Development of Poly (Ester Amide-Urethanes) from De-saturated Thevetia peruviana Seed Oil-FAMEs

This study present the synthesis of eco-friendly poly(ester amide-urethane) coating from Thevetia peruviana seed oil (TPSO). FT-IR, 1H NMR and 13C NMR spectral analyses were used in confirming the structure of compounds. Physico-chemical properties of desaturated N,N'-bis (2- hydroxyethyl) Thevetia peruviana seed oil fatty amide (DHETA), poly(ester amide) (PESA) and poly(ester amide urethanes) (PESAU), as well as chemical resistance, antibacterial studies and thermal analysis of PESAU were also examined. Aims: To evaluate the thermal stability and antibacterial activities of PESAU. Study Design: Extraction of seed oil from the air-dried seedlings of Thevetia peruviana seeds and preparation of polyol through urea fractionation. Followed by urethane synthesis using 4,4'- diisocyanatodicyclohexylmethane (H12MDI). Result: The 46.4 g ICI/100g Iodine value (I.V.) of the amide (DHETA) base polyol was reduced to 10.5 g ICI/100 g value for the urethane (PESAU). The zero percent value for PESAU hydroxyl value (H.V.) is an indication of complete reaction of the hydroxyl functional groups on PESA with H12MDI. Spectroscopic examinations carried out confirm the formation of synthesized compounds. Conclusion: The synthesized urethane (PESAU) shows excellent inhibitive activities against tested organisms

Thermal Stability and Antibacterial Activity of a Newly Prepared Organic Coating from a De-saturated Seed Oil of Thevetia Peruviana

Air drying polyesteramide-urethanes resins were synthesized from de-saturated fatty methyl ester (FAME) of Thevetia peruviana seed oil commonly known as Yellow oleanda (a tropical ornamental shrub) having about 68.8% unsaturated and 30.9% saturated fatty acids. Urea fractionation method was used to optimize the percentage of functional groups (in this case double bonds) by physio-sorption of the saturated fatty acids. The physico-chemical characterization of the optimized unsaturated FAME such as hydroxyl value, iodine value, saponification value, refractive index, inherent viscosity were carried out using standard methods. Through condensation reaction the N,N- bis(2-hydroxyethyl) Thevetia peruviana (HETA) prepared from the FAME react with isophthalic acid to form polyesteramide. The latter undergo urethanation with H1 • 2 MDI. The structural elucidation of the moisture cured polyesteramide-urethane urethane coating was based on FTIR, 1H-NMR and 13C-NMR spectroscopic methods. The coatings films were evaluated for its antibacterial activity and thermal stability properties on TGA and DSC. SEM of the coating films was also examine

A NOVEL METHOD FOR WATER AND WATER CANAL EXTRACTION FROM LANDSAT-8 OLI IMAGERY

Constituents of hydrologic network, River and water canals play a key role in Agriculture for cultivation, Industrial activities and urban planning. Remote sensing images can be effectively used for water canal extraction, which significantly improves the accuracy and reduces the cost involved in mapping using conventional means. Using remote sensing data, the water Index (WI), Normalized Difference Water Index (NDWI) and Modified NDWI (MNDWI) are used in extracting the water bodies. These techniques are aimed at water body detection and need to be complemented with additional information for the extraction of complete water canal networks. The proposed index MNDWI-2 is able to find the water bodies and water canals as well from the Landsat-8 OLI imagery and is based on the SWIR2 band. In this paper, we use Level-1 precision terrain corrected OLI imagery at 30 meter spatial resolution. The proposed MNDWI-2 index is derived using SWIR2 (B7) band and Green (B3) band. The usage of SWIR2 band over SWIR1 results in very low reflectance values for water features, detection of shallow water and delineation of water features with rest of the features in the image. The computed MNDWI-2 index values are threshold by making the values greater than zero as 1 and less than zero as zero. The binarised values of 1 represent the water bodies and 0 represent the non-water body. This normalized index detects the water bodies and canals as well as vegetation which appears in the form of noise. The vegetation from the MNDWI-2 image is removed by using the NDVI index, which is calculated using the Top of Atmosphere (TOA) corrected images. The paper presents the results of water canal extraction in comparison with the major available indexes. The proposed index can be used for water and water canal extraction from L8 OLI imagery, and can be extended for other high resolution sensors

Synthesis and Characterization of Polyamide-Urethane/Clay Nanocomposites from Yellow Oleanda (Thevetia Peruviana) Seed Oil

Thevetia peruviana commonly known as yellow oleanda or lucky nut seed oil was harvested in EmureEkiti, southwestern Nigeria. The extraction of the seed oil was carried out using n-hexane in a soxhlet extractor. The seed oil with high contents of 18:1 (48.24%), 16:0 (22.25%), 18:2 (19.76%) fatty acids and having the following physico-chemical parameters (I.V, 75.4; S.V, 192.5; P. V, 1.9; A.V, 2.0; specific gravity, 0.91175; density, 0.90905. The seed oil was used in the preparation of diethanolamide. The diethanolamide was subsequently used in the preparation of polyurethane/clay nanocomposite. The formation of the hybrid polymeric coating was monitored and confirmed using Fourier Transform Infrared Spectroscopy (Ff-IR), Nuclear Magnetic Resonance (IH-NMR and 13C-NMR), Electronspin ionization-mass spectroscopy (ESIMS), X-ray diffraction spectroscopy (XRD). The thermal stability of the product was studied by Thermal gravimetic analyser (TGA), Dynamic and mechanical thermal analyser (DMTA), Differential scanning calorimetry (DSC)

Angiographically borderline left main coronary artery lesions: correlation of transthoracic doppler echocardiography and intravascular ultrasound: a pilot study

<p>Abstract</p> <p>Background</p> <p>the clinical decision making could be difficult in patients with borderline lesions (visually assessed stenosis severity of 30 to 50%) of the left main coronary artery (LM). The aim of the study was to evaluate the relationship between transthoracic Doppler (TTDE) peak diastolic flow velocity (PDV) and intravascular ultrasound (IVUS) measurements in the assessment of angiographically borderline LM lesions.</p> <p>Methods</p> <p>27 patients (mean age 64 ± 8 years, 21 males) with borderline LM stenosis referred for IVUS examination were included in the study. We performed standard IVUS with minimal lumen area (MLA) and plaque burden (PB) measurement and routine quantitative coronary angiography (QCA) with diameter stenosis (%DS) and area stenosis (%AS) assessment in all. During TTDE, resting PDV was measured in the LM.</p> <p>Results</p> <p>interpretable Doppler signal could be obtained in 24 patients (88% feasibility); therefore these patients entered the final analysis. MLA was 7.1 ± 2.7 mm². TTDE measured PDV correlated significantly with IVUS-derived MLA (r = -0.46, p < 0.05) and plaque burden (r = 0.51, p < 0.05). Using a velocity cut-off of 112 cm/sec TTDE showed a 92% sensitivity and 62% specificity to identify IVUS-significant (MLA < 6 mm²) LM stenosis.</p> <p>Conclusion</p> <p>In angiographically borderline LM disease, resting PDV from transthoracic echocardiography is increased in presence of increased plaque burden by IVUS. TTDE evaluation might be a useful adjunct to other invasive and non-invasive methods in the assessment of borderline LM lesions. Further, large scale studies are needed to establish the exact cut-off value of PDV for routine clinical application.</p

Withanolides and related steroids

Since the isolation of the first withanolides in the mid-1960s, over 600 new members of this group of compounds have been described, with most from genera of the plant family Solanaceae. The basic structure of withaferin A, a C28 ergostane with a modified side chain forming a δ-lactone between carbons 22 and 26, was considered for many years the basic template for the withanolides. Nowadays, a considerable number of related structures are also considered part of the withanolide class; among them are those containing γ-lactones in the side chain that have come to be at least as common as the δ-lactones. The reduced versions (γ and δ-lactols) are also known. Further structural variations include modified skeletons (including C27 compounds), aromatic rings and additional rings, which may coexist in a single plant species. Seasonal and geographical variations have also been described in the concentration levels and types of withanolides that may occur, especially in the Jaborosa and Salpichroa genera, and biogenetic relationships among those withanolides may be inferred from the structural variations detected. Withania is the parent genus of the withanolides and a special section is devoted to the new structures isolated from species in this genus. Following this, all other new structures are grouped by structural types. Many withanolides have shown a variety of interesting biological activities ranging from antitumor, cytotoxic and potential cancer chemopreventive effects, to feeding deterrence for several insects as well as selective phytotoxicity towards monocotyledoneous and dicotyledoneous species. Trypanocidal, leishmanicidal, antibacterial, and antifungal activities have also been reported. A comprehensive description of the different activities and their significance has been included in this chapter. The final section is devoted to chemotaxonomic implications of withanolide distribution within the Solanaceae. Overall, this chapter covers the advances in the chemistry and biology of withanolides over the last 16 years.Fil: Misico, Rosana Isabel. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis y Métodos Físicos Aplicados a la Química Orgánica (i); ArgentinaFil: Nicotra, V.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Instituto Multidisciplinario de Biología Vegetal (p); Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; ArgentinaFil: Oberti, Juan Carlos María. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Instituto Multidisciplinario de Biología Vegetal (p); Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; ArgentinaFil: Barboza, Gloria Estela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Instituto Multidisciplinario de Biología Vegetal (p); Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; ArgentinaFil: Gil, Roberto Ricardo. University Of Carnegie Mellon; Estados UnidosFil: Burton, Gerardo. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis y Métodos Físicos Aplicados a la Química Orgánica (i); Argentin

An overlooked connection: serotonergic mediation of estrogen-related physiology and pathology

BACKGROUND: In humans, serotonin has typically been investigated as a neurotransmitter. However, serotonin also functions as a hormone across animal phyla, including those lacking an organized central nervous system. This hormonal action allows serotonin to have physiological consequences in systems outside the central nervous system. Fluctuations in estrogen levels over the lifespan and during ovarian cycles cause predictable changes in serotonin systems in female mammals. DISCUSSION: We hypothesize that some of the physiological effects attributed to estrogen may be a consequence of estrogen-related changes in serotonin efficacy and receptor distribution. Here, we integrate data from endocrinology, molecular biology, neuroscience, and epidemiology to propose that serotonin may mediate the effects of estrogen. In the central nervous system, estrogen influences pain transmission, headache, dizziness, nausea, and depression, all of which are known to be a consequence of serotonergic signaling. Outside of the central nervous system, estrogen produces changes in bone density, vascular function, and immune cell self-recognition and activation that are consistent with serotonin's effects. For breast cancer risk, our hypothesis predicts heretofore unexplained observations of the opposing effects of obesity pre- and post-menopause and the increase following treatment with hormone replacement therapy using medroxyprogesterone. SUMMARY: Serotonergic mediation of estrogen has important clinical implications and warrants further evaluation

Luminescent Tris(8-hydroxyquinolates) of Bismuth(III)

Luminescent homoleptic bismuth(III) complexes have been synthesized by adding several functionalized 8-hydroxyquinolate ligands to bismuth(III) chloride in a 3:1 mole ratio in either ethanol or tetrahydrofuran (THF) solvent. These complexes have been characterized by single-crystal X-ray diffraction (XRD) analysis, UV-vis spectroscopy, fluorescence spectroscopy, and density functional theory (DFT) calculations to determine their structures and photophysical properties. Reversible dimerization of the mononuclear tris(hydroxyquinolate) complexes was observed in solution and quantified using UV-vis spectroscopy. The fluorescence spectra show a blue shift for the monomer compared with homoleptic aluminum(III) hydroxyquinolate compounds. Four dimeric compounds and one monomeric isomer were characterized structurally. The bismuth(III) centers in the dimers are bridged by two oxygen atoms from the substituted hydroxyquinolate ligands. The more sterically hindered quinolate complex, tris(2-(diethoxymethyl)-8-quinolinato)bismuth, crystallizes as a monomer. The complexes all exhibit low-lying absorption and emission spectral features attributable to transitions between the HOMO (π orbital localized on the quinolate phenoxide ring) and LUMO (π* orbital localized on the quinolate pyridyl ring). Excitation and emission spectra show a concentration dependence in solution that suggests that a monomer-dimer equilibrium occurs. Electronic structure DFT calculations support trends seen in the experimental results with a HOMO-LUMO gap of 2.156 eV calculated for the monomer that is significantly larger than those for the dimers (1.772 and 1.915 eV). The close face to face approach of two quinolate rings in the dimer destabilizes the uppermost occupied quinolate π orbitals, which reduces the HOMO-LUMO gap and results in longer wavelength absorption and emission spectral features than in the monomer form