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1.
D. Bimberg C. Meuer M. Lammlin S. Liebich J. Kim E. Varene A. Kovsh I. Krestnikov G. Eisenstein 《中国光学快报(英文版)》2009,7(3):266-266
The authors regret that one of the coauthors was inadvertently omitted in the previous paper. E. Varene was a member of the Institut fur Festk6rperphysik at the Technische Universitat Berlin and contributed to the results on cross-phase modulation. 相似文献
2.
A multipurpose sampler (Gerstel MPS), designed for liquid large volume, gaseous and headspace samples was used for the GC-MS analysis of organic volatiles in human urine. Headspace sampling with a volume-, temperature- and speed-controlled gas-tight syringe was combined with a temperature-controlled cold injection system (CIS) for cold trapping, enrichment and focusing of analytes. Regular 2-ml GC vials filled with 1 ml acidified urine were used as headspace sampling vials. A 100-vial autosampler tray was equipped with an additional temperature and heating time controlled "preheating station" for five vials. Profiles of organic volatiles in human urine were determined and 34 components identified. Trimethylamine (TMA) and 4-heptanone as two metabolites of medical interest were quantified. Calibration curves and intra assay imprecision for 4-heptanone concentrations in the range of 40 to 800 ng/ml showed a correlation coefficient of r = 0.9980 and a relative standard deviation (RSD) between 3.0 and 3.4%. Calibration curves and intra-assay imprecision for TMA concentrations in the range of medical interest from 0.5 to 20 micrograms/ml showed a correlation coefficient of r = 0.9968 and a RSD between 4.1 and 6.8%. The high practicability of the multipurpose sampler for both gaseous and liquid samples together with the here shown good reproducibility and sensitivity make this single CIS-GC-MS system very attractive for routine clinical use in metabolic profiling of organic volatiles (headspace) and non-volatiles (liquid). 相似文献
3.
A review of sample preparation methods for organic acids in biological fluids, in particular serum and urine, is presented. It covers techniques on organic acid determination without sample preparation, release of organic acids from binding locations, removal of proteins by protein precipitation and ultrafiltration, isolation of the organic acids by liquid-liquid and liquid-solid extraction, purification of the extract, derivatization and pre-fractionation. The various alternative sample preparation steps are compared and critically discussed. Examples of applications including profile analysis of organic acids by gas chromatography (GC), determination of particular organic acids by GC or liquid chromatography and determination of fatty acids as a distinct chemical class of acids demonstrate that the kind of sample preparation chosen depends strongly on the analytical aims. 相似文献
4.
Hierarchical cluster analysis (HCA) and principal components analysis (PCA) were applied to find groups between similar depth-profiles in thin-layers investigated by Rutherford backscattering spectrometry (RBS).HCA yields in one run an objective hierarchy of similarity for several profiles. Among the similarity coefficients examined the linear measure, the Euclidean distance and the exponential measure respond with different sensitivity to overall shifts in direction of the concentration axis, whereas the correlation measure relates to parallelism of the profiles.For agglomerative HCA with Euclidean distance, a lowest significant linkage level has been defined by use of Fisher'sF-test. For divisive HCA based also on Euclidean distance, the maximum of a separating function marks the most separating cluster step. The outcomes of both proposals agree for the data set investigated.PCA is useful for verifying the results of HCA and yields additional information about the data structure. In the actual example quite different positions of features (concentrations at definite depths) in the space of the two first principal components hint at peculiarities during the metallurgical coating process. 相似文献
5.
Summary The information of distribution analyses considerably exceeds that of integral analyses because of the spatial resolution. Distribution-analytical procedures are characterized by the ideal information amount which is determined by the ideal spatial resolving power A* that is theoretically attainable by actual scanning or mapping. Compared with it, the real information amount of distribution-analytical results are determined by a practical spatial resolving power and therefore, among others, by the number of measuring points. In dependence on the stochastical properties of multi-phase materials an optimum area can be specified for distribution-analytical investigations with a maximum information content. Methods of testing homogeneity can be characterized by means of the information theory in dependence on the arrangement of measuring points, on the evaluation of concentration or measuring values, and on their univariate, multiple or multivariate character.Part II: see [5] 相似文献
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Hans Günther Wahl Silke-Yvonne Habel Norbert Schmieder Hartmut M. Liebich 《Journal of separation science》1994,17(7):543-548
Identification of cis/trans isomers of unsaturated fatty acids cannot usually be achieved by GC-MS (gas chromatography-mass spectrometry) without reference substances. In this study a GC-FTIR-MS system (gas chromatography-Fourier transform-mass spectrometry) was used to identify fatty acid methyl esters (FAMEs) and differentiate between the cis/trans isomers. Besides methyl esters, 2-alkenyl-4,4-dimethyloxazoline derivatives (DMOX), which have been used to locate double bond positions of unsaturated fatty acids, were examined with respect to their suitability for cis/trans differentiation. A combined GC-FTIR-MS system with a wide band (4000–550 cm?1) mercury cadmium telluride (MCT) detector was used in series and parallel to identify 31 reference unsaturated fatty acids, including 7 pairs of cis/trans isomers. Serum samples of healthy persons and commercially available fish oil were analyzed as examples of complex mixtures. Using splitless injection the detection limit for the less sensitive IR detector was 25 ng/μl in case of the weak cis and trans bands. In the FTIR spectra cis/trans isomers were identified by analysis of bands arising from C? H out-of-plane (oop) bending: for both the FAME and DMOX derivatives cis-1,2-disubstituted double bonds give a strong band near 720 cm?1 and the corresponding trans isomers near 967 cm?1. cis Isomers could be identified further by a band at 3012 cm?1. With the combined data of the GC-FTIR-MS system it is now possible to identify polyunsaturated fatty acids with regard to the discrimination of cis/trans isomers. 相似文献
10.
Werner Funcke Dieter Henneberg Clemens Von Sonntag Almuth Klemer 《Journal of mass spectrometry : JMS》1979,14(4):220-221
The TMS-ethers of four glycosylamines and seven Amadori compounds have been investigated by electron impact mass spectrometry. The mass spectra of glycosylamine-TMS derivatives and of their isomeric Amadori rearrangement products are quite characteristic. The two types of compounds can be distinguished by a few characteristic peaks. 相似文献