalinisation (p = 0.049; 95% CI 0.05-2.69) and increasing microscopic RPE abnormalities (p = 0.022; 95% CI 0.188-2.422). RPE abnormalities were more likely to be observed in eyes with increased BrM hyalinisation (p = 0.044; 95% CI 0.61-4.319). Conclusions: BLinD is most likely an age-related deposit rather than a specific lesion of AMD. Its accumulation is associated with increasing BrM hyalinisation and microscopic RPE abnormalities, suggesting a relationship with dysregulated RPE metabolism and/or transport.

The Cytotoxic Effects of Human Mesenchymal Stem Cells Induced by Uranium.

Bone is a major tissue for uranium deposition in human body. Considering mesenchymal stem cells (MSCs) play a vital role in bone formation and injury recovery, studying the mechanism of MSCs responding to uranium poisoning can benefit the understanding of bone damage and repair after uranium exposure. Cellular structural alterations were analyzed via transmission electron microscopy (TEM). Changes in cellular behaviors were assessed through cellular viability, apoptosis, and the production of DNA double-strand breaks (DSBs). In addition, the influence of gap junctional intercellular communication (GJIC) on uranium toxicity was assessed. The disruption of MSCs was elevated with the increase in uranyl nitrate concentration, as shown by TEM micrograph. This was verified by the results of cellular viability and DSB production. Interestingly, the results of apoptosis assay indicated significant apoptosis occurred, which was accompanied with an obvious disruption of cellular membranes. Furthermore, closely contacted cell confluence groups exhibited resistant to uranium poisoning in contrast to sparse growth groups, which can be eliminated with the pretreatment of a GJIC inhibitor in the close connection group. To verify the association between GJIC and cytotoxic effects of uranyl nitrate, GJIC function was evaluated by wound healing and cellular migration. The results showed an inhibition of the healing ratio and migration ability induced by the exposure of uranyl nitrate. The low transfer efficiency of the dye coupling experiment and depressed expression of gap functional protein connexins confirmed the impairment of GJIC function. These results suggest that uranium toxicity is involved with GJIC dysfunction.

The role of thermal treatment and formulation on modifying the structural nature and optimizing certain physical features of coprecipitated superparamagnetic Co–Mn–Cr spinel ferrite

Examining the composition and heat treatment effects of co-precipitated Co0.7Mn0.3CrxFe2-xO4 (x = 0.0, 0.2, 0.4, 0.6, 0.8, and 1) ferrite nanoparticles provides valuable insights into the structural, morphological, optical, magnetic, and electrical properties of these materials. X-ray diffraction (XRD) and Rietveld refinement analyses confirm the spinel cubic crystalline phase of the samples, indicating the formation of well-defined crystal structures. Transmission electron microscope micrographs manifest the nanoscale nature of the produced specimens and their narrow particle size distribution with a small standard deviation. This uniformity is often desirable in many applications because it confirms the similarity of the properties and behaviors of the nanoparticles. The Fourier transform infrared spectroscopy study suggests that the substitution of Cr3+ ions at octahedral sites influences molecular stability. Annealing causes a slight expansion in bond length and a subsequent decrease in stability. The presence of Cr3+ ions enhances the strength of the specimens, while annealing weakens them. This indicates a fine balance between composition and processing conditions in determining the strength of the materials. The estimated optical indirect bandgap undergoes a redshift by adding Cr3+ ions. Annealing at elevated temperatures reduces the bandgap due to the quantum confinement effect, indicating the tunability of optical properties through compositional and thermal control. Samples with x ≥ 0.6 exhibit nearly zero coercivity, indicating superparamagnetic behavior, which have promising applications. The preference of Cr3+ ions to occupy octahedral B-sites influences the magnetic behavior of the materials. The dielectric polarization and dielectric loss improved by adding Cr3+ ions, while the alternating current conductivity decreased. From impedance spectroscopy, the real and imaginary parts, Z’ and Z”, were increased by increasing Cr content. Furthermore, the annealing process greatly affects the electrical properties of the specimens. Overall, the study emphasizes the intricate relationship between composition, annealing conditions, and the resulting structural, magnetic, and electrical properties of Co–Mn–Cr ferrite nanoparticles, providing significant observations for the development of tailored materials for diverse applications in electronics, magnetics, and medicine.

New stable waterborne amorphous polylactic acid/organoclay nanocomposites prepared using emulsification solvent evaporation method

AbstractWater based polylactic acid (PLA)‐surface modified montmorillonite (MMt) nanocomposites as biobased formulations for paper coating were successfully developed using emulsification solvent evaporation method. Electrostatic and steric stabilization mechanisms have contributed to the production of stable emulsions up to 5 months at 23 ± 1°C, revealing strong repulsive forces generated between the nanoparticles as confirmed by zeta potential (ζ) and dynamic light scattering (DLS) analysis. MMt particles were fully encapsulated by PLA as demonstrated by transmission electron microscopy (TEM) micrographs. Meanwhile the film formation process highlighted the importance of emulsifier's type and solubility in the polymer matrix, as no films were obtained when sodium oleate was used alone compared with continuous, homogeneous, and free‐standing films obtained when the combination Tween 80 (80 wt%)—sodium oleate (20 wt%) was used. Scanning electron microscopy (SEM) micrographs of the cross‐section's surfaces showed homogeneous dispersion of the MMt particles with no clusters or agglomerates formed. Thermal analyses using differential scanning calorimetry and thermogravimetric analysis (DSC‐TGA) showed an overall reduction in the glass transition temperature (Tg) and the thermal stability of neat PLA, whoever this reduction was recovered when MMt was added due to the confinement effect. Thickened PLA and PLA/MMt emulsions using 1 wt% xanthan gum showed a non‐Newtonian behavior and shear thinning flow with suitable viscosity values for paper coating applications.Highlights Development of stable PLA/organoclay nanocomposite aqueous dispersions. Steric and electrostatic mechanisms provided excellent stability. Full encapsulation of organoclay platelets in nanometric PLA particles. Formation of free‐standing films from PLA/organoclay emulsions. Thickened PLA/organoclay emulsions using Xanthan gum for paper coatings.

Solvothermal Synthesis of Cu2ZnSnSe4 Nanoparticles and Their Visible-Light-Driven Photocatalytic Activity.

Cu2ZnSnSe4 (CZTSe) nanoparticles (NPs) were successfully synthesized via a solvothermal method. Their structural, compositional, morphological, optoelectronic, and electrochemical properties have been characterized by X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), Field-emission scanning electron microscopy (FE-SEM), transmission electron microscope (TEM), UV-vis absorption spectroscopy, and electrochemical impedance spectroscopy (EIS) techniques. Porosimetry and specific surface area in terms of the Brunauer-Emmett-Teller (BET) technique have also been studied. XRD indicates the formation of a polycrystalline kesterite CZTSe phase. Raman peaks at 173 and 190 cm-1 confirm the formation of a pure phase. TEM micrographs revealed the presence of nanoparticles with average sizes of ~90 nm. A BET surface area of 7 m2/g was determined. The CZTSe NPs showed a bandgap of 1.0 eV and a p-type semiconducting behavior. As a proof of concept, for the first time, the CZTSe NPs have been used as a visible-light-driven photocatalyst to Congo red (CR) azo dye degradation. The nanophotocatalyst material under simulated sunlight results in almost complete degradation (96%) of CR dye after 70 min, following a pseudo-second-order kinetic model (rate constant of 0.334 min-1). The prepared CZTSe was reusable and can be repeatedly used to remove CR dye from aqueous solutions.