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61.
R. Hertz‐Schünemann R. Dorfner C. Yeretzian T. Streibel R. Zimmermann 《Journal of mass spectrometry : JMS》2013,48(12):i-i
Resonance‐enhanced multiphoton ionisation time‐of‐flight mass spectrometry (REMPI‐TOFMS) enables the fast and sensitive on‐line monitoring of volatile organic compounds (VOC) formed during coffee roasting. On the one hand, REMPI‐TOFMS was applied to monitor roasting gases of an industrial roaster (1500 kg/h capacity), with the aim of determining the roast degree in real‐time from the transient chemical signature of VOCs. On the other hand, a previously developed μ‐probe sampling device was used to analyse roasting gases from individual coffee beans. The aim was to explore fundamental processes at the individual bean level and link these to phenomena at the batch level. The pioneering single‐bean experiments were conducted in two configurations: (1) VOCs formed inside a bean were sampled in situ, i.e. via a drilled μ‐hole, from the interior, using a μ‐probe (inside). (2) VOCs were sampled on‐line in close vicinity of a single coffee bean's surface (outside). The focus was on VOCs originating from hydrolysis and pyrolytic degradation of chlorogenic acids, like feruloyl quinic acid and caffeoyl quinic acid. The single bean experiments revealed interesting phenomena. First, differences in time–intensity profiles between inside versus outside (time shift of maximum) were observed and tentatively linked to the permeability of the bean's cell walls material. Second, sharp bursts of some VOCs were observed, while others did exhibit smooth release curves. It is believed that these reflect a direct observation of bean popping during roasting. Finally, discrimination between Coffea arabica and Coffea canephora was demonstrated based on high‐mass volatile markers, exclusively present in spectra of Coffea arabica. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
62.
Fabian Benz Christoph Roderburg David Vargas Cardenas Mihael Vucur Jérémie Gautheron Alexander Koch Henning Zimmermann J?rn Janssen Lukas Nieuwenhuijsen Mark Luedde Norbert Frey Frank Tacke Christian Trautwein Tom Luedde 《Experimental & molecular medicine》2013,45(9):e42
MicroRNA (miRNA) levels in serum have recently emerged as potential novel biomarkers for various diseases. miRNAs are routinely measured by standard quantitative real-time PCR (qPCR); however, the high sensitivity of qPCR demands appropriate normalization to correct for nonbiological variation. Presently, RNU6B (U6) is used for data normalization of circulating miRNAs in many studies. However, it was suggested that serum levels of U6 themselves might differ between individuals. Therefore, no consensus has been reached on the best normalization strategy in ‘circulating miRNA''. We analyzed U6 levels as well as levels of spiked-in SV40-RNA in sera of 44 healthy volunteers, 203 intensive care unit patients and 64 patients with liver fibrosis. Levels of U6 demonstrated a high variability in sera of healthy donors, patients with critical illness and liver fibrosis. This high variability could also be confirmed in sera of mice after the cecal ligation and puncture procedure. Most importantly, levels of circulating U6 were significantly upregulated in sera of patients with critical illness and sepsis compared with controls and correlated with established markers of inflammation. In patients with liver fibrosis, U6 levels were significantly downregulated. In contrast, levels of spiked-in SV40 displayed a significantly higher stability both in human cohorts (healthy, critical illness, liver fibrosis) and in mice. Thus, we conclude that U6 levels in the serum are dysregulated in a disease-specific manner. Therefore, U6 should not be used for data normalization of circulating miRNAs in inflammatory diseases and previous studies using this approach should be interpreted with caution. Further studies are warranted to identify specific regulatory processes of U6 levels in sepsis and liver fibrosis. 相似文献
63.
Lutz Kummer Chia-Wen Hsu Onur Dagliyan Christopher MacNevin Melanie Kaufholz Bastian Zimmermann Nikolay V. Dokholyan Klaus M. Hahn Andreas Plückthun 《Chemistry & biology》2013,20(6):847-856
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64.
S. Wohlfahrt M. Fischer M. Saraji-Bozorgzad G. Matuschek T. Streibel E. Post T. Denner R. Zimmermann 《Analytical and bioanalytical chemistry》2013,405(22):7107-7116
Comprehensive multi-dimensional hyphenation of a thermogravimetry device (i.e. a thermobalance) to gas chromatography and single photon ionization–time-of-flight mass spectrometry (TG–GC×SPI–MS) has been used to investigate two crude oil samples of different geographical origin. The source of the applied vacuum ultraviolet radiation is an electron beam pumped rare gas excimer lamp (EBEL). The soft photoionization favors the formation of molecular ions. Introduction of a fast, rapidly modulated gas chromatographic separation step in comparison with solely TG–SPI–MS enables strongly enhanced detection especially with such highly complex organic matrices as crude oil. In contrast with former TG–SPI–MS measurements, separation and identification of overlying substances is possible because of different GC retention times. The specific contribution of isobaric compounds to one mass signal is determined for alkanes, naphthalenes, alkylated benzenes, and other compounds. Figure
Specific characteristics of a two-dimensional TG–GC×SPI–MS contour plot obtained from Turkish crude oil. The complete m/z and TG temperature ranges are displayed in a. The magnified region from m/z 50–250 and 140–170 °C reveals the “pixilated” structure (b). Parts c and d reveal the system’s ability to investigate compounds in a broad m/z range with limitations for very-high and very-low boiling compounds as shown for m/z 260 and m/z 70, respectively 相似文献
65.
66.
The complexity of technical products increases significantly, due to an increasing number of interacting design variables of many components and subsystems. At the same time, the need for separated development processes is increasing due to specialization and outsourcing. Solution space methods are designed to solve this conflict. The requirements from an upper level, e.g. performance measures of the whole system, can be cascaded down to requirements on a lower level, e.g. performance measures of the subsystems or components, as it is done in the V-model approach. The method does not only take the numerous interactions into account but also guarantees the resulting intervals of different parameters to be independent of each other. Unfortunately, the computational cost of the state-of-the-art stochastic approach is high. The approach in this paper shows that the computational effort can be reduced considerably using a gradient based optimization approach for constraint problems. We demonstrate that the approach reduces the required number of function evaluations for a chassis design problem by a factor of 30, but more important, the CPU time for solving the problem by a factor of 20. (© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
67.
Ben Ali K Lafon O Zimmermann H Guittet E Lesot P 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2007,187(2):205-215
We describe several homo- and heteronuclear 2D NMR strategies dedicated to the analysis of anisotropic (2)H spectra of a mixture of dideuterated unlike/like stereoisomers with two remote stereogenic centers, using weakly orienting chiral liquid crystals. To this end, we propose various 2D correlation experiments, denoted "D(H)(n)D" or "D(H)(n)C" (with n=1, 2), that involve two heteronuclear polarization transfers of INEPT-type with one or two proton relays. The analytical expressions of correlation signals for four pulse sequences reported here were calculated using the product-operators formalism for spin I=1 and S=1/2. The features and advantages of each scheme are presented and discussed. The efficiency of these 2D sequences is illustrated using various deuterated model molecules, dissolved in organic solutions of polypeptides made of poly-gamma-benzyl-L-glutamate (PBLG) or poly-epsilon-carbobenzyloxy-L-lysine (PCBLL) and NMR numerical simulations. 相似文献
68.
69.
Paola Zimmermann Crocomo Takahito Kaihara Soki Kawaguchi. Dr. Patrycja Stachelek Prof. Dr. Satoshi Minakata Prof. Dr. Piotr de Silva Prof. Dr. Przemyslaw Data Prof. Dr. Youhei Takeda 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(53):13390-13398
Novel electron donor–acceptor–donor (D-A-D) compounds comprising dibenzo[a,j]phenazine as the central acceptor core and two 7-membered diarylamines (iminodibenzyl and iminostilbene) as the donors have been designed and synthesized. Investigation of their physicochemical properties revealed the impact of C2 insertion into well-known carbazole electron donors on the properties of previously reported twisted dibenzo[a,j]phenazine-core D-A-D triads. Slight structural modification caused a drastic change in conformational preference, allowing unique photophysical behavior of dual emission derived from room-temperature phosphorescence and triplet–triplet annihilation. Furthermore, electrochemical analysis suggested sigma-dimer formation and electrochemical polymerization on the electrode. Quantum chemical calculations also rationalized the experimental results. 相似文献
70.