Review on the interactions between dopamine metabolites and α-Synuclein in causing Parkinson's disease.

Parkinson's disease (PD) is characterized by an abnormal post-translational modifications (PTM) in amino acid sequence and aggregation of alpha-synuclein (α-Syn) protein. It is generally believed that dopamine (DA) metabolite in dopaminergic (DAergic) neurons promotes the aggregation of toxic α-Syn oligomers and protofibrils, whereas DA inhibits the formation of toxic fibers and even degrades the toxic fibers. Therefore, the study on interaction between DA metabolites and α-Syn oligomers is one of the current hot topics in neuroscience, because this effect may have direct relevance to the selective DAergic neuron loss in PD. Several mechanisms have been reported for DA metabolites induced α-Syn oligomers viz. i) The reactive oxygen species (ROS) released during the auto-oxidation or enzymatic oxidation of DA changes the structure of α-Syn by the oxidation of amino acid residue leading to misfolding, ii) The oxidized DA metabolites directly interact with α-Syn through covalent or non-covalent bonding leading to the formation of oligomers, iii) DA interacts with lipid or autophagy related proteins to decreases the degradation efficiency of α-Syn aggregates. However, there is no clear-cut mechanism proposed for the interaction between DA and α-Syn. However, it is believed that the lysine (Lys) side chain of α-Syn sequence is the initial trigger site for the oligomer formation. Herein, we review different chemical mechanism involved during the interaction of Lys side chain of α-Syn with DA metabolites such as dopamine-o-quinone (DAQ), dopamine-chrome (DAC), dopamine-aldehyde (DOPAL) and neuromelanin. This review also provides the promotive effect of divalent Cu2+ ions on DA metabolites induced α-Syn oligomers and its inhibition effect by antioxidant glutathione (GSH).

Efficient catalytic activity of BiVO4 nanostructures by crystal facet regulation for environmental remediation.

Controlled growth of BiVO4 nanostructures along (121) and (040) crystal facets plays a crucial role in enhancing their catalytic performance. In this regard, the visible light active photocatalyst BiVO4 was synthesized concerning the effect of pH and surfactants by hydrothermal method. The morphology and size of BiVO4 are strongly dependent on the concentration of H+ and Bi3+ in the reaction system while varying the pH. Further, the significant role of cationic surfactant for obtaining the morphology of the spherical nanoparticles of BiVO4 powders with size 55 nm was analyzed. Adsorption behavior of as-synthesized samples was investigated through Langmuir isotherm model. The catalytic performance of BiVO4 photocatalyst with the degradation efficiency of 98.79% and 15.58% over the methylene blue (MB) and methyl orange (MO) dyes were noticed within 60 min of light irradiation respectively. The enhanced and declined catalytic activity was well correlated with the surface charge of BiVO4 photocatalyst towards the MB and MO dyes respectively. Further, the photocatalytic activity of mixed anionic and cationic dyes was performed. The degradation pathway of MB dye was analyzed by LC-MS for the identification of intermediate products. From the obtained results, the proposed possible photocatalytic mechanism reported.

Suppression of intrinsic thermal conductivity in Sr1-x Gd x TiO3 ceramics via phonon-point defect scattering for enhanced thermoelectric application.

A substantial reduction in the thermal conductivity for strontium titanate (ABO3) perovskite structure was realized for the A-site substitution of gadolinium (rare earth element) in SrTiO3 ceramics. The effect of Gd3+ substitution on the structure, composition, and thermoelectric properties of SrTiO3 was investigated. The substitution of Gd3+ in the SrTiO3 matrix resulted in the minimalization of thermal conductivity. The thermal conductivity followed a similar trend as that of thermal diffusivity, but specific heat capacity exhibited a non-monotonic trend. The thermal conductivity is reduced to 1.05 W m-1 K-1 for the minimal substitutional composition (Sr0.99Gd0.01TiO3) which is 30% less than that of SrTiO3 at 303 K. The variation in the ionic radii and atomic mass of the heavier rare earth Gd3+ substituted over Sr2+ resulted in the reduction of thermal conductivity of SGTO ceramics caused by the corresponding boundary scattering at low temperatures and temperature-independent phonon-impurity scattering at high temperatures.

A novel strategy of nanosized herbal Plectranthus amboinicus, Phyllanthus niruri and Euphorbia hirta treated TiO2 nanoparticles for antibacterial and anticancer activities.

Titanium dioxide nanoparticles exhibit good anticancer and antibacterial activities. They are known to be environmentally friendly, stable, less toxic, and have excellent biocompatibility nature. Due to these properties, they are well suited for biological applications particularly in biomedical applications such as drug delivery and cancer therapy. In this research article, three medicinal herbs namely, Plectranthus amboinicus (Karpooravalli), Phyllanthus niruri (Keezhanelli), and Euphorbia hirta (Amman Pacharisi), were used to modify the surface of the TiO2 nanoparticles. The synthesized nanoparticles were subjected to various characterization techniques. The samples are then subjected to MTT assay to determine cell viability. KB oral cancer cells are used for the determination of the anticancer nature of the pure and bio modified nanoparticles. It is observed that Plectranthus amboinicus-Phyllanthus niruri modified TiO2 nanoparticles exhibit excellent anticancer activities among other bio modified and pure samples. The samples are then examined for antibacterial activities against three Gram-negative bacterial strains namely, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and two Gram-positive bacterial strains namely, Staphylococcus aureus and Streptococcus mutans, respectively. Among the modified and pure samples, Plectranthus amboinicus showed good antibacterial activity against Gram-positive and Gram-negative bacteria. In the Flow cytometry analysis, the generation of p53 protein expression from Plectranthus amboinicus-Phyllanthus niruri modified TiO2 nano herbal particles shows the anti-cancerous nature of the sample. Then to determine the toxic nature of the Plectranthus amboinicus-Phyllanthus niruri modified TiO2 nano herbal particles against normal cells, the NPs were subjected to MTT assay against normal L929 cells, and it was found to be safer and less toxic towards the normal cells.

Interface enriched highly interlaced layered MoS2/NiS2 nanocomposites for the photocatalytic degradation of rhodamine B dye.

In the past few decades, air and water pollution by organic dyes has become a serious concern due to their high toxicity. Removal of these organic dyes from polluted water bodies is a serious environmental concern and the development of new advanced photocatalytic materials for decomposing organic dyes can be a good solution. In this work, layered molybdenum disulfide/nickel disulfide (MoS2/NiS2) nanocomposites with various NiS2 content was synthesized by a one-step hydrothermal method using citric acid as a reducing agent. The X-ray diffraction pattern shows the hexagonal and cubical crystal structure of MoS2 and NiS2, respectively. Morphological analysis confirms the formation of MoS2/NiS2 nanosheets. The elemental composition of the samples was carried out by XPS, which shows a significant interaction between NiS2 and MoS2. The photocatalytic performance of MoS2/NiS2 nanocomposites was studied by the degradation of rhodamine B (RhB). Ni-4 sample shows higher photocatalytic activity with a maximum degradation of 90.61% under visible light irradiation for 32 min.

Oxide-based catalysis: tailoring surface structures via organic ligands and related interfacial charge carrier for environmental remediation.

Hierarchical nanostructures and the effects of ligands on their structure formation were investigated. Morphological analysis showed the change in the morphology from nanospindles to hollow hexagonal nanodisks with the change in ligands. Structural analysis exhibited the formation of both hexagonal ZnO and monoclinic CuO structures in the composition. The elemental composition confirms the presence of CuO and ZnO in the composition. An ultra-fast degradation was achieved for the nanocomposites. The ZnO/CuO composite with ethylenediamine showed the best activity by degrading 98.77% of the methylene blue dye in 36 min. A possible photocatalytic mechanism is proposed.

Interface driven energy-filtering and phonon scattering of polyaniline incorporated ultrathin layered molybdenum disulphide nanosheets for promising thermoelectric performance.

The hybrid of organic conducting polymers and inorganic materials with ultralow thermal conductivity, which is a promising strategy for the realization of polymer based effective thermoelectric (TE) applications. In this work, ultrathin layered molybdenum disulphide (MoS2) nanosheets/PANI nanocomposites are prepared by hydrothermal route. The effect of varying PANI wt% in the nanocomposites and its interface effect on thermoelectric properties are well investigated. The successful incorporation of PANI between the MoS2 layers confirmed by high resolution transmission electron microscope (HRTEM). The significantly enhanced potential difference of MoS2/ PANI nanocomposites with increasing PANI content is well clarified by the increased Seebeck value. The variable range hopping property is identified and conductivity is raised up highly due to insertion of PANI in layered van der Waal's gap of MoS2. The effective interface facilitates charge for fast transport. The reduced thermal conductivity is observed of about 0.248 W*m-1*K-1 for 2.5 wt% addition of PANI. The key factor is that the stability of the sample is improved for MoS2/ PANI nanocomposites than pristine MoS2. Our work paved a new approach to improve TE performance by preparing TE MoS2 material through simple chemical route.

Bio-modified TiO2 nanoparticles with Withania somnifera, Eclipta prostrata and Glycyrrhiza glabra for anticancer and antibacterial applications.

Titanium dioxide nanoparticles exhibit good anticancer and antibacterial activities. They are known to be environmentally friendly and stable, less toxic and excellent biocompatibility nature. In this paper we report the biological properties of pure TiO2 nanoparticles modified with Withania somnifera (Ashwagandha), Eclipta prostrata (Karisalankanni) and Glycyrrhiza glabra (Athimathuram) for biological applications. X-ray diffraction results revealed the anatase nature of the samples. From the TEM analyses, it is observed that there is an increase in the particle size of the bio modified samples. UV results show the red shift for the bio modified samples when compared with the pure samples. The samples are then subjected to MTT assay to determine the cell viability. KB oral cancer cells are used for the determination of anticancer nature of the pure and bio modified nanoparticles. It is observed that Withania somnifera - Eclipta prostrate modified TiO2 nanoparticles exhibit excellent anticancer activities among other bio modified and pure samples. The samples are then examined for their antibacterial activities against three Gram-negative bacterial strains namely, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and two Gram-positive bacterial strains namely, Staphylococcus aureus and Streptococcus mutans. Among the modified and pure samples, Withania somnifera - Eclipta prostrata showed good antibacterial nature against Gram-positive and Gram-negative bacteria.

The effects of HIV/AIDS on the clinical profile and outcomes post pericardiectomy of patients with constrictive pericarditis: a retrospective review.

OBJECTIVE: The clinical profile and surgical outcomes of patients with constrictive pericarditis were compared in HIV-positive and -negative individuals. METHODS: This study was a retrospective analysis of patients diagnosed with constrictive pericarditis at Inkosi Albert Luthuli Central Hospital, Durban, over a 10-year period (2004-2014). RESULTS: Of 83 patients with constrictive pericarditis, 32 (38.1%) were HIV positive. Except for pericardial calcification, which was more common in HIV-negative subjects (n = 15, 29.4% vs n = 2, 6.3%; p = 0.011), the clinical profile was similar in the two groups. Fourteen patients died preoperatively (16.9%) and three died peri-operatively (5.8%). On multivariable analysis, age (OR 1.17; 95% CI: 1.03-1.34; p = 0.02), serum albumin level (OR 0.63; 95% CI: 0.43-0.92; p = 0.016), gamma glutamyl transferase level (OR 0.97; 95% CI: 0.94-0.1.0; p = 0.034) and pulmonary artery pressure (OR 1.49; 95% CI: 1.07-2.08; p = 0.018) emerged as independent predictors of pre-operative mortality rate. Peri-operative complications occurred more frequently in HIV-positive patients [9 (45%) vs 6 (17.6%); p = 0.030]. CONCLUSIONS: Without surgery, tuberculous constrictive pericarditis was associated with a high mortality rate. Although peri-operative complications occurred more frequently, surgery was not associated with increased mortality rates in HIV-positive subjects.

Atmospheric Oxidation Mechanism and Kinetics of Hydrofluoroethers, CH3OCF3, CH3OCHF2, and CHF2OCH2CF3, by OH Radical: A Theoretical Study.

In the present work, the reaction mechanism of two segregated hydrofluoroethers (HFEs), CH3OCF3 (HFE-143a) and CH3OCHF2 (HFE-152a), and a nonsegregated HFE, CHF2OCH2CF3 (HFE-245fa2), with OH radical is studied using electronic structure calculations. The initial reaction between HFE and OH radical is studied by considering two (three for CHF2OCH2CF3) pathways, H-atom abstraction and C-O bond breaking, OH addition reaction and C-C bond breaking, and OH addition reaction, which leads to the formation of alkyl radical intermediate. The dominant atmospheric fate of initially formed alkyl radical intermediate is its reaction with O2. The peroxy radicals thus formed exit through the reaction with HO2 radical and NO radical resulting in the formation of products, carbonyl fluoride (COF2), trifluoromethylformate, trifluoro(hydroperoxymethoxy)methane, difluoro(hydroperoxy methoxy)methane, difluoromethylformate, 2-(difluoromethoxy)-1,1,1-trifluoro-2-hydroperoxyethane, and difluoromethyl ester. The rate constant is calculated for the initial H-atom abstraction reaction using canonical variational transition state theory with small curvature tunnelling corrections over the temperature range 272-350 K. The atmospheric lifetime and global warming potential of HFEs are obtained from the calculated reaction potential energy surface and rate constant. The results are discussed with respect to the atmospheric implications of CH3OCF3 (HFE-143a), CH3OCHF2 (HFE-152a), and CHF2OCH2CF3 (HFE-245fa2).

Ultrathin layered MoS2 nanosheets with rich active sites for enhanced visible light photocatalytic activity.

Edge-rich active sites of ultrathin layered molybdenum disulphide (MoS2) nanosheets were synthesized by a hydrothermal method. The effect of pH on the formation of MoS2 nanosheets and their photocatalytic response have been investigated. Structural and elemental analysis confirm the presence of S-Mo-S in the composition. Morphological analysis confirms the presence of ultrathin layered nanosheets with a sheet thickness of 10-28 nm at pH 1. The interplanar spacing of MoS2 layers is in good agreement with the X-ray diffraction and high-resolution transmission electron microscopy results. A comparative study of the photocatalytic performance for the degradation of methylene blue (MB) and rhodamine B (RhB) by ultrathin layered MoS2 under visible light irradiation was performed. The photocatalytic activity of the edge-rich ultrathin layered nanosheets showed a fast response time of 36 min with the degradation rate of 95.3% of MB and 41.1% of RhB. The photocatalytic degradation of MB was superior to that of RhB because of the excellent adsorption of MB than that of RhB. Photogenerated superoxide radicals were the key active species for the decomposition of organic compounds present in water, as evidenced by scavenger studies.

Controlled synthesis of organic ligand passivated ZnO nanostructures and their photocatalytic activity under visible light irradiation.

Zinc oxide (ZnO) nanostructures were synthesized and their photocatalytic activity was evaluated using methylene blue (MB) as a model pollutant. Ethylenediamine (EDA) was used as a passivating agent to control the morphology and size of the ZnO nanostructures. In the absence of EDA, agglomerated ZnO nanoparticles were obtained. The addition of EDA at varying concentrations considerably influenced the morphological size. The as-prepared samples were extensively characterized using various techniques. The morphology- and size-dependent photocatalytic degradation of MB was studied under visible light irradiation. The maximum degradation efficiency was observed for ZnO nanoflakes; the MB-related absorbance peak completely disappeared after 15 min of irradiation. Furthermore, the effect of various photocatalytic reaction parameters, such as pH (3-12) of the solution, the concentration of the dye (5, 10, 15, and 20 ppm), and the dosage of the photocatalyst (25, 50, 75, and 100 mg L(-1)), on the photodegradation of MB was investigated to determine the maximum degradation efficiency. The optimum values of solution pH, dye concentration, and photocatalyst dosage were 11, 10 ppm, and 75 mg L(-1), respectively.

Effect of organic-ligands on the toxicity profiles of CdS nanoparticles and functional properties.

CdS nanoparticles are one among the most promising agents for fluorescent imaging. Hence, it is essential to develop new strategies to overcome the cytotoxicity of these nanoparticles. Surface modification is one of the simplest and effective techniques. This paper assesses the effect of surface modification on toxicity of the CdS nanoparticles. Unmodified CdS and surface-modified CdS nanoparticles were synthesized in an aqueous medium using a wet chemical route at room temperature. The surface modification of the CdS nanoparticles with polyvinylpyrrolidone (PVP) and cysteine was confirmed using infrared absorption studies. The diameters of unmodified CdS, PVP-modified CdS, and cysteine-modified CdS nanoparticles were determined using HRTEM. They exhibited luminescence in the range from 500 to 800 nm. The cytotoxic effects of these CdS nanoparticles were investigated in cultures of Vero cells. The results indicated that Vero cell viability was higher for the surface-modified CdS nanoparticles than for the unmodified CdS nanoparticles. The reduction in the toxicity was related to the nature of the capping agents used for the surface modification, and the particle size.

Amino acid-mediated synthesis of zinc oxide nanostructures and evaluation of their facet-dependent antimicrobial activity.

ZnO nanostructures (ZnO-NSs) of different morphologies are synthesized with the amino acids L-alanine, L-threonine, and L-glutamine as capping agents. X-ray diffraction (XRD) shows the formation of a crystalline wurtzite phase of ZnO-NSs. The surface modification of ZnO-NSs due to the capping agents is confirmed using Fourier transform infrared (FTIR) spectroscopy. Photoluminescence spectroscopy reveals that the concentration of surface defects correlates positively with the number of polar facets in ZnO-NSs. The antimicrobial activity of the ZnO-NSs has been tested against Escherichia coli and the common pathogens Staphylococcus aureus, Klebsiella pneumoniae, and Bacillus subtilis. Culture-based methods in rich medium show up to 90% growth inhibition, depending on the ZnO-NSs. Flow cytometry analyses indicate that the reactive oxygen species (ROS) generated by ZnO-NSs contribute mostly to the antibacterial activity. Control experiments in minimal medium show that amino acids and other reducing agents in Luria-Bertani (LB) medium quench ROS, thereby decreasing the antimicrobial activity of the ZnO-NSs.

Morphology-directed synthesis of ZnO nanostructures and their antibacterial activity.

Zinc oxide (ZnO) nanostructures of various morphologies were produced in an aqueous system, with pyridine as a shape-directing agent. X-ray diffraction (XRD) and selected-area electron diffraction (SAED) revealed hexagonal wurtzite crystal structure. Variation in surface morphology was analyzed using transmission electron microscopy (TEM). Changes in surface morphology were attributed to the absence of steric stabilization in pyridine during synthesis process. Pyridine concentration affected morphology and optical properties. Fourier transform infrared spectroscopy (FTIR) confirmed the presence/absence of pyridine on the surface of ZnO nanostructures (ZnO-NSs). Optical measurements carried out using UV-visible spectrophotometer (UV-vis) and photoluminescence (PL) indicated the presence of defects. All the samples exhibited two PL peaks, at 350-370 nm and 560-624 nm. Variation in the intensities of PL peaks corresponded to the changes in the surface morphology from nanoparticles to rods and origin of deep-level defect luminescence is attributed to surface recombination. The toxicity of the nanostructures was tested on model Gram-negative and Gram-positive pathogens. Smaller nanorods were most toxic among the nanostructures tested.

Uniaxial growth of <100> zinc (tris) thiourea sulphate (ZTS) single crystal by Sankaranarayanan-Ramasamy (SR) method and its characterizations.

<100> directed single crystals of zinc (tris) thiourea sulphate, a semi-organic compound, have been grown at an average growth rate of 2mm per day by Sankaranarayanan-Ramasamy (SR) method. Transparent ZTS crystal of size 70mm length and 15mm diameter was grown. The growth conditions have been optimized. Chemical etching, Vickers microhardness, UV-Vis NIR, dielectric constant and dielectric loss analysis were made on conventional and SR method grown ZTS crystals. Thermo gravimetric and differential thermal analysis was carried out to determine the thermal properties of the grown crystal. The NLO efficiency of the crystal has been confirmed using the Kurtz powder technique. The comparative study indicates that the crystal quality of unidirectional grown ZTS crystal is better compared to conventional slow evaporation method grown crystal.

Growth and characterization of novel organic optical crystal: Anilinium D-tartrate (ADT).

A novel organic nonlinear optical (NLO) crystal of anilinium d-tartrate (abbreviated as ADT) has been grown by the solution growth (slow evaporation) method at room temperature. Transparent crystals of dimensions 4mm×2mm×1mm were obtained. The grown single crystal was subjected to different characterization analyses in order to find out its suitability for device fabrication. Single crystal X-ray diffraction analysis reveals that ADT crystallizes in triclinic system with non-centrosymmetric space group P1. FTIR spectrum was recorded to explore information of the functional groups. The placement of protons and carbon was determined using (1)H NMR and (13)C NMR spectral analyses. The SHG output of ADT was recorded by Kurtz-Perry powder technique. The range of optical absorption was ascertained by recording UV-vis spectrum. The PL spectrum of ADT shows green emission. The dielectric behavior of ADT was investigated at 30°C, 70°C and 105°C are reported. Thermal properties were investigated by thermo gravimetric, differential thermal and differential scanning calorimetric analyses.

Kodamaea ohmeri tricuspid valve endocarditis with right ventricular inflow obstruction in a neonate with structurally normal heart.

The yeast Kodamaea (Pichia) ohmeri is a rare human pathogen with infrequent report of neonatal infection. Native valve endocarditis by Kodamaea ohmeri is extremely rare. The current case report describes a case of fatal nosocomial native valve endocarditis without any structural heart defects in a 40dayold baby. The patient was referred to our institute after having ICU stay of 18 days in another hospital for necrotizing enterocolitis and was found to have obstructive tricuspid valve mass and fungemia with Kodamaea ohmeri. In spite of the treatment, patient developed sepsis with disseminated intravascular coagulation and could not be revived.

Synthesis and characterization of a new organic nonlinear optical crystal: L-phenylalaninium maleate.

l-Phenylalaninium maleate (abbreviated as LPM) chemical formula C(9)H(12)NO(2)(+).C(4)H(3)O(4)(-), a new organic nonlinear optical crystal was grown by slow evaporation technique. Transparent needle shaped crystal of dimensions 7mmx1mmx0.5mm was obtained. Single crystals of LPM have been subjected to X-ray diffraction analysis to estimate the lattice parameters and the space group. The powder X-ray diffractogram of the crystal has been recorded and the reflections from various planes are identified. The XRD studies confirm the crystalline nature. The qualitative analysis on the crystal has been carried out using Fourier transform infrared (FTIR) and Fourier transform Raman (FTRaman) spectral measurements. The presence of hydrogen and carbon in the grown crystal was confirmed by using proton and carbon nuclear magnetic resonance (NMR) spectral analyses. Optical behaviour of the crystal was investigated using UV-vis spectroscopy. The thermal stability of the crystal was analysed with the aid of thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The nonlinear optical (NLO) property of the crystal was tested by Nd:YAG laser source.