藏药镰形棘豆总黄酮苷元抑菌活性的研究(英文)

镰形棘豆是中国应用的传统藏药,由于该植物的很多生物活性与其黄酮类有关,本研究提取了镰形棘豆中的总黄酮苷元,选择了9种病原菌对其抑菌活性进行了体外抑菌试验的评估。试验结果表明,镰形棘豆分离得到的总黄酮苷元对试验所用的病原菌均有较强的抑菌作用,其中对金黄色葡萄球菌的最低抑菌浓度为MIC=0.38 mg/mL,其他各菌的MIC和MBC范围在0.75~3 mg/mL之间。通过此研究可为镰形棘豆黄酮类活性组分的进一步研究提供依据。     

藏药镰形棘豆对缺氧/复氧H_9C_2心肌细胞损伤的保护作用

探讨藏药镰形棘豆(OFB)提取物对缺氧/复氧(H/R)H_9C_2心肌细胞损伤的保护作用。方法:采用三气培养箱培养法建立H_9C_2心肌细胞缺氧/复氧损伤模型。实验分为3组:正常细胞对照组;缺氧/复氧损伤组(H/R);7个药物加缺氧/复氧损伤组(H/R+OFB);于缺氧/复氧开始时分别加入终浓度为0.1 mg/L、1 mg/L、10 mg/L、100 mg/L、300 mg/L、600 mg/L、1 000 mg/L的镰形棘豆提取物,以细胞活力为指标,利用MTS法测定药物对细胞活力的影响。检测镰形棘豆乙酸乙酯水甲醇压柱组分与氯仿萃取组分不同给药剂量对H_9C_2心肌细胞缺氧/复氧损伤的影响。结果:与模型组相比药物处理组显著升高缺氧/复氧H_9C_2心肌细胞活力(p0.05)。结论:藏药镰形棘豆对H_9C_2心肌细胞的缺氧/复氧损伤有保护作用。     

镰形棘豆的一个新变型——白花镰形棘豆

描述了豆科棘豆属镰形棘豆(Oxytropis falcata Bunge)的一个新变型:白花镰形棘豆(Oxytropis falcataBunge form.atbiflora Y.H.Wu).原变型的花冠为蓝紫色或紫红色,而新变型花冠为白色.     

固相微萃取-气质法测定土壤挥发性抑菌物质*

运用固相微萃取 气相色谱 质谱法 (SPME GC MS) ,测定了参与土壤抑真菌作用的土壤挥发性成分和土壤细菌挥发性代谢物。通过比较土壤来源和土壤细菌来源的挥发性抑菌成分 ,发现在强挥发性抑菌土壤和土壤细菌代谢物中普遍存在着三甲胺、二甲基二硫醚、3 甲基 2 戊酮、甲基吡嗪、 2 ,5 二甲基吡嗪、N ,N 二甲基辛胺、十九烷等化合物。这些化合物很有可能就是参与土壤抑菌作用 ,特别是挥发性物质抑菌作用的主要成分。另外 ,为深入了解土壤中参与抑菌作用的挥发性化合物提供了简便有效的方法。     

不同温度竹荪品种挥发性成分及风味特性分析

[目的]分析研究不同温度竹荪品种挥发性成分及风味特性。[方法]选生长温度、子实体形态有明显差异的两个代表性竹荪品种:红托竹荪、棘托竹荪,采用顶空固相微萃取(HS-SPME)和气相色谱-质谱联用(GC-MS)技术,分析其挥发性成分。[结果]两种竹荪挥发性成分涵盖醛、醇、酯、酮、烃、杂环等类,两个品种所含化合物种类、含量有差异。中温品种挥发性成分72种,含量95. 279%,气味表现成分36种,含量27. 713%,占其挥发性成分的29. 086%。中高温品种挥发性成分55种,含量94. 392%,气味表现成分29种,含量15. 916%,占其挥发性成分的16. 862%。[结论]不同温度竹荪品种,其所含挥发性成分不同,气味表现物质不同,其风味特征不同。     

固相微萃取气质联用分析百里香花和叶挥发性成分

利用顶空固相微萃取技术(SPME)采集百里香Thymus mongolicus花和叶的挥发性成分,采用GC/MS技术分析鉴定,并用峰面积进行归一化定量。结果表明,从百里香花和叶总离子流图中分别鉴定出24、14种化合物,分别占总峰面积的99.573%和97.187%。百里香花和叶主要成分包括酚类和萜烯类,其中百里香酚在百里香花和叶中分别占35.38%和49.13%。     

贵州产辣蓼挥发性成分分析

采用固相微萃取法和水蒸气蒸馏法提取出贵州产辣蓼的挥发性成分,运用GC-MS联用技术对挥发性成分进行分析鉴定,并采用峰面积归一法确定各成分的相对含量。固相微萃取物中鉴定出48个化合物,主要有β-石竹烯(27.02%),正癸醇(14.39%),十二醛(12.96%)等,水蒸气蒸馏物中鉴定出27个化合物,β-红没药烯(19.00%),补身树醇(15.25%),十二醛(14.41%)等。辣蓼中挥发性成分经两种不同提取方法成分存在明显差异。与文献数据比较,不同省区产的辣蓼挥发性成分差异很大。体外抗菌试验表明,辣蓼挥发性成分具有抑菌作用,这些研究结果为辣蓼的有效利用提供了依据。     

连翘花蕾与花的挥发性成分研究

本文采用顶空固相微萃取和气相色谱质谱联用(HS-SPME-GC-MS)技术比较分析了连翘花蕾和花的挥发性成分。从连翘花蕾和花中共鉴定了83个化合物,其中40个化合物是共有的。连翘花蕾的挥发性成分以烃类(41.04%)为主,而连翘花的挥发性成分以醇、醛和酮类化合物(26.46%)为主;酯类化合物在花蕾中的含量为8.11%,在花中下降到2.12%;而酸类化合物则从3.56%上升到5.18%。结果表明,随着花蕾的开放,酯类成分逐渐被水解为酸。     

温郁金超临界萃取物的化学成分研究

采用超临界流体萃取技术萃取温郁金中的挥发性成分,通过L9(34)正交设计对萃取条件进行优化,结果表明55℃,35 MPa,240 min为较优条件。GC-MS联用技术对挥发性成分进行定性及半定量分析,首次从温郁金中检测到香橙烯氧化物、喇叭烯氧化物、卡拉烯环氧化物等11种化合物。与水蒸汽蒸馏工艺相比,超临界萃取工艺的收率较之高出3倍,萃取时间缩短4倍,抗癌有效活性成分榄香烯、莪二酮、莪术醇和吉马酮的得率分别高出32%,23%,105%和15%。     

镰形棘豆正丁醇提取物对小鼠的致突变试验

目的:评价镰形棘豆的正丁醇提取物对小鼠的致突变性.方法:小鼠随机分成6组,设阴性对照组(Ⅰ组)、阳性对照组(Ⅱ组)和4个剂量组(Ⅲ组、Ⅳ组、Ⅴ组和Ⅵ组),4个剂量组经口给予镰形棘豆正丁醇提取物的剂量分别为800mg/kg、100mg/kg、2000mg/kg、4000mg/kg,于给药后第2d取材观察小鼠骨髓嗜多染红细胞(PCE)微核率,于第35d取材来观察精子畸形率的变化.结果:镰形棘豆正丁醇提取物对小鼠微核细胞的产生及致精子畸形存在剂量-效应关系.Ⅲ组、Ⅳ组与Ⅰ组比较差异不显著(P＞0.05);Ⅴ组、Ⅵ组与Ⅰ组比较均差异显著(P＜0.05).结论:低浓度的镰形棘豆正丁醇提取物对小鼠的骨髓嗜多染红细胞和精子没有致突变作用,而高浓度的对小鼠的骨髓嗜多染红细胞和精子具有致突变作用.     

石香薷挥发油提取的比较研究

利用GC-MS对石香薷挥发油进行了定性、定量分析。采取超临界CO2萃取、水蒸气蒸馏和有机溶剂石油醚萃取这三种方法提取石香薷挥发油。这三种方法提取石香薷挥发油的主要成分基本相似,主要为含氧化合物(香薷酮、百里香酚和香荆芥酚)等,采取超临界CO2萃取和水蒸气蒸馏的石香薷挥发油品质较优。超临界CO2萃取法为提取石香薷挥发油的理想方法。     

Comprehensive two‐dimensional gas chromatography–mass spectrometry analysis of volatile constituents in Thai vetiver root oils obtained by using different extraction methods

Introduction – Vetiver root oil is known as one of the finest fixatives used in perfumery. This highly complex oil contains more than 200 components, which are mainly sesquiterpene hydrocarbons and their oxygenated derivatives. Since conventional GC‐MS has limitation in terms of separation efficiency, the comprehensive two‐dimensional GC‐MS (GC × GC‐MS) was proposed in this study as an alternative technique for the analysis of vetiver oil constituents. Objective – To evaluate efficiency of the hyphenated GC × GC‐MS technique in terms of separation power and sensitivity prior to identification and quantitation of the volatile constituents in a variety of vetiver root oil samples. Methodology – Dried roots of Vetiveria zizanioides were subjected to extraction using various conditions of four different methods; simultaneous steam distillation, supercritical fluid, microwave‐assisted, and Soxhlet extraction. Volatile components in all vetiver root oil samples were separated and identified by GC‐MS and GC × GC‐MS. The relative contents of volatile constituents in each vetiver oil sample were calculated using the peak volume normalization method. Results – Different techniques of extraction had diverse effects on yield, physical and chemical properties of the vetiver root oils obtained. Overall, 64 volatile constituents were identified by GC‐MS. Among the 245 well‐resolved individual components obtained by GC × GC‐MS, the additional identification of 43 more volatiles was achieved. Conclusion – In comparison with GC‐MS, GC × GC‐MS showed greater ability to differentiate the quality of essential oils obtained from diverse extraction conditions in terms of their volatile compositions and contents. Copyright © 2009 John Wiley & Sons, Ltd.     

鱼腥草挥发油的化学成分

The volatile oils from Houttuynia cordata Thunb. were obtained with supereritical CO2, steam distillation and petroleum ether extraction and analyzed qualitatively and quantitatively by GC-MS. The results showed that the chemical constituents of the volatile oils by three different methods are very different. The extraction rates of volatile oil by above-mentioned three extraction methods are 1.764%, 0.040% and 0.082%, respectively. The volatile oil extracted by supercritical CO2 extraction, which the content of houttuyninum reached 14.393 %, is better than those with traditional methods.     

Profiles of the Essential Oils and Headspace Analysis of Volatiles from Mandragora autumnalis Growing Wild in Tunisia

Mandragora autumnalis Bertol . (Solanaceae family), synonym of M. officinalis Mill ., occurs in North Africa and grows natively in Northern and Central Tunisia, in humid to sub‐arid climates. The ripe fruits of mandrake are odiferous with a particular, indescribable, specific odor, shared, to a lesser extent, by the leaves and roots. We carried out an investigation of the essential oils (EOs) and of the aromatic volatiles emitted by fresh leaves, roots and ripe fruits of M. autumnalis growing wild in Central Tunisia. The EOs were obtained from freshly collected plant material by hydrodistillation, while the volatile emissions from the powdered M. autumnalis tissues were sampled by headspace solid phase microextraction (HS‐SPME); both types of samples were analyzed by gas chromatography‐mass spectrometry (GC/MS). Fifty‐one compounds representing 96.2–98.6 % of the total oil compositions were identified in the three tissues and belonged to different chemical classes specifically in 16 esters, 12 alcohols, 12 hydrocarbons, 6 ketones, 3 aldehydes and 3 acids. The main constituents were pentadecanoic acid (34.2 %) and hexadecanol (26.3 %). A total of 78 volatile compounds emanating from M. autumnalis tissues, representing 94.1–96.4 % of the total volatile compositions, were identified: 22 esters, 11 alcohols, 9 aldehydes, 14 ketones, 7 nitrogen, 10 hydrocarbons, 2 lactones, 1 sulfur and 2 ethers. Ethyl hexanoate (12.3 %) and 1,3‐butanediol (12.3 %) were at the highest relative percentages. This study characterizes and distinguishes M. autumnalis from Tunisia and attributes the compounds responsible for the intoxicating and particular odor of fruits. Chemosystematic of Mandragora autumnalis based on the identification of essential oils and headspace volatiles of each of its organ can be used to characterize this species according to its geographic distribution.     

A method for the solvent extraction of low-boiling-point plant volatiles

A new method has been developed for the extraction of volatiles from plant materials and tested on seedling tissue and mature leaves of Arabidopsis thaliana, pine needles and commercial mixtures of plant volatiles. Volatiles were extracted with n-pentane and then subjected to quick distillation at a moderate temperature. Under these conditions, compounds such as pigments, waxes and non-volatile compounds remained undistilled, while short-chain volatile compounds were distilled into a receiving flask using a high-efficiency condenser. Removal of the n-pentane and concentration of the volatiles in the receiving flask was carried out using a Vigreux column condenser prior to GC-MS. The method is ideal for the rapid extraction of low-boiling-point volatiles from small amounts of plant material, such as is required when conducting metabolic profiling or defining biological properties of volatile components from large numbers of mutant lines.     

迷迭香植物精油对白纹伊蚊的驱避作用及其化学成分

应用水蒸气蒸溜法和超临界二氧化碳萃取法提取生长于云南的迷迭香茎叶植物精油,测试2种精油对白纹伊蚊Aedes albopictus Skuse的驱避作用,并利用GC/MS联用仪分析2种精油的化学成分。结果表明:超临界二氧化碳提取的迷迭香精油对白纹伊蚊的驱避时间是(5.82±1.13)h,达到国标驱避剂评价的B级标准。2种精油化学成分中都含有驱纹活性物质:柠檬烯、樟脑、Eucalyptol、(+)-4-Carene、1-methyl-4-(1-methyle thylidene)-cyclohexene、Beta-pinene等,且驱蚊活性成分在挥发油中占有较高比例,显示该植物精油在驱蚊方面有一定开发价值。     

侧柏树干的超临界CO_2萃取物组分分析及双条杉天牛的EAG反应

利用超临界CO2萃取法和索氏提取法分别提取侧柏Platycladus orientalis(L.)的韧皮部和木质部挥发物,经GC/MS分析其成分,结果表明:超临界CO2萃取物中检测到的21种组分中以倍半萜烯及其氧化物为主,没有检测到单萜类物质;索氏提取法检测到23种组分,韧皮部中检测到的组分以高沸点的树脂酸和二萜等为主,单萜烯和倍半萜及其氧化物含量较低;木质部中以倍半萜烯及其氧化物为主。将不同提取样品进行双条杉天牛Semanotus bifasciatus(Motschulsky)的触角电位反应,结果表明:2种方法的萃取物均能引起天牛的EAG反应,但以超临界萃取物引起的EAG反应较强,且与索氏提取物的反应值差异显著。罗汉柏烯和雪松醇可能是侧柏植物中引诱双条杉天牛的重要活性组分。     

芹菜子的超临界CO2流体萃取物的化学成分研究

本文采用ＧＣ和ＧＣ－ＭＳ技术,就芹菜子的超临界ＣＯ２流体萃取法（ＳＦＥ－ＣＯ２）精油和水汽蒸馏法（ＳＤ）精油的化学组成作了对比研究。结果表明,ＳＤ法精油的主要成分为单萜烯烃类物质,而ＳＦＥ－ＣＯ２法精油为苯并呋喃酮类化合物。共有３２种化合物被鉴定,其中两种为首次在芹子油中被发现。     

超临界CO_2和微波辅助萃取艾叶挥发油工艺的研究

通过超临界CO2萃取均匀设计实验和微波辅助萃取艾叶挥发油的正交实验比较,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:萃取压力16MP,萃取温度31℃,CO2流量20kg/h和时间80min,得率3.75%;微波萃取最佳工艺条件为:辐射功率720w,辐射时间200s,溶剂量400mL,洗涤剂量50mL,得率4.85%。水蒸馏法提取率为1.87%。结果表明超临界CO2和水蒸馏法萃取艾叶挥发油品质最好;微波萃取收率最高,但品质较差。     

超临界CO2萃取茉莉净油化学成分的研究

利用 GC和 GC- MS联用仪对超临界 CO2 萃取茉莉浸膏的净油进行化学成分分析 ,分离出 131个组分 ,鉴定出其中的 35个化合物 ,所鉴定的成分占分离成分的 85%以上。同时将分析结果与普通溶剂法制取的茉莉净油进行比较。