Synthesis of Cholesterol-Conjugated Magnetic Nanoparticles for Purification of Human Paraoxonase 1

Human serum paraoxonase 1 (PON1) is known as an antioxidant and is also involved in the detoxification of many compounds. In this study, a novel purification strategy was employed to purify the PON1 by using cholesterol-conjugated magnetic nanoparticles. Magnetic nanoparticles were synthesized and conjugated with cholesterol through diazotized p-aminohippuric acid. In Fourier transform infrared spectrum of cholesterol-p-aminohippuric acid-Fe₃O₄ nanoparticles, the appearance of peaks at 3,358.3, 1,645 cm⁻¹, and at 2,334.9 cm⁻¹ confirmed the conjugation. The molecular weight of purified PON1 was nearly 45 kDa on sodium dodecyl sulfate (SDS)–polyacrylamide gel electrophoresis (PAGE), and isoelectric point was 5.3. The specific activity was 438 U mg⁻¹ protein, and the purification fold was 515 with 73% yield. The K _m values were 1.3 and 0.74 mM with paraoxon and phenyl acetate, respectively. Western blot of 2D-PAGE confirmed the homogeneity and stability of the enzyme. Mg⁺², Mn⁺², glycerol, (NH₄)₂SO₄, PEG 6000, Triton X-100, and phenylmethylsulfonyl fluoride did not show any effect on activity. Pb⁺², Co⁺², Zn²⁺, ethanol, β-mercaptoethanol, and acetone reduced the activity while Ni²⁺, Cd²⁺, Cu²⁺, iodoacetic acid, SDS, dimethylformamide, DMSO inhibited the activity. In vitro enzyme activity was slightly reduced by acetyl salicylic and acetaminophen and reduced 50% with amino glycosides and ampicillin antibiotics at concentrations of 0.6 and 30 mg ml⁻¹, respectively. This is the first report for the synthesis of cholesterol-conjugated magnetic nanoparticles for simple purification of PON1 enzyme.     

The rôle of countercurrent chromatography in the fractionation of complex mixtures

The biologically active pricipals in nature are frequently present as only a few parts per million of complex mixtures of non-volatile components and often have limited stability. Their isolation often requires the application of all available techniques, such as adsorption chromatography, ion exchange procedures, size exclusion techniques, and solvent partition methods consistent with their physical properties and stability. The process of countercurret chromatography is essentially liquid-liquid chromatography in which the stationary liquid bed is retained in the column by a force field rather than by a solid supporting matrix. Adsorption effects are thereby eliminated. The technique is particularly advantageous in the preparative separation of milligram to gram quantities of polar and labile organic compounds and bio-particulate materials such as cells and cell fragments. Virtually any twophase solvent system, either aqueous or non-aqueous may be employed. Countercurrent chromatography (CCC) provides a convenlent alternative to adsorption chromatography for fractionation of natural products or other complex mixtures. In some cases, this high resolution method offers advantages with regard to the avoidance of contamination from solid adsorbents, versatility, and relatively inexpensive operation. The article covers some of the applications, selection of solvents, and advantages of CCC.     

Synthesis and characterization of 2,7-dihydro-1H-dinaphtho[c,e]tellurepin: a new heterocyclic telluride

Synthesis of the racemic cyclic telluride, i.e., 2,7-dihydro-1H-dinaphtho-[c,e]tellurepin (1), possessing a C₂ axis was based on the reaction of 2,2^′-bis(bromomethyl)-1,1^′-binaphthalene with potassium tellurocyanate in dry DMSO. Reaction of halogens with 1 gave the diiodo (2), dibromo (3) and dichloro (4) derivatives. Treatment of 1 with iodomethane and iodoethane gave the methyl- and ethyl tellurepinium iodides, 5 and 6, respectively.Compound 1 reduced the carbonyl groups in DDQ and TCQ to hydroxyl groups. Mononuclear palladium(II) complex, [(C₂₂H₁₆Te)₂PdCl₂], was prepared by reaction of 1 with [PdCl₂(NCPh)₂].All new compounds were characterized by elemental analysis and spectroscopic techniques.     

60Co-v Radiolysis of a Mixture of Benzene and Cyclohexane in Presence of Diphenyl Mercury

In the radiolysis of cyclohexane in presence of 4×10^?3M diphenylmercury (Hg φ₃) three isomers of hexane, methylcyclopentane (G=0.018), benzene (G=0.42) and cyclohexene (G=0.047) were detected. Addition of benzene in the mixture of cyclohexane and Hg φ₃ formed two isomers of pentane, hexene and one isomer of hexane as additional products, while cyclohexene was eliminated completely. Normally, eight products were detected in presence of 10 to 50% benzene. Total radiolytic yield of products increased in presence of 15 to 25% benzene but in presence of 35 to 50% benzene G values became very low. Considerable amount of hexene is formed in a mixture of benzene and cyclohexane but neither benzene nor cyclohexane in presence of Hg φ₂ formed this compound. In the presence o. benzene and φ₂Hg hexane yield is very much reduced. Protection is observed in presence of 10% as well as 35 to 50% benzene in this system. The plot of benzene concentration in moles/litre versus methylcyclopentane is linear and from the slope of the straight line, the values of rate constants were found to be 2.65×10^?2 litre/mole sec., 5.25×10^?3 litre mole sec., 9×10^?7 litre/mole sec. for methylcyclopentane, cyclohexane and benzene respectively. A plot of G(–c-C₆H₁₂) versus 1/[C₆H₆] also gave a straight line which confirms the sponge type protection in this multicomponent system.     

加权ebyev-Ostrowski型不等式

关于著名的ebyev不等式,已有众多的研究成果.通过建立积分不等式,来建立全新的加权ebyev型积分不等式.给予了独立的证明,并给出了此类不等式的新评价.     

Polymer dispersed liquid crystal device with integrated luminescent solar concentrator

Polymer dispersed Liquid crystal (PDLC) windows are regarded as a good choice for curtain-free windows. However, conventional PDLC needs external electricity to operate, which causes extra energy consumption. These devices cannot be combined with traditional solar cells for energy savings. In this study, a new design of luminescent solar concentrator (LSC)-based PDLC device is presented. In particular, we successfully demonstrate that the PDLC can be integrated with LSC as its back scatter and potentially contributes towards the enhancement of power output by minimising backside light losses. Multi-luminophore LSC is employed to increase the absorption of air mass 1.5 solar irradiance. The edge emission measurements show multiple-luminophore-based PDLC-LSC gives the maximum edge emission power which is 1.7 times more than that of single luminophore-based PDLC-LSC device. Photocurrent measurements are also performed as an additional evidence for the improved performance of PDLC-LSC device. Finally, the visual properties of PDLC-LSC devices are evaluated to realise the compatibility of using such devices in the built environment.