UV Absorption Spectra Research Articles

Influence of starch capping effect on optical absorption and photoluminescence behaviour of ZnS nanoparticles

The green chemical of route synthesis followed and the precursor compounds taken during the synthesis of ZnS nanoparticles (NPs) play an imperative role on their structural and photo physical properties. The green chemical route of synthesis of NPs is proved to be an advantageous method imparting novel properties to the synthesized NPs. Present study involves the synthesis of uncapped and starch capped ZnS NPs by a facile chemical coprecipitation technique. ZnS NPs have been synthesized using zinc acetate and sodium sulfide as precursors. The structural and morphological features of the samples were studied by Xray diffraction (XRD) and field emission electron microscopy (FESEM). Fourier transform infra red spectra (FTIR) was carried out to confirm capping by starch. Compositional analysis was done by electron dispersive spectroscopy (EDS). Optical properties were analyzed using UVabsorption spectra and photoluminescence (PL) measurements. Formation of ZnS NPs with cubic phase was revealed by XRD and quantum confinement effect by the UV absorption. With increase in capping agent (starch) concentration PL intensity decreased. Such heavy metal free, nontoxic ZnS nanoparticles are suitable for optoelectronic applications.

Photoisomerization of 1,2-Di(4-pyridyl)ethylene According to NMR and UV Spectroscopy Data and Density Functional Modeling.

Photoisomerization of 1,2-di(4-pyridyl)ethylene under UV irradiation was studied by NMR and UV spectroscopy in solutions of acetone, acetonitrile and chloroform. It has been established that in the studied solutions under irradiation, geometric photoisomerization occurs: the trans-isomer transforms into the cis-isomer and then cyclization occurs. DFT modeling of the listed processes, states and UV absorption spectra of the sample in an acetonitrile solution was performed.

Dinuclear Phenoxo-Bridged Nickel(II) and Copper(II) Complexes of Phenolate-Based Tripodal Ligand: Theoretical and Experimental Insights

Three dinuclear complexes of composition [NiII 2(L)2][ClO4]2 and [CuII 2(L)2(OClO3)2] . 3H2O have been synthesized using a new tripodal ligand [(2-pyridyl)methyl](2-benzyl)-aminomethyl}-phenol (HL)], in its deprotonated form, providing a N2O donor set. Crystallographic analyses reveal that [CuII 2(L)2(OClO3)2] . 3H2O has a diphenoxo-bridged structure. In [CuII 2(L)2(OClO3)2] . 3H2O, each metal center is MIIN2O3-coordinated with a square-pyramidal environment for each copper(II) center. In this work, the molecular structure, harmonic vibrational frequencies and UV-Vis of [NiII 2(L)2]2+ and [CuII 2(L)2]2+ has been explored. With the help of density functional theory (DFT)/B3LYP techniques and LANL2DZ as a basis set, the ground-state molecule shape and vibrational frequencies were computed. The basic vibrations were allocated using the VEDA program to compute the potential energy distribution (PED) of the vibrational modes. The band gap energies of the title complexes ([NiII 2(L)2]2+ and [CuII 2(L)2]2+) are 3.21 eV and 1.59 eV, respectively, according to HOMO-LUMO energies. The maximal absorption wavelength and band gap energy of the title complexes were calculated theoretically using the UV absorption spectra. MEP analysis identifies electrophilic and nucleophilic sites. Hirshfeld surface analysis was used to characterize the 3D intermolecular interactions in ([NiII 2(L)2]2+ and [CuII 2(L)2]2+) of the crystal surface, whereas fingerprint plots were used to explain the 2D interactions. The biological activity of the complexes was investigated using molecular docking.

Hg(II) immobilization and detection using gel formation with tetra-(4-pyridylphenyl)ethylene and an aggregation-induced luminescence effect

Tetra-(4-pyridylphenyl)ethylene (TPPE), featuring an aggregation-induced luminescence effect (AIE), has been synthesized and used for selective detection of Hg2+ in DMF/H2O (3:7, v/v) binary solutions. There was a color change from colorless to yellow in the detection of the Hg2+ ions, in addition to an increased fluorescence emission. This shows that TPPE will function as an excellent “turn-on” fluorescence probe in the detection Hg2+. Moreover, the interference of Al3+, Ba2+, Mn2+, Ca2+, Fe3+, Cu2+, Ag+, Cd2+, Co2+, Ni2+, Mg2+, Pb2+, Zn2+, and Cr3+ ions was found to be negligible under optimized solvent conditions. Cysteine and EDTA were also found to form TPPE-based fluorescent switches with the Hg2+ ions. The practical use of the TPPE sensor was also demonstrated by using a specific test kit. Characterization using FT-IR, NMR titration, UV titration, EDS, and HR-MS techniques showed that Hg2+ will form a 1:1 complex with TPPE. Also, the observation of a Tyndall effect, in addition to UV absorption and fluorescence spectra, did clearly demonstrate the presence of an AIE. More noteworthy, TPPE and Hg2+ were found to form a metal–organic gel (MOG) in the DMF solution. The SEM, TEM, ICP, and Zeta potential analyses confirmed that the fluorescent MOG could further adsorb an excess of Hg2+ ions. The BET analyses revealed that the MOG showed a type IV-H3 hysteresis loop according to the International Union of Pure and Applied Chemistry classification. The results of the XRD analysis and of the spectroscopic titrations show that a π–π stacking may be the auxiliary driving force for the gel formation, after that a coordination has taken place. These results indicate that further research on structurally simple metal ion fluorescent probes, which are based on the AIE, is promising for the achievement of a simultaneous fluorescent detection and adsorption of heavy metal pollutants.

Changes of dissolved organic matter fractions and formation of oxidation byproducts during electrochemical treatment of landfill leachates: Development of spectroscopic indicators for process optimization

Electrochemical oxidation (EO) is an attractive option for treatment of dissolved organic matter (DOM) in landfill leachate but concerns remain over the energy efficiency and formation of oxidation byproducts ClO3− and ClO4−. In this study, EO treatment of landfill leachates was carried out using representative active and nonactive anode materials, cell configurations and current densities. Size exclusion chromatograms coupled with 2D synchronous and asynchronous correlation analysis showed that the sensitivity of DOM fractions to EO degradation was dependent on the anode material. The nonactive boron-doped diamond (BDD) anode demonstrated the best performance for DOM oxidation. The humic acid-like fraction (HA, 2.5–20 kDa) predominated the visible absorbance of landfill leachates at λ ≥400 nm, and it generally had the highest reaction rates except the occurrence of the pH-induced denaturation and precipitation of the proteinaceous biopolymer fraction (BP, >20 kDa). During the EO treatment of landfill leachate with BDD anode, the UV absorbance spectra of landfill leachates at wavelengths <400 nm were affected by the formation of free chlorine. Instead, the decrease of Abs420 was found to be a good indicator of the shift of the oxidation from predominantly HA fraction to the proteinaceous BP fraction. The behavior of the Abs420 parameter was also indicative of the transition from the energy-efficient oxidation of DOM to the dominance of side reactions of chlorine evolution and the subsequent formation of ClO3− and ClO4−. These findings suggest that the EO treatment of landfill leachate can be optimized by adjusting the current density with feedback signals from the online monitoring of Abs420, to achieve a trade-off between degradation of DOM and control of ClO3− and ClO4−.

Variation in the Optical Properties of PEO-Based Composites via a Green Metal Complex: Macroscopic Measurements to Explain Microscopic Quantum Transport from the Valence Band to the Conduction Band.

In this study, a green chemistry method was used to synthesize polymer composites based on polyethylene oxide (PEO). The method of the remediation of metal complexes used in this study is an environmentally friendly procedure with a low cost. Zinc metal ion (Zn2+)-polyphenol (PPHNL) complexes were synthesized for two minutes via the combination of a black tea leaf (BTL) extract solution with dissolved Zn-acetate. Then, UV-Vis and FTIR were carried out for the Zn-PPHNL complexes in a liquid and solid. The FTIR spectra show that BTLs contain sufficient functional groups (O-H, C-H, C=O, C=C, C-O, C-N, and N-H), PPHNL, and conjugated double bonds to produce metal complexes by capturing the cations of Zn-acetate salt. Moreover, FTIR of the BTL and Zn-PPHNL complexes approves the formation of the Zn-PPHNL complex over the wide variation in the intensity of bands. The UV absorption spectra of BTL and Zn-PPHNL indicate complex formation among tea PPHNL and Zn cations, which enhances the absorption spectra of the Zn-PPHNL to 0.1 compared to the figure of 0.01 associated with the extracted tea solution. According to an XRD analysis, an amorphous Zn-PPHNL complex was created when Zn2+ ions and PPHNL interacted. Additionally, XRD shows that the structure of the PEO composite becomes a more amorphous structure as the concentration of Zn-PPHNL increases. Furthermore, morphological study via an optical microscope (OM) shows that by increasing the concentration of Zn-PPHNL in a PEO polymer composite the size of the spherulites ascribed to the crystalline phase dramatically decreases. The optical properties of PEO: Zn-PPHNL films, via UV-Vis spectroscopy, were rigorously studied. The Eg is calculated by examining the dielectric loss, which is reduced from 5.5 eV to 0.6 eV by increasing the concentration of Zn-PPHNL in the PEO samples. In addition, Tauc's form was used to specify the category of electronic transitions in the PEO: Zn-PPHNL films. The impact of crystalline structure and morphology on electronic transition types was discussed. Macroscopic measurable parameters, such as the refractive index and extinction coefficient, were used to determine optical dielectric loss. Fundamental optical dielectric functions were used to determine some key parameters. From the viewpoint of quantum transport, electron transitions were discussed. The merit of this work is that microscopic processes related to electron transition from the VB to the CB can be interpreted interms of measurable macroscopic quantities.

Beneficial effect of ζ-carotene-like compounds on acute UVB irradiation by alleviating inflammation and regulating intestinal flora.

ζ-Carotene is a key intermediate in the carotenoid pathway, but owing to its low content and difficulties in isolation, its application is restricted. In this study, three genes (pnCrtE, pnCrtB, and pnCrtP) in the carotenoid pathway of Antarctic moss were identified, recombined, and expressed in Escherichia coli (E. coli) BL21(DE3). The expression product was identified as one of the ζ-carotenes by UV absorbance spectrum, thin layer chromatography (TLC), and super-high-performance liquid chromatography-mass spectrum (UPLC-MS), and was called a ζ-carotene-like compound (CLC). Excessive exposure to ultraviolet B (UVB) irradiation is one of the main risk factors for skin photodamage. The purpose of this study was to investigate the preventive and therapeutic effects of CLC on UVB-induced skin photodamage in mice. In this paper, through histological examinations (hematoxylin-eosin, HE; Masson and TdT-mediated dUTP Nick-End Labeling, Tunel), biochemical index detection (reactive oxygen species, ROS; inflammatory factors; cyclobutyl pyrimidine dimers, CPDs and hyaluronic acid, HA), quantitative real time polymerase chain reaction (qRT-PCR), immunohistochemistry and intestinal content flora, etc., it is concluded that CLC has the potential to enhance skin antioxidant capacity by activating the nuclear transcription factor/antioxidant reaction element (Nrf2/ARE) pathway and also reduce skin inflammation and aging by inhibiting the mitogen-activated protein kinase (MAPK) pathway. Moreover, the regulation of intestinal flora may potentially mitigate skin damage induced by UVB radiation. This research not only developed a green and sustainable platform for the efficient synthesis of CLC but also laid a foundation for its application in functional food and medicine for skin resistance against UVB damage.

P-type β-Ga2O3 films were prepared by Zn-doping using RF magnetron sputtering

The XRD patterns show that the peak position of the Zn-doped β-Ga 2 O 3 films shifts to lower angles with the substrate temperature decreasing from 700℃ to room temperature, indicating the incorporation of Zn into Ga 2 O 3 films. Because the ion radius of Ga 3+ is 0.61Å and Zn 2+ is 0.74Å, the lattice spacing expanses with the increase of Zn concentration and thus the diffraction angle of the characteristic peak becomes smaller. The photoelectric response measurements show that the Zn-doped β-Ga 2 O 3 film based photodetectors manifest much lower dark-current and higher photo-to-dark current ratio. • P-type Ga 2 O 3 films were obtained by Zn doping using radio frequency magnetron sputtering method. • The doping concentration of Zn has a close relationship with temperature. • Zn-doped β-Ga 2 O 3 based photodetector manifested much lower dark-current and higher photo-to-dark current ratio. Zn-doped Ga 2 O 3 films were prepared using RF magnetron sputtering method at various deposition temperatures. Hall measurement demonstrated the present Zn-doped β-Ga 2 O 3 film was p -type conductivity. The XRD and XRF measurements showed the Zn dopant concentration increased with the decrease of temperature so that the position of the characteristic peak shifted to lower angles. The UV absorption spectra showed that the bandgaps became narrower with the doping concentration of Zn atom increasing. The pure and Zn-doped β-Ga 2 O 3 films were used to fabricate the photodetectors with MSM structure, respectively. The photoelectric response measurements showed that the Zn-doped specimen manifested much lower dark-current and higher photo-to-dark current ratio, but slower photoresponse speed.

Bioavailability and systemic transport of oleanolic acid in humans, formulated as a functional olive oil.

Evidence of the pharmacological activity of oleanolic acid (OA) suggests its potential therapeutic application. However, its use in functional foods, dietary supplements, or nutraceuticals is hindered by limited human bioavailability studies. The BIO-OLTRAD trial is a double-blind, randomized controlled study with 22 participants that received a single dose of 30 mg OA formulated as a functional olive oil. The study revealed that the maximum serum concentration of OA ranged from 500 to 600 ng mL-1, with an AUC0-∞ value of 2862.50 ± 174.50 ng h mL-1. Furthermore, we discovered a physiological association of OA with serum albumin and triglyceride-rich lipoproteins (TRL). UV absorption spectra showed conformational changes in serum albumin due to the formation of an adduct with OA. Additionally, we demonstrated that TRL incorporate OA, reaching a maximum concentration of 140 ng mL-1 after 2-4 hours. We conjecture that both are efficient carriers to reach target tissues and to yield high bioavailability.

Photodissociation dynamics and UV absorption spectrum of acetone oxide (CH3)2COO.

The photodynamics and B1A' ← X1A' absorption spectrum of acetone oxide, (CH3)2COO, are studied theoretically from first principles. The underlying adiabatic potential energy curves (and surfaces) are computed by a second-order multireference perturbation theory method and diabatized using a diabatization by ansatz scheme. To confirm the results, for selected geometries EOM-CCSD and XMS-RS2C calculations were also performed. The dynamical calculation rests on the multi-configuration time-dependent Hartree wavepacket propagation method. The experimental absorption spectrum is reproduced satisfactorily. This result serves to validate the Hamiltonian model built within the quasi-diabatic representation. Contrary to the smallest Criegee intermediate, CH2OO, it is found that the vibronic coupling between the B and C states of (CH3)2COO plays an essential role in reproducing the experimental absorption spectrum. Time-dependent electronic populations reveal a faster decay than for the smaller system CH2OO. This is interpreted in terms of the stronger coupling between the B and C states in the larger system leading to a shorter lifetime for the B state than in CH2OO.

Synthesis and characterization of some Lanthanide (III) Complexes based on 2, 6-Diphenylisonicotinic acid

This paper presents the synthesis of four mononuclear lanthanide (III) complexes, possessing 2, 6-Diphenylisonicotinate as a ligand.The complexes were synthesized in aqueous solution at room temperature in a one to three molar ratios of the Ln (III) salt and the ligand, respectively.The white or grayish powdered complexes that formed were characterized by elemental analysis, ftir, uv, and Fluorescence spectroscopy. The ftir absorption spectra indicated that 2, 6-Diphenylisonicotinate acts as a bidentate ligand and coordinates to Ln (III) through the carboxylate oxygen and the adjacent carbonyl oxygen (–C=O).The UV absorption spectra of the complexes are similar in band profile and shape to the spectrum of the ligand except a slight blue shift of the absorption maxima. The excitation and emission spectra of the complexes are very much similar to that of the ligand with minor differences in excitation and emission wavelengths.The elemental analysis results show a good agreement between the calculated and found percentages of chn. Based on the elemental analysis andspectroscopic resultsof the four complexes, wesuggestthat the compounds formed are nine coordinate around the metal center and have the general formulaLn(C18H12NO2)3.3H2O.

Primula vulgaris'ten Sentezlenen Gümüş Nanopartiküllerin Antimikrobiyal ve Antioksidan Potansiyeli

In this study, biosynthesis and in vitro phytochemical composition, antibacterial and antioxidant activities of silver nanoparticles were investigated by using aqueous leaf, flower and root extracts of Primula vulgaris (P. vulgaris subsp. vulgaris). The synthesized silver nanoparticles (AgNPs) were confirmed by color conversion and ultraviolet-visible (UV-visible) spectrophotometry. The appearance of a dark brown color and a UV absorption spectrum range at 440 nm confirmed the synthesized silver nanoparticles. The antimicrobial activity of silver nanoparticles synthesized from the leaf of P. vulgaris; S. aureus 25±1, S. epidermidis 20±1, P. aeruginosa 20±1, A. hydrophila 21±1, C. albicans 25±1, C. tropicalis 25±1, C. parapsilosis 22±1 and C. glabrata 20±1 mm zone diameter was determined. The most antimicrobial effect of P. vulgaris leaf aqueous extract; S. aureus 20±1, S. epidermidis 18±1, A.hydrophila 15±1, P. aeruginosa 12±2, C. albicans 18±1, C. glabrata 18±1, C.tropicalis15±2, and C. parapsilosis 15±2 mm zone diameter was revealed. The presence of flavonoids, terpenoids, protein, and carbohydrates was found to be higher in silver nanoparticles synthesized in the flower part of P. vulgaris, according to phytochemical screening. While saponins were detected in P. vulgaris root extracts, tannins and protein were detected in the leaf extract. The flower had the highest total phenolic extract content of the silver nanoparticle (29.08±0 mg GAE/g DW), while the leaf and root had the lowest total phenolic content of 9.06±0.5 and 8.64±3.3 mg GAE/g DW, respectively. The flower had the highest total phenolic extract content of the plant aqueous extracts (25.10±0.2 mg GAE/g DW), while the leaf and root had the lowest (8.28±0.5 and 5.20±0.0 mg GAE/g DW, respectively).The DPPH (1,1-Diphenyl-2-picrylhydrazil) assay was used to assess free radical scavenging activity. The antioxidant activity of AgNPs biosynthesized using P. vulgaris flower extract was 90.6 %, while P. vulgaris flower aqueous extracts were 86.3 %. This can be concluded that silver nanoparticles synthesized using P. vulgaris flower extract are useful in the preparation of pharmacologically useful drugs.

Extraction and characterisation of type I collagen from the skin offcuts generated at the commercial fish processing centres.

Effective use of underutilised fish processing by-products could open avenues for new industries if they are used to extract high-valued bioactive compounds. Therefore, discarded skin offcuts of three main commercial fish species of Sri Lanka were used to extract collagen with acetic acid and the extracted collagen was evaluated for industrial suitability. The yields of acid-soluble collagens from Yellowfin tuna (Thunnus albacares), Seer fish (Scomberomorus commerson) and Asian sea bass (Lates calcarifer) were 61.26%, 58.21% and 59.31%, respectively on a dry-weight basis. Fourier Transform Infra-Red spectra and X-ray Diffraction spectra confirmed that all collagens were in type I and preserved the native triple-helical structure during extraction. The UV absorption spectra confirmed a high collagen purity in all species. These results confirm that the extracted collagen consists of the characteristics required for collagen-based industries such as food, pharmaceutical, and biomedical. The high availability of skin offcuts from the processing industry and the higher collagen yields revealed in this study confirm the possibility of using discarded skin offcuts of the three fish species as a potential source of type I collagen for industrial purposes.

Synthesis of Hollow Calcium Carbonate Microspheres by a Template Method for DOX Loading and Release with Carbon Dots Photosensitivity.

Calcium carbonate, as the main inorganic component of human bones and teeth, has good biocompatibility and bioactivity and finds increasing applications in the field of bone drug carriers. In this study, hollow calcium carbonate microspheres were synthesized by a water hydrothermal method using folic acid as a template. Before drug loading, the prepared calcium carbonate microspheres were subjected to aminidation, carboxylation, and vinylenimine modification. The hollow calcium carbonate microspheres loaded with doxorubicin hydrochloride (DOX) were further incorporated with light-emitting carbon quantum dots(CQDs) and hyaluronic acid (HA). The result showed that the drug loading capacity in the as-prepared calcium carbonate was 179.064 mg/g. In the simulated solutions of cellular metabolism containing various concentrations of reduced glutathione(GSH), the sustained release of DOX was confirmed qualitatively by the luminescence of the CQDs. The DOX release rate was measured quantitively by UV absorption spectra. The highest release rate reached 85.99% in a simulated solution of 0.005 mol/L GSH solution, and the release rate could vary intelligently with the concentration.

High charge collection efficiency detector based on plasma purified high-quality diamond

Diamond radiation detector is an ideal choice for the next-generation radiation detection in harsh environments, due to its small size, high irradiation resistance and fast response. However, high-purity single crystal diamond is hard to be prepared at the high growth rate due to the inevitable impurity incorporation. In this paper, based on the high-quality high-temperature/high-pressure (HPHT) single crystal diamond substrate, detector-grade single crystal diamonds material with high purity and low defect density were epitaxially grown at growth rate of about 4 μm/h by using plasma environment purification technology. It showed that the full width at half maximum of X-ray rocking curve of high-quality single crystal diamond could reach 0.007°, there was no nitrogen related impurity in PL spectrum, and the substitutional nitrogen content estimated by UV absorption spectrum was less than 10 ppb. After metallization and packaging process, the diamond detectors were prepared and the detector response under irradiation with 241 Am α-particles was realized. For the sample with fewer dislocations, the charge collection efficiency and energy resolution of this detector were 86.8 % and 7.85 % for electrons, and 96.7 % and 2.48 % for holes. The product of mobility and lifetime of electrons and holes were 1.7 × 10 −4 cm 2 V −1 and 3.7 × 10 −4 cm 2 V −1 , respectively. The high performances of the detector indicate that the current diamond detector can meet the application requirements of commercial diamond detectors. • Detector-grade diamond was prepared by plasma environment purification technology. • The high-purity single crystal diamond was grown at growth rate of about 4 μm/h. • The diamond detector with charge collection efficiency of 96.7 % was realized. • The products of mobility and lifetime of electrons and holes were 1.7 × 10 −4 and 3.7 × 10 −4 cm 2 V −1 .

Kinetic Salt Effect on Base-Catalyzed Isomerization of d-Glucose into d-Fructose.

Isomerization of d-glucose (Glc) into d-fructose (Fru) is of great importance for food sector as well as for valorization of lignocellulosic biomass. Soluble and solid bases exhibit high catalytic activity for the isomerization. Here, we report a salt effect on the base-catalyzed aqueous-phase Glc-Fru isomerization. Addition of soluble salts (Na2 SO4 , NaNO3 , K2 SO4 , and NaCl) results in an increased apparent reaction rate (factors of 1.5 to 6). The salt effect was observed both in the presence of soluble base NaOH at constant pH value and solid bases MgO, Li3 PO4 , and Mg-Al hydrotalcite. Apparent activation energy and UV absorption spectra were not significantly influenced by addition of salts. Potentiometric titration showed that the acidity constants of the saccharides increase in the presence of electrolytes. Since the rate of the isomerization depends on the thermodynamic acidity constant of Glc, the isomerization is accelerated by the presence of electrolytes.

Synthesis, characterization, DFT studies, and molecular modeling of hydrazinelidene‐3‐oxo‐3‐(p‐olyl) propanal derivatives as potential candidate for Hepatitis B and C treatment

AbstractSerious liver conditions including cirrhosis, hepatocellular carcinoma, and liver failure can be brought on by hepatitis B and C (HBV and HCV) infection. In our study, compound H_B and H_E were synthesized, spectroscopically, theoretically characterized, and investigated as potential drug for HBV and HCV. The stability of the investigated compounds as well as their Inter‐ and intramolecular interactions were investigated using the density functional theory with the B3LYP/6‐311+G (d, p) basis set. Lower energy gaps for studied compounds indicate compound ds to be reactive. The maximal absorption wavelengths of the substances under investigation were ascertained using the UV absorption spectrum. The optical property of the compounds under investigation was also calculated. Various vibrational modes displayed by functional groups present in the examined compounds were considered. Thereafter, docking was performed to determine the compatibility of compounds in study with selected hepatitis B and C proteins in comparison to recommended drugs Sofosbuvir and lamivudine. The results of molecular docking were based on binding affinity. Compound H_E, with a binding affinity of ‐7.6 kcal/mol has more potential in treating hepatitis than H_B, which has a binding affinity of ‐7.1 kcal/mol and is also a better anti‐hepatic agent than standard drugs sofosbuvir and lamivudine with lower binding affinities. Hence, H_E has the potential to treat HBV and HCV.

Investigating the structure and optical characteristics of two new organic-inorganic hybrid crystals

Using the solvent evaporation approach at room temperature (RT), we produced transparent single crystals of two new organic-inorganic hybrid materials: (C5H6NO)SO3NH2 (crystal 1: reaction by sulfamate and 4-hydroxypyridine) and (C3H5N2)SO3NH2 (crystal 2: reaction by sulfamate and imidazole). Both crystals have the same space structure and belong to the P21/c space group of the monoclinic crystal system, according to the results of X-ray single crystal diffraction. In crystals 1 and 2, sulfamic acid and organics (4-hydroxypyridine, imidazole) are alternatively positioned by hydrogen bonds to create a layered structure. Hydrogen bonds and electrostatic Coulomb forces connect the layers to one another. Powder XRD demonstrates the remarkable phase purity of both crystals. Furthermore, the optical properties of both crystals, including IR, UV absorption, and fluorescence spectra, have been investigated in detail. The presence of functional groups such as NH2 and CC in the grown crystals was confirmed by Fourier transform infrared analysis. The optical band gaps for crystals 1 and 2 are about 4.33 and 4.31 eV, respectively, and the UV absorption findings show a low light absorption. According to the photoluminescence spectra, the two crystals have distinct fluorescence characteristics, with emission peaks of approximately 433 nm and 442 nm, apiece.

ZnO and cobalt decorated ZnO NPs: Synthesis, photocatalysis and antimicrobial applications

The rapid growth of pollutants, both biological and non-biological, puts environmental systems in jeopardy. In view of this, the current study demonstrates the synthesis of undoped and Cobalt-doped zinc oxide nanoparticles (Co doped ZnO NPs) via co-precipitation method. The confirmation of incorporation of the Co dopant into ZnO NPs was verified through various spectroscopic and microscopic techniques. UV-absorption spectra of cobalt-doped ZnO NPs revealed a red shift with change of absorption spectra from 356 nm to 377 nm as compared to undoped ZnO NPs. XRD studies inferred that the average crystallite size of 0.5% and 1% Co-doped ZnO powder was obtained to be ∼16 nm and 14 nm respectively. A drop in band gap value from 3.48 eV to 3.30 eV provided as substantive evidence of the successful integration of Co2+ ions inside the ZnO matrix. FESEM and HRTEM studies revealed that the obtained ZnO NPs are in narrow size distribution (15–20 nm) with a wurtzite crystal structure. The synthesized ZnO and Co–ZnO NPs showed excellent photocatalytic and antimicrobial potency towards reactive brown dye (RB-1) and two bacterial strains, respectively. 1% Co-doped ZnO demonstrated the maximum photocatalytic activity (∼95%), in contrast to 0.5% Co-doped ZnO and undoped ZnO. Thus, the findings of this work support the developed system has a dual role as the photocatalyst, and antibacterial agent for efficient environmental remediation.

Targeted Therapy of Non-Small Cell Lung Cancer and Liver Cancer: Functional Nanocarriers for the Delivery of Cisplatin and Tissue Factor Pathway Inhibitor-2

Introduction: The aim of the study was to construct folic acid-modified PEGylated paramagnetic nanoparticles (MNPs) co-carrying tissue factor pathway inhibitor-2 (TFPI-2) and cisplatin (CDDP), and to study the molecular-targeting and inhibitory effects of the nanocomposite on non-small cell lung cancer (NSCLC) and liver cancer. Methods: Nanocomposites were prepared using amino-modified iron oxide nanoparticles as carriers, co-loading CDDP and PEGylated FA/TFPI-2. Transmission electron microscopy, UV absorption spectrum, and dynamic light scattering were employed to characterize the morphology, structure, particle size, and zeta potential of the nanocomposite. The phenylenediamine method was used to detect the loading of CDDP, and the CCK-8 assay was used to detect the toxic effect of the nanocomposite on HUVECs, A549, and NCI-H460 cells. In tumor-bearing mice models, the antitumor effects of the nanocomposites were assessed using TUNEL staining (at the molecular level), reverse transcriptase quantitative polymerase chain reaction (at the gene level), hematoxylin and eosin staining (at the cellular level), and the appearance of the mice models. Results: The synthesized FA-MNP/CDDP/TFPI-2 nanocomposite was uniformly dispersed and spherical in shape (approximate diameter: 10 nm). The zeta potential of particles was −9.44 mV, and the average particle size was 25 nm. The loading amount of CDDP was 70.24 μg/mL (23.33%). The nanocomposite was nontoxic to HUVECs, while it showed a favorable inhibitory effect on A549 and NCI-H460 cells. In vivo experiments in mice demonstrated satisfactory imaging properties and therapeutic effects of nanocomposite against liver cancer. Discussion: FA-MNP/CDDP/TFPI-2 may provide insights for the development of new chemotherapeutic drugs.