Ultraviolet-visible Spectroscopy Research Articles

Preparation and characterization of grouper bone peptides-calcium complex by lactic acid bacteria fermentation

In this study, grouper bone peptides-calcium complex (GPs-Ca) was prepared by lactic acid bacteria fermentation, and its structure and stability were analyzed. Response surface methodology (RSM) optimization was used to determine the optimal fermentation conditions as follows: 4% (v/v) inoculum size, 4.5 g/100mL glucose addition and fermentation time 75 h,under which the soluble calcium content was 5953.61 mg/L and the peptide content was 21.75 mg/mL. The results of ultraviolet-visible absorption spectroscopy (UV) and fluorescence spectroscopy (Fs) showed a significant spectral shift for GPs-Ca relative to grouper bone peptides (GPs), indicating that peptide combined with calcium to produce a new substance after fermentation. Fourier transform infrared spectroscopy (FTIR) showed that carboxyl groups participated in the formation of GPs-Ca. Scanning electron microscopy (SEM) showed that calcium ions were embedded or adsorbed on the peptide surface. According to the stability analysis, GPs-Ca was stable during heating, alkaline environment and intestinal digestion, but easily dissociated in acidic environment. GPs-Ca prepared by lactic acid bacteria fermentation has the potential to be used as a new type of calcium supplement product, which provides a scientific basis for the high-value utilization of grouper bone.

A review of the antimicrobial benefits of naturally extracted nanomaterials

Nanotechnology finds immense potential due to the unique characteristics of nanomaterials. Though noble metal nanoparticles, particularly gold and silver nanoparticles possess advanced properties their conventional production methods pose environmental hazards. This paper explores the eco-friendly approaches using natural sources for synthesizing gold and silver nanoparticles. Rose and pomegranate extracts were used to synthesize gold nanoparticles. Evaluation using ultraviolet-visible (UV-Vis) spectroscopy confirmed the nanoparticle formation, and Fourier transform infrared spectroscopy (FT-IR) analysis recognized the presence of plant-derived compounds for stabilizing these particles. In-depth observations of their size and form were provided using electron microscopy, and these findings were aligned with the inferences made from the UV-Vis data. Silver nanoparticles were produced using Ocimum gratissimum leaf extract (OGE), exhibiting dose-dependent antimicrobial effects against bacterial strains. A comparative analysis demonstrated the distinct antibacterial characteristics of silver and gold nanoparticles against several bacterial strains. These nanoparticles demonstrated enhanced inhibitory effects when employed in combination with antibiotics, suggesting the possibility of dealing with antibiotic resistance. The study presents opportunities for producing nanomaterials with minimal impact on the environment and for addressing antibiotic resistance. Further research can enhance the process and find more useful applications as this green synthesis approach can bring about significant improvements in many areas.

Ultrasound-Assisted Extraction, Characterization and Assessment of Vegetable Tannins from Guava (Psidium guajava) Leaves for Leather Tanning

For commercial leather processing, chrome tanning is the most used approach but it significantly contributes to environmental pollution. Vegetable tannins, which are large polyphenolic compounds, form strong interactions with proteins and carbohydrates, thereby enhancing the adaptability and value of vegetable-tanned leather as well as reducing environmental impact. In this study, vegetable tannins were extracted from the leaves of Guava plants (Psidium guajava) using ethanol as the solvent, facilitated by ultrasound. Extracted tannins were quantified using the Folin–Ciocâlteu reagent with ultraviolet-visible spectroscopic method. Ultrasound enhanced the extraction process producing a high yield in less time due to its mechanical, thermal, and cavitation impacts. The extracted tannins were characterized by a variety of spectroscopic techniques, including Proton (1H) Nuclear magnetic resonance, Fourier-transform infrared, and ultraviolet-visible spectroscopy. The effect of various process variables, such as temperature, solid-liquid ratio, ultrasonic power, extraction period, and powder fineness, were also investigated to optimize the extraction process. Finally, the extracted tannins were employed in leather tanning processes to assess their potential as tanning agents. The extracted tannins ensured uniform diffusion of tannins, improved thermal stability and reduced the number of tannins in effluent by 68% making it an environmentally friendly leather tanning process.

Exploring the potential of Nauclea latifolia for sustainable synthesis of ZnO nanoparticles: characterization and antibacterial assessment

The work presents a report on Zinc oxide nanoparticles (ZnO NPs) synthesized through a green approach using Nauclea latifolia fruit extracts, with a view to investigating the prepared nanoparticles for their antimicrobial activities. The ZnO NPs synthesized were characterized using various analytical instruments, including X-ray Diffraction (XRD), Fourier Transform Infrared (FTIR), Ultraviolet-Visible (UV-Vis) spectroscopy, Dynamic Light Scattering (DLS), and Transmission Electron Microscopy (TEM). The instruments provided valuable information on the characteristics of the Zn ONPs. The antibacterial activities of the synthesized ZnO NPs were evaluated with Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli). The maximum absorption was observed at 379 nm. The average hydrodynamic size and the polydispersity index (PDI) were measured as 81.77 nm and 0.401, respectively. The nanomaterial has a hexagonal wurtzite structure, and the Zn–O bond was detected at 537 cm–1. The nanoparticles were in the nano range with sizes ranging from 10.02 nm to 28.50 nm. The N. latifolia fruit extract-mediated ZnO NPs showed excellent performance against the two bacteria at all concentrations of ZnO NPs. The highest inhibition zones for E. coli and S. aureus at 8 mg/L of ZnO NPs are 21 and 16 mm, respectively. This study provides valuable insights into an efficient, simple, and environmentally friendly route for synthesizing ZnO NPs with a potential application in the biomedical field.

Ferroheme/Ferriheme Directly Involved in the Synthesis and Decomposition of Hydrazine as an Electron Carrier during Anammox.

Anammox bacteria performed the reaction of NH4+ and NO with hydrazine synthase to produce N2H4, followed by the decomposition of N2H4 with hydrazine dehydrogenase to generate N2. Ferroheme/ferriheme, which serves as the active center of both hydrazine synthase and hydrazine dehydrogenase, is thought to play a crucial role in the synthesis and decomposition of N2H4 during Anammox due to its high redox activity. However, this has yet to be proven and the exact mechanisms by which ferroheme/ferriheme is involved in the Anammox process remain unclear. In this study, abiotic and biological assays confirmed that ferroheme participated in NH4+ and NO reactions to generate N2H4 and ferriheme, and the produced N2H4 reacted with ferriheme to generate N2 and ferroheme. In other words, the ferroheme/ferriheme cycle drove the continuous reaction between NH4+ and NO. Raman, ultraviolet-visible spectroscopy, and X-ray absorption fine structure spectroscopy confirmed that ferroheme/ferriheme is involved in the synthesis and decomposition of N2H4 via the core FeII/FeIII cycle. The mechanism of ferroheme/ferriheme participation in the synthesis and decomposition of N2H4 was proposed by density functional theory calculations. These findings revealed for the first time the heme electron transfer mechanisms, which are of great significance for deepening the understanding of Anammox.

Combining analytical techniques to assess the translocation of diesel particles across an alveolar tissue barrier in vitro

BackgroundDuring inhalation, airborne particles such as particulate matter ≤ 2.5 μm (PM2.5), can deposit and accumulate on the alveolar epithelial tissue. In vivo studies have shown that fractions of PM2.5 can cross the alveolar epithelium to blood circulation, reaching secondary organs beyond the lungs. However, approaches to quantify the translocation of particles across the alveolar epithelium in vivo and in vitro are still not well established. In this study, methods to assess the translocation of standard diesel exhaust particles (DEPs) across permeable polyethylene terephthalate (PET) inserts at 0.4, 1, and 3 μm pore sizes were first optimized with transmission electron microscopy (TEM), ultraviolet-visible spectroscopy (UV-VIS), and lock-in thermography (LIT), which were then applied to study the translocation of DEPs across human alveolar epithelial type II (A549) cells. A549 cells that grew on the membrane (pore size: 3 μm) in inserts were exposed to DEPs at different concentrations from 0 to 80 µg.mL− 1 ( 0 to 44 µg.cm− 2) for 24 h. After exposure, the basal fraction was collected and then analyzed by combining qualitative (TEM) and quantitative (UV-VIS and LIT) techniques to assess the translocated fraction of the DEPs across the alveolar epithelium in vitro.ResultsWe could detect the translocated fraction of DEPs across the PET membranes with 3 μm pore sizes and without cells by TEM analysis, and determine the percentage of translocation at approximatively 37% by UV-VIS (LOD: 1.92 µg.mL− 1) and 75% by LIT (LOD: 0.20 µg.cm− 2). In the presence of cells, the percentage of DEPs translocation across the alveolar tissue was determined around 1% at 20 and 40 µg.mL− 1 (11 and 22 µg.cm− 2), and no particles were detected at higher and lower concentrations. Interestingly, simultaneous exposure of A549 cells to DEPs and EDTA can increase the translocation of DEPs in the basal fraction.ConclusionWe propose a combination of analytical techniques to assess the translocation of DEPs across lung tissues. Our results reveal a low percentage of translocation of DEPs across alveolar epithelial tissue in vitro and they correspond to in vivo findings. The combination approach can be applied to any traffic-generated particles, thus enabling us to understand their involvement in public health.

Investigation of the electronic band gap tuning by Si doping on BeO using UV–VIS spectroscopy and density functional theory

BeO with tissue equivalent features promising dosimetric properties, making BeO particularly suitable for being used in all dosimetry applications. In this work, BeO was synthesized and doped with Si using sol-gel and solid-state methods, respectively. To find the optical band gap of Si-doped BeO nanoparticles (BeO:Si) experimentally, the ultraviolet-visible (UV–Vis) spectroscopy was used. To simulate the electronic band structure of BeO and Si-doped BeO, we used the QUANTUM ESPRESSO code based on density functional theory (DFT). The calculated electronic band structure exhibited insulator behavior and the band gap decreased with Si doping in two potential types. Compared to BeO, a shift toward lower energies was determined from the UV–Vis absorption spectrum of BeO:Si, the simulated and the experimental band gaps were found to be in good agreement. These findings offer insights into the dopant syntheses of BeO and their widespread use for fundamental studies as well as their potential applications.

Ultrasonically Assembled 0-D Zirconium Oxide on TiO2 Nanorod for a Sensitive Determination of Antibiotic Drug in Biological Samples

Abstract Biological, food, and water samples were used to determine the amount of Furazolidone (FUZ) in a variety of applications, including health and nutrition, diagnosis/treatment, pharmacological research, and food/drug quality monitoring. Using hydrothermal and ultrasonication strategies, new type of TiO2 (1D) and ZrO2 (0D) (TiO2/ZrO2) nanocomposites were prepared for FUZ determination. Then the prepared nanocomposite was characterization under X-ray diffraction, field emission scanning electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, ultra violet visible spectroscopy, and the electrochemical property of the material was characterized by electrochemical impedance spectroscopy and cyclic voltammetry (CV). In addition, detection of FUZ was analyzed by electroanalytical studies such as CV and differential pulse voltammetry (DPV). This proposed TiO2/ZrO2/GCE sensor exhibits excellent electrochemical characteristics, including excellent linearity (0.01 – 537.22 µM), nanomolar detection limit (19 nM), and encouraging sensitivity (0.35 µA µM-1cm-2) and it shows greater selectivity, repeatability, and longer storage stability. Along with concerned realizability, the primed sensor was analyzed over biological samples that reveal good recovery in real samples.

The potential biological activities of Aspergillus luchuensis-aided green synthesis of silver nanoparticles

Biosynthetic metals have attracted global attention because of their safety, affordability, and environmental friendliness. As a consequence, the cell-free filtrate (CFF) of Dill leaf-derived endophytic fungus Aspergillus luchuensis was employed for the extracellularly synthesis silver nanoparticles (AgNPs). A reddish-brown color shift confirmed that AgNPs were successfully produced. The obtained AgNPs were characterized by UV–Vis (ultraviolet–visible spectroscopy), Transmission electron microscopy (TEM), FTIR, EDX, and zeta potential. Results demonstrated the creation of crystalline AgNPs with a spherical shape at 427.81 nm in the UV–Vis spectrum, and size ranged from 16 to 18 nm as observed by TEM. Additionally, the biogenic AgNPs had a promising antibacterial activity versus multidrug-resistant bacteria, notably, S. aureus, E. coli, and S. typhi. The highest growth reduction was recorded in the case of E. coli. Furthermore, the biosynthesized AgNPs demonstrated potent antifungal potential versus a variety of harmful fungi. The maximum growth inhibition was evaluated from A. brasinsilles, followed by C. albicans as compared to cell-free extract and AgNO3. In addition, data revealed that AgNPs possess powerful antioxidant activity, and their ability to scavenge radicals increased from 33.0 to 85.1% with an increment in their concentration from 3.9 to 1,000 μg/mL. Furthermore, data showed that AgNPs displayed high catalytic activity of safranin under light irradiation. The maximum decolorization percentage (100%) was observed after 6 h. Besides, the biosynthesized AgNPs showed high insecticidal potential against 3rd larval instar of Culex pipiens. Taken together, data suggested that endophytic fungus, A. luchuensis, is an attractive candidate as an environmentally sustainable and friendly fungal nanofactory.

Green synthesis of silver nanoparticles using leaf extract of Calluna vulgaris: Characterizations, properties, and photocatalytic activities

Green synthesis of silver nanoparticles was carried out using leaf extract from Calluna vulgaris. The formation of nanoparticles was confirmed through the emergence of a surface plasmon resonance band in ultraviolet-visible spectroscopy. The characterization conducted using various microscopic techniques revealed that the nanoparticles mostly ranged in size from approximately 20 to 70 nm. Analysis, including Fourier transform infrared spectrometry, X-ray diffraction, and energy-dispersive X-ray spectroscopy, confirmed the chemical, crystalline structure, and presence of silver, respectively. The synthesized nanoparticles exhibited notable stability with an average zeta potential of -23.1 ± 0.6 mV. Evaluation of their antibacterial activity against Staphylococcus aureus and Escherichia coli demonstrated significant efficacy with diameters of inhibition zones measuring 10.23 ± 0.54 mm and 15.38 ± 0.32 mm, respectively. Additionally, the nanoparticles displayed a remarkable inhibition of approximately 88% against E. coli biofilm formation at a concentration of 100 μg/mL. They also exhibited unique photocatalytic performances. This research contributes to the literature in this field by producing new silver nanoparticles with cost-effectiveness, stability, antibacterial, antioxidant, antibiofilm, and photocatalytic properties, while using a previously untapped plant extract for this purpose.

Valorizing the potential of saffron petals extract for aluminium corrosion control: An integrated approach involving extraction, experimental and computational analysis

Our study focuses on enhancing the antioxidant potential of saffron petals extract (SPE) as a sustainable corrosion inhibitor for aluminium (Al) in a 3.5% NaCl solution. The phytochemical screening and antioxidant activity are identified. Various investigative methodologies, including experimental techniques such as Electrochemical Impedance Spectroscopy (EIS) and Potentiodynamic Polarization (PDP), were employed to evaluate the effectiveness of this compound in inhibiting corrosion. Computational analysis, involving Density Functional Theory (DFT) and Molecular Dynamics (MD) simulations, were utilized to carry out a Theoretical study on the main constituents of SPE. The surface characteristics and composition of the corroded Al were examined using a combination of Scanning Electron Microscopy (SEM), Energy-Dispersive X-ray Spectroscopy (EDX) and Fourier Transform Infrared Spectroscopy (FT-IR). The Electrochemical results suggest that the effectiveness of the inhibitor was dependent on its concentration, reaching 95.11% at 500 ppm of SPE. The PDP indicates that mixed inhibition control effectively slowed down the corrosion of Al. Furthermore, the adsorption behaviour of SPE onto Al follows to the Langmuir isotherm model. SEM, EDX and FT-IR analyses further verified significant alterations in the surface morphology and roughness of Al and confirming the successful formation of a protective layer on the Al surface. Ultraviolet-Visible spectroscopy (UV-Vis) reveals evidence of interaction between Al and the SPE molecules. Computational studies substantiated these observations, demonstrating the reactivity and adsorption patterns of the evaluated major bioactive molecules of SPE on the Al surface.

Effect of Oligoricinoleic Acid on Degradation of Polylactic Acid

ABSTRACT The objective of this research is to explore the impact of oligoricinoleic acid (ORA) on the degradation of polylactic acid (PLA). ORA was synthesized from ricinoleic acid using tin (II) 2-ethylhexanoate as a catalyst. The chemical structures of the obtained ORA were confirmed by Fourier-transform infrared spectrometer (FT-IR) and proton nuclear magnetic resonance spectroscopy (1H-NMR). PLA/ORA films were prepared through the casting method by varying ORA concentrations as 0.1%wt, 0.3%wt, 0.5%wt, 1.0 wt%, and 3.0%wt. Degradation of the films via hydrolysis was studied by soaking the films in deionized water and stirring at 120 rpm in an incubator at 37°C. Alterations in the structure and properties of the films were investigated after soaking for 7, 14, 21, and 28 days using ultraviolet-visible spectroscopy (UV-Vis), Fourier-transform infrared spectrometer (FTIR), scanning electron microscope (SEM), X-ray diffraction (XRD), differential scanning calorimeter (DSC), thermogravimetric analysis (TGA), and universal testing machine (UTM). Gel permeation chromatography (GPC) was performed to confirm the decrease in molecular weight (MW). The presence of 3%wt ORA could promote both ductility and degradation of PLA films. ORA further enhances thermal stability, indicating potential for prevention of thermal degradation during melt processing.

Improved Synthesis of Cu2O NPs and Ascorbic Acid-Modified Derivatives for Adsorption of Brilliant Cresyl Blue: Surface and Reusability Studies

This study addresses the critical need for efficient and recyclable photocatalysts for water treatment applications by presenting a novel approach for the synthesis and characterization of copper (I) oxide (Cu2O) nanoparticles modified with ascorbic acid (Cu2O/AA). The motivation for this research stems from the increasing concern about environmental pollution caused by organic pollutants, such as Brilliant Cresyl Blue (BCB), and the necessity for sustainable solutions to mitigate this issue. Through comprehensive characterization techniques including Ultraviolet–Visible spectroscopy (UV-Vis), Fourier Transform Infrared spectroscopy (FTIR), X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), zeta potential measurements, and Brunauer–Emmett–Teller (BET) analysis, we demonstrate a significant modification to the electronic structure, enhancing the photocatalytic activity of Cu2O/AA. BET analysis revealed a mesoporous structure with a specific surface area of 2.7247 m2/g for Cu2O/AA, further emphasizing its potential for enhanced catalytic performance. The photocatalytic degradation studies showcased remarkable efficiency improvements, with degradation coefficients of 30.8% and 73.12% for Cu2O NPs and Cu2O/AA NC, respectively, within a 120 min timeframe. Additionally, recyclability experiments indicated sustained efficiency over five consecutive cycles, with both catalysts retaining crystalline integrity. These findings underscore the promising potential of Cu2O/AA nanoparticles as highly efficient and recyclable photocatalysts for the degradation of organic pollutants, offering superior performance compared to pure Cu2O NPs and addressing the pressing need for sustainable water treatment solutions.

Cu/Co Bimetallic Carbon Catalyst as a Highly Efficient Promoter for Reactive Dyes Degradation with PMS.

The synergistic effect between bimetallic catalysts has been confirmed as an effective method for activating persulfate (PMS). Therefore, we immobilized copper-cobalt on chitosan to prepare bimetallic carbon catalysts for PMS activation and degradation of reactive dyes. Experimental results demonstrate that the CuCo-CTs/PMS catalytic degradation system exhibits excellent degradation performance toward various types of reactive dyes (e.g., Ethyl violet, Chlortalidone, and Di chlorotriazine), with degradation rates reaching 90% within 30 min. CuCo-CTs exhibit high catalytic activity over a wide pH range of 3-11 at room temperature and under static conditions, degrading over 92% of RV5 within 60 min. ultraviolet-visible (UV-vis) spectroscopy and color changes in the dye solution confirm the effective degradation of RV5, with a degradation rate of 97.2% within 10 min. Additionally, CuCo-CTs demonstrate good stability and reusability, maintaining a degradation rate of 92.8% after eight cycles. Kinetic studies indicate that the degradation follows pseudo-first-order kinetics. Furthermore, based on the results of radical scavenging experiments, the catalytic degradation mechanism of the dye involves both radical and nonradical pathways, with 1O2 identified as the primary active species. This study provides insights and experimental evidence for the application of persulfate oxidation in the treatment of dyeing wastewater.

Discrimination of Brazilian green canephora coffee beans by ultraviolet–visible spectroscopy as a non-target analysis: A tool for recognizing geographical indications

Specialty green coffee beans have a higher commercial value and some of them have recently been classified in Brazil based on the indication of provenance and denomination of origin. In this context, the classification of the type of coffee bean is still a challenge, using traditional analytical techniques. Thus, alternative analytical techniques, such as ultraviolet–visible spectroscopy (UV–Vis), as non-target analysis can be applied as a quick and reliable method of coffee classification using data science, such as chemometric tools. In the present study, UV–Vis were evaluated as a new strategy for discrimination of green beans of Brazilian specialty canephora coffees with recognized geographical indications (Robusta Amazônico and Conilon from state of Espírito Santo), for the first time. Spectra obtained from the aqueous extract of 222 samples. The Principal Component Analysis (PCA) was performed and subsequently Partial Least Squares with Discriminant Analysis (PLS-DA) model developed. The PCA indicated tendency to group the samples in their respective classes, pointing to the similarities in the spectra of samples of the same origin. The PLS-DA model obtained showed figures of merit values starting at 89.3% in the test set. The VIP scores showed that the variables associated with chlorogenic acids, caffeine and chlorophyll are the most important for differentiating the studied coffees. The results obtained showed that UV–Vis fingerprint − non-targeted analysis associated with PLS-DA is appropriate for the discrimination of green beans of Brazilian specialty coffee from different origins, in a simple way, using common equipment in several laboratories.

Synthesis, Characterization, and Properties of a Titanium(IV)-Tetrathiafulvalene-Based Complex.

To deeply investigate the interaction between a tetrathiafulvalene (TTF) unit and a Ti(IV) center, a monomeric heteroleptic octahedral Ti(IV) complex containing a diimine ligand composed of a 1,10-phenanthroline core fused with a TTF fragment (ligand 2a) was prepared. The stable complex formulated as Ti(1)2(2a), where 1 is a 2,2'-biphenolato derivative, was efficiently synthesized by following a one-step approach. This complex and its model species [Ti(1)2(2b)] were fully characterized in solution, and their solid-state structures were established by single-crystal X-ray diffraction analysis. Density functional theory calculations allowed the assignment of the frontier orbitals involved in the electronic transitions characterized by ultraviolet-visible absorption spectroscopy. Electrochemical and spectroelectrochemical studies revealed that the TTF unit within Ti(1)2(2a) can undergo two reversible one-electron oxidation processes; a reversible one-electron reduction of the Ti(IV) atom was highlighted. The photophysical measurements performed for this donor-acceptor molecular system indicated that an electron transfer process upon light excitation occurred within Ti(1)2(2a).

Optimization of ultrasonic pretreatment and analysis of chlorogenic acid in potato leaves

Chlorogenic acid (CA) is an effective ingredient that can strengthen immunity during following the COVID-19 era. The current cost of CA is high owing to its complex purification process and low yield (approximately 2%). In this study, a one-step path orthogonal experiment was designed based on the results from Gauss calculation, which consisted of acidity, coordination, and hydrolysis in molecules. The optimized extraction conditions were 60 ℃, 60 min, 1:20 liquid ratio, and 40% ethanol in a nitrogen atmosphere controlled using a device of our own design, which led to CA yields of up to 6.35% from potato leaves. The purified CA was analyzed using high-performance liquid chromatography, thin-layer chromatography, ultraviolet–visible spectroscopy, and molecular fluorescence. This accurate and reproducible method can not only be used to obtain high yields of CA but can also be used for the quality control of active plant products and their isomers.

The role of reduced graphene oxide on mitigation of lead phytotoxicity in Triticum aestivum L.plants at morphological and physiological levels

Rapid global industrialization and an increase in population have enhanced the risk of heavy metals accumulation in plant bodies to disrupt the morphological, biochemical, and physiological processes of plants. To cope with this situation, reduced graphene oxide (rGO) NPs were used first time to mitigate abiotic stresses caused in plant. In this study, rGO NPs were synthesized and reduced with Tecoma stans plant leave extract through modified Hummer's methods. The well prepared rGO NPs were characterized by ultra-violet visible spectroscopy (UV–Vis), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Zeta potential, and scanning electron microscopy (SEM). However, pot experiment was conducted with four different concentrations (15, 30, 60, 120 mg/L) of rGO NPs and three different concentrations (300, 500,700 mg/L) of lead (Pb) stress were applied. To observe the mitigative effects of rGO NPs, 30 mg/L of rGO NPs and 700 mg/L of Pb were used in combination. Changes in morphological and biochemical characteristics of wheat plants were observed for both Pb stress and rGO NPs treatments. Pb was found to inhibit the morphological and biochemical characteristics of plants. rGO NPs alone as well as in combination with Pb was found to increase the chlorophyll content of wheat plants. Under Pb stress conditions and rGO NPs treatments, antioxidant enzyme activities like ascorbate peroxidases (APX), superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT) were observed. Current findings revealed that greenly reduced graphene oxide NPs can effectively promote growth in wheat plants under Pb stress by elevating chlorophyll content of leaves, reducing the Pb uptake, and suppressing ROS produced due to Pb toxicity.

Fabrication of sulfobutylether-β-cyclodextrin/glabridin inclusion complex for promoting bioactivities.

As the main active compound of Glycyrrhiza glabra L., glabridin (GLD) has been shown to have multiple bioactivities, whereas the clinical application of GLD is restricted by its low water solubility. In this study, GLD was encapsulated into a sulfobutylether-β-cyclodextrin (SBE-β-CD)-based inclusion complex (SBE-β-CD/GLD) by the freeze-drying method. The materials characterization, antibacterial activity, stimulated cellular behavior and in vivo full-thickness diabetic wound healing ability of the hydrogels were assessed and analyzed. The successful encapsulation of the inclusion complex was confirmed by ultraviolet (UV) visible spectroscopy, Fourier transform infrared (FT-IR), X-ray diffractometer (XRD), scanning electron microscope (SEM), and nuclear magnetic resonance (NMR). SBE-β-CD as an excipient significantly enhances the water solubility of GLD, and SBE-β-CD/GLD showed excellent biocompatibility on human vascular endothelial cells (HUVECs) and erythrocytes. The SBE-β-CD/GLD inclusion complex exerted a pronounced antibacterial activity on Staphylococcus aureus and Escherichia coli in vitro. The SBE-β-CD/GLD inclusion complex markedly enhanced the antioxidant activity compared with free GLD. The SBE-β-CD/GLD inclusion complex potently accelerates the healing of full-thickness skin defects by inhibiting inflammation. The outcomes suggest that SBE-β-CD could be used as a promising drug delivery system for the clinical application of GLD.

Novel green synthesis of Value-Added graphene quantum dots from bagasse and pith for biological applications

The continuing rush for potential biomedical applications has sparked the fabrication of graphene quantum dots (GQDs) particularly from agricultural waste. GQDs are unique among carbon-based nanomaterials due to their flexibility, chemical stability, size control, and non-toxic nature. In this study, we have developed Graphene Quantum dots from sugarcane bagasse (GQDs-SB) and sugarcane bagasse pith (GQDs-SBP) by carbonization followed by microwave pyrolysis. The optical properties of the synthesized GQDs-SB and GQDs-SBP were characterized by Ultraviolet–Visible spectroscopy and Photoluminescence (PL) analysis and the surface functional groups were determined by FT- IR analysis. The High resolution transmission electron microscopy (HR-TEM) was used to examine dimensions and structure of GQDs-SB and GQDs-SBP. The storage stability of GQDs-SB and GQDs-SBP was monitored using Ultraviolet–Visible spectroscopy. The synthesized GQDs-SB and GQDs-SBP were evaluated for biological applications like anti-oxidant activity, anti inflammatory activity and cytotoxic effect was also assessed. GQDs-SB and GQDs-SBP demonstrated significant antioxidant and anti-inflammatory effects due to their great ability to scavenge free radicals and extraordinary water solubility. The synthesized GQDs-SB and GQDs-SBP were less toxic in nature.