白术挥发油的提取、氧化分解及抗肿瘤研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
白术挥发油是白术的主要活性成分,因其抗肿瘤作用确切、不良反应小,具有开发成中药抗肿瘤新药的良好前景。挥发油性质不稳定、易氧化分解,给新药研发带来困难。针对上述,我们解决挥发油稳定性的研究思路是,让其尽快氧化分解,获得性质稳定的、具有抗肿瘤作用的白术挥发油。具体研究内容如下:
     1.筛选出白术挥发油最佳提取溶剂和不同提取方法的提取率,分别是乙酸乙酯(2.56%)和超临界CO2萃取(安徽产2.76%);筛选出最佳氧化分解条件为室外光照(19-27℃),HPLC跟踪检测苍术酮的分解率为98.08%。
     2.通过HPLC测定氧化分解前后白术挥发油中苍术酮、γ-榄香烯、β-桉叶醇、白术内酯Ⅰ和白术内酯Ⅲ五种抗肿瘤成分的含量。结果表明,氧化后苍术酮和γ-榄香烯的含量降为零,其它三种成分含量显著增加,其中β-桉叶醇的含量是超临界CO2萃取安徽产最高,是氧化分解前的1527.56倍,白术内酯Ⅰ、白术内酯Ⅲ的含量是水蒸气蒸馏提取河北产最高,是氧化分解前的4.30倍。
     3.采用GC-MS技术,对氧化分解前后及不同提取方法的白术挥发油化学成分及含量变化进行了分析比较。研究表明,氧化分解后主要抗肿瘤成分苍术酮和γ-榄香稀的含量平均分别降低了95%和98%,而白术内酯Ⅰ、白术内酯Ⅲ、广木香内酯、β-桉叶醇和Isovelleral五种成分的总增加量是氧化分解前的3.68-11.04倍。
     4.采用电感耦合等离子体发射光谱(ICP-AES)对白术生药、挥发油和氧化分解挥发油中Mg, Al、Fe、Cr、Cu、Mn、Ni、Sr、Ti和Zn10种微量元素的含量进行了测定。结果在不同提取方法中,各微量元素含量变化较大。
     5.采用细胞生物学方法研究氧化分解前后白术挥发油对人源卵巢癌细胞SKOV-3的抗肿瘤作用。结果表明,抑制细胞增殖与诱导凋亡呈时间和剂量依赖关系,MTT法测定表明以挥发油浓度200mg/L抑制率最高,不同浓度以作用72h抑制率最明显;采用流式细胞仪测定氧化分解前后白术挥发油对SKOV-3细胞凋亡和细胞周期的影响,结果挥发油浓度为150mg/L凋亡率最高,细胞周期分别阻滞在G2/M期和S期。
Volatile oil is the main active ingredient of the Atractylodes macrocephala Koidz. Because of its exact antitumor effects and small side effects, it has a good prospect in antitumor drugs. However, the unstableness and easy oxidation make the drug discovery difficult. In response to these, the approach we are taking to solve the stability problem of volatile oil is to let it go through quick oxidation and decomposition, turning into volatile oil with anti-tumor effects. The specific contents of the research are as follows.
     1. It was found that the best extraction solvent of Volatile oil is ethyl acetate (2.56%) and the best extraction methods is supercritical CO2 extraction (2.76%). The optimum conditions of oxidation and decomposition is outdoor light (19-27℃), The decomposition rate of atractylone is 98.08%.
     2. Five anti-tumor components of Volatile Oil before and after oxidative decomposition from Atractylodes macrocephala Koidz were determinated by HPLC. The results showed that atractylone andγ-elemene content was zero after oxidation, the other three components were significantly increased,β-eudesmol content in Volatile Oil by supercritical CO2 extraction was the highest from Anhui,1527.56 times higher than that before oxidative decomposition. AtractylenolideⅠ、Ⅲcontent was the highest by steam distillation from Hebei and 4.30 times higher than that before oxidation.
     3. GC-MS were employed to analsis ingredients and contents of Volatile Oil before and after oxidative from Atractylodes macrocephala Koidz with different method. The results show that the main anti-tumor component of Volatile Oil after oxidative decomposition, the content of atractylone andγ-elemene was decreased by 95% and 98%, while the increment of atractylenolideⅠ, atractylenolideⅢ, costunolide,β-eudesmene and Isovelleral is 3.68-11.04 times more than that before oxidation Volatile Oil.
     4. Content of 10 kinds of trace elements(Mg,Al,Fe,Cr,Cu,Mn,Ni,Sr,Ti,Zn)in Atractylodes macrocephala Koidz, volatile oils and volatile oil of Oxidative decomposition was determined by ICP-AES. The results indicate that there existed greatly difference in different extraction conditions.
     5. This experiment researched the effect on the ovarian cancer cell SKOV-3 of Volatile Oil before and after oxidative decomposition from Atractylodes macrocephala Koidz. The volatile oil has the function of proliferation inhibition of ovarian cancer cell, and this effect is in dose and time dependent manner. Affer dealing with the concentrations of 200mg/L, it had highest inhibition rate,and it were significant after 72 hours at different concentrations. Effects on skov-3 apoptosis and cell cycle induced by volatile oil of atractylodes macrocephala koidz before and after oxidative decomposition was studied by Flow Cytometry. Affer dealing with the concentrations of 200mg/L it had highest apoptosis rate, a cell cycle-specific in G2/M and S phase, respectively.
引文
[1]王郁金,苏衍进,郑广娟.白术挥发油对小鼠H22肝癌淋巴道转移模型的影响[J].现代中医药,2009,29(4):74-75.
    [2]段启,许冬谨,刘传祥,李成龙.白术的研究进展[J].中草药,2008,39(5):4-6.
    [3]中华人民共和国药典委员会.中华人民共和国药典一部[M].北京:化学工业出版社,2005:68-69.
    [4]张宗,张鸿翔,史天良,刘玉瑛.白术挥发油抗肿瘤作用的研究[J].肿瘤研究与临床,2006,18(12):799-800
    [5]杜永辉,史天良,米振国.白术挥发油对人类膀胱肿瘤细胞T24生物学行为的研究[J].肿瘤研究与临床,2008,20(2):80-82.
    [6]张强,李章万.白术挥发油成分的分析[J].华西药学杂志,1997,12(2):119-120.
    [7]陈柳蓉,邵青.紫外分光光度法测定白术中苍术酮含量[J].浙江医科大学学报,1996,25(6):270-271.
    [8]乔小云,李俏,陆晓和.白术挥发油提取工艺研究[J].医药导报,2001,9(20)551-552.
    [9]崔庆新,董岩,王怀生.白术挥发油化学成分的GC/MS分析[J].药物分析杂志,2006,26(1):124-126.
    [10]邱琴,崔兆杰,刘廷礼,张善东.白术挥发油化学成分的GC-MS研究[J].中草药,2002,33(11):980-981.
    [11]闫克里,刘玉英,史天良.气-质联用对不同提取法的白术油化学成分的分析[J].中国药物与临床,2002,2(5):339-340.
    [12]周日宝,吴佳,童巧珍,刘叶曼,刘湘丹.不同提取方法中白术挥发油成分的比较研究[J].中药材,2008,31(2):229-232.
    [13]吴佳,周日宝,童七珍,潘清平,刘湘丹,陈玉秀.不同采收时期白术挥发油比较研究[J].湖南中医药大学学报,2007,27(4):40-42.
    [14]吴素香,吕圭源,李万里.白术超临界CO2萃取工艺及萃取物的化学成分研究[J]. 中成药,2005,27(8):885-887.
    [15]王芳.白术挥发油有效成分提取及氧化动力学研究[D].西北大学,2005,12-13.
    [16]郑建珍,刘文涵.不同白术栽培品种挥发油化学成分的GC-MS分析[J].中国药房,2010,21(31):2924-2926.
    [17]周枝凤,沈菊文,龚范,梁逸曾,邱细敏.白术挥发油成分分析及其色谱指纹图谱研究初探[J].中草药,2004,31(1):5-8.
    [18]彭万仁,成诚GC-MS法分析白术挥发油化学成分的探讨[J].四川职业技术学院学报,2006,16(3):114-115.
    [19]刘磊,杨艳.电感耦合等离子体-原子发射光谱法测定中药中微量元素[J].光谱实验室,2010,27(5):1964-1967.
    [20]惠坚.微量元素与中药功效[J].中国医院药学杂志,1991,11(6):268-269.
    [21]汤洪波,周健,李君邻.原子吸收分光光度法测定赣产白术中微量元素[J].微量元素与健康研究,2008,25(6):55-56.
    [22]姚艳红,许桂花,张敬东,李承范,李东浩.长白山区野生、种植贝母和白术中微量元素的ICP-MS对比分析[J].光谱学与光谱分析,2008,28(5):1165-1167.
    [23]霍建中,季文月.微波消解ICP-AES法测定白术中常量及微量元素[J].精细石油化工,2007,24(2):62-64.
    [24]曾亮,陈孟兰,汪延磊,余丹.黄芪、白术、防风及玉屏风散中微量元素研究[J].时珍国医国药,2007,18(8):1849-1850.
    [25]朱庆均,郑广娟,等.白术对S180荷瘤小鼠瘤组织p53基因表达的影响[J].山东中医药大学学报,2004,28(5):387-388
    [26]王郁金.白术挥发油抗肿瘤增殖和转移的实验研究[D].济南:山东中医药大学,2004.
    [27]杜永辉,史天良,米振国.白术挥发油对人类膀胱肿瘤细胞T24生物学行为的研究[J].肿瘤研究与临床,2008,20(2):80-82.
    [28]关晓辉,曲娴,杨志萍,等.白术挥发油对小鼠免疫功能的影响[J].北华大学学报(自然科学版),2001,2(2):122-124.
    [29]朱庆均.白术挥发油对人肺癌细胞株增殖和细胞周期的影PG细胞响[J].中国中医药科技,2008,15(6):428-429.
    [30]Wang CC, Chen LG, Yang LL. Cytotoxic activity of sesquiterpenoids from At ractylodes ovata on leukemia cell lines.[J]. Plant Med.,2002,68 (3):204-8.
    [31]Wang C C, Lin S Y,Cheng H C,et al. Pro-oxidant and cytotoxic activities of atractylenolide I in human promyeloleukemic HL-60 cells[J]. Food and Chemic al Toxicology,2006,44:1308-1315.
    [32]Liu Y, Jia Z, Dong L, et al. A Randomized Pilot Study of Atractylenolide I on Gastric Cancer Cachexia Patients[J]. Evid Based Complement Alternat Med. 2008,5(3):337-344.
    [33]刘呋,叶峰,邱根全等.白术内酯Ⅰ对肿瘤恶病质患者细胞因子和肿瘤代谢因子的影响[J].第一军医大学学报,2005,25(10):1308-1311.
    [34]Hiroshi Tsuneki, En-Long Ma, Shinjiro Kobayashi, et al.Antiangiogenic acti vity of β-eudesmol in vitro and in vivo. European Journal of Pharmacology 5 12 (2005) 105-115.
    [35]Isabelle Aujard, Daniel Ro"me, Erwan Arzel, Martin Johansson, Dick de Vos, Olov Sterner. Tridemethylisovelleral, a potent cytotoxic agent[J]. Bioorga nic & Medicinal Chemistry,2005,13:6145-6150.
    [36]Jung-Hye CHOI, Kyung-Tae LEE. Costunolide-Induced Apoptosis in Human L eukemia Cells:Involvement of c-Jun N-Terminal Kinase Activation[J]. Biol. Pha rm. Bull,2009,32(10):1803-1808.
    [37]许浪,刘丹,晏丹,李玉红.榄香稀对肺癌细胞凋亡的影响[J].数理医药学杂志,2009,22(2):154-155.
    [38]Li CQ,He LC,J in J Q, et al 1At ractylenolide I and At r-actylenolide III inhibit lipopolysaccharide-induced TNF-αand NO production in macrop ha ges [J]. Phy -tot he rapy Research,2007,21 (4):347.
    [39]李伟,文红梅,崔小兵等.白术健脾有效成分研究[J].南京中医药大学学报,2006,22(6):366.
    [40]马恩龙[3-Eudesmol抗血管形成及抗肿瘤作用的研究[D].沈阳药科大学,2005.
    [41]王金华,薛宝云,梁爱华,王岚,付梅红,叶祖光.苍术有效成分β-桉叶醇对小鼠小肠推进功能的影响[J].中国药学杂志,2002,37(4):266-268.
    [42]郝延军,桑育黎,李宝林,等.苍术酮的常温稳定性研究[J].中成药,2007,29(6):895-896.
    [43]杨美华,龚红梅.储存温度对白术药材中苍术酮含量的影响[J].江西中医学院学报,2005,17(3):46.
    [44]王小芳,王芳,张亚环,等.白术挥发油中苍术酮氧化反应的动力学[J].应用化学,2007,24(3):301-305.
    [45]朱秀卿,阎克里,赵丽.白术挥发油及其有机溶液稳定性动力学研究[J].中国药物与临床,2010,10(6):632-634.
    [46]HikinoH, Hikino Y, Yosioka I. Studies on the constituents ofAtractylodesⅣ. S tructure and autoxidation of atractylone[J]. Chem Pharm Bull,1964,12(7):755.
    [47]刘友平,秦春梅,鄢丹.β-环糊精包合物在中药学领域中的应用进展[J].中草药,2003,34(7):61.
    [48]荣立新,孙晖,王克君.环糊精在药剂学上的应用[J].中国药学杂志,2000,35(10):7091.
    [49]陈晓灵,李祥.正交试验法研究白术挥发油提取及β-环糊精包合工艺[J].河北医药,2006,28(3):228-229.
    [50]王宇环,居明乔,王红,丰衍增.β-环糊精包合白术挥发油的工艺研究[J].制剂于质量,2000,23(12):767-768.
    [51]葛亮,张志国.白术挥发油β-环糊精包合物的工艺研究[J].中国药业,2008,17(3):27-28.
    [52]王艳霞,彭善祥.正交法优选β-环糊精包合白术挥发油的工艺研究[J].广西中医药,2004,27(3):59-60.
    [53]徐先顺,夏厚林,彭玉秀.白术挥发油包合前后化学成分的研究[J].西南民族大学学报自然科学版,2004,30(6):718-720.
    [54]余丽丽,杨星昊,李春成.白术挥发油/β2环糊精包合物的表征[J].中国药学杂志,2005,40(2):90-93.
    [1]崔庆新,董岩,王怀生.白术挥发油化学成分的GC/MS分析[J].药物分析杂志,2006,26(1):124-126.
    [2]陈柳蓉,邵青.紫外分光光度法测定白术中苍术酮含量[J].浙江医科大学学报,1996,25(6):270-271.
    [3]汤得芳,郝玉珩,刘佐雅.平江白术根茎挥发油的成分及其抑瘤作用研究[J].药学通报,1984,19(9):43.
    [4]李伟,文红梅,张爱华,葛建华,吴皓.白术质量标准研究-HPLC法测定2种白术内酯的含量[J].药物分析杂志,2001,21(3):170-172.
    [5]Li CQ,He LC,J in J Q, et al 1 At ractylenolide I and At r-actylenolide III inhibit lipopolysaccharide-induced TNF -αand NO production in macrop hages [J]. Phy-tot he rapy Research,2007,21 (4):347.
    [6]Hiroshi Tsuneki, En-Long Ma, Shinjiro Kobayashi, et al.Antiangiogenic activity of β-eudesmol in vitro and in vivo. European Journal of Pharmacology 512 (2005) 105-115.
    [7]汤秀红,秦叔逵,谢恬.榄香烯注射液抗肿瘤作用基础研究的现状和进展[J].临床肿瘤学杂志,2010,15(3):266-273.
    [8]周日宝,吴佳,童巧珍,刘叶曼,刘湘丹.不同提取方法中白术挥发油成分的比较研究[J].中药材,2008,2(31):229-232.
    [9]国家药典委员会,中华人民共和国药典,一部,北京:化学工业出版社,2005: 68-69.
    [10]乔小云,李俏,陆晓和.白术挥发油提取工艺研究[J].医药导报,2001,9(20):551-552.
    [11]刘胜姿,魏万之,邱细敏,凌晓.不同提取方法对白术油气相-质谱指纹图谱的影响[J].湖南师范大学学报(医学版),2004,1(1):53-55.
    [1]张强,李章万,白术挥发油成分的分析[J].华西药学杂志,1997,12(2):119-120.
    [2]张晓川,陈琴华,朱军.白术超临界C02流体萃取部位脂溶性成分的GC/MS分析[J].中国药房,2006,17(23):1836.
    [3]周枝凤,沈菊文,龚范,梁逸曾,邱细敏.白术挥发油成分分析及其色谱指纹图谱研究初探[J].中草药,2004,1(35):5-8.
    [4]崔庆新,董岩,王怀生.白术挥发油化学成分的GC/MS分析[J].物分析杂志,2006,26(1):124-126.
    [5]邱琴,崔兆杰,刘廷礼,张善东.白术挥发油化学成分的GC-MS研究[J].中草药,2002,11(33):980-981.
    [6]周日宝,吴佳,童巧珍,刘叶曼,刘湘丹.不同提取方法中白术挥发油成分的比较研究[J].中药材,2008,2,2(31):229-232.
    [1]赵先文,韩存芝,荆洁线.微量元素与肺癌的关系及临床应用[J].中华流行病学杂志,1998,19(5):286-289.
    [2]Gupea SK, Shukla VK, Vaidya M P, etal. Serum t race element s and CU/ZN ratio in breast cancer patients [J]. J Surg Oncol,1991,46(3):178-181.
    [3]单金缓,王秀梅,丁良.中草药中硒的生物功能及测定方法研究进展[J].中草药,2003,34(3):280.
    [4]陈国翠,张达生,张光明,刘遗德.血清微量元素铜锌与卵巢肿瘤关系的初步探讨[J].医学新知杂志,1994,4(1):15-17.
    [5]李光城,吴应荣,黄宇营.肺癌、宫颈癌细胞凋亡前后微量元素的变化[J].光谱学与光谱分析,2000,20(2):240-242.
    [6]张颖,李秀.微量元素铜锌硒与肺癌的关系探讨[J].微量元素与健康研究,2000,17(3):15-17.
    [7]成慧娟,靳白玉.微量元素对癌症的影响[J].甘肃医药,2008,27(5):13-14.
    [8]贺祝英,魏惠芬,邱德文,张元利,梁光义.大果木姜子无机元素的测定与其精油中无机元素的分析比较[J].微量元素与健康研究,1995,12(4):38-39.
    [9]张丙生,王钦源.大黄挥发油中金属元素分析[J].微量元素与健康研究,1999,16(1):53-54.
    [1]Wang KF, Cui H, Feng J, et al. Effect of reduced expression of Her2 by RNA interference on the biological characters of ovarian carcinoma cells[J]. Zhonghua Fu Chan Ke Za Zhi, 2008 Aug,43 (8):622-625.
    [2]陈刚,李静,等.反义PTTG真核表达载体对人卵巢癌细胞SKOV-3恶性表形的抑制作用[J].癌症,2003,22(10):1009-1013.
    [3]Wang C C, Lin S Y, Cheng H C, et al. Pro-oxidant and cytotoxic activities of atractylenolide I in human promyeloleukemic HL-60 cells[J]. Food and Chemical Toxicology,2006,44:1308-1315.
    [4]Li C Q, He L C, Jin J Q. Atractylenolide I and Atractylenolide III Inhibit Lipopolysaccharide-induced TNF-a and NO Production in Macrophages[J]. Phytotherapy Research,2007,21(4):3471.
    [5]Ohshima H, Tatemichi M, Sawa T. Chemical basis of inflammation-induced carcinogenesis. Arch Biochem Biophys.2003,417:3-11.
    [6]Anna JM, Jacek S, Tomasz S, Jakub G, Witold L.Antitumor effects of sulindac in ovarian cell cultures.[J]. GINEKOLOGIA POLSKA,,2011,82(3):195-199.