Determination of unsaturated fatty acid composition by high-resolution nuclear magnetic resonance spectroscopy

High-resolution nuclear magnetic resonance (NMR) spectroscopy provides useful data for analyzing fatty acid compositions of edible vegetable oils. Quantitation of each fatty acid was carried out by evaluation of particular peaks. According to the ¹H NMR method, terminal methyl protons, divinyl protons, and allyl protons are useful to calculate linolenic acid, linoleic acid, and oleic acid, respectively. The ω-2 carbon, divinyl carbon, and allylic carbons were used for calculation of these acids by the ¹³C NMR method. Compositional results obtained by NMR coincided well with those of the conventional gas chromatography (GC) method. Results from ¹³C NMR were in better agreement with those from GC than were the results obtained by the ¹H NMR method.     

Iodine Excess as an Environmental Risk Factor for Autoimmune Thyroid Disease

The global effort to prevent iodine deficiency disorders through iodine supplementation, such as universal salt iodization, has achieved impressive progress during the last few decades. However, iodine excess, due to extensive environmental iodine exposure in addition to poor monitoring, is currently a more frequent occurrence than iodine deficiency. Iodine excess is a precipitating environmental factor in the development of autoimmune thyroid disease. Excessive amounts of iodide have been linked to the development of autoimmune thyroiditis in humans and animals, while intrathyroidal depletion of iodine prevents disease in animal strains susceptible to severe thyroiditis. Although the mechanisms by which iodide induces thyroiditis are still unclear, several mechanisms have been proposed: (1) excess iodine induces the production of cytokines and chemokines that can recruit immunocompetent cells to the thyroid; (2) processing excess iodine in thyroid epithelial cells may result in elevated levels of oxidative stress, leading to harmful lipid oxidation and thyroid tissue injuries; and (3) iodine incorporation in the protein chain of thyroglobulin may augment the antigenicity of this molecule. This review will summarize the current knowledge regarding excess iodide as an environmental toxicant and relate it to the development of autoimmune thyroid disease.     

Formal Nucleophilic Boryl Substitution of Organic Halides with Silylborane/Alkoxy Base System

Boryl substitution of organohalides with a silylborane and alkoxy bases is described. This reaction can be applied to various functionalized aryl halides. Alkyl and alkenyl halides, and even sterically congested aryl bromides also provided the corresponding borylated products in high yields. Mechanistic studies indicated that neither trace transition-metal impurities nor aryl radical species involved in this reaction.     

Copper‐ion adsorption and gold‐ion reduction by polyphenols prepared by the enzymatic reaction of horseradish peroxidase

Polyphenols were synthesized via a horseradish peroxidase reaction from phenol, catechol, and pyrogallol for use as copper‐ion adsorbents. The molecular weights of the polyphenols ranged from about 1000 to 3000 g/mol. The hydroxyl group contents in the polyphenols from phenol, catechol, and pyrogallol were 5.9, 4.0, and 0.94 mol/kg, respectively, as determined by titration. The saturation binding capacity for copper ions of the polyphenols from phenol, catechol, and pyrogallol were calculated to be 1.44, 0.88, and 0.22 mol/kg, respectively, at pH 4.5. Copper ions were efficiently adsorbed via an ion‐exchange interaction by the synthesized polyphenols with vicinal hydroxyl groups, and those polyphenols could be applied to metal adsorption. Gold ions were selectively reduced by the phenol group in polypyrogallol in acid media to form gold particles. The reduced gold particles were eluted with a solution of 1.0M thiourea plus 0.5M HCl. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Gamma-ray and neutron dosimetry by EPR and AMS, using tooth enamel from atomic-bomb survivors: a mini review

The electron paramagnetic resonance (EPR, or electron spin resonance) method was used to measure CO??· radicals recorded in tooth enamel by exposure to atomic-bomb gamma rays. The EPR-estimated doses (i.e. ??Co gamma-ray equivalent dose) were generally in good correlation with cytogenetic data of the same survivors, whereas plots of EPR-estimated dose or cytogenetically estimated dose against DS02 doses turned out to scatter more widely. Because those survivors whose EPR doses were higher (or lower) than DS02 doses tended to show also higher (or lower) responses for cytogenetic responses, the apparent variation appears primarily due to problems in individual DS02 doses rather than the measurement errors associated with the EPR or cytogenetic technique. A part of the enamel samples were also used for evaluation of neutron doses by measuring ?1Ca/??Ca ratios using the accelerator mass spectrometry technique. The results for the measured ratios were on average ~85 % of the calculated ratios by DS02 (but within the 95 % confidence bounds of the simulated results), which lends support to DS02-derived neutron doses to the survivors.     

Nonlinear motion correction of respiratory-gated lung SPECT images

We propose a method for correcting the motion of the lungs between different phase images obtained by respiratory-gated single photon emission computed tomography (SPECT). This method is applied to SPECT images that show a preserved activity distribution in the lungs such as 99m-Tc macro aggregated albumin (99m-Tc-MAA) perfusion images and 99m-Tc-Technegas ventilation images. In the proposed method, an objective function, which consists of both the degree of similarity between a reference image and a deformed image, and the smoothness of deformation is defined and optimized using a simulated annealing algorithm. For the degree of similarity term in the objective function, an expansion ratio, defined as the ratio of change in local volume due to deformation, is introduced to preserve the total activity during the motion correction process. This method was applied to data simulated from computer phantoms, data acquired from a physical phantom, and 17 sets of clinical data. In all cases, the motion correction between inspiration and expiration phase images was successfully achieved.     

Thermoplastic Acrylic Rubber Physically Crosslinked by Tiny Poly(vinylidene fluoride) Crystals

Summary: Acrylic rubber showed greatly improved mechanical properties and very nice elasticity when blended with small amount of PVDF. PVDF crystallized into very sparse and loose spherulites in the blends with ACM molecular chains incorporated into the PVDF lamellae. These micro‐crystals were precisely dispersed in the ACM matrix and acted as the physical crosslink points for the matrix upon stretching. Therefore, the ACM/PVDF blends containing small amounts of PVDF display the typical properties of thermoplastic elastomers with large elongation at break, high tensile strength, and excellent strain recovery from the highly deformed state.

Schematic diagram of physically crosslinked ACM by the tiny PVDF crystals in ACM‐rich PVDF/ACM blends.     

Analyses of homo-oligomer interfaces of proteins from the complementarity of molecular surface, electrostatic potential and hydrophobicity

To extract the general structural features of interacting protein pairs, the non-redundant homo-oligomer interfaces (393 interfaces) in the PDB were analyzed using the fine-grained molecular surface, electrostatic potentials and the hydrophobicity calculated as the solvation free energy using empirical parameters. For each property, statistical analyses of the degree of complementarity were carried out, and we developed a method to judge whether interfaces were shape-complementary, electrostatic-complementary and/or hydrophobic-complementary or not. In order to search for the correlation between the property complementarity and structure of the interfaces, at first, we roughly classified all the interfaces into the following five groups according to the structure of the interface and surveyed the correlation between the shape classification and the complementary: cyclic-oligomer (69), twisted-dimer (27), dimer-parallel (14), dimer-perpendicular (109) and dimer-circular (174), where the number in the parenthesis is the number of interfaces in each group. As a result, we found the new characteristic trends as the possible necessary conditions in the formation of homo-oligomer interfaces, especially from the viewpoint of electrostatic complementarity. In addition, we also show that complementarity analyses can be used to discriminate the biological-interface from the crystallographic-interface in homo-oligomer proteins.