Biogenic synthesis of nickel cobaltite nanoparticles via a green route for enhancing the photocatalytic and electrochemical performances.

Green synthesis aligns with the global demand for eco-friendly and sustainable technologies, reducing the dependency on harmful chemicals and high-energy processes typically used in conventional synthesis techniques. This study highlights a novel green synthesis route for nickel cobaltite nanoparticles (NiCO2O4 NPs) utilizing Hyphaene thebaica extract as a natural reducing and stabilizing agent. The synthesized NiCO2O4 NPs, with sizes ranging from 20 to 30 nm, exhibited uniform diamond-like structures as confirmed by SEM and TEM imaging. XRD analysis verified the polycrystalline nature of these nanoparticles, while EDS measurements confirmed the elemental composition of Ni and Co. The presence of functional groups was subsequently verified through FT-IR analysis, and Raman spectroscopy further confirmed phase formation. Electrochemical evaluations revealed significant pseudocapacitive behavior, showing a specific capacitance of 519 F/g, demonstrating their potential for high-performance supercapacitors. To further assess the applicability of the synthesized NiCO2O4 NPs, their photocatalytic activity against methylene blue (MB) dye was investigated, resulting in a 99% degradation rate. This impressive photocatalytic efficiency highlights their potential application in environmental remediation. Overall, this work underscores the significant potential of green synthesis methods in producing high-performance nanomaterials while simultaneously reducing environmental impact and promoting sustainable development.

Potential nanomedicinal applications and physicochemical nature of Hyphaene thebaica-reduced nano-samaria.

Herein we described the biofabrication of samarium oxide nanoparticles (HT-Sm2O3 NPs) by applying the aqueous fruit extract of Hyphaene thebaica was utilized as an eco-friendly chelating agent. The prepared NPs were subjected to various physicochemical properties and potential in biomedical applications. X-ray Diffraction (XRD) pattern revealed sharp peaks that corroborated with the Joint Committee on Powder Diffraction Standards (JCPDS) card no. 00-042-1464. Crystallite size obtained from Debye-Scherrer approximation and Williamson-Hall (W-H) plot was 28.73 and 69.3 nm, respectively. Optical bandgap was calculated by employing Kubelka-Munk (K-M) function and was found to be ~4.58 eV. Raman shift was observed at 121, 351, 424-, and 561 cm-1. Photoluminescence (PL) spectra revealed two major peaks positioned at 360 and 540 nm. The high-resolution transmission electron microscopy (HR-TEM) analysis of HT-Sm2O3 nanoparticles (NPs) showed that they predominantly have spherical to cuboidal shapes. Additionally, the selected area electron diffraction (SAED) pattern presented spotty rings, indicating a high level of crystallinity in these NPs. The potential nanomedicine applications were studied using diverse bioassays using different treatments. The antioxidant activity demonstrated 45.71% ± 1.13% inhibition at 1000 µg/mL. Brine shrimp lethality assay revealed the highest cytotoxicity of 46.67% ± 3.33% at 1000 µg/mL and LC50 value of 1081 µg/mL. HT-Sm2O3 NPs exhibited inhibition of angiogenesis (20.41% ± 1.18%) at of 1000 µg/mL. MTT assay results indicated that HT-Sm2O3 NPs exhibit inhibitory effects on cell lines. Specifically, these NPs showed an IC50 value of 104.6 µg/mL against 3T3 cells. Against MCF-7 cells, the NPs demonstrated an IC50 value of 413.25 µg/mL. Additionally, in the inhibition of acetylcholinesterase (AChE), the newly synthesized NPs showed an IC50 value of 320 µg/mL. The antidiabetic assessment through α-glucosidase and α-amylase inhibition assays revealed, an IC50 value of 380 µg/mL for α-glucosidase and 952 µg/mL for α-amylase was calculated. Overall, our study suggested that the Sm2O3 NPs possess moderate anticancer, cholinesterase inhibition, and antidiabetic potential, however, needs further assessment. RESEARCH HIGHLIGHTS: In this work, nano-samaria is synthesized using an eco-friendly and green approach. The nanoparticles were characterized using techniques such as Raman, HR-TEM, FTIR, DRS, XRD, and so on, and the applications were studied using multiple in vitro bioassays for Diabetes, Alzheimer, and Cancer. The nano-samaria revealed good potential for potential biomedical applications.

In-vitro cytotoxicity of biosynthesized nanoceria using Eucalyptus camaldulensis leaves extract against MCF-7 breast cancer cell line.

Cerium oxide nanoparticles possess unique properties that make them promising candidates in various fields, including cancer treatment. Among the proposed synthesis methods for CNPs, biosynthesis using natural extracts, offers an eco-friendly and convenient approach for producing CNPs, particularly for biomedical applications. In this study, a novel method of biosynthesis using the aqueous extract of Eucalyptus camaldulensis leaves was used to synthesize CNPs. Scanning electron microscopy and Transmission electron microscopy (TEM) techniques revealed that the synthesized CNPs exhibit a flower-like morphology. The particle size of CNPs obtained using Powder X-ray diffraction peaks and TEM as 13.43 and 39.25 nm. Energy-dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy confirmed the effect of biomolecules during the synthesis process and the formation of CNPs. The cytotoxicity of biosynthesized samples was evaluated using the MTT method demonstrating the potential of these samples to inhibit MCF-7 cancerous cells. The viability of the MCF-7 cell line conducted by live/dead imaging assay confirmed the MTT cytotoxicity method and indicated their potential to inhibit cancerous cells. Furthermore, the successful uptake of CNPs by MCF-7 cancer cells, as demonstrated by confocal microscopy, provides evidence that the intracellular pathway contributes to the anticancer activity of the CNPs. In general, results indicate that the biosynthesized CNPs exhibit significant cytotoxicity against the MCF-7 cancerous cell line, attributed to their high surface area.

Neurotoxicity and Developmental Neurotoxicity of Copper Sulfide Nanoparticles on a Human Neuronal In-Vitro Test System.

Nanoparticles (NPs) are becoming increasingly important novel materials for many purposes, including basic research, medicine, agriculture, and engineering. Increasing human and environmental exposure to these promising compounds requires assessment of their potential health risks. While the general direct cytotoxicity of NPs is often routinely measured, more indirect possible long-term effects, such as reproductive or developmental neurotoxicity (DNT), have been studied only occasionally and, if so, mostly on non-human animal models, such as zebrafish embryos. In this present study, we employed a well-characterized human neuronal precursor cell line to test the concentration-dependent DNT of green-manufactured copper sulfide (CuS) nanoparticles on crucial early events in human brain development. CuS NPs turned out to be generally cytotoxic in the low ppm range. Using an established prediction model, we found a clear DNT potential of CuS NPs on neuronal precursor cell migration and neurite outgrowth, with IC50 values 10 times and 5 times, respectively, lower for the specific DNT endpoint than for general cytotoxicity. We conclude that, in addition to the opportunities of NPs, their risks to human health should be carefully considered.

DFT study on CO 2 capture using boron, nitrogen, and phosphorus-doped C 20 in the presence of an electric field.

Burning fossil fuels emits a significant amount of CO 2 , causing climate change concerns. CO 2 Capture and Storage (CCS) aims to reduce emissions, with fullerenes showing promise as CO 2 adsorbents. Recent research focuses on modifying fullerenes using an electric field. In light of this, we carried out DFT studies on some B, N, and P doped C 20 ( C 20 - n X n , n = 0, 1, 2, and 3; X = B, N, and P) in the absence and presence of an electric field in the range of 0-0.02 a.u.. The cohesive energy was calculated to ensure their thermodynamic stability showing, that despite having lesser cohesive energies than C 20 , they appear in a favorable range. Moreover, the charge distribution for all structures was depicted using the ESP map. Most importantly, we evaluated the adsorption energy, height, and CO 2 angle, demonstrating the B and N-doped fullerenes had the stronger interaction with CO 2 , which by far exceeded C 20 's, improving its physisorption to physicochemical adsorption. Although the adsorption energy of P-doped fullerenes was not as satisfactory, in most cases, increasing the electric field led to enhancing CO 2 adsorption and incorporating chemical attributes to CO 2 -fullerene interaction. The HOMO-LUMO plots were obtained by which we discovered that unlike the P-doped C 20 , the surprising activity of B and N-doped C 20 s against CO 2 originates from a high concentration of the HOMO-LUMO orbitals on B, N and neighboring atoms. In the present article, we attempt to introduce more effective fullerene-based materials for CO 2 adsorption as well as strategies to enhance their efficiency and revealing adsorption nature over B, N, and P-doped fullerenes and in the end, hope to encourage more experimental research on these materials within growing electric field for CO 2 capture in the future.

Localized surface plasmon resonance sensing of Trenbolone acetate dopant using silver nanoparticles.

In this work, localized surface plasmon resonance (LSPR) sensing as applicable in the detection of Trenbolone acetate dopant is demonstrated. We show that the LSPR of the Trenbolone acetate/silver nanoparticle (Tren Ac/AgNPs) complex is sensitive to changes in the adsorbent concentration. The results show an average redshift of + 18 nm in the LSPR peak with variations in intensity and broadening behavior of the LSPR band of the Tren Ac/AgNPs complex. AgNPs were synthesized using laser ablation in liquid (LAL) technique with water as the solvent. UV-Vis spectroscopy was used for absorbance measurements and particle size and morphology were monitored using scanning electron microscopy (SEM). The aggregation behavior of the Tren Ac/AgNPs complex was monitored using energy-dispersive X-ray spectroscopy (EDS). Molecular Electrostatic Potential (MEP) and the HOMO-LUMO orbitals of the optimized Trenbolone acetate structure were obtained using Density Function Theory (DFT). The molecule was optimized at the B3LYP level of theory using the 6-311 basis set carried out using the Gaussian 09 software package. The results showed that O2- is Trenbolone acetate's active site that would interact with Ag+ to form a complex that would influence the plasmon behavior. The results presented in this work demonstrate the feasibility of LSPR for anabolic androgenic steroid detection.

Ionome mapping and amino acid metabolome profiling of Phaseolus vulgaris L. seeds imbibed with computationally informed phytoengineered copper sulphide nanoparticles.

This study reports the effects of a computationally informed and avocado-seed mediated Phyto engineered CuS nanoparticles as fertilizing agent on the ionome and amino acid metabolome of Pinto bean seeds using both bench top and ion beam analytical techniques. Physico-chemical analysis of the Phyto engineered nanoparticles with scanning-electron microscopy, transmission electron microscopy, X-ray diffraction, and Fourier Transform Infrared Spectroscopy confirmed the presence of CuS nanoparticles. Molecular dynamics simulations to investigate the interaction of some active phytocompounds in avocado seeds that act as reducing agents with the nano-digenite further showed that 4-hydroxybenzoic acid had a higher affinity for interacting with the nanoparticle's surface than other active compounds. Seeds treated with the digenite nanoparticles exhibited a unique ionome distribution pattern as determined with external beam proton-induced X-ray emission, with hotspots of Cu and S appearing in the hilum and micropyle area that indicated a possible uptake mechanism via the seed coat. The nano-digenite also triggered a plant stress response by slightly altering seed amino acid metabolism. Ultimately, the nano-digenite may have important implications as a seed protective or nutritive agent as advised by its unique distribution pattern and effect on amino acid metabolism.

Phyto-fabrication of ultrafine nanoscale holmium oxide HT-Ho2O3 NPs and their biomedical potential.

In this study holmium oxide nanoparticles (Ho2O3 NPs) are fabricated using Hyphaene thebaica extracts as a bioreductant. The XRD pattern of HT-Ho2O3 NPs (product from phyto-reduction) suggested that the nanoparticles are crystalline with no impurities. Scherrer approximation revealed grain sizes of ∼10 nm. The HR-TEM revealed HT-Ho2O3 NPs possessed a quasi-spherical morphology complemented by SEM and the particle sizes were in the range of 6-12 nm. The infrared spectra revealed characteristic Ho-O bonding at ∼603 cm-1. Raman spectra indicated five main peaks positioned at 156 cm-1, 214 cm-1, 328 cm-1, 379 cm-1 and 607 cm-1. Eg (optical bandgap) was found to be 5.1 eV. PL spectra indicated two major peaks at 415 nm and 607 nm. EDS spectra confirmed the elemental presence of holmium (Ho). Spotty rings were obtained during the SAED measurement which indicated crystallinity of HT-Ho2O3 NPs. The HT-Ho2O3 NPs were further analyzed for their antioxidant, anti-angiogenic and cytotoxic properties. The antioxidant potential was moderate i.e., 43.40 ± 0.96% at 1000 µg mL-1 which decreased in a dose dependent manner. Brine shrimp lethality was highest at 1000 µg mL-1 with the LC50 320.4 µg mL-1. Moderate anti-angiogenic potential was observed using in ova CAM assay. MTT bioassay revealed that the HT-Ho2O3 NPs inhibited the 3T3 cells (IC50 67.9 µg mL-1), however, no significant inhibition was observed against MCF-7 cells. α-Amylase and ß-glucosidase inhibition revealed that the HT-Ho2O3 NPs can be of use in controlling blood glucose levels. Overall, it can be concluded that biosynthesis using aqueous extracts can be a suitable alternative in finding ecofriendly paradigms for the synthesis of nanoparticles. We suggest extended research into the bioreduced Ho2O3 NPs for establishing their biomedical potential and toxicity.

Biosynthesis of magnesium oxide and calcium carbonate nanoparticles using Moringa oleifera extract and their effectiveness on the growth, yield and photosynthetic performance of groundnut (Arachis hypogaea L.) genotypes.

Small-scale crop production has been significantly impacted by the heavy price, limited supply, and frequent shortage of inorganic fertilisers, which is partly attributable to the Covid-19 pandemic outbreak and led to rising oil and food prices. Thus, integrating environmentally friendly agricultural practices that can improve crop productivity and advance the sustainability of agricultural cropping systems is critical. This study synthesized and characterised MgO and CaCO3Moringa oleifera nanoparticles and assessed their effects on groundnut genotypes. The effect of biosynthesized MgO and CaCO3 nanoparticles using Moringa oleifera extract on the growth and yield of groundnut genotypes exposed to different concentrations of 50, 100 and 200 mg/L was examined. The experiment was carried laid out in a 3 × 8 factorial completely randomized design (CRD) with eight replicates per treatment. Each plant was sprayed with 5 ml of the solution crystalline size of the MgO and CaCO3 nanoparticles 2.48 nm and 10.30 nm, respectively. Foliar application of nanoparticle treatments was applied weekly except for the negative control. The collected data were subjected to a two-way analysis of variance (ANOVA). Mean separations were done using Tukey's Honest Significant Difference (HSD) at P < 0.05. The findings demonstrated that foliar application of MgO and CaCO3 nanoparticles positively affected groundnut biomass production. The results further revealed that the concentration of 50 mg/L of MgO and 100 mg/L of CaCO3 considerably improved groundnut plant growth, yield, and nodulation in comparison with other treatments. There is a great deal of evidence signifying that foliar applications of 50 mg/L of MgO 100 mg/L CaCO3 contributed greatly to plant growth and crop production. Therefore, 50 mg/L of MgO and 100 mg/L CaCO3 nanoparticles foliar application could be recommended as nano-fertilisers application rate for groundnut production.

Effect of extraction methods on phytochemical constituents and antioxidant activity of de-kernelled Sclerocarya birrea seeds.

BACKGROUND: Marula (Sclerocarya birrea) is an indigenous African fruit-bearing tree with many commercial uses; however, de-kernelled seeds generated from marula fruit-processing are wasted. The phytochemical constituents of de-kernelled marula seeds have not been investigated previously and its extract/tea may potentially serve as a promising source of antioxidants and phytochemicals. This study aimed to investigate the effect of different extraction methods (maceration and decoction) on the recovery of phenolic compounds, sugars, organic acids, and antioxidants from de-kernelled marula seeds. RESULTS: Extracts produced from decoction for 30 min contained the highest phenolic content (2253.93 ± 25.72 mg gallic acid equivalent kg-1 extract), flavonoid content (1020.99 ± 23.90 mg rutin equivalent kg-1 extract), as well as combined sugars and organic acids (1884.03 mg kg-1 extract). Fourier-transform infrared spectroscopy analysis confirmed the presence of functional groups typically present in phenolic compounds, sugars, and organic acids in the extracts obtained from decoction. CONCLUSION: The characterization revealed that decoction extraction increased solubility, variety, and yield of phytochemical and antioxidant compounds recovered from de-kernelled marula seeds. The highest concentrations of phytochemicals were obtained using the decoction method. This study may therefore pave the way for extract composition and future utilization of de-kernelled marula seeds in the food industry. © 2023 Society of Chemical Industry.

Theoretical study of chemical reactivity descriptors of some repurposed drugs for COVID-19.

This study focuses on computational studies of chemical reactivity descriptors of some proposed drugs for COVID-19. Density functional theory calculations were used to optimize the structure and investigate the frontier orbitals and the chemical reactivity descriptors of these drugs. The frontier orbitals, which include both the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), play an essential role in molecular interactions and chemical reactivity of molecule. Polarizability, which determines the response of the susceptibility of a molecule to an approaching charge, is higher in the more complex drugs such as Hydroxychloroquine, Remdesivir, and Ivermectin compare to the smaller drugs. The HOMO and LUMO orbital energies were calculated to obtain the energy gap of the studied drugs, which is in the following order: Favipiravir < Hydroxychloroquine, Remdesivir < Ivermectin < Artesunate < Artemether < Artemisinin. Generally, molecules with a larger energy gap have lower chemical reactivity and higher kinetic stability.

Antimicrobial, antioxidant, and cytotoxic properties of biosynthesized copper oxide nanoparticles (CuO-NPs) using Athrixia phylicoides DC.

Nanoparticles produced from various metal elements including copper have been used in the treatment of infectious diseases in response to antibiotic failure due to microbial resistance. Copper is recommended for use in the production of nanoparticles largely because of its accessibility and affordability. This study aimed to synthesise copper oxide nanoparticles (CuO-NPs) using leaf extracts of Athrixia phylicoides and assess their antibacterial, antioxidant and cytotoxicity properties. The characterization of the obtained NPs was done through X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR), Scanning electron microscopy (SEM) and Energy-dispersive spectroscopy (EDS). Our results showed that the NPs had a highly crystalline, quasi-spherical shape with an average diameter of 42 nm. Also, gram-positive bacteria Bacillus cereus and Staphylococcus aureus were the most susceptible to CuO-NPs with MIC values of 0.62 mg/mL and 0.16 mg/mL, respectively, as shown by the broth microdilution method. In addition, CuO-NPs demonstrated strong radical 2,2-diphenyl-1-picrylhydrazyl (DPPH) inhibitory activity with an IC50 value of 10.68 ± 0.03 µg/mL. However, the cytotoxicity activity determined by (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide) (MTT) assay revealed that the CuO-NPs were not toxic to human embryonic kidney cells (HEK 293 cells) at an LC50 value of 66.08 ± 0.55 µg/mL. The synthesised CuO-NPs showed high antibacterial, and antioxidant potency and less toxicity. Therefore, they could be a feasible alternative source of therapeutic agents in treating bacterial and oxidative stress-induced diseases.

Fabrication of surface-enhanced Raman spectroscopy substrates using silver nanoparticles produced by laser ablation in liquids.

This research describes the use of surface-enhanced Raman spectroscopy (SERS) substrates based on colloidal silver nanoparticles (AgNPs) produced by laser ablation of silver granules in pure water that are inexpensive, easy to make, and chemically stable. Here, the effects of the laser power, pulse repetition frequency, and ablation duration on the Surface Plasmon Resonance peak of AgNPs solutions, were used to determine the optimal parameters. Also, the effects of the laser ablation time on both ablation efficiency and SERS enhancement were studied. The synthesized AgNPs were characterized by UV-Vis spectrophotometer, Scanning Electron Microscope (SEM), and Raman spectrometer. The Surface Plasmon Resonance peak of AgNP solutions was centered at 404 nm confirming their synthesis and they were noted to be spherical with 34 nm in diameter. Using Raman spectroscopy, they had main bands centered at 196 cm-1 (O = Ag2/Ag-N stretching vibrations), 568 cm-1 (NH out of plane bending); 824 cm-1 (symmetric deformation of the NO2); 1060 cm-1 (NH out of plane bending); 1312 cm-1 (symmetric stretching of NO2); 1538 cm-1 (NH in-plane bending); and 2350 cm-1 (N2 vibrations). Their Raman spectral profiles remained constant within the first few days of storage at room temperature implying chemical stability. The Raman signals from blood were enhanced when mixed with AgNPs and this depended on colloidal AgNPs concentration. Using those generated by 12 h ablation time, an enhancement of 14.95 was achieved. Additionally, these substrates had an insignificant impact on the Raman profiles of samples of rat blood when mixed with them. The Raman peaks noted were attributed to CC stretching of glucose (932 cm-1); CC stretching of Tryptophan (1064 cm-1); CC stretching of ß Carotene (1190 cm-1); CH2 wagging of proteins (1338 and 1410 cm-1); carbonyl stretch for proteins (1650 cm-1); CN vibrations for glycoproteins (2122 cm-1). These SERS substrates can be applied to areas such as forensics to distinguish between human and other animal blood, monitoring of the efficacy of drugs, disease diagnostics such as diabetes, and pathogen detection. All this can be achieved by comparing the Raman spectra of the biological samples mixed with the synthesized SERS substrates for different samples. Thus, the results on the use of inexpensive, simple-to-prepare Raman substrates have the possibility of making surface-enhanced Raman spectroscopy available to laboratories with scarce resources in developing nations.

Advancements in electrochemical technologies for the removal of fluoroquinolone antibiotics in wastewater: A review.

In recent times, the need to make water safer and cleaner through the elimination of recalcitrant pharmaceutical residues has been the aim of many studies. Fluoroquinolone antibiotics such as ciprofloxacin, norfloxacin, enrofloxacin, and levofloxacin are among the commonly detected pharmaceuticals in wastewater. Since the presence of these pharmaceuticals in water bodies poses serious risks to living organisms, it is vital to adopt effective wastewater treatment techniques for their complete removal. Electrochemical technologies such as photoelectrocatalysis, electro-Fenton, electrocoagulation, and electrochemical oxidation have been established as techniques capable of the complete removal of organics including pharmaceuticals from wastewater. Hence, this review presents discussions on the recent progress (literature within 2018-2022) in the applications of common electrochemical processes for the degradation of fluoroquinolone antibiotics from wastewater. The fundamentals of these processes are highlighted while the results obtained using the processes are critically discussed. Furthermore, the inherent advantages and limitations of these processes in the mineralization of fluoroquinolone antibiotics are clearly emphasized. Additionally, appropriate recommendations are made toward improving electrochemical technologies for the complete removal of these pharmaceuticals with minimal energy consumption. Therefore, this review will serve as a bedrock for future researchers concerned with wastewater treatments to make informed decisions in the selection of suitable electrochemical techniques for the removal of pharmaceuticals from wastewater.

Using Nanomaterials as Excellent Immobilisation Layer for Biosensor Design.

The endless development in nanotechnology has introduced new vitality in device fabrication including biosensor design for biomedical applications. With outstanding features like suitable biocompatibility, good electrical and thermal conductivity, wide surface area and catalytic activity, nanomaterials have been considered excellent and promising immobilisation candidates for the development of high-impact biosensors after they emerged. Owing to these reasons, the present review deals with the efficient use of nanomaterials as immobilisation candidates for biosensor fabrication. These include the implementation of carbon nanomaterials-graphene and its derivatives, carbon nanotubes, carbon nanoparticles, carbon nanodots-and MXenes, likewise their synergistic impact when merged with metal oxide nanomaterials. Furthermore, we also discuss the origin of the synthesis of some nanomaterials, the challenges associated with the use of those nanomaterials and the chemistry behind their incorporation with other materials for biosensor design. The last section covers the prospects for the development and application of the highlighted nanomaterials.

Physicochemical and nanomedicine applications of phyto-reduced erbium oxide (Er2O3) nanoparticles.

Hyphaene thebaica fruits were used for the fabrication of spherical erbium oxide nanoparticles (HT-Er2O3 NPS) using a one-step simple bioreduction process. XRD pattern revealed a highly crystalline and pure phase with crystallite size of ~ 7.5 nm, whereas, the W-H plot revealed crystallite size of 11 nm. FTIR spectra revealed characteristic Er-O atomic vibrations in the fingerprint region. Bandgap was obtained as 5.25 eV using K-M function. The physicochemical and morphological nature was established using Raman spectroscopy, reflectance spectroscopy, SAED and HR-TEM. HT-Er2O3 NPS were further evaluated for antidiabetic potential in mice using in-vivo and in-vitro bioassays. The synthesized HT-Er2O3 NPS were screened for in vitro anti-diabetic potentials against α-glucosidase enzyme and α-amylase enzyme and their antioxidant potential was evaluated using DPPH free radical assay. A dose dependent inhibition was obtained against α-glucosidase (IC50 12 µg/mL) and α-amylase (IC50 78 µg/mL) while good DPPH free radical scavenging potential (IC50 78 µg mL-1) is reported. At 1000 µg/mL, the HT-Er2O3 NPS revealed 90.30% and 92.30% inhibition of α-amylase and α-glucosidase enzymes. HT-Er2O3 NPs treated groups were observed to have better glycemic control in diabetic animals (503.66 ± 5.92*** on day 0 and 185.66 ± 2.60*** on day 21) when compared with positive control glibenclamide treated group. Further, HT-Er2O3 NPS therapy for 21 days caused a considerable effect on serum total lipids, cholesterol, triglycerides, HDL and LDL as compared to untreated diabetic group. In conclusion, our preliminary findings on HT-Er2O3 NPS revealed considerable antidiabetic potential and thus can be an effective candidate for controlling the post-prandial hyperglycemia. However, further studies are encouraged especially taking into consideration the toxicity aspects of the nanomaterial.

Optical and Thermal Behavior of Germanium Thin Films under Femtosecond Laser Irradiation.

In this study, we theoretically investigate the response of a germanium thin film under femtosecond pulsed laser irradiation. Electron and lattice temperatures, as well as material-specific optical properties such as dielectric function and reflectivity, were calculated during the irradiation using an extended two-temperature model coupled with the carrier density rate equation and the Drude model. Melting and ablation fluence thresholds were also predicted, resulting in 0.14 J cm-2 and 0.35 J cm-2, respectively. An ultrafast change in both optical and thermal properties was detected upon laser irradiation. Results also indicate that thermal melting occurs after germanium takes on a metallic character during irradiation, and that the impact ionization process may have a critical role in the laser-induced thermal effect. Therefore, we suggest that the origin of the thermal modification of germanium surface under femtosecond laser irradiation is mostly due the impact ionization process and that its effect becomes more important when increasing the laser fluence.

Effect of Optimized Precursor Concentration, Temperature, and Doping on Optical Properties of ZnO Nanoparticles Synthesized via a Green Route Using Bush Tea (Athrixia phylicoides DC.) Leaf Extracts.

Nanoparticles possess several properties, such as antimicrobial, anti-inflammatory, wound healing, catalytic, magnetic, optical, and electronic properties, that have allowed them to be used in different fields. Among them, zinc oxide (ZnO) has received copious consideration due to its technological and medicinal applications. Plant-mediated synthesis of ZnO nanoparticles has provided a cost-effective and eco-friendly method. Therefore, the objective of the study is to assess the effect of the precursor concentration and silver and cerium doping on the optical properties of ZnO nanoparticles synthesized via a green process using bush tea leaf extract as the chelating agent. Zinc nitrate hexahydrate was used as the precursor. Quasi-spherical-shaped ZnO nanoparticles were obtained with an average crystallite size ranging between 24.53 and 63.02 nm. The crystallite size was found to decrease with the increase of precursor concentration at 43.82 nm (0.05 g), 37.25 nm (0.10 g), 26.53 nm (0.50 g), and 24.53 nm (1 g); thereafter, the size increases with an increase in precursor concentration. The optimum precursor concentration was 1 g with the smallest grain size and a high purity level. The increase in annealing temperature induced an increase in the crystallite size of ZnO nanoparticles from 24.53 nm (600 °C) to 34.24 nm (800 °C), however, increasing the level of purity of the nanopowders. The band gap energies were 2.75 and 3.17 eV as calculated using the Tauc plot with variations due to the precursor concentrations. Doping with both silver and cerium increased the band gap of ZnO nanoparticles up to 3.19 eV and the increase in annealing temperature slightly augmented the band gap energy from 3.00 and 3.16 eV, respectively. Hence, doping with Ag and Ce induced the formation of nanorods at higher concentrations. This study successfully demonstrated that the natural plant extract of bush tea can be used in the bioreduction of zinc nitrate hexahydrate to prepare pure ZnO nanoparticles, thus extending the use of this plant to the nano producing industry.

Insights into the molecular mechanism of triazolopyrimidinone derivatives effects on the modulation of α1ß2γ2 subtype of GABAA receptor: An in silico approach.

Due to the importance of benzodiazepine drugs in clinical practice, such as the treatment of anxiety disorders, depression, and insomnia and the side effects of classical benzodiazepines, the study of new benzodiazepine agonists has received much attentions. In this work, we used in silico methods to explore the molecular mechanism of 1,2,4-triazolo [1,5-a] pyrimidinone derivatives in the modulation of α1ß2γ2 subtype of GABAA receptor. To this aim, molecular docking, molecular dynamics simulation (MD), post-MD analysis, binding free energy calculation, and prediction of ADME properties were performed. Results showed that all new compounds have a better binding affinity for the Benzodiazepine (BZD) site of the receptor than diazepam and compound 4c had the highest affinity among them. Moreover, a good agreement was observed between the calculated ΔGbinding and experimental IC50 values. Also, we noticed that residues in loop regions (particularly loop C and D-F in α1 and γ2 subunits, respectively) forming BZD binding site, take part in forming several H-bonds between the agonists and the receptor. Ser205, Thr207, Tyr160, and His102 of α1 subunit and Thr207 of γ2 subunit are mainly involved in forming H-bonds. Also, the orientation of agonists in the BZD binding site leads to π-π interactions with hydrophobic residues in loops A-F. Based on the DCCM analysis, the correlated motions in the γ2 subunit residues are greater than those of α1 subunit residues. Further, predicted ADME results indicated that all agonists meet the criteria. The triplicate MD simulation showed the reproducibility of the results and strengthened the study. Our results provide a comprehensive insight into the receptor-agonist interactions and clues for designing future BZD agonists.

Laser-enabled delivery of antiretroviral drugs into HIV-1 infected TZM-bl cells.

The use of femtosecond laser to create sub-microscopic transient pores on the cell membrane allowing exogenous material into mammalian cells has become a very efficient optical delivery method over the past decade. This study focuses on laser-enabled delivery of antiretroviral (ARV) drugs into HIV-1 infected TZM-bl cells in vitro. A 1 kHz femtosecond laser emitting at a wavelength of 800 nm was used to photoporate cells at 6.5 µW. Trypan blue was used for characterisation and its uptake was quantified using Matlab software. Cell membrane damage was assessed using the lactate dehydrogenase (LDH) assay while HIV-1 infection was assessed using luciferase assay. Our results showed successful delivery of ARVs into HIV-1 infected cells without compromising their cell membranes, subsequently reducing the level of infection. The LDH assay showed no significant cell membrane damage of laser-treated cells, and the luciferase assay demonstrated significant reduction in the level of HIV-1 infection.