Characterization of the surface properties of xylan by FT-Raman spectroscopy and wicking technique

Using FT-Raman spectroscopy, column wicking technique and the equations of Washburn as well as van Oss et al., the surface properties of xylan, the main component in hemicelluloses, has been characterized and estimated. Raman spectrum showed that xylan has been structured by acetyl group and methyl-bonded glucurono group. Obtained results show that the surface free energy of xylan is higher in comparison with literature reported values for cellulose because the former has a larger Lifshitz–van der Waals component than the latter. However, xylan has been found to have very smaller polarity and orientation data than that of cellulose.     

Determination of mangiferin, jateorrhizine, palmatine, berberine, cinnamic acid, and cinnamaldehyde in the traditional Chinese medicinal preparation Zi-Shen pill by high-performance liquid chromatography

High-performance liquid chromatography is employed to determine the contents of six marker components such as mangiferin, jateorrhizine, palmatine, berberine, cinnamic acid, and cinnamaldehyde in the traditional Chinese medicinal preparation Zi-Shen pill. The separation is performed on a C(18) column by stepwise gradient elution with water (0.2%, v/v, triethylamine adjusted to pH 4 with phosphoric acid)-methanol-acetonitrile (0.01 min, 98:0:2; 20 min, 80:5:15; 30 min, 65:13:22; and 55 min, 65:13:22) as the mobile phase at a flow rate of 0.9 mL/min, with UV detection at 280 nm. Six regression equations show good linear relationships between the peak area of each marker and concentration. The recoveries of the markers listed are 95.5%, 98.3%, 96.8%, 99.5%, 101.7%, and 102.1%, respectively. The repeatability and reproducibility (relative standard deviation) of the method are less than 2.5% and 3.3%, respectively.     

A simplified approach for evaluation of the polarity parameters for polymer using the K coefficient of the Mark-Houwink-Sakurada equation

Since two solvent polarity parameters, e.g., the Et(30) defined by Reichardt and the pi* defined by Kamlet and Taft, respectively, plotted with the K coefficient of the Mark-Houwink-Sakurada equation, presented good linear fits, this paper suggests applying the extrapolating method in the same way as the Zisman plot to obtain similar polarity parameters for polymers. In order to verify those obtained polarity parameter values for various polymers, literature-reported polarity values determined using other techniques are referenced and indicate that this paper introduced a simplified approach that can be applied to evaluate the polarity parameters for polymers. In this paper, since we observe that various polymers are of interest to present absolutely different slope tendencies, e.g., positive and negative, it is also suggested that polarity properties of polymers may be reinterpreted.     

A rapid two-step chromatographic method for the quantitative determination of vitellogenin in fish plasma

By combining anion-exchange membrane purification with high-performance size-exclusion chromatography (HPSEC) analysis, a two-step chromatographic method was developed for the determination of vitellogenin (Vtg) in fish plasma. Most plasma protein interferences can be removed during anion-exchange membrane purification process. Vtg is eluted from the size-exclusion chromatography column with a retention time of about 9 min and is characterized based on the native molecular weight, with a limit of quantification of 20 g Vtg mL^–1 plasma. The spiked recovery and interassay variability were better than 80% and 4.8%. This method was successfully applied to analyze the plasma Vtg levels of loach (Misgurnus angaillicaudatus) and sea catfish (Enchelyopus elongatus). In addition to all the female fish, Vtg is detected in 75% of male loaches and 100% of male sea catfish. The result indicates that some chemicals or unknown factors with estrogenic activity have induced male fish to produce Vtg.     

The Quasiapproximate $(\mathcal{U} + \mathcal{K})$ –Invariants of Essentially Normal Operators

For a class of essentially normal operators, we characterize their norm closures of –orbits. Moreover, we introduce a notion of the quasiapproximate – equivalence of essentially normal operators and determine completely the quasiapproximate –invariants. Finally, we give the canonical forms of essentially normal operators under this quasiapproximate –equivalence.     

Nonlinear Internal Damping of Wave Equations with Variable Coefficients

For wave equations with variable coefficients on regions which are not necessarily smooth, we study the energy decay rate when a nonlinear damping is applied on a suitable subrigion.     

Preparation of microcapsules containing two-phase core materials

Urea-formaldehyde (UF) microcapsules containing two-phase core materials in which phthalocyanine blue BGS (beta-CuPc) particles were homodispersed in tetrachloroethylene (TCE) were prepared by in situ polymerization. The effects of the various process parameters, including the type of surface modifier, the viscosity of UF prepolymer, the type of water-soluble surfactant, and the concentration of oil-soluble surfactant in the capsule core on the dispersity of beta-CuPc particles in TCE and the properties of the capsule wall and the adsorption of beta-CuPc particles on the internal surface of capsule wall were experimentally investigated. It was shown that using octadecylamine (ODA) to modify beta-CuPc particles resulted in a significant increase of the dispersing extent (DE) and the electrophoresis velocity of the particles in TCE (about 4 and 20 times more than that of unmodified). In addition, the optimal reaction conditions of the synthesis UF prepolymer were obtained by the orthogonal test. On the other hand, as the oil/water interfacial tension of emulsion was big enough, the microcapsule formed. The concentration of Span-80 in TCE was no less than 0.062 mM; the adsorption of beta-CuPc particles on internal surface of wall were restrained. Finally, the microcapsules in which beta-CuPc particles possess reversible response to dc electric field were obtained.     

Effect of surface roughness on determination of bulk tissue optical parameters

Monte Carlo simulations have been conducted to investigate the effect of surface roughness on the inverse determination of bulk optical parameters. Results show that mus, mua, and g can be overestimated by an order of magnitude for thin slab tissue samples with a moderate index mismatch at the interfaces if typical surface roughness is neglected. Measurements of Intralipid samples between glass windows with smooth and rough surfaces have been carried out and agreement was found between the numerical and the experimental data. This study suggests that the surface roughness should be taken into account for both in vitro and in vivo determination of bulk tissue optical parameters.     

激光导致的透明固体损伤模型

详细分析了描述激光导致损伤的"移动的损伤"模型,发现该模型不适用于常见的飞秒激光对绝缘性透明固体材料处理的情况(如:800nm的100fs激光脉冲,0.65NA紧聚焦系统),此时脉冲与物质间相互作用区域和聚焦系统的瑞利长度可以比拟.对模型做了改进,改进后的模型可以很好地预期飞秒激光脉冲在固体中产生损伤的时间和空间形态.     

Chemical synthesis of CD52 glycopeptides containing the acid-labile fucosyl linkage

Glycopeptide 1 with the fucosylated trisaccharide, beta-d-GlcNAc(1-->4)[alpha-l-Fuc(1-->6)]-beta-d-GlcNAc, linked to the Asn of CD52 peptide was prepared by two methods, both of which used the free glycosyl Asn 12 and glycotripeptide 21 as key intermediates. Thus, after the trisaccharide was prepared and linked to Asn, the carbohydrate moiety was deprotected to give 12. From 12, 21 was constructed in homogeneous NMP solutions by elongating the peptide chain alone the N-terminus. Though the glycopeptides were easily soluble in NMP, they were barely soluble in diethyl ether, because of the free trisaccharide. Consequently, addition of diethyl ether to the reaction mixtures could precipitate the glycopeptides, and the products were conveniently isolated and purified in the solid form. The coupling of 21 with a free nonapeptide 24 in NMP afforded 1. 1 was also prepared by solid-phase synthesis, using the acid-sensitive 2-chlorotrityl resin. In this case, 21 was attached to the nonapeptide on the resin, and the resulting glycopeptide was then released with dilute acetic acid. Deprotection of the peptide under moderate acidic conditions gave 1. The acid-labile alpha-fucose was not affected in these syntheses.