Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0432222 (SEM)
 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Specific effects of the cytotoxic secondary lipid oxidation product, 4-hydroxynonenal (10(-8)-10(-4) M), on intact sheets of rat jejunum were measured as changes in short circuit current (delta(I)sc) following cumulative addition to either the mucosal or serosal side, using the analogous aldehyde, nonenal, as reference. 4-Hydroxynonenal stimulated I(sc) from the serosal side (maximal delta(I)sc = 27.2 +/- 3.5 microA/cm2, mean +/- SEM, N = 32) while nonenal stimulated I(sc) primarily from the mucosal side (maximal delta(I)sc = 16.2 +/- 3.4 microA/cm2, N = 20). Inhibition by 100 microM bumetanide (4-hydroxynonenal: 88.9 +/- 3.0%, N = 6, p < 0.05, nonenal: 69.3 +/- 2.9%, N = 6, P < 0.05) indicated chloride secretion. Nonenal-induced delta(I)sc was inhibited (72.5 +/- 1.2%, N = 8, P < 0.05) by a combination of nordihydroguaiaretic acid (100 microM) and piroxicam (10 microM), while 4-hydroxynonenal-induced delta(I)sc, was abolished by piroxicam (N = 8, P < 0.001) and inhibited by 1 microM tetrodotoxin (69.8 +/- 9.7%, N = 6, P < 0.001). These data indicate that 4-hydroxynonenal stimulates chloride secretion mediated by prostaglandins and the enteric nervous system. The site of action (serosal) being opposite to the reference aldehyde.
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PMID:Oxidant-stimulated chloride secretion in rat jejunum in vitro is mediated by eicosanoids. 1275 76

Antigen-sampling M cells are found in the follicle-associated epithelium above organized lymphoid tissue in many mucosae. They play a key role in initiating the mucosal immune response and act as a site of entry for opportunistic pathogens. This study investigates the presence of M cells in the Guinea pig conjunctiva. Maackia amurensis leukoagglutinin I and II (MAL-I and MAL-II) were identified as potential conjunctival M cell markers based on a screening of 12 lectins and 5 carbohydrate epitope antibodies on aldehyde-fixed follicles. Biotinylated or fluorescein-conjugated MAL-I was then instilled into conjunctival sacs in vivo for 15-60 min. Specimens were assessed by epi-fluorescence stereomicroscopy, confocal scanning laser microscopy and transmission and scanning electron microscopy (TEM and SEM). Selective labelling of a subset of epithelial cells overlying lymphoid follicles was observed following in vivo exposure to MAL-I. MAL-I labelling was restricted to cells with sparse, irregular microvilli. Cells preferentially labelled with MAL-I were found to internalize the lectin during a 60 min in vivo exposure. MAL-I was transcytosed to basolateral membranes of cells filled with intracellular vesicles during a 45 min in vivo incubation. This study demonstrates that the Guinea pig conjunctiva contains a cell with morphological and functional characteristics of antigen-sampling M cells.
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PMID:Conjunctival M cells selectively bind and translocate Maackia amurensis leukoagglutinin. 1578 Dec 82

An optimized procedure was designed for the preparation of the microporous metal-organic framework (MOF) [Cu3(btc)2] (BTC=benzene-1,3,5-tricarboxylate). The crystalline material was characterized by X-ray diffraction, optical microscopy, SEM, X-ray photoelectron spectroscopy, N2 sorption, thermogravimetry, and IR spectroscopy of adsorbed CO. CO adsorbs on a small number of Cu2O impurities, and particularly on the free CuII coordination sites in the framework. [Cu3(btc)2] is a highly selective Lewis acid catalyst for the isomerization of terpene derivatives, such as the rearrangement of alpha-pinene oxide to campholenic aldehyde and the cyclization of citronellal to isopulegol. By using the ethylene ketal of 2-bromopropiophenone as a test substrate, it was demonstrated that the active sites in [Cu3(btc)2] are hard Lewis acids. Catalyst stability, re-usability, and heterogeneity are critically assessed.
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PMID:Probing the Lewis acidity and catalytic activity of the metal-organic framework [Cu3(btc)2] (BTC=benzene-1,3,5-tricarboxylate). 1688 Oct 30

XAD copolymer resins may be functionalized with heavy metal ion-selective ligands either by covalent linkage to the polymer backbone or by impregnation. These resins may be tailored to be specific for certain heavy metals by adjusting the retention and elution parameters. For the synthesis of immobilized Amberlite XAD-4 copolymer resins that are expected to preconcentrate a number of transition and heavy metals, the Schiff base method was chosen. For this purpose the copolymer was nitrated, reduced to the corresponding amine and converted to the imine compounds via a Schiff base reaction using different organic aldehyde compounds. The interactions of 8 elements (Cd, Co, Cu, Mn, Ni, Pb, U and Zn) with the resins were qualitatively investigated. Optimal pH for retention was typically 6-8 for most resins although one could be used at pH 5 and elution was achieved using 0.1 M HNO3. The resins were characterized by FTIR, SEM and elemental analysis. It was demonstrated that the resins could be used to preconcentrate ultra-trace analytes from natural waters, and analysis of environmental certified reference materials using FI-ICP-MS showed good agreement with the certified values. Metal retention capacities were also calculated using a batch system and were found to compare favorably with other resins reported in the literature.
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PMID:Comparison of some newly synthesized chemically modified Amberlite XAD-4 resins for the preconcentration and determination of trace elements by flow injection inductively coupled plasma-mass spectrometry (ICP-MS). 1706 92

The absorption and fluorescence spectral characteristics of 4-hydroxy-3-methoxybenzaldehyde (HMB) have been studied in different solvents, pH and beta-cyclodextrin (beta-CD) and compared with 4-hydroxy-3,5-dimethoxybenzaldehyde (HDMB). The inclusion complex of HMB with beta-CD is analysed by UV-vis, fluorimetry, FT-IR, (1)H NMR, SEM and AM1 methods. In HMB, the normal emission (B band) is originates from a locally excited state and the longer emission (A band) is due to intramolecular charge transfer state (ICT). The OH group of HMB is present in the interior part of the beta-CD cavity and aldehyde group present in the upper part of the beta-CD cavity.
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PMID:Intramolecular charge transfer effects on 4-hydroxy-3-methoxybenzaldehyde. 1762 56

In orthopaedics and cardiovascular surgery, titanium has become the metal of choice, due to its excellent mechanical properties and biocompatibility. In many surgical operations, chemicals and/or biomolecules (such as antibiotics or growth factors) are used in conjunction with prostheses, so as to avoid or stimulate targeted biological events. Often, immobilization instead of release of such molecules is preferred to optimize their effects, thus avoiding ectopic transformations. A versatile method for the functionalization of pure Ti is shown here, which allows the covalent immobilization of polypeptides. In order to avoid the hydrolysable Ti-O-Si bond found in directly silanized Ti, we use organic/inorganic silica colloids, derived from commercially available 25 nm Ludox silica nanoparticles. Prior to deposition onto Ti-Cp, the silica nanoparticles are functionalized by a propylsemicarbazide moiety by silanization. After spin-coating onto the Ti substrates, the colloids were shown by SEM to form a uniform layer, and to be very strongly adsorbed; the reactivity of the supported semicarbazide (Sc) functionalities being maintained. Chemoselective reaction of semicarbazide groups on the surface with aldehyde moieties present on the polypeptide of interest was chosen in this work due to its efficiency, to its compatibility with the proteinogenic amino acids and in particular cystein and to the use of mild experimental conditions. Aldehyde groups are also easily introduced onto polypeptides by synthesis, oxidation of N-terminal Ser residue or polysaccharide moieties of glycoproteins. Biological assays with MC3T3-E1 osteoblasts revealed an excellent cytocompatibility as shown by the assessment of cell viability, vitality and morphology.
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PMID:Ti-Cp functionalization by deposition of organic/inorganic silica nanoparticles. 1786 78

In this work, polyvinilydene fluoride (PVDF) microcapsules were prepared by using combined emulsion and phase inversion techniques. With this method, microcapsules with different diameters and porosities have been obtained by just controlling the diameter of the membrane used during the preparation. Using a PVDF solution containing the oxidation catalyst ammonium molybdate (20 wt %), catalytic polymeric microcapsules with diameters ranging from 600 to 1,200 microm have been obtained. Characterization of catalytic microcapsules by means of SEM, BSE, and EDX analyses showed a uniform ammonium molybdate dispersion in the polymeric matrix. Catalytic microcapsules have been tested in the oxidation of aromatic primary alcohols to corresponding aldehydes. In the range 600-1,200 microm, the microcapsule diameter influences the formation of oxidation products: in particular, microcapsule diameters >900 microm slightly diminish the formation of aldehyde due to a beginning diffusion limitation. An interesting structure-reactivity behavior, induced by the interaction between the polymeric membrane and the substituted aromatic alcohol, has been observed.
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PMID:Combined emulsion and phase inversion techniques for the preparation of catalytic PVDF microcapsules. 1870 84

A series of 12-phosphotungstic acid (PWA) supported on various porous carriers, such as silica, alumina, titania, clay, and carbon were prepared, and their catalytic performance evaluated in the synthesis of imidazoles in solvent-free condition. It was found that PWA supported on silica (PWA/SiO(2)) showed higher activity compared to other catalysts. The observed behavior has more or less correlated with the acidic characteristic found through the potentiometrically titrated acidic sites and proton availability. The catalyst was characterized by FTIR, XRD, TGA/DSC, BET, and SEM. The presence of the Keggin structure can be followed by the above techniques, eliminating any doubt about the collapse of the supported anion. It can be observed that the process tolerates both electron donating and electron withdrawing substituents on the aldehyde with both benzil and benzoin. The general applicability of the method is demonstrated by using both benzylic and aromatic amines. The yields obtained were excellent without forming any side products such as trisubstituted imidazoles, which are normally produced in the presence of strong acids. The protocol developed using PWA/SiO(2) is superior in terms of process simplicity, reusable catalyst, high yields, short reaction time, and preclusion of toxic solvent.
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PMID:Supported heteropoly acids offering strong option for efficient and cleaner processing for the synthesis of imidazole derivatives under solvent-free condition. 2010 58

It is reported that catalytic hydrogenation of cinnamaldehyde to cinnamyl alcohol is a structural sensitive reaction dependent on size and type of metal doper of unsupported platinum nanocrystals used. Smaller sizes of platinum nanocrystals are found to give lower selectivity to cinnamyl alcohol, which suggests the high index Pt sites are undesirable for the terminal aldehyde hydrogenation. A plot of reaction selectivity across the first row of transition metals as dopers gives a typical volcano shape curve, the apex of which depicts that a small level of cobalt on platinum nanocrystals can greatly promote the reaction selectivity. The selectivity towards cinnamyl alcohol over the cobalt doped Pt nanocrystals can reach over 99.7%, following the optimization in reaction conditions such as temperature, pressure and substrate concentration. Detailed studies of XRD, CO chemisorption (for FTIR), TEM, SEM, AES and XPS of the nanostructure catalyst clearly reveal that the decorated cobalt atoms not only block the high index sites of Pt nanocrystals (sites for Co deposition) but also exert a strong electronic influence on reaction pathways. The d-band centre theory is invoked to explain the volcano plot of selectivity versus metal doper.
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PMID:Geometric and electronic effects on hydrogenation of cinnamaldehyde over unsupported Pt-based nanocrystals. 2121 7

The Schiff base ligand, N,N'-bis-(4-isopropylbenzaldimine)-1,2-diaminoethane (L), obtained by the condensation of 4-isopropylbenzaldehyde and 1,2-diaminoethane, has been used to synthesize the complexes of the type [ML(2)X(2)] [M = Co(II), Ni(II) and Zn(II); X = Cl and OAc]. The newly synthesized ligand (L) and its complexes have been characterized on the basis of elemental analyses, mass, (1)H and (13)C-NMR, molar conductance, IR, UV-vis, magnetic moment, CV and thermal analyses, powder XRD and SEM. IR spectral data show that the ligand is coordinated to the metal ions in a bidentate manner. The geometrical structures of these complexes are found to be octahedral. Interestingly, reaction with Cu(II) ion with this ligand undergoes hydrolytic cleavage to form ethylenediamine copper(II) complex and the corresponding aldehyde. The antimicrobial results indicate that the chloro complexes exhibit more activity than the acetato complexes. The complexes bind to CT-DNA by intercalation modes. Novel chloroform soluble ZnL(2)Cl(2) complex exhibits tremendous antimicrobial, DNA binding and cleaving properties.
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PMID:Synthesis, spectroscopic, antimicrobial, DNA binding and cleavage studies of some metal complexes involving symmetrical bidentate N, N donor Schiff base ligand. 2185 99


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