野生与栽培羌活药材挥发油含量及组分的比较分析

分析野生和栽培羌活药材挥发油含量及其组分的变化,为羌活药材的引种栽培及进一步的开发利用提供了依据。采用水蒸气蒸馏法提取羌活药材中的挥发油,通过GC-MS对挥发油成分进行分析鉴定;利用聚类分析对测定结果进行分类;通过相关分析研究海拔对羌活药材挥发油含量的影响。6份药材样品挥发油含量范围为1.60～7.98 mL/100g,6份羌活药材挥发油成分经GC-MS分析,共鉴定出57个化合物,共有成分12个;基于挥发油成分种类及相对含量的聚类分析显示了羌活药材挥发性成分种类及含量的种间差异;相关分析结果表明,海拔高度与挥发油含量存在显著正相关。野生和栽培羌活药材挥发油含量存在差异,总体上野生羌活药材的挥发油含量高于栽培种;羌活药材挥发油含量随海拔升高而增加。     

阔叶箬竹叶和箬竹叶中挥发油的提取及成分分析

采用水蒸气蒸馏法分别提取阔叶箬竹叶和箬竹叶中的挥发油,用乙醚作溶剂进行多次萃取,利用气相色谱-质谱(GC-MS)联用分析二者的化学成分并进行比较。从阔叶箬竹叶提取的挥发油中共鉴定出37种化合物,主要成分为叶醇、1-己醇、苯甲醇、己醛、2-乙基呋喃、β-紫罗兰酮等。从箬竹叶提取的挥发油中共鉴定出49种化合物,主要成分为叶醇、苯甲醇、β-紫罗兰酮、2-己烯醛、苯乙醇、2-甲氧基-4-乙烯基苯酚、2-乙基呋喃等。两种箬叶挥发油中相对含量最高的成分都为叶醇,都含有酮、醛、醇、酚、酯类化合物,且酮、醛、醇的含量明显高于其他成分。     

超临界CO_2萃取连翘挥发油的正交试验和GC-MS分析

采用正交试验法对超临界CO2萃取连翘挥发油的条件进行了研究；结果显示最佳萃取条件为萃取压力30MPa，萃取温度35℃，解析压力6．7MPa，解析温度50℃，粉碎度0．55mm；按对结果的影响大小依次排列为萃取温度，粉碎度，萃取压力，解析压力，解析温度；用气相色谱－质谱联用技术测定了最佳萃取条件所得连翘挥发油的化学成分，从中鉴定出21种成分，并测定了其相对含量，主要成分为α－蒎烯、β－蒎烯、萜品醇－4、α－萜品醇、苯甲醇等。     

同时蒸馏萃取GC-MS分析刺异叶花椒叶挥发油化学成分

研究黔产刺异叶花椒叶挥发油的化学成分，采用同时蒸馏萃取提取并用气相色谱-质谱进行分离测定，共分离出67种成分，鉴定出37个化合物，主要成分为萜烯化合物及其衍生物，柠檬烯为19．31％，里哪醇为15．26％，桧烯为13．60％。     

姜科姜黄属植物有效成分的研究

研究不同产地姜科姜黄属植物挥发油的化学成分,了解不同产地姜科姜黄属植物挥发性成分的差别,为控制其药材质量提供理论依据。采用水蒸气蒸馏法提取不同产地姜科姜黄属植物的挥发油,用气相色谱—质谱联用仪对其进行分离测定,结合计算机检索对分离的化合物进行结构鉴定,应用色谱峰面积归一化法测定各成分的相对百分含量。结果发现,不同产地姜科姜黄属植物的水蒸气蒸馏提取物得率在0．20％～2．13％之间,分别鉴定出24～40个化学成分。不同品种、不同产地姜科姜黄属植物的挥发油含量和其所含成分有较大差别,文献报道的某些有效成分如莪术酮、莪术二酮、莪术醇和表莪术酮在某些供试品中未检测到。实验中10个供试品药材中挥发性成分主要为单萜类及倍半萜类化合物及其衍生物,倍半萜类化合物的百分含量(44．57％～88．65％)明显高于单萜类化合物的百分含量(1．63％～26．69％)。     

超临界CO2萃取柚子叶挥发油的研究及GC-MS分析

采用超临界CO2萃取技术提取柚子叶的挥发性成分,以挥发油得率为衡量工艺参数的指标,通过正交试验法考察超临界CO2萃取过程中萃取温度、萃取压力、CO2的流量及萃取时间4个因素对柚子叶挥发油得率的影响。结果表明20MPa、萃取温度45℃、CO2流量7kg·h-1、萃取时间120min为最佳工艺。通过GC-MS对挥发油进行分析,从柚子叶挥发油中分离出144个组分,鉴定了61种成分,占化合物检出总量的90.4%。     

气相色谱-质谱法分析山柰挥发油化学成分

采用水蒸气蒸馏法从山柰中提取挥发油。采用不同类型的毛细管桩进行分析,找出最佳分析条件,用归一化法测定其质量分数用并用相色谱－质谱法对化学成分进行鉴定。共鉴定了３４种成分,占挥发油总成分的９１％以上。     

苍术挥发油成分的分析

用色谱－质谱－计算机联用法分析了南苍术挥发油的化学成分和相对百分含量，分离出６２种组分，鉴定出２２种化合物，占其挥发油总量的８９２％。     

人参挥发油的提取和分析

应用ＧＣ－ＭＳ－ＤＳ联机分析人参挥发油是当前较好的方法，但人参挥发油的提取方法和ＧＣ－ＭＳ条件的选择明显影响人参挥发油这一复杂天然混合物的分离和鉴定。本工作严格控制提取条件，提高了挥发油收率，达０．９５％；选择最佳ＧＣ－ＭＳ条件，鉴定出７６种化合物，该法稳定重现性好。     

唇形科植物挥发油化学成分的GC/MS研究

在运用GC/MS技术的基础上采用HELP(直观推导式演进特征投影法)方法研究了九种唇形科植物的化学成分, 并以唇形科植物半枝莲为例详细介绍了HELP的解析过程. 应用总体积积分法测定各成分的相对百分含量. 鉴定出相对共有成分达70余种, 大多数为萜类化合物及其衍生物. 不同的唇形科植物的挥发油化学成分与特征成分有明显差异. 九种药材挥发性成分中均含有桉油精(Eucalyptol, 含量0.10%～1.01%)和芳樟醇(Linalool, 0.11%～3.05%). 利用GC/MS分析法结合化学计量学分辨方法鉴定挥发油化学成分, 比单独使用GC-MS法结果更准确、可靠.     

Chemical composition and possible in vitro antigermination activity of three Hypericum essential oils

The essential oils of Hypericum perforatum, H. perfoliatum and H. hircinum, growing in Southern Italy, were analyzed by GC and GC/MS. In the three oils, 111 compounds in all were identified: 53 for the oil of H. hircinum (93.7% of the total oil), 55 for H. perforatum (96.5% of the total oil) and 63 for H. perfoliatum (98.7% of the total oil). The major fraction of the essential oils of H. perforatum and H. hircinum was represented by sesquiterpene hydrocarbons, while the monoterpene alpha-pinene, and the phenol thymol were the most abundant compounds in the essential oil of H. perfoliatum. The oils were evaluated for their potential in vitro phytotoxic activity against germination and early radicle elongation of Raphanus sativus and Lepidium sativum. The germination of this latter was significantly inhibited by the essential oil of H. hircinum, at the highest doses tested, whereas radicle elongation of garden cress was significantly inhibited by the essential oils of H. perfoliatum and H. hircinum. The radicle elongation of radish was inhibited by the essential oil of H. hircinum to a major extent and by H. perforatum and perfoliatum in a minor measure.     

High performance liquid chromatography/electrospray mass spectrometry of Hypericum perforatum extracts

Hypericum perforatum L. (St. John's Wort) is a widely distributed herbaceous perennial plant which has been well known as a medicinal plant since antiquity. In recent years, H. perforatum has received increasing attention for the treatment of depression and other neuralgic disorders. The main constituents of H. perforatum extract include flavonoids, naphthodianthrones, phloroglucinols, essential oils and xanthones. The present work reports the analysis of naphthodianthrones and phloroglucinols in H. perforatum extracts by means of high performance liquid chromatography (HPLC) coupled simultaneously to a diode array detector (DAD) and electrospray mass spectrometry (ESI-MS). Hypericin, pseudohypericin, hyperforin and adhyperforin were separated and identified on the base of their on-line UV and mass spectra. Quantitative analysis of hypericin derivatives in different extracts of H. perforatum using DAD and MS detectors was performed. In addition, direct infusion ESI-MS of H. perforatum extracts was applied to obtain rapid mass fingerprints of constituents present in the sample.     

Volatile constituents of two Hypericum species from Tunisia

The chemical composition of the essential oils obtained by hydrodistillation from the aerial parts of the Tunisian Hypericum perforatum and H. ericoides ssp. roberti was elucidated by a combination of GC and GC-MS analyses. The main constituents of the oil of H. perforatum were alpha-pinene (11.8%), alpha-ylangene (10.4%), germacrene-D (9.5%), n-octane (6.5%) and alpha-selinene (5.9%). The oil of H. ericoides ssp. roberti exhibited a higher amount of aliphatic and branched hydrocarbons and the main constituents were n-octane (29.1%), alpha-pinene (10.9%), pulegone (7.7%) and acetophenone (7%). Both qualitative and quantitative differences were observed between the studied oils. This chemical variability seems likely to result from the genetic variability, since samples of both species were collected at the same location and processed under the same conditions.     

改进的微波辅助无溶剂法提取薄荷和陈皮中的挥发油组分

An improved solvent free microwave extraction, in which a kind of microwave absorption medium （carbonyl iron powder） was used, was applied to the extraction of essential oil from dried menthol mint and orange peel without addition of any solvent and pretreatment. It took much less time of extraction （30 min） than microwave-assisted hydrodistillation （90 min） and conventional hydrodistillation （180 min）. The kinds of chemical compositions in essential oil extracted by different methods were almost the same and such improved solvent free microwave extraction can be a feasible way in extraction of essential oil from dried plant materials.     

Rapid analysis of the essential oils from dried Illicium verum Hook. f. and Zingiber officinale Rosc. by improved solvent-free microwave extraction with three types of microwave-absorption medium

A new method of extracting essential oils from dried plant materials has been studied. By adding a microwave-absorption medium (MAM) to a reactor, solvent-free microwave extraction (SFME) was improved and can be used to extract essential oils from dried plant material without pretreatment. With a microwave irradiation power of 85 W it took only approximately 30 min to extract the essential oils completely. The whole extraction process is simple, rapid, and economical. Three types of MAM, iron carbonyl powder (ICP), graphite powder (GP), and activated carbon powder (ACP), and two types of dried plant material, Illicium verum Hook. f. and Zingiber officinale Rosc., were studied. The results were compared with those obtained by use of conventional SFME, microwave-assisted hydrodistillation (MAHD), and conventional hydrodistillation (HD), and the conclusion drawn was that improved SFME was a feasible means of extracting essential oils from dried plant materials, because there were few differences between the composition of the essential oils extracted by improved SFME and by the other methods.     

Liquid-phase microextraction utilising plant oils as intermediate extraction medium--towards elimination of synthetic organic solvents in sample preparation

Hollow fibre based liquid-phase microextraction (LPME) using fatty oils and essential oils as the organic phase was evaluated to develop sample preparation technology eliminating the use of hazardous organic solvents. Basic drugs were extracted from different aqueous samples (0.2 to 1 mL) through approximately 15 microL of either almond oil, arachis oil, olive oil, soy-bean oil, anise oil, fennel oil, lavender oil, or peppermint oil (organic phase) immobilised within the pores of a polypropylene hollow fibre and into 20 microL of 10 mM HCOOH (acceptor phase) present inside the lumen of the hollow fibre. The extraction performance of the essential oils was comparable with the solvents normally used in LPME (dihexyl ether, n-octanol, and dodecyl acetate) in terms of extraction recovery and extraction speed. Whereas all essential oils tested were compatible with human urine, only anise oil was successful for plasma. The fatty oils provided lower recoveries than the essential oils due to higher viscosity, but all the fatty oils were compatible both with urine and plasma samples. In spite of the multi-component nature of the oils tested, they were not found to seriously contaminate the acceptor phases during extraction. In conclusion, fatty oils and essential oils may serve as alternative organic phase in LPME, eliminating the use of hazardous organic solvents.     

Improved solvent-free microwave extraction of essential oil from dried Cuminum cyminum L. and Zanthoxylum bungeanum Maxim

Solvent-free microwave extraction (SFME) is a recently developed green technique which is performed in atmospheric conditions without adding any solvent or water. SFME has already been applied to extraction of essential oil from fresh plant materials or dried materials prior moistened. The essential oil is evaporated by the in situ water in the plant materials. In this paper, it was observed that an improved SFME, in which a kind of microwave absorption solid medium, such as carbonyl iron powders (CIP), was added and mixed with the sample, can be applied to extraction of essential oil from the dried plant materials without any pretreatment. Because the microwave absorption capacity of CIP is much better than that of water, the extraction time while using the improved SFME is no more than 30 min using a microwave power of 85 W. Compared to the conventional SFME, the advantages of improved SFME were to speed up the extraction rate and need no pretreatment. Improved SFME has been compared with conventional SFME, microwave-assisted hydrodistillation (MAHD) and conventional hydrodistillation (HD) for the extraction of essential oil from dried Cuminum cyminum L. and Zanthoxylum bungeanum Maxim. By using GC-MS system the compositions of essential oil extracted by applying four kinds of extraction methods were identified. There was no obvious difference in the quality of essential oils obtained by the four kinds of extraction methods.     

玫瑰花提取工艺、化学成分及其生物活性研究进展

玫瑰花具有重要的观赏和药用价值, 主要的化学成分有玫瑰精油、黄酮类、多糖类和酚酸类等, 具有心肌保护、抗氧化、抑菌、抗肿瘤、抗病毒、镇静催眠作用、调节血脂和降血糖等生物活性.玫瑰精油是高级香水、香料和化妆品不可取代的原料, 其提取工艺是工业研究的重点.对玫瑰花中的化学成分和生物活性进行了综述, 并重点总结了玫瑰精油的提取工艺、成分和生物活性, 为玫瑰花, 特别是玫瑰精油的研究和开发提供参考.     

Comparison of MAHD with UAE and Hydrodistillation for the Analysis of Volatile Oil From Four Parts of Perilla frutescens Cultivated in Southern China

Three different isolation techniques, specifically microwave-assisted hydrodistillation (MAHD), ultrasound-assisted extraction (UAE), and conventional hydrodistillation (HD) were employed to obtain essential oils from whole plants, leaves, roots, and stems of Perilla frutescens. The essential oils were analyzed using gas chromatography with flame ionization detection and gas chromatography with mass spectrometry. Variations in chemical composition were observed; these were attributed to differences in plant organs. Variations in the percentages of the main constituents of the oils extracted based on plant organ were irregular and affected the quantity and composition of the oils. Oil yields were affected by the method of extraction and extraction organ variation. The maximum volume of oil was extracted from leaves via MAHD and the minimum was extracted from roots via UAE. Oil yields ranged from 0.05% to 0.53%. The contents of essential oil varied significantly with the plant organ. In the essential oils of the plant parts studied were showed a predominance of oxygenated monoterpenes. Variation of extraction methods and organs may influence the oil components either qualitatively or quantitatively.     

Separation and Chemical Characterization of Wetting Crude Oil Compounds

To improve the understanding of wettability, especially the influence of colloidal stability and composition of crude oil, wetting experiments on quartz sand were performed with an asphaltene-rich oil, a resin-rich oil, and with model oils containing different colloid compositions. A two-step procedure was developed to investigate the wetting behavior. In the first step those crude oil components were extracted, which preferentially wet solid surfaces. The extracted crude oil components were characterized in the second step. The amount of adsorbed oil components correlates with the stability of the crude oil colloids: low colloidal stability of crude oil leads to larger amounts of adsorbed components than does high colloidal stability. The addition of resins and/or low molecular weight asphaltenes to the crude oil stabilizes the crude oil colloids; i.e., a lower amount of wetting components are isolated by extraction in such systems. To find out, which fraction of the adsorbed oil components determines the wetting behavior of a crude oil, the wetting properties of the toluene solutions of these fractions were compared to those of the toluene solutions of the precipitated crude oil colloids. The fractions extracted with the solvent systems chloroform and methanol/chloroform showed nearly the same wetting behavior as the crude oil colloids. These fractions are characterized by the highest molecular weights, higher sulfur compositions, and the lowest H/C ratios. On the other hand, the nitrogen compounds predominate in the acetone fraction.