UV-Vis Analysis Research Articles

Enhanced photocatalytic degradation of antiviral drugs lopinavir and ritonavir by Ni doped ZnO/SiO2 nanocomposites

Enhanced photocatalytic degradation of antiviral drugs lopinavir and ritonavir by Ni doped ZnO/SiO2 nanocomposites

Detection of presence of Bioactive metabolites in CCFE (Co cultured Cell Free Extracts) of Microbacterium barkeri (LMA4), Corynebacterium argentoratense (LMA5) and Streptomyces shenzhenensis (LMA6)

The members of actinomycetes, versatile microspecies with dynamic source of bioactive molecules, are the nodal attraction of researchers. Continuous efforts are streaming to detect and launch new or derivetatised antibiotics to defend against the reemerged drug resistant infectious agents. This communication is dealt with detection of bioactive molecules from three strains of novel actinomycetal strains, namely, Microbacterium barkeri (LMA4), Corynebacterium argentoratense (LMA5) (Gene bank No. OP023130) and Streptomyces shenzhenensis (LMA6) (Gene bank No. OQ092768) isolated from pond soil of near by locality. The strains were cocultured with laboratory maintained bacteria, Staphylococcus aureus (BMS4) and a Gram negative, Escherichia coli (BME4) and the co cultured cell free extract (CCFE) of respective actinobacterial strains were subjected to UV-visible and LC MS analysis. The preliminary observation could note about similar peak pattern with Streptomycin, Doxorubicin, Pyrazine, Pyrrolizidines, Oxacillin, Ciprofloxacin, Allistatin, Gentamycin, Chlorellin, Penicillin, Penicillin G, Kanamycin, Levofloxacin, Amikacin, Ofloxacin, Imipenem and more over Ampicillin, as inferred from UV visible, followed by Liquid chromatography. The conclusive result was inferred from the LC-MS (m/z) spectrum analysis. It was noted that the peak with ID-53, eluted from the CFE, of co-culture broth of LMA4 with BMS4, with retention time (RT) 26.99 (min), of m/z 751.3, carried out with Electrospray Ionisation (ES) in +ve mode (ES+), Peaks with IDs, 45, 54 (24.65 and 27.11respective RTs), having resultant m/z, 749.8and 751.7 in ES-, and the CFE containing LMA6 and BMS4, with eluted peak Ids 12, 42 (RTs, 5.71, 20.55), having m/z 752.4 and 749.8 and 749.8 in ES+ mode, which could be assigned with structure of Azithromycin.

Passivator materials based on the benzothiazole-sulfonamide hybrid: Synthesis, optical, electrochemical properties, and molecular modeling for perovskite solar cells

Passivator materials based on the benzothiazole-sulfonamide hybrid: Synthesis, optical, electrochemical properties, and molecular modeling for perovskite solar cells

Eco-friendly Synthesis of Gold Nanoparticles of Methanolic Extract of Bauhinia vahlii Leaves and Evaluation of Tyrosinase Inhibitory Activity

Background: The green synthesis of gold nanoparticles (AuNPs) using natural materials has gained significant attention in recent years due to their eco-friendliness and potential applications in various fields. Methods: The present study aimed at the green synthesis and anti-hyperpigmentation potential of gold nanoparticles (AuNPs) using a methanolic extract of Bauhinia vahlii. Furthermore, the green synthesis of the AuNPs was confirmed by UV-visible, FT-IR, XRD, and EMDEX analysis. The size and surface topological significance of green synthesized AuNPs were evaluated through Scanning Electron Microscope and Field Emission Scanning Electron Microscopy. Results: The size of the synthesized AuNPs was found to be in the range of 100-1000 nm. The tyrosinase inhibitory activity of AuNPs was evaluated through the mushroom tyrosinase inhibitory assay method. The tyrosinase inhibitory activities of crude extract, AuNPs, and Kojic acid were found to be 98.7 ±0.7, 75±1.3 and 41±1.1 μg/ml, respectively. Conclusion: Hence, green synthesized AuNPs of B. vahlii leaf extract may be used as a potent antihyperpigmentation agent in the market of nano cosmeceuticals.

Green synthesis of anethole-loaded zinc oxide nanoparticles enhances antibacterial strategies against pathogenic bacteria.

The threat of antibiotic resistance is escalating, diminishing the effectiveness of numerous antibiotics due to the rapid development of resistant bacteria. In response, the use of green-synthesized nanoparticle, alone or combined with antimicrobial agents, appears promising. This study explores the effectiveness of zinc oxide nanoparticles (ZnONPs) synthesized using Loranthus cordifolius leaf extracts and subsequently coated with anethole. The fabrication of these nanoparticles was confirmed via UV-Vis, FTIR and TEM analyses, ensuring the nanoparticles were produced as intended. Utilizing a nanoprecipitation process that excludes evaporation and drying, a high drug loading capacity of 16.59% was accomplished. The encapsulation efficiency for anethole was recorded at 88.23 ± 4.98%. Antibacterial efficacy was assessed by com paring the green-synthesized ZnONPs (average size: 14.47nm), anethole-loaded ZnONPs (average size: 14,75nm), and commercially sourced ZnONPs. The ZnONPs with anethole demonstrated superior inhibition against all tested bacterial strains, including Gram-negative species like Pseudomonas aeruginosa and Escherichia coli, and Gram-positive species like Bacillus subtilis and Staphylococcus aureus, outperforming the commercially available ZnONPs. Additionally, anethole-coated ZnONPs showed the greatest inhibition of Gyr-B activity (IC50 = 0.78 ± 0.2M), better than both green-synthesized and commercially available ZnONPs. These findings emphasize the enhanced antimicrobial properties of ZnONPs, particularly when combined with green synthesis and anethole loading, highlighting their potential in various biomedical applications.

Photocatalytic degradation of ampicillin antibiotics in aqueous solution utilizing ZnFe2O4/MWCNTs/TiO2 ternary nanocomposite under solar light irradiation

Photocatalytic degradation of ampicillin antibiotics in aqueous solution utilizing ZnFe2O4/MWCNTs/TiO2 ternary nanocomposite under solar light irradiation

Green synthesis of Tacrine modified Schiff bases as anti-Alzheimer Agents: An effective strategy validated through in-silico and in-vitro analysis

Green synthesis of Tacrine modified Schiff bases as anti-Alzheimer Agents: An effective strategy validated through in-silico and in-vitro analysis

Unveiling Fluorescence Spectroscopy, Molecular Docking and Dynamic Simulations: Interactions Between Protein and 2, 4-Dinitrophenylhydrazine Schiff Base.

In this study, we aimed to explore the interaction mechanism between bovine serum albumin (BSA) and a Schiff base compound derived from 2,4-dinotrophenyl hydrazine (L) using various spectroscopic techniques. The interaction between BSA and synthesizing molecule can provide insights into binding affinity, conformational changes and potential applications in drug delivery or biochemistry. The interaction between BSA and L was studied by using UV-Vis and fluorescence titration analysis. The fluorescence quenching emission was observed at 343nm, upon addition of L to the buffer solution of BSA. The binding between BSA and ligand is static in nature using fluorescence quenching emission. The thermodynamic parameters were calculated from the temperature-dependent binding constants (i.e., ∆H = -0.318kcal/mol, ∆G = -7.857kcal/mol and ∆S = 0.023kcal/mol), which indicated that the protein-ligand complex formation between L and BSA is mainly due to the electrostatic interactions. The experimental and theoretical results showed excellent agreement with respect to the mechanism of binding and binding constants. The molecular docking and molecular dynamic analysis experiments were performed to establish the interaction between protein and ligand.

DFT study of electronic and nonlinear optical properties of alkaline earth metals and superalkalis doped all-cis-1, 2, 3, 4, 5, 6-hexafluorocyclohexane as an efficient excess electron system

Continual advancements are being pursued to discover innovative strategies for developing materials with remarkable nonlinear optical (NLO) response. Herein, electronic, geometric, thermodynamic and NLO properties of excess electron systems based on stacked Janus dimer, all-cis-1,2,3,4,5,6-hexafluorocyclohexane (C6H6F6)2 are thoroughly investigated. The excess electron systems are designed by doping alkaline earth metals (AEMs) on fluorine face and superalkalis on hydrogen face of Janus dimer. The higher values of vertical ionization energies (VIE) and interaction energies (Eint), confirm the electronic and thermodynamic stabilities of the designed complexes, respectively. Natural bond orbital (NBO) analysis is performed, and the excess electron character of the complexes is confirmed through frontier molecular orbital (FMO) analysis by highest occupied molecular orbital (HOMO) iso-densities. FMO shows a significant decrease in energy gaps (Egap) of the complexes (i.e., Eg = 1.80–3.12 eV), compared to the stacked Janus dimer (i.e., Eg = 9.41 eV). The transparency of the complexes to UV region is confirmed through UV–vis analyses, revealing their maximum absorption in visible and near-IR regions. The higher NLO response of the designed excess electron systems is further proved by the greater values of first hyperpolarizability (β o ) i.e., up to 1.70 × 106 au. Moreover, the time dependent-density functional theory (TD-DFT) computations and two-level model are employed to investigate the controlling factors of hyperpolarizability, illustrating the contribution of transition energy (∆E3), change in dipole moment (∆μ) and oscillator strength (f o ) in controlling the β o . Ab-initio molecular dynamics (AIMD) simulation further confirm that the designed superalkalide complexes are kinetically and thermally stable. The thorough investigation of these excess electron systems proves them an appropriate candidate for NLO applications.

Synthesis and assessment of the Mo/MoO3/CZTS/Ag diode fabricated by one-pot hydrothermal route: impact of temperature

A facile one-step hydrothermal method was utilized to prepare Cu2ZnSnS4 film employing EDTA as a complexing agent. An effective Molybdenum oxide layer was also formed in the same approach for forming the Cu2ZnSnS4 film. The influence of preparation temperature on structural, morphology, and optical characteristics was studied. The formation of crystalline kesterite phase Cu2ZnSnS4 films with preferred orientation along the (112) plane was confirmed by X-ray diffraction and Raman spectroscopy, and it was also demonstrated that structure property changes with preparation temperatures: kesterite phase Cu2ZnSnS4 is formed at lower preparation temperatures and kesterite phase Cu2ZnSnS4 and Cu2S are formed with increasing preparation temperature. Also, Raman analysis confirmed the formation of a Molybdenum oxide layer on the Mo substrate. Field emission scanning electron microscopy revealed that surface morphology changes from leaves of trees to flake-flowers. According to UV-visible analysis, Cu2ZnSnS4 films exhibited high and wide absorbance spectra in the visible and infrared regions and a band gap between (1.67-1.9) eV. Photoluminescence analysis revealed emission peaks at (1.569, 1.55, and 1.56) eV for samples prepared at (160, 200, and 230)0C, respectively, which is very close to the band's gap of Cu2ZnSnS4. Finally, the electrical study of Mo/MoO3/CZTS/Ag junctions was performed by using current-voltage (I-V) measurement.

Green Synthesis of Luminescent Carbon Dots from Ficus benghalensis Aerial Roots for Bioimaging.

In this work, carbon quantum dots (CQDs) were prepared using a one-step hydrothermal green synthesis method from a low-cost and eco-friendly renewable biomass, specifically the Ficus benghalensis aerial roots (FB-AR). For the past two decades, CQDs have been noted for their tunable emission spectrum, quantum yield, biocompatibility, photostability, and unique optoelectronic properties such as photoluminescence (PL), and fluorescence. The synthesized Ficus benghalensis carbon quantum dots (FB-CQDs) were characterized for their physical, structural, and chemical properties using XRD, Raman, HRTEM, XPS, FTIR, TG-DTG, UV-visible, and photoluminance analysis. XPS analysis confirmed the presence of phytoconstituent functionalities and the composition of components. The FB-CQDs, which exhibit long-range emissions, have potential applications in various biological and therapeutic fields. Their bioimaging capability is tested in Escherichia coli bacteria. However, despite their promising characteristics, the FB-CQDs showed no antibacterial inhibition against Escherichia coli and Staphylococcus aureus, likely due to its carbonization temperature.

Electrochemical hydrogen storage using SrFe12O19 surface-immobilized polyoxometalate

Electrochemical hydrogen storage using SrFe12O19 surface-immobilized polyoxometalate

Highly sensitive and selective ratiometric fluorescence and colorimetric detection of Cr(VI) via in situ encapsulation of green/red carbon quantum dots in zeolite

Highly sensitive and selective ratiometric fluorescence and colorimetric detection of Cr(VI) via in situ encapsulation of green/red carbon quantum dots in zeolite

Solvent assisted mechanochemical synthesis, antimicrobial and antioxidant studies of Ni2+, Mn2+, Cr<sup>2+</sup> , and Cu<sup>2+</sup> Metal complexes of some ligands derived from l-histidine and l-alanine

Mechanochemistry enables rapid, quantitative reactions to occur at or close to 27℃. It is a one-step process that allows for reactant homogenization, product nucleation, and particle growth. These processes use little or no solvent, making them less wasteful and more environmentally friendly than solvent-based reactions. Ni2+ , Mn2+, Cr2+and Cu2+ metal ions were synthesized by grinding in an agate mortar with pestle using ligands derived from amino acids (Histidine &Alanine) which were further synthesized to form complexes. The entire experiment was carried out by solvent solvent-assisted mechanochemical process and ethanol was used as liquid liquid-assisted solvent. The complexes were characterized by IR spectroscopy, U-V spectroscopy, X-ray analysis, melting point, solubility test, and conductivity measurement. The Solubility test showed that the complexes are soluble in DMSO, DMF, and ethanol and are insoluble in both hexane and tetrachloromethane. The molar conductivity values are in the range of (6.05-28.56) Ω-1cm2mol-1 ) indicating the complexes behave as non-electrolytes. IR analysis showed a vibrational frequency band observed at (1620-1625) cm-1 which is assigned to the ʋ(C=N) of the azomethine, also the new bands M=N, M=O indicate the coordination reaction between the metal and the ligands. The UV visible analysis shows various transitions, the metal complexes showed adsorption bands at λ of 420 and 575nm respectively because of the ligand-to-metal charge transfer (LMCT). The XRD analysis showed that there was a change in phase between the starting material and the product which indicate that a reaction occurred, also the nature of the spectra showed that the compounds are all crystalline. The Antimicrobial activity showed that both the complexes and the ligands have good activity against the bacterial isolates. Antioxidant activity was also tested and the compound appeared to have moderate scavenging activities compared to the reference used. The values indicated that the activities are more pronounced when coordinated with metal ions.

Studi penambahan chemical pada produk migas guna mengurangi dampak negatif terhadap lingkungan proses distribusi

The distribution of fuel impacts the environment through emissions and combustion residues. This study evaluates hydrocarbon compounds in petroleum products with ethanol addition to enhance octane ratings and reduce emissions. Gravimetric methods assessed ash content, FTIR analyzed organic compound absorption via functional groups, and UV-Vis spectrophotometry measured toluene levels through absorbance. Results showed ethanol blending with biodiesel reduced ash content from 74.48 mg/L to 64.99 mg/L, a 9.4% decrease, indicating a positive environmental impact. UV-Vis analysis revealed increased toluene content, reflecting higher octane value and potential emission reductions. Additionally, blending Pertamax with ethanol showed increased oxygenated compounds, such as alcohols and esters, at a 1600 nm wavelength. In conclusion, adding ethanol positively affects the environment by reducing emissions and improving octane ratings. However, further analysis is needed to comprehensively assess its environmental impact.

Investigating the effect of Cu underlayer and FTO etching towards photoelectrochemical performance enhancement of Cu2O photoelectrode

Investigating the effect of Cu underlayer and FTO etching towards photoelectrochemical performance enhancement of Cu2O photoelectrode

H2S gas sensing behavior of 2-D V2O5 nanowire network structure

H2S gas sensing behavior of 2-D V2O5 nanowire network structure

Structural phase transition from rhombohedral to monoclinic phase and physical properties of (1-x) Bi0.85La0.15FeO3 – (x) Ca0.5Sr0.5TiO3 ceramics prepared by the solid-state route

Structural phase transition from rhombohedral to monoclinic phase and physical properties of (1-x) Bi0.85La0.15FeO3 – (x) Ca0.5Sr0.5TiO3 ceramics prepared by the solid-state route

Eco-Friendly Photocatalytic Treatment of Dyes with Ag Nanoparticles Obtained through Sustainable Process Involving Spirulina platensis

The development of efficient photocatalysts is crucial in addressing water pollution concerns, specifically in the removal of organic dyes from wastewater. In this context, the use of silver nanoparticles (Ag NPs) might represent a method to achieve high dye degradation efficiencies. On the other hand, the classical Ag NP production process involves several reactants and operating conditions, which make it poorly sustainable. In the present work, Ag NPs were synthesized according to a new sustainable process involving the use of natural extracts of Spirulina platensis and milder operating conditions. The material was also calcined to determine the influence of organic content on the properties of Ag NPs. The X-ray diffraction (XRD) analysis displayed the AgCl and Ag phases with a crystalline size of 11.79 nm before calcination. After calcination, only the Ag phase was present with an increased crystalline size of 24.60 nm. Fourier Transform Infrared Spectroscopy (FTIR) confirmed the capping role of the metabolites from the extract. Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) revealed the spherical or quasi-spherical morphologies with agglomeration due to the calcination. Energy-dispersive X-ray spectroscopy (EDX) and Thermogravimetric (TGA) analyses further confirmed the involvement of metabolites in the synthesis of Ag NPs. The optical changes in the products were observed in a UV-Vis analysis. The Ag NPs were tested for their photocatalytic activity against the laboratory dye brilliant blue r in visible light in various conditions. The highest degradation efficiency of 81.9%, with a kapp value of 0.00595 min−1, was observed in alkaline medium after 90 min of light irradiation.

Nanopriming with phytofabricated selenium nanoparticles alleviates arsenite-induced oxidative stress in Spinacia oleracea L.

Arsenic (As) contamination of agricultural soil has become a major concern due to its adverse effects on plant growth and human health. Selenium nanoparticles (SeNPs), a novel selenium (Se) source, are characterised by their exceptional biocompatibility, degradability, and bioactivities. In the present study, SeNPs were biogenically synthesised and further characterised using UV-visible spectroscopy, XRD, FTIR, and TEM analysis. Different concentrations of the synthesised SeNPs were used to treat Spinacia oleracea L. (spinach) seeds to determine their impact on growth profile, gas exchange, photosynthetic pigments, oxidative stress, and antioxidant enzyme status upon arsenite (AsIII) treatment. The findings revealed that SeNP supplementation at a concentration of 100µM (SeNPs100) led to a significant reduction in As accumulation by twofold in roots and 1.5-fold in leaves when compared to plants exposed to AsIII100 (µM) alone. Interestingly, the photosynthetic efficiency was also remarkably enhanced upon SeNPs100 treatment, associated with increased activities of the defence enzymes (ascorbate peroxidase, catalase, and glutathione peroxidase) in the AsIII + SeNP-exposed spinach plants as compared to AsIII treatment alone. Overall, the present study highlights the potential of biogenic SeNP supplementation in promoting plant growth and mitigating As toxicity in spinach under AsIII stress. This study could have significant implications for the use of SeNPs as a nanofertiliser in regions grappling with As-contaminated soils for sustainable agriculture and human health.