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Nitrogen Stream (nitrogen + stream)
Selected AbstractsOdour-active compounds of Jinhua hamFLAVOUR AND FRAGRANCE JOURNAL, Issue 1 2008Huanlu Song Abstract Using DHS, SAFE, GC,O and GC,MS, the odour-active compounds of Jinhua ham were identified and ranked according their odour potencies. For DHS, the ham powder was purged with a nitrogen stream at a flow rate of 50 ml/min for 25 min, 5 min and 1 min, respectively. The effluent of sample headspace was trapped by a Tenax tube, which was placed onto the vessel for GC,O. The most important odorants (FD factor = 125) in Jinhua ham headspace were ethyl 2-methylbutanoate/ethyl 3-methylbutanoate, hexanal, 1-hexen-3-one, 1-octen-3-one, 2-acetyl-1-pyrroline and 2-methoxyphenol, followed by the following odorants (FD factor = 25): 3-methyl butanal, dimethyl trisulphide, 1-nonen-3-one, butanoic acid, phenylacetaldehyde, 3-methylbutanoic acid, 2-methyl(3-methyldithio)furan, , -nonalctone and 4-methylphenol (p -cresol). For SAFE, the ham powder was extracted with diethyl ether, distilled by SAFE and then separated into neutral/basic and acidic fractions. Both fractions were subjected to AEDA. The relatively high-odour impact compounds (Log3FD Factor ,5) of the N/B fraction of SAFE extract of Jinhua ham were 1-octen-one, ethyl 3-methylbutanoate, methional, phenylacetaldehyde, 2-phenylethanol, (E)-4,5-epoxy-(E)-decenal, p -cresol (4-methylphenol); 3-methylbutanal, hexanal, 2-acetyl-1-pyrroline, decanal, (E,Z)-2,6-nonadienal and (E,E)-decadienal. The important odorants of the Ac fraction of SAFE extract of Jinhua ham were butanoic acid, 3-methylbutanoic acid, hexanoic acid, phenylacetic acid and an unknown. It was shown that the aroma of Jinhua ham consisted of a variety of compounds having different odour properties; a single compound could not characterize the aroma of Jinhua ham. Copyright © 2008 John Wiley & Sons, Ltd. [source] Simultaneous determination of maraviroc and raltegravir in human plasma by HPLC-UVIUBMB LIFE, Issue 4 2009Stefania Notari Abstract Therapeutic drug monitoring is pivotal to improve the management of HIV infection. Here, a new HPLC,UV method to quantify simultaneously maraviroc and raltegravir levels in human plasma is reported. Remarkably, this is the first method for maraviroc determination in human plasma. The volume of the plasma sample was 600 ,L. This method involved automated solid-phase extraction with Oasis HLB Cartridge 1 cc (30 mg divinylbenzene and N -vinylpyrrolidone) and evaporation in a water bath under nitrogen stream. The extracted samples were reconstituted with 200 ,L 50/50 of mobile-phase solution (0.01 M KH2PO4 and acetonitrile). Twenty microliters of these samples were injected into a HPLC,UV system, the analytes were eluted on an analytical dC18 Atlantis column (150 mm × 4.6 mm I.D.) with a particle size of 5 ,m. The mobile phase (0.01 M KH2PO4 and acetonitrile) was delivered at 1.0 mL/min with isocratic elution. The total run time for a single analysis was 10 min; maraviroc and raltegravir were detected by UV at 197 and 300 nm. The calibration curves were linear up to 2,500 ng/mL. The absolute recovery ranged between 93 and 100%. The HPLC,UV method reported here has been validated and is currently applied to monitor plasma levels of maraviroc and raltegravir in HIV-infected patients. © 2009 IUBMB IUBMB Life, 61(4):470,475, 2009 [source] High-throughput determination of atrasentan in human plasma by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometryBIOMEDICAL CHROMATOGRAPHY, Issue 9 2005Perry G. Wang Abstract Atrasentan (A-147627) is an endothelin antagonist receptor being developed at Abbott Laboratories for the treatment of prostate cancer. A quick and sensitive method for the determination of atrasentan in human plasma has been developed and validated using high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry. A dual-column, single mass spectrometer system is used to provide a reliable and routine means to increase sample throughput. The analytical method involves liquid,liquid extraction and internal standard (A-166790). The plasma samples and internal standard are acidified with 0.3 m hydrochloric acid prior to being extracted into 1:1 (v[sol ]v) hexanes,methyl t -butyl ether. The organic extract was evaporated to dryness using heated nitrogen stream and reconstituted with mobile phase. Atrasentan and internal standard were separated with no interference in a Zorbax SB-C18 analytical column with 2.1 × 50 mm, 5 µm, and a Zorbax C8 guard column using a mobile phase consisting of 50:50 (v:v) acetonitrile,0.05 m ammonium acetate, pH 4.5, at a flow rate of 0.30 mL[sol ]min to provide 4 min chromatograms. For a 250 µL plasma sample volume, the limit of quantitation was approximately 0.3 ng[sol ]mL. The calibration was linear from 0.30 to 98.0 ng[sol ]mL (r2 > 0.995). A significant advantage of the method is the ability to employ parallel HPLC separations with detection by a single MS[sol ]MS system to provide sensitivity and selectivity sufficient to achieve robust analytical results with a lower limit of quantitation of 0.30 ng[sol ]mL and high throughput. Copyright © 2005 John Wiley & Sons, Ltd. [source] Separation of VOCs from N2 using poly(ether block amide) membranesTHE CANADIAN JOURNAL OF CHEMICAL ENGINEERING, Issue 3 2009Li Liu Abstract This work deals with the separation of volatile organic compounds (VOCs) from nitrogen streams for organic vapour emission control by poly(ether block amide) membranes. As representative air pollutant VOCs, n -pentane, n -hexane, cyclohexane, n -heptane, methanol, ethanol, n -propanol, n -butanol, acetone, dimethyl carbonate, and methyl tert -butyl ether were used in this study. The separation of both binary VOC/N2 and multicomponent VOCs/N2 gas mixtures was carried out, and the membranes exhibited good separation performance. A VOC concentration of more than 90 mol% was achieved at a feed VOC concentration of 5 mol%. It was found that the permeances of the VOCs were mainly dominated by their solubilities in the membrane, whereas the permeance of N2 was affected by the presence of the VOCs. The permeance of N2 in the VOC/N2 mixtures was shown to be higher than pure N2 permeance due to membrane swelling induced by the VOCs dissolved in the membrane. Nevertheless, theVOC/N2 selectivity increased with an increase in the feed VOC concentration. Among the VOCs studied, the membrane showed a higher permeance to alcohol VOCs than paraffin VOCs. The effects of feed VOC concentration, temperature, stage cut, and permeate pressure on the separation performance were investigated. Ce travail porte sur la séparation des composés organiques volatils (COV) présents dans des courants d'azote pour le contrôle des émissions de vapeur organique par des membranes de poly(éther amide bloc). Comme polluants atmosphériques représentatifs des COV, on a utilisé dans cette étude le n-pentane, le n-hexane, le cyclohexane, le n-heptane, le méthanol, l'éthanol, le n-propanol, le n-butanol, l'acétone, le carbonate de diméthyle et le méthyl tertio-butyl. On a procédé à la séparation du mélange de gaz de COV/N2 binaire et du mélange de gaz multicomposant COV/N2, et les membranes montrent une bonne performance de séparation. Une concentration de COV de plus de 90% en poids moléculaire a été obtenue à une concentration d'alimentation de COV de 5% en poids moléculaire. On a trouvé que les perméances de N2 était sensibles à la présence de COV. La perméance de N2 dans les mélanges de COV/N2 s'avère plus élevée que la perméance du N2 pur en raison du gonflement de la membrane provoqué par les COV dissous dans la membrane. Néanmoins, la sélectivité des COV/N2 augmente avec la concentration de COV d'alimentation. Parmi les COV étudiés, la membrane montre la plus haute perméance aux COV d'alcool qu'aux COVde paraffine. Les effets de la concentration de COV d'alimentation, de la température, la coupure de phase et la pression des perméats ont été étudiés. [source] |