小叶臭黄皮叶挥发油化学成分的研究

采用水蒸气蒸馏法提取小叶臭黄皮叶挥发油,运用毛细管气相色谱-质谱联用法对挥发油成分进行了分析,共分离出84个峰,鉴定了其中的66种成分,所鉴定成分占挥发油总量的94.52%.其主要化学成分为α-芹子烯(15.76%)、石竹烯(15.05%)、β-芹子烯(9.54%)、α-蒎烯(6.43%)和α-石竹烯(5.39%)等.     

中国砂仁属植物精油化学成分的研究(一)——阳春砂仁和广宁绿壳砂仁

阳春砂仁为我国著名中药材,广宁绿壳砂仁亦可入药,功效与阳春砂仁相仿,单产比阳春砂仁高。我们应用色谱和色谱/质谱联用方法,分析了它们的种子精油化学成分,分别鉴定出23和25个化学成分。两者相同的成分有α-蒎烯,β-菰烯,樟脑,龙脑,乙酸龙脑酯等16个,其中主要化学成分如樟脑,香叶烯,柠檬烯,樟脑烯,乙酸龙脑酯,龙脑等含量一致     

不同生长年限巨尾桉叶挥发性成分GC-MS分析

为了分析不同年限巨尾桉叶挥发油的化学成分及生长年限对化学成分组成的影响,采用水蒸气蒸馏法,分别提取2006～2010年种植的巨尾桉叶片中的挥发性成分,并用气相色谱质谱联用技术分析鉴定其化学成分。结果表明:不同生长年限的巨尾桉叶片挥发油产量在0.55%～1.35%之间,随生长年限的增加而升高。利用GC-MS共鉴定出63个化合物,占总挥发油的93.00%～97.07%。其中相对含量较高的物质为:1,8-桉叶油素(55.72%～63.47%)、α-松油醇(9.78%～14.15%)、乙酸松油酯(4.96%～7.06%)、α-蒎烯(0.99%～4.31%)、龙脑(2.40%～4.89%)。由于生长年限的不同,挥发油中物质的组成及相对含量均存在差异。     

连翘挥发油成分分析

从连翘果实中提取了挥发油,用气相色谱-质谱联用法分析其挥发油的化学成分,鉴定出β-蒎烯、香桧烯、α-蒎烯等56个化合物,并用气相色谱测定了挥发油中各成分的相对含量,其鉴定率达93.37％。     

中药法落海挥发油化学成分研究

目的：分析和鉴定法落海中挥发油的化学成分。方法：用蒸馏法提取法落海中的挥发油，借助GC-MS法将挥发油中各化学成分进行分离和鉴定，用峰面积归一化法测定其相对含量。结果：法落海挥发油离子流图共有99个峰，鉴定出了77种化合物，占挥发油总量96.1%，其中主要成分为：α-蒎烯（27.33%）、α-水芹烯（9.87%），十二烷醇（8.41%）、罗勒烯（7.24%）、4,4,6,6-四甲基-二环[3.1.0]己-2-烯（5.55%）、肉豆蔻脑酸（3.58%）、蛇麻烯（2.76%）等。结论：本实验采用GC-MS联用技术分析了法落海中所含挥发油成分，使用峰面积归一化法计算挥发油中的相对含量，该方法操作简单，灵敏度高，检测效果好。简要讨论主要成分中化学成分的药理作用，为开发利用法落海提供理论依据。     

五种柏科植物挥发油成分的GC-MS分析

柏科植物是园林绿化中常用的常绿树种,具有种数多、分布广的特点。该研究采用水蒸气蒸馏法提取5种柏科植物叶片中的挥发油,利用气相色谱-质谱(GC-MS)与计算机检索联用技术对其化学成分进行分析和鉴定,并用面积归一法测定各组分的相对含量。结果表明:用水蒸气蒸馏法提取柏科植物挥发油得油率较高,除偃柏外4种柏树的得油率都在0.5%以上;5种柏科植物挥发油中共检测出了80种萜类物质,其中日本花柏中萜类物质最多含有54种,日本扁柏次之含有51种,柏木含有47种,线柏含有42种,偃柏则只含有35种;挥发油中含量较高的成分有乙酸龙脑酯、α-蒎烯、3-蒈烯、D-柠檬烯、松油烯-4-醇、桧烯和萜品油烯等,一些植物还含有龙脑、β-月桂烯、石竹烯、β-紫罗兰酮和Verticiol等一些重要的药用成分;柏科植物挥发油具有成分及相对含量差异大、成分较简单、化合物种类以萜烯类为主的特点。研究结果可为进一步开发利用柏科植物资源提供理论依据。     

下田菊挥发油化学成分的研究

利用水蒸汽蒸馏法、两相溶剂萃取法提取下田菊(Adenostemma lavenia(L.)O.Ktze.)地上部分的挥发油,提取10h的挥发油得率为0.990%。采用毛细管气相色谱-质谱联用(GC-MS)技术结合计算机检索对该挥发油的化学成分进行了分析和鉴定,采用色谱峰面积归一化法计算了各成分的相对含量。从挥发油中共分离出36个峰,鉴定了其中的35种成分,占总量的99.56%,其中α-荜澄茄油烯(32.62%)、石竹烯(24.97%)和γ-榄香烯(5.53%)为主要成分,此外α-石竹烯(3.97%)、α-恰米烯(3.57%)、双环[4,3,0]-7-亚甲基-2,4,4-三甲基-2-乙烯基-壬烷(3.41%)、γ-萜品烯(3.07%)、d-柠檬烯(2.57%)、α-蒎烯(2.49%)及2-蒈烯(2.28%)的含量也较高。     

滨海前胡不同部位挥发油化学成分GC-MS分析

采用水蒸气蒸馏法分别提取滨海前胡Peucedanum japonicum根、茎叶、花及果实中挥发油,使用GC-MS分析挥发油并鉴定其化学成分,比较不同部位挥发油的化学成分及含量差异。结果显示,从根、茎叶、花和果实挥发油中分别鉴定出58、36、40和45种化学成分, 分别占各部位挥发油总量的95.60%、98.03%、95.82%和95.36%。四个部位共鉴定出79个化学成分, 其中有相同化合物20种,主要成分为α-侧柏烯、α-蒎烯、β-月桂烯、β-蒎烯等。     

石油菜挥发油和超临界流体萃取物化学成分的GC-MS分析

首次利用水蒸气蒸馏法和超临界流体萃取法(SFE)对石油菜地上部位进行提取,分别获得挥发油和SFE萃取物,采用气相色谱-质谱联用技术(GC-MS)结合计算机数据库检索对这两种提取物的化学成分进行了分析鉴定,采用峰面积归一化法测定了其中各个化学成分的相对含量。从挥发油中共分离出39个色谱峰,鉴定了其中28个化学成分,已鉴定出的成分的相对含量总和占化合物检出总量的91.90%,化合物类型均为萜类。从SFE萃取物中共分离出136个色谱峰,鉴定了其中65个化学成分,已鉴定出的成分的相对含量总和占化合物检出总量的58.17%,化合物类型包括萜类、芳香族类和脂肪族类。挥发油和SFE萃取物均含有α-蒎烯、石竹烯和桉油烯醇,其他成分则存在较大差异。     

乌榄叶挥发油化学成分分析

采用气相色谱-质谱联用(GC-MS)方法首次对乌榄叶挥发油成分进行了测试分析,并应用色谱峰面积归一化法计算各成分的相对含量。分离出19个峰,确认了19种化合物,所鉴定的组分占挥发油总量的100%,主要成分是石竹烯(33.47)、α-蒎烯(18.03%)、d-柠檬烯(16.82%)、α-侧柏烯(11.74%)和α-水芹烯(6.51%)。     

江西迷迭香精油的成分分析及抗氧化、抑菌活性研究

为了研究江西迷迭香精油的化学成分及抗氧化、抑菌活性,采用水蒸气蒸馏法提取迷迭香精油,利用气相色谱-质谱联用法(GC-MS)对迷迭香精油成分进行分析,通过对DPPH自由基、羟基自由基的清除活性和还原力来研究迷迭香精油的体外抗氧化活性;通过以枯草芽孢杆菌、金黄色葡萄球菌和大肠杆菌为供试菌,测定抑菌圈大小和最低抑菌浓度(MIC)来研究迷迭香精油的抑菌活性。实验结果表明,从迷迭香精油中鉴定出40种化学成分,占精油总量的99.46%,其主要化学成分有α-蒎烯(39.05%)和1,8-桉叶素(16.86%),其次是莰烯(4.22%)、D-柠檬烯(3.87%)、龙脑(3.74%)、β-石竹烯(3.11%)等,α-蒎烯的含量高于国内其他产地;迷迭香精油对DPPH、羟基自由基和还原力的半数清除率IC₅₀值分别为76.42、51.40和49.15μL/mL;精油对枯草芽孢杆菌、金黄色葡萄球菌和大肠杆菌的抑菌圈大小分别为14.40±0.66、11.41±0.19、11.70±0.27 mm,最低抑菌浓度(MIC)分别为2.50、10.00、10.00μL/mL,对枯草芽孢杆菌的抑制作用明显强于金黄色葡萄球菌和大肠杆菌。结果表明迷迭香精油具有较好的抗氧化、抑菌活性。     

椪柑精油及其主要抑菌组分对菌核青霉的抑制作用

采用水蒸气蒸馏法提取椪柑(Citrus reticulate Blanco)果皮精油,并用GC-MS对其成分进行分析,共鉴定出46种成分,主要包括柠檬烯(57.67%)、β-芳樟醇(5.36%)、2-蒈烯(4.47%)、β-蒎稀(4.31%)、γ-松油烯(4.08%)、α-蒎烯(3.27%)、1,2-二异丙烯基环丁烷(2.87%)、β-月桂烯(2.77%)、α-侧柏烯(2.40%)、β-水芹烯(2.24%)、癸醛(1.80%)和香茅醇(1.49%)等。采用污染食物技术(poisoned food technique)和液体培养法(liquid culture)测定了不同浓度椪柑精油以及主要抑菌组分对菌核青霉的抑制作用。结果表明:不同浓度(0.5~20μl/ml)的椪柑精油对菌核青霉生长均有一定的抑制,且抑菌效果与浓度呈正相关。无论是采用污染食物技术还是液体培养法,20μl/ml椪柑精油均能完全抑制菌核青霉生长;随着培养 时间延长到7d, 20μl/ml椪柑精油抑菌效果有所下降,但仍能显著抑制菌核青霉生长。采用污染食物技术考察了椪柑精油中7种常见抑菌成分对菌核青霉的影响。结果表明,0.04μl/ml柠檬醛和1.07μl/ml β-芳樟醇能显著抑制菌核青霉生长,而其他组分无明显作用。实验结果表明,椪柑精油的抑菌作用可能归功于其所含的柠檬醛和β-芳樟醇。     

THE CHEMICAL CONSTITUENTS OF THE ESSENTIAL OIL FROM THE ROOTS OF VALERIANA OFFICINALIS VAR.LATIFOLIA

Ahstract In order to find the aroma characteritics of Valeriana officinalis var. latifolia, the chemical composition of the essential oil of this plant have been examined. This essential oil was analysed by GC-MS on the Finnigan -4510 instrument. As a resu1t (see Tab1e 1 and Fig. 1 ) 21 compounds were identified. The major components are bornyl acetate (50.56 % ), α-pinene (6.76% ), camphene (16. 17% ), β-pinene (6. 48% ), limonene (1.77% ), carveyl acetate (5.47% ), dihydrocarveyl acetate (1.62%) etc. This essential oil having a delicious aroma shows to be suitable for compounding perfume of cigar and food flavor, and cosmetic flavor too.     

Antioxidant and Antibacterial Activities of Crude Extracts and Essential Oils of Syzygium cumini Leaves

This research highlights the chemical composition, antioxidant and antibacterial activities of essential oils and various crude extracts (using methanol and methylene chloride) from Syzygium cumini leaves. Essential oils were analyzed by gas chromatography-mass spectrometry (GC-MS).The abundant constituents of the oils were: α-pinene (32.32%), β-pinene (12.44%), trans-caryophyllene (11.19%), 1, 3, 6-octatriene (8.41%), delta-3-carene (5.55%), α-caryophyllene (4.36%), and α-limonene (3.42%).The antioxidant activities of all extracts were examined using two complementary methods, namely diphenylpicrylhydrazyl (DPPH) and ferric reducing power (FRAP). In both methods, the methanol extract exhibited a higher activity than methylene chloride and essential oil extracts. A higher content of both total phenolics and flavonoids were found in the methanolic extract compared with other extracts. Furthermore, the methanol extract had higher antibacterial activity compared to methylene chloride and the essential oil extracts. Due to their antioxidant and antibacterial properties, the leaf extracts from S. cumini may be used as natural preservative ingredients in food and/or pharmaceutical industries.     

鸭儿芹根、茎、叶挥发油的化学成分

采用水蒸气蒸溜法提取其根、茎、叶中的挥发油,利用GC-MS联用仪对其化学成分进行分析,以归一化法计算各个化学成分的相对含量.鸭儿芹根挥发油中共分离出11个峰,鉴定出11种化合物,占总离子峰的98.61％,主要成分为α-芹子烯、γ-芹子烯等;茎中共分离出25个峰,鉴定出25种化合物,占总离子峰的100.00％,主要成分为...     

Studies on Chemical Compositions of Volatile Oil from Seeds of Cuminum cyminum L.

This paper deals with the determination of chemical compositions of volatile oil of Cuminum cyminum L. in Xinjiang area. Using capillary gas chromatography and GG/MS, the following components have been identified: α-pinene, β-pinene, camphene, myrcene, γ-terpinene, ρ-cymene, terpinolene, linalool, pulegone, cuminaldehyde, 2,3-dihydrocuminal and myrtenal etc. Besides, silica gel column chromatography as well as some spectrum methods such as IR, MS, NMR, etc. were used to elucidate the structure of 2,3-dihydrocuminal or 4-isopropyldelta-1,3-cyclohexadiene-l-carbaldehyde.     

阔叶百里香鲜、干茎叶精油成分及其抑菌效果

采用水蒸气蒸馏法和气相色谱-质谱联用技术(GC-MS)分析阔叶百里香(Thymus pulegioides)鲜、干茎叶精油含油率、化学组成及其相对含量的差异,并比较精油对链格孢(Alternaria alternata)、粉红单端孢(Trichothecium roseum)和意大利青霉(Penicillium italicum)的抑制效果。鲜、干茎叶含精油率分别为0.53%、0.37%,分别鉴定出35、40种化合物,其主要化学成分相同,均含有百里香酚(鲜样31.30%,干样26.82%)、麝香草酚甲醚、右旋龙脑和邻伞花烃等,只是相对含量略有差异;在抑菌实验中,百里香精油对链格孢菌的抑制作用最为明显,其次是意大利青霉和粉红单端孢。鲜、干阔叶百里香精油的组分较为接近,相对含量略有差异;阔叶百里香精油对3种真菌具有较好的抑制效果,且鲜样精油的抑菌效果好于干样精油。     

Anti-fungal activity of crude extracts and essential oil of Moringa oleifera Lam

Investigations were carried out to evaluate the therapeutic properties of the seeds and leaves of Moringa oleifera Lam as herbal medicines. Ethanol extracts showed anti-fungal activities in vitro against dermatophytes such as Trichophyton rubrum, Trichophyton mentagrophytes, Epidermophyton floccosum, and Microsporum canis. GC-MS analysis of the chemical composition of the essential oil from leaves showed a total of 44 compounds. Isolated extracts could be of use for the future development of anti-skin disease agents.     

Chemical composition of essential oils of four Eucalyptus species and their phytotoxicity on silverleaf nightshade (Solanum elaeagnifolium Cav.) in Australia

Phytotoxicity and chemical composition of essential oils from four selected Eucalyptus species in Australia were investigated. Essential oils had stronger inhibitory effects on germination and seedling growth of silverleaf nightshade (Solanum elaeagnifolium Cav.) when compared with a commercial eucalyptus oil and with 1,8-cineole. E. salubris oil had the highest inhibition index for silverleaf nightshade germination, root growth and shoot growth, while E. spathulata had the lowest inhibitory effect except root growth. Gas chromatography-mass spectrometry analysis revealed 56 compounds present in E. salubris oil, with 1,8-cineole (57.6?%), ??-pinene (10.9?%) and p-cymene (8.3?%) predominant. E. dundasii oil contained 55 identified compounds with 1,8-cineole (65.5?%) and ??-pinene (19.9?%) being the richest fractions. There were 56 compounds identified from E. brockwayii oil with ??-pinene (31.1?%), isopentyl isovalerate (20.2?%) and 1,8-cineole (16.9?%) as the most abundant components. E. spathulata oil contained 60 compounds, predominantly 1,8-cineole (52.9?%) and ??-pinene (31.0?%). Further study is required to determine the phytoxicity of the individual identified compounds on silverleaf nightshade and whether the observed phytotoxicity is attributable to a single compound or to the synergistic effects of several compounds.     

Chemical variability of the wood essential oil of Cedrus atlantica Manetti from Corsica

The composition of 48 samples of essential oil isolated from the wood of Cedrus atlantica growing in Corsica was investigated by GC (in combination with retention indices), GC/MS, and (13) C-NMR. Twenty-three compounds accounting for 73.9-96.0% of the oil composition were identified. The oils consisted mainly of monoterpene hydrocarbons and sesquiterpenes, in particular α-pinene (5; up to 79.4%), himachalol (4; up to 66.2%), β-pinene (up to 21.4%), β-himachalene (2; up to 19.3%), γ-himachalene (3; up to 11.0%), and α-himachalene (1; up to 10.9%). The 48 oil compositions were submitted to k-means partitioning and principal-component analysis, which allowed the distinction of two groups within the oil samples. The composition of Group I (44% of the samples) was dominated by 5, while the samples of Group II (56% of the samples) contained mainly 4.