原花青素提取及微胶囊化研究

作为葡萄加工的副产物,葡萄籽中富含葡萄籽油和低聚原花青素。作者利用超临界二氧化碳萃取葡萄籽后所得的残渣为原料,以含有0.8%醋酸的乙醇溶液为提取剂来提取其中的原花青素,在55℃条件下进行两次重复提取,葡萄籽残渣与提取液的比例控制在1∶8(W/V),每次提取60 min,原料中原花青素的提取率可以达到98.2%;为提高产品的贮藏稳定性,还对以阿拉伯胶与麦芽糊精组合作为原花青素微胶囊壁材来进行微胶囊化的工艺进行研究,结果表明在阿拉伯胶占壁材40%、芯壁材比为3∶7,混合液中固形物含量为20%的条件下,经喷雾干燥后所得原花青素的产率为88.84%,微胶囊化效率达到99.2%。检测结果表明,原花青素紫外吸收光谱在微胶囊化前后没有变化,而其贮藏稳定性得到提高。     

刺葡萄籽油功效成分及其动物学药理作用研究

目的:研究刺葡萄籽油中的功效成分及其动物学药理作用.方法:使用GC/MS对甲酯化和未经甲酯化处理的刺葡萄籽油进行分析,研究籽油中的功效成分,并以小白鼠为研究对象进行刺葡萄籽油的喂食.结果:超临界CO2萃取的刺葡萄籽油的GC/MS分析结果表明,刺葡萄籽油成分以脂肪酸为主,其中不饱和脂肪酸含量占87%,不饱和脂肪酸主要为亚油酸,其含量达82.32%,高于已有报道的葡萄籽油中亚油酸含量;未经甲酯化处理的籽油经GC/MS分析发现,刺葡萄籽油中含有一种具有较强生物活性的成分-角鲨烯,而赤霞珠葡萄的GC/MS分析中没有发现,也未见葡萄属植物中舍有角鲨烯成分的研究报道.通过动物学药理作用实验发现,刺葡萄籽油不仅能显著降低血清总胆固醇(TC)、甘油三脂(TG)含量,还能够在降低低密度脂蛋白胆固醇(LDL-C)的同时,提高高密度脂蛋白胆固醇(HDL-C)的含量.结论:刺葡萄籽油中含有多种对人体有益的功效成分,值得人们进一步地研究.     

干姜超临界CO2萃取与水蒸气蒸馏工艺比较研究

目的：比较干姜的超临界CO2萃取与水蒸气蒸馏两种工艺的差别,为其在复方制剂中的应用提供工艺设计参考。方法：分别用超临界CO2萃取和水蒸气蒸馏处理干姜药材,采用GC、TLC对产物进行分析比较。结果：超临界CO2萃取产物得率为8．0％,水蒸气蒸馏得率为0．2％,GC、TLC显示超临界CO2萃取物比水蒸气蒸馏样品有较多的成分。结论：干姜的超临界CO2萃取工艺较水蒸汽蒸馏工艺的产物量高,成分较多。     

均匀设计法优选芝麻油提取新工艺

本文通过超临界CO2提取芝麻油的均匀设计实验和微波和超声波诱导提取芝麻油的正交实验比较,考察影响提取的主要因素,寻求最佳萃取工艺。超临界CO2萃取最佳工艺条件为：压力32MPa,温度60℃,CO2流量31kg／h,萃取时问80min,得率46．39％;微波萃取最佳工艺条件为：溶剂为丙酮,物料与溶剂比例1：7,辐射时间7min,辐射功率810W,得率23．01％。超声波萃取最佳工艺条件为：物料与溶剂比例1：7,溶剂为石油醚,浸泡时间30h,得率23．99％。结果表明超临界CO2萃取芝麻油品质最好,而且萃取也最高,质量最稳定。     

山葡萄籽中原花青素的提取

研究了提取溶剂、温度、时间、料液比4个因素对山葡萄籽中原花青素得率的影响。确定最佳提取工艺：以70％丙酮为提取荆,在60℃条件下,提取120min,料液比为1：7,原花青素的得率为2．31％     

超临界CO2萃取百合花挥发油的工艺研究

本文介绍了超临界CO2萃取百合花中挥发油的提取分离工艺,重点研究了超临界CO2萃取压力、温度、时间对出油率的影响。正交试验结果表明：影响超临界CO2萃取的主要因素为C3〉A2〉B2（A为萃取压力,B为萃取温度,C为萃取时间）;最佳工艺参数：SC-CO2萃取压力为18MPa,温度为50℃,时间为90min,流量为25L／min,所得百合花挥发油的出油率高达2．92％。     

原花青素对亚硝化反应的抑制作用研究

研究了葡萄籽原花青素的最佳提取条件,及其对亚硝化反应的抑制作用。结果表明：原花青素的最佳提取条件为60％乙醇,料液比1：5,50℃水浴回流1h,其对亚硝胺合成的最大阻断率为91．2％,对亚硝酸钠的最大清除率为88．3％。     

微孔草籽油的超临界CO2流体萃取及HPLC—MS分析

利用超临界CO2萃取微孔草籽油,并对籽油进行了HPLC／MS分析。实验确定的最佳超临界CO2流体萃取条件是：萃取温度45℃,萃取压力20MPa,CO2流量为35-40kg／h,萃取时间120min,在此条件下白刺籽油的萃取率为16．12％。利用HPLC／MS对微孔草籽油分析,发现其不饱和脂肪酸的相对含量高达73．19％。比较了超临界CO2萃取微孔草籽油油样和石油醚萃取微孔草籽油油样的理化性质,发现超临界CO2流体萃取的籽油质量优于传统溶剂萃取的籽油。     

葡萄籽中原花青素的提取及应用现状

原花青素（proanthocyanidins,PC)是目前国际上公认的清除人体内自由基最有效的天然抗氧化剂,广泛分布于多种天然植物中。阐述了葡萄废弃物中原花青素的功能,分析了其应用开发现状。结合常用的提取方法,并综合国内外关于原花青素的研究进展,对葡萄籽中原花青素提取的工艺参数进行优化,从而得出葡萄籽中原花青素最优提取方案。以期为葡萄籽的全面利用和原花青素的工业化生产提供科学依据,使原花青素拥有更广泛的应用。     

生姜的超临界CO2提取分离工艺的研究

本文研究了超临界CO2流体萃取生姜的工艺,探讨了萃取压力、温度扣时问等因素对生姜萃取率的影响,通过正交实验确定了生姜超临界CO2流体萃取最佳工艺：生姜原料切成薄片,含水率15％以下,萃取条件为压力24Mpa、温度40℃、时间2h。     

Physicochemical and biological properties of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose (6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin)

A unique multibranched cyclomaltooligosaccharide (cyclodextrin, CD) of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose [6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin, (G(2))(3)-betaCD] was prepared. The physicochemical and biological properties of (G(2))(3)-betaCD were determined together with those of monobranched CDs (6-O-alpha-D-glucopyranosyl-alpha-cyclodextrin (G(1)-alphaCD), 6-O-alpha-D-glucopyranosyl-beta-cyclodextrin (G(1)-betaCD), and 6-O-alpha-maltosyl-beta-cyclodextrin (G(2)-betaCD)). NMR spectra of (G(2))(3)-betaCD were measured using various 2D NMR techniques. The solubility of (G(2))(3)-betaCD in water and MeOH-water solutions was extremely high in comparison with nonbranched betaCD and was about the same as that of the other monobranched betaCDs. The formation of an inclusion complex of (G(2))(3)-betaCD with stereoisomers (estradiol, retinoic acid, quinine, citral, and glycyrrhetinic acid) depends on the cis-trans isomers of guest compounds. The cis isomers of estradiol, retinoic acid, and glycyrrhetinic acid were included more than their trans isomers, while the trans isomers of citral and quinine fit more tightly than their cis isomers. (G(2))(3)-betaCD was the most effective host compound in the cis-trans resolution of glycyrrhetinic acid. Among the branched betaCDs, (G(2))(3)-betaCD exhibited the weakest hemolytic activity in human erythrocytes and showed negligible cytotoxicity in Caco-2 cells up to 200 microM. These results indicate unique characteristics of (G(2))(3)-betaCD in some biological responses of cultured cells.     

Spectral and thermodynamic properties of Ag(I), Au(III), Cd(II), Co(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(IV), and Zn(II) binding by methanobactin from Methylosinus trichosporium OB3b

Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV–visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ.     

Circular dichroism spectra of DNA quadruplexes [d(G(5)T(5))](4) as formed with G(4) and T(4) tetrads and [d(G(5)T(5)). d(A(5)C(5))]2 as formed with Watson-Crick-like (G-C)(2) and (T-A)(2) tetrads

We utilize electrophoresis and find that a thermally treated equimolar mixture of the oligonucleotide d(G(5)T(5)) and its complementary oligonucleotide d(A(5)C(5)) exhibits either two bands or a single band in one lane, depending on the conditions of the incubation solutions. The thermally treated d(G(5)T(5)) solution loaded in a different lane exhibits a single band of the parallel quadruplex [d(G(5)T(5))](4), which is composed of homocyclic hydrogen-bonded G(4) and T(4) tetrads previously proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(A(5)C(5)), the fast band is assigned to a Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex, so that the slow band with the same low mobility as that of [d(G(5)T(5))](4) may be assigned to either [d(G(5)T(5))](4) itself or a [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex. If the latter compound is true, this may be the antiparallel quadruplex composed of the heterocyclic hydrogen-bonded G-C-G-C and T-A-T-A tetrads proposed previously. After removing these three bands for the duplex and two kinds of hypothetical quadruplexes, we electrophoretically elute the corresponding compounds in the same electrophoresis buffer using an electroeluter. The eluted compounds are ascertained to be stable by electrophoresis. The circular dichroism (CD) and UV absorption spectra measured for the three isolated compounds are found to be clearly different. For the electrophoretic elution of the hypothetical [d(G(5)T(5))](4) quadruplex, the result of the molecularity of n = 4 obtained from the CD melting curve analysis provides further support for the formation of the parallel [d(G(5)T(5))](4) quadruplex already proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(C(5)A(5)), the fast band with a molecularity of n = 2 corresponds to the Watson-Crick duplex, d(G(5)T(5)). d(A(5)C(5)). The slow band with a molecularity of n = 4 indicates the antiparallel quadruplex [d(G(5)T(5)). d(A(5)C(5))](2), whose observed CD and UV spectra are different from those of [d(G(5)T(5))](4). By electrophoresis, after reannealing the eluted compound [d(G(5)T(5)). d(A(5)C(5))](2), a distinct photograph showing the band splitting of this quadruplex band into the lower duplex and upper quadruplex bands is not possible; but by a transilluminator, we occasionally observe this band splitting with the naked eye. The linear response polarizability tensor calculations for the thus determined structures of the [d(G(5)T(5))](4) quadruplex, the McGavin-like [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex, and the Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex are found to qualitatively predict the observed CD and UV spectra.     

Synthesis and luminescence properties of a blue-emitting Sr(3.5) Y(6.5) O(2) (PO(4) )(1.5) (SiO(4) )(4.5) :Eu(2+) phosphor

A novel blue‐emitting Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:Eu²⁺ phosphor was synthesized via a solid‐state reaction. Powder X‐ray diffraction (XRD) analysis demonstrated that the Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5 host had a hexagonal crystal structure in the space group P6₃/m and unit cell parameters a = 9.418 Å, c = 6.900 Å. The as‐prepared phosphor showed a blue emission and all the main emission peaks were located at around 466 nm for different excitation wavelengths of 297, 333 and 391 nm. The temperature dependence of the photoluminescence property was investigated in the range 20–250 °C, and the emission intensity decreased to 71% of the initial value at room temperature on increasing the temperature to 150 °C. According to the classical theory of fluorescent thermal quenching, the activation energy (ΔE) for the thermal quenching luminescence of the as‐prepared Sr_3.45Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:0.05Eu²⁺ phosphor was determined to be 0.20 eV. Copyright © 2011 John Wiley & Sons, Ltd.     

The frequencies of Gm(1), Gm(2), Gm(4), Gm(12), and Inv(1) in Hessen (Germany)

Summary The serum groups Gm(1) [Gm(a)], Gm(2) [Gm(x)], Gm(4) [Gm(f)]. Gm(12) [Gm(b)] and Inv(1) [Inv(1)] of 2000 sera of healthy blood donors from the land Hesse were examined. The results obtained were compared with those known until now. Three persons, not related to each other, possessed the extremely rare phenotype Gm(-1, 2, 4, 12) [Gm (a-x+b+f+)]. In 0.75% of the cases we found a discordant behaviour of the factors Gm(4) and Gm(12) [Gm(f) and Gm(b)].

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Zusammenfassung 2000 Seren von gesunden Blutspendern aus Hessen wurden bezüglich der Gamma-Globulin-Serumgruppen Gm(1) [Gm(a)], Gm(2) [Gm(x)], Gm(4) [Gm(f)]. Gm(12) [Gm(b)] und Inv(1) [Inv(1)] untersucht. Die gefundenen Resultate wurden mit den bisher bekannten verglichen. Drei miteinander nicht verwandte Personen wiesen den äußerst seltenen Phänotyp Gm(-1, 2, 4, 12) [Gm(a-x+b+f+)] auf. In 0.75% der Fälle fanden wir ein diskordantes Verhalten der Faktoren Gm(4) und Gm(12) [Gm(f) und Gm(b)].

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Director: Prof. Dr. W. Wachsmuth

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Director: Prof. Dr. W. Spielmann

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The nomenclature suggested by WHO at a round-table conference over genes, genotypes and allotypes of immunglobulins is used. The conference took place in Geneva on the 1965 31. 5. to the 5. 6. [5].

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With technical assistance of S. Mohs.