|
| ||
|
|
||
Caproic Acid (caproic + acid)
Selected AbstractsSuperparamagnetic Hyperbranched Polyglycerol-Grafted Fe3O4 Nanoparticles as a Novel Magnetic Resonance Imaging Contrast Agent: An In Vitro AssessmentADVANCED FUNCTIONAL MATERIALS, Issue 16 2009Liang Wang Abstract Hyperbranched polyglycerol-grafted, magnetic Fe3O4 nanoparticles (HPG-grafted MNPs) are successfully synthesized by surface-initiated ring-opening multibranching polymerization of glycidol. Reactive hydroxyl groups are immobilized on the surface of 6,9,nm Fe3O4 nanoparticles via effective ligand exchange of oleic acid with 6-hydroxy caproic acid. The surface hydroxyl groups are treated with aluminum isopropoxide to form the nanosized macroinitiators. The successful grafting of HPG onto the nanoparticles is confirmed by infrared and X-ray photoelectron spectroscopy. The HPG-grafted MNPs have a uniform hydrodynamic diameter of (24.0,±,3.0) nm, and are very stable in aqueous solution, as well as in cell culture medium, for months. These nanoparticles have great potential for application as a new magnetic resonance imaging contrast agent, as evidenced by their lack of cytotoxicity towards mammalian cells, low uptake by macrophages, excellent stability in aqueous medium and magnetic fields, and favorable magnetic properties. Furthermore, the possibility of functionalizing the hydroxyl end-groups of the HPG with cell-specific targeting ligands will expand the range of applications of these MNPs. [source] Volatile fatty acid production during anaerobic mesophilic digestion of solid potato wasteJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 7 2004Wilson Parawira Abstract The production of volatile fatty acids by anaerobic digestion of solid potato waste was investigated using a batch solid waste reactor with a working capacity of 2 dm,3 at 37°C. Solid potato waste was packed into the digester and the organic content of the waste was released by microbial activity by circulating water over the bed, using batch loads of 500 g or 1000 g potato waste. The sequence of appearance of the volatile fatty acids was (acetic, propionic); (n -butyric); (n -valeric, iso-valeric, caproic); (iso-butyric). After 300 h digestion of potato waste on a small scale, the fermentation products were chiefly (mg g,1 total VFAs): acetic acid (420), butyric acid (310), propionic acid (140) and caproic acid (90), with insignificant amounts of iso-butyric acid, n -valeric and iso-valeric acids. When the load of potato solids was increased, the volatile fatty acid content was similar, but butyric acid constituted 110 mg g,1 and lactic acid 400 mg g,1 of the total volatile fatty acids. The maximum soluble chemical oxygen demand (COD) achieved under the experimental conditions used was 27 and 37 g COD dm,3 at low and high loadings of potato solids, respectively. The total volatile fatty acids reached 19 g dm,3 of leachate at both loads of potato solid waste. Gas production was negligible, indicating that methanogenic activity was effectively inhibited. Copyright © 2004 Society of Chemical Industry [source] Influence of "Alternative" C-terminal amino acids on the formation of [b3 + 17 + Cat]+ products from metal cationized synthetic tetrapeptides,JOURNAL OF MASS SPECTROMETRY (INCORP BIOLOGICAL MASS SPECTROMETRY), Issue 5 2004V. Anbalagan Abstract The aim of this study was to investigate the dissociation patterns, and in particular the relative abundance of [b3 + 17 + Cat]+, for peptides with C-termini designed to allow transfer of the ,OH required to generate the product ion, but not necessarily as the most favored pathway. Working with the hypothesis that formation of a five-membered ring intermediate, including intramolecular nucleophilic attack by a carbonyl oxygen atom, is an important mechanistic step, several model peptides with general sequence AcFGGX were synthesized, metal cationized by electrospray ionization and subjected to collision-induced dissociation (CID). The amino acid at position X was one that either required a larger ring intermediate (,-alanine, ,-aminobutyric acid and ,-amino- n -caproic acid to generate six-, seven- or nine- membered rings, respectively) to transfer ,OH, lacked a structural element required for nucleophilic attack (aminoethanol) or prohibited cyclization because of the inclusion of a rigid ring (p - and m -aminobenzoic acid). For Ag+, Li+ and Na+ cationized peptides, our results show that amino acids requiring the adoption of larger ring intermediates suppressed the formation of [b3 + 17 + Cat]+, while amino acids that prohibit cyclization eliminated the reaction pathway completely. Formation of [b3 , 1 + Cat]+ from the alkali metal cationized versions was not a favorable process upon suppression or elimination of the [b3 + 17 + Cat]+ pathway: the loss of H2O to form [M , H2O + Cat]+ was instead the dominant dissociation reaction observed. Multiple-stage dissociation experiments suggest that [M , H2O + Cat]+ is not [b4 , 1 + Cat]+ arising from the loss of H2O from the C-terminus, but may instead be a species that forms via a mechanism involving the elimination of an oxygen atom from an amide group. Copyright © 2004 John Wiley & Sons, Ltd. [source] Cometary glycine detected in samples returned by StardustMETEORITICS & PLANETARY SCIENCE, Issue 9 2009Jamie E. Elsila Here, we present the stable carbon isotopic ratios of glycine and ,-amino- n -caproic acid (EACA), the two most abundant amino acids identified in Stardust-returned foil samples measured by gas chromatography-mass spectrometry coupled with isotope ratio mass spectrometry. The ,13C value for glycine of +29 ± 6, strongly suggests an extraterrestrial origin for glycine, while the ,13C value for EACA of ,25 ± 2, indicates terrestrial contamination by Nylon-6 during curation. This represents the first detection of a cometary amino acid. [source] Detection of cometary amines in samples returned by StardustMETEORITICS & PLANETARY SCIENCE, Issue 1-2 2008Daniel P. Glavin A suite of amino acids and amines including glycine, L-alanine, ,-alanine (BALA), ,-amino- n -butyric acid (GABA), ,-amino- n -caproic acid (EACA), ethanolamine (MEA), methylamine (MA), and ethylamine (EA) were identified in acid-hydrolyzed, hot-water extracts of these Stardust materials above background levels. With the exception of MA and EA, all other primary amines detected in comet-exposed aerogel fragments C2054,4 and C2086,1 were also present in the flight aerogel witness tile that was not exposed to the comet, indicating that most amines are terrestrial in origin. The enhanced relative abundances of MA and EA in comet-exposed aerogel compared to controls, coupled with MA to EA ratios (C2054,4: 1.0 ± 0.2; C2086,1: 1.8 ± 0.2) that are distinct from preflight aerogels (E243,13C and E243,13F: 7 ± 3), suggest that these volatile amines were captured from comet Wild 2. MA and EA were present predominantly in an acid-hydrolyzable bound form in the aerogel, rather than as free primary amines, which is consistent with laboratory analyses of cometary ice analog materials. It is possible that Wild 2 MA and EA were formed on energetically processed icy grains containing ammonia and approximately equal abundances of methane and ethane. The presence of cometary amines in Stardust material supports the hypothesis that comets were an important source of prebiotic organic carbon and nitrogen on the early Earth. [source] Rapid determination of short-chain fatty acids in colonic contents and faeces of humans and rats by acidified water-extraction and direct-injection gas chromatographyBIOMEDICAL CHROMATOGRAPHY, Issue 8 2006Guohua Zhao Abstract Short-chain fatty acids (SCFAs) have attracted much attention recently because of their positive physiological effects. In this work, a rapid and reliable gas chromatographic method for determination of eight SCFAs, in colonic and faecal samples from rats and humans has been developed and validated. The methodology involves extraction of the SCFAs in water before a direct injection procedure on a FFAP capillary column. A stock standard solution containing acetic acid, propionic acid, n -butyric acid, i -butyric acid, n -valeric acid, i -valeric acid, n -caproic acid and n -heptanoic acid was prepared and used. A high line-arity (r2 > 0.9990), low quantification limit (2.38,30.14 µm) and high recovery for most acids were obtained. Acidification of faecal samples was found to be crucial for quantitative determination of the SCFAs, and adjustment of pH to 2,3 was regarded as necessary. Glass wool inserted in the glass liner of the injection port proved effective in preventing the contamination of the column by non-volatiles, and 12% formic acid reduced the ghost peak that appeared gradually after several injections. After validation, the methodology was applied on two faecal samples from rats fed diets containing different amount of dietary fibre and one faecal sample from human fed a normal diet to test the accuracy of the developed method. Copyright © 2005 John Wiley & Sons, Ltd. [source] | ||||||||||