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A high performance liquid chromatographic (HPLC) system is described for determination of the unsaturated disaccharide (delta Di-HA) derived from hyaluronic acid (HA) in human urine by digestion with hyaluronidase SD. The effects of eluents on the separation of delta Di-HA and delta Di-0S, which is derived from the reaction of chondroitin with the enzyme, have been studied. The established chromatographic conditions were as follows--column: a stainless steel tube (4 mm i.d. x 250 mm) packed with TSKgel NH2-60; eluent: a mixture of acetonitrile and 0.1 M Tris-HCl buffer containing 0.1 M boric acid and 10 mM sodium sulphate, pH 7.0 (64:36, v/v). The strong fluorescence of unsaturated disaccharide after the reaction with 2-cyanoacetamide in alkaline medium was used for post-column detection. The calibration curve for delta Di-HA was linear in the range 5 pmol-5nmol with a practical detection limit of 2 pmol. The assay coefficients of variation (n = 5) at 200 pmol for delta Di-HA and delta Di-0S were 1.7 and 1.5%, respectively. This HPLC system has been applied to the determination of HA in human urine.  相似文献   
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A new analytical method of designing two-aspherical-mirror anastigmats was developed and applied to searching solution groups of soft X-ray microscopes of a large misalignment tolerance. The two-mirror anastigmat configurations were expressed by a practical variable related to pupil obstruction limiting the system throughput. Axial coma and other aberrations caused by a slight decenter of the system were then formulated to represent sensitivity to misalignment. These formulations enabled a global survey of solution groups as demonstrated by a designing example of soft X-ray microscopes with a magnification m = −1/50, which resulted in four solutions more insensitive to misalignment than a standard Schwarzschild optics in the soft X-ray region. Some solutions were also found to have much larger fields of view suitable for high resolution imaging as confirmed by computer ray tracing.  相似文献   
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Mori I  Fujita Y  Toyoda M  Hasegawa Y 《Talanta》1992,39(5):535-539
The colour development between 4-(2-pyridylazo)-resorcinol(PAR) and osmium(VIII) in the presence of cationic and nonionic surfactants in a weakly acidic medium was more stable and reproducible than in the absence of surfactant (PAR-alone method). An improved spectrophotometric determination of osmium(VIII) with PAR was investigated in the presence of mixed surfactants of N-hexadecyltrimethylammonium chloride (HTAC) and Brij 58 [poly(oxyethylene)lauryl ether] as cationic and nonionic surfactants at pH 6.0-7.2. The calibration graph was linear in the range 0-110 microg/10 ml osmium(VIII), and the apparent molar absorptivity was 2.4 x 10(4) l.mole(-1).cm(-1) with a Sandell sensitivity of 0.0079 microg/cm(2) osmium(VIII).  相似文献   
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A new type of multi-turn time-of-flight mass spectrometer was constructed, consisting of four cylindrical electric sectors and 28 electric quadrupole lenses, the size of the vacuum chamber being 60 x 70 x 20 cm. It was demonstrated that the mass resolution can be increased according to the number of cycles of the ions through the ion optical system.  相似文献   
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Infrared and Raman spectra of 1,2-dibromoethane CH2BrCH2Br and CD2BrCD2Br were observed in the liquid state, and the fundamental frequencies were determined by comparison with those of related molecules. Infrared absorption intensities of fundament bands were measured in the liquid state, and the intensity data were interpreted on the basis of the valence-optical theory. From the converged value of a population ratio, the energy difference between the trans and gauche isomers was determined, which was in good agreement with the value obtained from the temperature effect of the IR spectrum.  相似文献   
9.
Treatment of alkyl allyl carbonates derived from various alcohols with a palladium catalyst in MeCN affords ketones and aldehydes in high yields. This new method of oxidation of alcohols can be applied to various alcohols except simple primary alcohols.  相似文献   
10.
Isotropie Raman spectra of the symmetric C—H stretching bands of several organic molecules are measured in the neat liquid and in solvents including water. The linewidths are interpreted on the basis of the vibrational dephasing model, and intermolecular interactions between the solutes and solvents are discussed.  相似文献   
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