千里光和额河千里光化学成分及生物活性研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
千里光(Senecio scandens Buch.-Ham.)为菊科(Compositae)千里光属(Senecio L.)植物,主要分布于我国华东、中南、西南地区以及陕西和甘肃等地。千里光是我国应用历史悠久的常用中药,其性味苦、寒,入肺、肝、大肠经,具有清热解毒、凉血消肿、清肝明目等功效,主治疮疖痛肿、虫蛇咬伤、上呼吸道感染、扁桃体炎、咽喉炎、肺炎、眼结膜炎、痢疾以及骨髓造血功能障碍、脑炎、贫血等。额河千里光(Senecio argunensis Turcz.),又名羽叶千里光,斩龙草等,分布于我国东北、西北和华南等地区。地方药志中多有收载,以全草入药,具有清热解毒的功效,主治虫蛇咬伤、急性结膜炎、疮疖痈肿、骨髓造血功能障碍、脑炎、贫血等。本文初步研究了千里光和额河千里光的抗氧化及抗菌等生物活性,并对其溶性和挥发性化学成分进行了分析,主要研究结果如下:
     (1)千里光和额河千里光茎、叶和花中挥发性成分的提取和分析挥发性成分采用水蒸馏法进行提取,气相色谱-质谱(GC-MS)联用技术进行分析和鉴定。从千里光茎中鉴定出30种挥发性成分(主要为棕榈酸50.2%、亚油酸23.12%和亚麻酸甲酯15.52%),叶中鉴定出35种挥发性成分(主要为棕榈酸38.43%、亚麻酸甲酯18.35%、植醇11.13%和亚油酸9.02%),花中鉴定出36种挥发性成分(主要为棕榈酸37.14%和亚油酸7.47%);从额河千里光茎中鉴定出43种挥发性成分(主要为棕榈酸43.74%、β-荜澄茄烯21.38%和亚油酸13.15%),叶中鉴定出36种成分(主要为棕榈酸39.62%、亚麻酸甲酯23.39%和亚油酸14.85%),花中鉴定出36种成分(主要为β-荜澄茄烯18.68%和芹子烯内酯15.52%)。
     (2)千里光和额河千里光根、茎、叶和花中溶性成分的提取和分析利用索氏提取法分别提取千里光和额河千里光根、茎、叶和花中的溶性成分,甲酯化处理之后,运用气相色谱-质谱(GC-MS)联用技术对其成分进行了分析和鉴定。从千里光根中鉴定出28种溶性成分(主要为亚油酸48.03%、棕榈酸22.19%和油酸10.51%),茎中鉴定出31种溶性成分(主要为亚油酸45.55%、棕榈酸20.05%和油酸18.85%),叶中鉴定出41种溶性成分(主要为亚麻酸34.27%、亚油酸27.75%和棕榈酸15.92%),花中鉴定出33种溶性成分(主要为亚油酸26.53%、棕榈酸24.06%和油酸22.53%);从额河千里光根中鉴定出32种溶性成分(主要为亚油酸50.69%和棕榈酸20.84%),茎中鉴定出33种溶性成分(主要为亚油酸45.76%、棕榈酸19.85%和亚麻酸14.39%),叶中鉴定出14种溶性成分(主要亚麻酸27.08%、亚油酸19.09%和棕榈酸15.97%),花中鉴定出21种溶性成分(主要为亚油酸18.44%、二十四烷13.78%和棕榈酸12.23%)。
     (3)千里光和额河千里光提取物的体外抗氧化活性研究以千里光和额河千里光的根、茎、叶、花为材料,分别测定了两种植物不同器官以及额河千里光叶的不同极性溶剂提取物的总多酚含量、对DPPH·自由基的清除能力和对β-胡萝卜素/亚油酸体系的抗氧化作用。结果表明:在千里光和额河千里光不同器官提取物中,叶甲醇提取物的总多酚含量较高,在DPPH·自由基清除体系和β-胡萝卜素/亚油酸体系中抗氧化活性也较好。其中,千里光叶甲醇提取物对DPPH·自由基的清除能力与人工合成抗氧化剂BHT相当,其EC_(50)值分别为0.0209±0.0005(mg/mL)和0.0206±0.0004(mg/mL),额河千里光叶甲醇提取物的EC_(50)值为0.0354±0.0005(mg/mL)。在额河千里光叶三个不同极性溶剂的提取物中,乙酸乙酯提取物对DPPH·自由基的清除能力和在β-胡萝卜素/亚油酸体系中的抗氧化活性最强。
     (4)千里光和额河千里光提取物的抑菌活性评价采用牛津杯法评价其根、茎、叶、花提取物的抑菌活性。实验结果表明,千里光和额河千里光的提取物对所试细菌均有不同程度的抑制作用。在所试浓度下,千里光不同器官甲醇提取物对表皮葡萄球菌的抑制作用均强于阳性对照盐酸四环素;额河千里光叶甲醇提取物对肺炎克雷伯氏菌的抑菌圈直径为16.3±1.2mm,接近盐酸四环素的抑菌圈(17.6±0.7mm);额河千里光叶乙酸乙酯提取物对所试细菌和酵母均有不同程度的抑制作用,其抑制效果明显优于石油醚、正丁醇和水提物,其中以普通变形菌最敏感,抑菌圈直径达22.0±2.4mm。
Senecio scandens Buch. -Ham., as one species of Senecio genus of Compositae family, distributes mainly in the East, South, South west, Shannxi and Gansu Province of Chian. The taste of this plant is biter and cool. It is a traditional Chinese medicine with the functions of clearing away heat and removing toxic substances, cooling blood to dissipate blood stasis and liver-clearing and improving acuity of sight. As one kind of folk medicines, it's usually used to treat furunculosis edema pain, bites of pest and snake, upper respiratory tract infection, tonsillitis, laryngopharyngitis, pneumonia, eye conjunctivitis, dysentery, bone marrow hematopoietic dysfunction, encephalitis and anemia. Senecio argunensis Turcz., whose another name is "Zhan Long Cao", as one species of Senecio genus of Compositae family, distributes mainly in the North east, North west and South of China. It has been registered in some local pharmacopeia. The whole herb has medicinal uses with the functions of clearing away heat and removing toxic substances. It's usually used to treat bites of pest and snake, acute conjunctivitis, furunculosis edema pain, bone marrow hematopoietic dysfunction, encephalitis and anemia. Modern pharmaceutical studies showed that S. scandens possesses the effects on antibiotic, antivirus and antioxidant etc.. This paper preliminary studied the antimicrobial and antioxidant activities of the extracts of S. scandens and S. argunensis using DPPH·free radical-scavenging systems,β-carotene/linoleic acid system and Oxford cup method. We also analyzed the fat-soluble constituents and volatile components of different parts of S. scandens and S. argunensis by gas chromatography-mass Spectrometry (GC-MS). The main results were as follows:
     (1) Volatile components from the stems, leaves and flowers of S. scandens and S. argunensis were obtained by hydrodistillation and analyzed by gas chromatography-mass Spectrometry (GC-MS), respectively. 30, 35 and 36 compounds were identified in stems, leaves and flowers of S. scandens, respectively.The main volatile compounds in stems of S. scandens were palmitic acid (50.2%), linoleic acid (23.12%) and linolenic acid methyl ester (15.52%). The main volatile compounds in leaves of S. scandens were palmitic acid (50.2%), linolenic acid methyl ester (18.35%), phytol (11.13%) and linoleic acid (9.02%). The main volatile compounds in flowers of 5. scandens were palmitic acid (37.14%) and linoleic acid (7.47%). 43, 36 and 36 compounds were identified in stems, leaves and flowers of S. argunensis, respectively. The main volatile compounds in stems of S. argunensis were palmitic acid (43.74%),β-cubebene (21.38%) and linoleic acid (13.15%). The main volatile compounds in leaves of S. argunensis were palmitic acid (39.62%), linolenic acid methyl ester (23.39%) and linoleic acid (14.85%). The main volatile compounds in flowers of S. argunensis wereβ-cubebene (18.68%) and selina-6-en-4-ol (15.52%).
     (2) Fat-soluble constituents from the roots, stems, leaves and flowers of S. scandens and S. argunensis were obtained by Soxlet extraction, derivated by methyl esterification and identified by gas chromatography-mass Spectrometry (GC-MS), respectively. 28, 31, 41 and 33 compounds were identified in roots, stems, leaves and flowers of S. scandens, respectively. The main fat-soluble compounds in roots of S. scandens were linoleic acid (48.03%), palmitic acid (22.19%) and oleic acid (10.51%). The main fat-soluble compounds in stems of S. scandens were linoleic acid (45.55%), palmitic acid (20.05%) and oleic acid (18.85%). The main fat-soluble compounds in leaves of S. scandens were linolenic acid (34.27%), linoleic acid (27.75%) and palmitic acid (15.92%). The main fat-soluble compounds in flowers of S. scandens were linoleic acid (26.53%), palmitic acid (24.06%) and oleic acid (22.53%). 32, 33, 14 and 21 compounds were identified in roots, stems, leaves and flowers of S. argunensis, respectively. The main fat-soluble compounds in roots of S. argunensis were linoleic acid (50.69%) and palmitic acid (20.84%). The main fat-soluble compounds in stems of S. argunensis were linoleic acid (45.76%), palmitic acid (19.85%) and linolenic acid (14.39%). The main fat-soluble compounds in leaves of S. argunensis were linolenic acid (27.08%), linoleic acid (19.09%) and palmitic acid (15.97%). The main fat-soluble compounds in flowers of S. argunensis were linoleic acid (18.44%), tetracosane (13.78%) and palmitic acid (12.23%).
     (3) The extracts from different organs (roots, stems, leaves and flowers) of S. scandens and S. argunensis, and extracts of different solevents from leaves of S. argunensis were subjected to screening for their possible in vitro antioxidant activities by using 2,2-diphenylpicrylhydrazyl (DPPH·) free radical-scavenging assays andβ-carotene /linoleic acid system. And the contents of total phennolic compounds of different extracts were also determined. The results showed that all the extracts have dose-effect relationship in DPPH·free radical-scavenging assays. Among them, the extracts of the leaves both from S. scandens and S. argunensis exhibited the highest antioxidant activities among all of the extracts. The EC_(50) value of the extracts from leaves from S. scandens is 0.0209±0.0005 (mg/mL), which is equivalent to synthetic antioxidant BHT (EC_(50): 0.0206±0.0004 (mg/mL)). And the EC_(50) value of extracts from leaves of S. argunensis is 0.0354±0.0005 (mg/mL). Among the extracts with different polarity solevents from leaves of S. argunensis and extracts with acetoacetate have the highest antioxidant activities both in DPPH·free radical-scavenging system andβ-carotene/linoleic acid system.
     (4) The extracts from different organs (roots, stems, leaves and flowers) of S. scandens and S. argunensis, and extracts of different solevents from leaves of S. argunensis were subjected to a screening for their possible antimicrobial activities by using the method of Oxford cup. The results showed that all the extracts were found to inhibit the growth of tested bacteria in some extent. At the tested concentration, the antimicrobial activities of extracts from different organs of S. scandens to Staphylococcus epidermidis are better than positive control Tetracycline hydrochloride. The Klebsiella pneumoniae subsp. pneumoniae was sensitive to methanol extracts from leaves of S. argunensis, and the inhibition zone is 16.3±1.2 mm, which is close to Tetracycline hydrochloric-de(17.6±0.7 mm). The results also showed that the ethyl acetate extracts were found to inhibit the growth of all bacteria tested. And the inhibition effect of ethyl acetate extracts is better than n-butanol, water and petroleum ether extracts. Among these, Proteus vulgaris was the most sensitive bacteria, and it's inhibition zone is 22±2.4 mm.
引文
[1]中国科学院植物研究所主编.中国高等植物科属检索表[M].北京:科学出版社,1987.
    [2]陈进军,王建华,耿果霞,等.千里光的化学成分鉴定及体外抗菌试验[J].动物医学进展,1999,20(4):35-37.
    [3]《中药辞海》编写组编.中药辞海[M].北京:中国医药科技出版社,1993年,第一卷,551.
    [4]M.Ruth Grue,J.Richard Liddell.Pyrrolizidine alkaloids from Senecio chrysocoma[J].Phytochemistry,1993,33(6):1517-1519.
    [5]曾美怡,李敏民,赵秀文.含吡咯双烷生物碱中草药的毒性(二)—款冬花和伪品蜂斗菜等的毒性反应[J].中药新药与临床药理,1996,7(4):51-52.
    [6]Bull L.B.,C.C.J.Culvenor,A.Y.Dick.The Pyrrolizidine alkaloids[M].Amsterdam:Northholland Publishing Company,1968,293.
    [7]Mclean E.K.The toxic actions of pyrrolizidine(Senecio) alkaloids[J].Pharmacal,1970,22:429.
    [8]袁继丽.中草药致肝损害的研究近况[J].中草药,1999,30(9):711-714.
    [9]胡金峰,冯孝章,贾忠建.篙属和千里光属植物中桉烷型倍半萜的光谱特征[J].天然产物与开发,1999,11(4):95.
    [10]Antoaneta B.Trendafilova,Elena T.Tsankova,Ljuba N.Evstaticva.Seco-eremophilanolides from Senecio macadonicus[J].Phytochemistry,1995,40(1):329-330.
    [11]S.Dupre,M.Grenz,J.Jakupovic,F.Bohlmann,H.M.Niemeyer.Eremophilane,germacrane and shikimic acid derivatives from chilean Senecio species.[J].Phytochemistry,1991,30(4):1211-1220.
    [12]G.Riicker,E.P.Schenkel,D.Manna,R.Mayer,et al.Sesquiterpene peroxide from Senecio selloi and Eupatorium rufescens[J].Pianta Med,1996,62:565.
    [13]吴斌,吴立军.千里光属植物的化学成分研究进展[J].中国中药杂志,2003,28(2):97-100.
    [14]Ferdinand Bohlmann,Christa Zdero.Sandaracopimarene derivatives from Senecio subrubrilorus[J].Phytochemistry,1982,21(7):1697-1700.
    [15]Ferdinand Bohlmann,Christa Zdero,Robert M.King,Harold Robinson.The first acetylenic monoterpene and other constituents from Senecio clevelandii[J].Phytochemistry,1981,20(10):2425-2427.
    [16]C.Zdero,F.Bohlmann,J.R.Liddell.Seco-eremophilanes and other constituents from south African Senencio species[J].Phytochemistry,1989,28(12):3532-3534.
    [17]Dond-Liang Cheng,Xiao-Ping Cao,Jie-Kai Cheng,E.Roeder.Diterpene glycosides from Senecio rufus[J].Phytochemistry,1992,32(1):151-153.
    [18]N De Tommasi,L.Rastrelli,M.R.Lauro,R.Aquino.Polyhydroxylated triterpenes from Senecio pseudotites[J].Phytochemistry,1998,49(4):1123-1125.
    [19]Josef Jizba,Milos Budesinsky,Tomas Vanek,et al.Components of Senecio pancicii Degen var.amautorum(Velen.) Stoj.,Stef.Et Kit.And S.pancicii Degen var.pancicii[J].Collection Czechoslovak Chem.Commun.1982,47:664.
    [20]Gerhard Rucker,Detlef Maims,Eloir P.Schenkel,et al.Triterpenes with a new 9-epi-cucurbitan skeleton from Senecio selloi[J].Phytochemistry,1999,52(8):1587-1591.
    [21]程卫强,隋长惠,袁久志,等。额河千里光黄酮类成分的研究[J].中草药,1999,30(10):727-729
    [22]S.Pena Betancourt,A.Proliac,J.Rayhaud.Quatre mono-O-glycosyl flavonoids des tiges feuillees de Senecio sanguisorbae DC.(Composees).Pharmazie,1988,43:142-143.
    [23]Toshio Goto,Tadao Kondo,Takatoshi Kawai,et al.Structure of cinerann,a tetra-acylated anthocyanin isolated from the blue garden cineraria,Senecio cruentus.Tetrahedron Leters,1984,25(2):6021-6024.
    [24]I.Piegay,J.Reynaud,J.Raynaud.Les flavonoides de Senecio aureus L.(C omposdes).Pharmazie,1996,41:524-525.
    [25]Serena Catalano,Stefano Luschi,Guido Flamini,et al.A xanthone from Senecio mikanioides leaves.Phytochemistry,1996,42(6):1605-1607.
    [26]Mario D'Agostino,Vincenzo De Feo,Francesco De Simone,et at.Three chalcones from Senecio pseudolites.Phytochemistry,1991,30(7):2440-2441.
    [27]Kenjiro Toki,Norio Saito,Harumitsu Kuwano,et al.Acylated pelargonidin 3,7-glycosides from pink flowers of Senecio cruentus.Phytochemistry,1995,38(6):1509-1512.
    [28]吴斌,吴立军,张磊,金哲实.麻叶千里光抗菌化学成分的研究(Ⅰ)[J].沈 阳药科大学学报,2004,21(5):341-345.
    [29]B Nan Dooren,R Bos,D H E Tattje.Composition of essential oil of some Senecio species[J].Planta Med.,1981,42:385.
    [30]Susana Abdo,Maria de Bernardi,Giulio Marinoni,et al.Furanoeremophilanes and other constituents from Senecio canescens[J].Phytochemistry,1992,31(11):3937-3941.
    [31]Cristina Perez,Alicia Mariel Agnese,Jose Luis Cabrera.The essential oil of Senecio graveolens(Compositae):chemical composition and antimicrobial activity tests[J].Journal of Ethnopharmacology,1999,66:91-96.
    [32]Ferdinand Bohlmann,Wolfgang Kramp,Harold Robinson,Robert M.King.A norsesquiterpene from Senecio humillimus[J].Phytochemistry,1981,20(7):1739-1740.
    [33]Elizabeth A.Jares,Maria Cristina Tettamanzi,Alicia B.Pomilio.Sitosterol 3-O-β-D-glucuranopyranoside from Senecio bonariensis[J].Phytochemistry,1990,29(1):340-341.
    [34]Th M Pinchon,M Pinkas.Les amino-acides libred des capitules de Senecio bicolor (Willd) Tod ssp cineraria(DC) Chater.Pharmazie,1991,46:232.
    [35]Hussein N S.Benzofuranes from Senecio desfontainei[J].Pharmazie,1992,47:468.
    [36]刘方,武子斌,牛淑敏,等.中药材抗氧化及自由基清除活性的研究[J].中国药学杂志,2001,36(7):442-445.
    [37]尹洪萍,袁红,华春珍,等.10种中药对耐药性肺炎链球菌的抑菌作用[J].医药导报,2003,22(7):483-484.
    [38]袁昌衡,周启贵,杨飞,等.80种中药水煎液对淋球菌的抑制试验[J].中国医院药学杂志,1997,17(11):508-509.
    [39]李丽静,王继彦,王本祥,荣大奇,房金荣.返魂草提取物及其有效成分抗病毒机制的研究[J].陕西中医学院学报,2004,27(6):65-66.
    [40]Yu Zhao,Peng Wang,Xiaojiang Hao,et al.Enantiomeric sesquiterpene lactones from Senecio tsoongianus[J].Chinese Chemical Letters,2002,13(8):754-757.
    [41]Qijun Zhang,Hui Dou,Qunxiong Zheng,et al.Two cytotoxic eremophilanolides from Senecio tsoongianus[J].Chinese Chemical Leters,2005,16(3):362-364.
    [42]Leslie T.Gelbaum,Leon H.Zalkow,Darrell Hamilton.Cytotoxic agent from Senecio anonymus Wood[J].Journal of Natural Products,1982,45(3),370.
    [43]李时珍.本草纲目,校点本上册,北京:人民出版社,1341.
    [44]程卫强.千里光属三种植物的生药学研究[D].沈阳:沈阳药科大学,1998.
    [45]田小雁.四种中草药的活性成分研究[D].北京:中国协和医科大学,2006.
    [46]王雪芬,屠殿君.九里明化学成分的研究[J].药学学报,1980,15(8):503-504.
    [47]周欣,赵超,杨小生.气相色谱-质谱分析黔产千里光挥发油的化学成分[J].中草药,2001,32(10):880-881.
    [48]Ferdinand Bohlmann,Christa Zdero,Jasmin Jakupovic,et al.Further pyrrolizidine alkaloids and furoeremophilanes from Senecio species[J].Phytochemistry,1986,25(5):1151-1159.
    [49]Veera Batra,T.R.Rajagopalan.Alkaloidal constituents of Senecio scandens Curr.Sci.1977,46(5):141.
    [50]L.R.G.Valadon,Rosemary S.Mummery.Carotenoids of certain compositae flowers[J].Phytochemistry,1967,6(7),983-988.
    [51]王耕,刘强.千里光中微量元素的测定[J].第一军医大学分校学报,2002,25(2):140.
    [52]程卫强,韦新贵,袁久志,隋长惠.额河千里光地下部分生物碱的研究[J].中草药,2001,32(9):783-784.
    [53]K.Liu,E.Roder.Pyrrolizidine alkaloids from Senecio argunensis.Phytochemistry,1991,30(4):1303-1305.
    [54]李宁,张朝凤,张勉.额河千里光中一个新的黄酮[J].中国药科大学,2008,39(1):20-22.
    [55]陈梅荣,丁惠堂,王晖,梁金星.千里光不同方法提取物抑菌作用的研究[J].江西中医学院学报,2002,14(4):15.
    [56]F.Liu,T.B.Ng.Antioxidative and free radical scavenging activities of selected medicinal herbs[J].Life Science,2000,66(8):725-735.
    [57]尚遂存,武雪芬,杨林莎.中草药食品抗氧化剂的筛选[J].天然产物研究与开发,1994,6(1):36-391.
    [58]刘因华,曹志红.抗艾滋病药物的发展近况[J].云南中医中药杂志,2004,25(6):44-45.
    [59]R.A.Collins,T.B.Ng,W.P.Fong,et al.A comparison of human immunodeficiency virus type 1 inhibition by partially purified aqueous extracts of Chinese medicinal herbs[J].Life Science,1997,60(23):PL345-PL351.
    [60]谭宗建,田汉文,彭志英.千里光保肝作用的实验研究[J].四川生理科学杂志, 2000,22(1):20-23.
    [61]国家中医药管理局《中华本草》编委会.中华本草[M].上海:上海科技出版社.1999,1390.
    [62]薄U坤,周燕,王玉华.紫外可见分光光度法测定额河千里光中总黄酮的含量[J].内蒙古医学院学报,2007,29(5):356-359.
    [63]李艳辉,格桑索朗,阿萍,等.双花千里光花精油的GC-MS分析[J].分析实验室,2006,25(7):42-45.
    [64]Peter Y.Y.Wong,David D.Kitts.Studies on the dual antioxidant and antibacterial properties of parsley(Petroselinum crispum) and cilantro(Coriandrum sativum)extracts[J].Food Chemistry,2006,97:505-515.
    [65]Sung-Sook Chun,Dhiraj A.Vattem,Yuan-Tong Lin,et al.Phenolic antioxidants from clonal oregano(Origanum vulgate) with antimicrobial activity against Helicobacter pylori[J].Process Biochemistry,2005,40:809-816.
    [66]E.L.Souza,T.L.M Stamford,E.O.Lima,V.N.Trajano.Effectiveness of Origanum vulgare L.essential oil to inhibit the growth of food spoiling yeasts[J].Food Control,2007,18:409-413.
    [67]张伟刚,印遇龙,黄瑞林,等.多不饱和肪酸的营养作用及其基因表达调控[J].食品科学,2006,27(1):273-277.
    [68]纳智.滇南红厚壳种子油的肪酸成分[J].热带亚热带植物学报,2005,13(6):505-506。
    [69]吕亮.蚕砂提取植醇工艺[J].广西化工,2002,31(1):42-43.
    [70]Yang ZH,Liu S P,Chen X D.Induction of apoptotic cell death and invivo growth inhibition of human cancer cells by a saturated branched-chain fatty acid 13-methyltetradecanoic acid[J].Cancer Res.,2000,60:505-509.
    [71]兰文智,陈超,黄雅芬,等.磷酶A_2在诱导红豆杉细胞产生活性氧中的作用[J].西北植物学报,2004,24(7):1286-1291.
    [72]周德文,周立勇.术类的药理和药效[M].国外医学·植物药分册,1996,11(3):120.
    [73]王金华,薛宝云,梁爱华,等.仓术有效成分β-桉叶醇对小鼠小肠推进功能的影响中国药学杂志,2002,37(4):266-268.
    [74]刘存芳,田光辉.抱茎蓼挥发油成分及其抗菌活性的研究[J].天然产物研究与开发,2007,19:447-451.
    [75]孙文基,等.天然活性成分简明手册[M].北京:中国医药科技出版社,1998: 149.
    [76]徐年军,白海波,严小军,等.黄金茶原植物山腊梅中挥发油性成分分析[J]分析测试学报,2006,25(1):90-93.
    [77]Leopold J.,Gerhard B.,Albera S.,et al.Composition quality control and antmicrobial activity of the essential oil of long-time Dill seeds from Bulgaria[J].Chemistry of Natural Compounds,2003,51:3854-3857.
    [78]鲍忠定,秦志荣,许荣年,等.杭白菊挥发油化学成分的气相色谱——质谱联用技术分析[J].食品科学,2003,24(6):120-121.
    [79]徐年军,白海波,严小军,等.山腊梅中挥发油成分分析[J].分析测试学报,2006,25(1):90-93.
    [80]孟祥颖,李向高,张宏.国产西洋参花蕾中挥发油的分离与鉴定[J].分析化学,2001,29(5):542-545.
    [81]孙文基,绳金芳.天然活性成分手册[M].北京:中国医药科学技术出版社,1998.
    [82]Shivaji V.More,M.N.V.Sastry,Chieh-Chieh Wang,et al.Molecular iodine:a powerful catalyst for the easy and efficient synthesis of quinoxalines[J].Tetrahedron Lett,2005,46:6345-6348.
    [83]黄凤洪,黄庆德,刘昌盛.肪酸的营养与平衡[J].食品科学,2004,25(增刊):262-265.
    [84]于海芹,张天柱,魏春雁,等.3种碱蓬属植物种子含油量及其肪酸组成研究[J].西北植物学报,2005,25(10):2077-2082.
    [85]Horrobin D.F.High levels of polyunsaturated fat may inhibit cancer growth[J].BMJ,1996,312(7029):511.
    [86]徐年军,白海波,严小军,等.山腊梅中挥发油成分分析[J].分析测试学报,2006,25(1):90-93.
    [87]陈华,辛广,张兰杰,等.没药中挥发性成分的酶提取及GC-MS分析[J].质谱学报,2007,28(3):152-157.
    [88]阎丽萍,高维平,曹玉波,等.由α-蒎烯异构β-蒎烯的合成方法[J].吉林化工学院学报,1997,14(2):6-8.
    [89]周永红,王延,宋湛谦.α-蒎烯合成杀虫增效剂的研究[J].林产化学与工业,1998,18(1):1-11.
    [90]曹兵,徐有仁,吕文,等.几种抗虫树种的化学成分分析及其抗虫机理的研究(Ⅳ)——几种生物活性物质的化学标样对天牛的毒杀作用[J].宁夏农林科 技,1997,(6):1-3.
    [91]胡喜兰,韩照祥,陶莹,等.DPPH·法测定17种植物的抗氧化活性[J].食品科技,2006,10:264-268.
    [92]Silva F A,Borges F,Guimaraes C,et al.Phenolic acids and derivatives:studies on the relationship among structure,radical scavenging activity,and physicochemical parameters[J].J Agric Food Chem,2000,48:2122-2126.
    [93]Frankel E N,Meyer A S.The problem of using one dimensionalmethods to evaluate multifunctional food and biological antioxidants[J].J Sci Food Agric,2000,8:1925-1941.
    [94]Cuvelier M E,Richard H,Berset C.Comparison of the antioxidative activity of some acid-phenols:structure-activity relationship[J].Biosci Biotechnol Biochem,1992,26:322-325
    [95]陈梅荣,丁惠堂,王晖,等.千里光不同方法提取物抑菌作用的研究[J].江西中医学院学报,2002,14(4):15.
    [96]汪劲松,潘继承.中草药千里光有效成分的提取及抑菌作用的研究[J].湖北师范学院学报(自然科学版),2000,20(3):48-50.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700