远志药材及其炮制品的质量研究
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摘要
目前中药的质量控制研究是中药热点研究问题之一。远志为大宗常用药材,临床应用以制远志为主要规格。近年来由于市场需求猛增,而野生资源急剧减少,栽培品供应有限,商品质量明显下降,直接影响到远志的临床疗效。因此,远志药材及其炮制品的质量控制研究就成为行业亟待解决的问题。本文采用单一指标成分测定、指纹图谱技术结合现代统计学方法,对远志及制远志进行了质量控制研究,期望为远志药材及其饮片的质量控制提供参考。本文共分四章,作者的主要贡献如下:
     1.采集了18个产地野生远志样品和5个主产区的栽培样品,采用HPLC法测定了其中远志皂苷元的含量,野生品含量在0.13%~0.50%之间,栽培品含量在0.32%~0.42%之间;建立了远志药材的HPLC指纹图谱,并对色谱峰进行了聚类分析,结果野生和栽培远志的指纹谱一致,聚类结果与传统道地产区的记载相一致。在此基础之上,采用多元逐步回归法对远志不同药用部位和商品规格进行成分群分析,获得远志质量等级的拟合评价公式。本研究可用于远志的质量评价及新资源开发。
     2.以远志皂苷元(C_(30)H_(45)O_6Cl)和甘草酸(C_(42)H_(62)O_(16))为指标,采用L_9(3~4)正交试验法,考察了制远志的炮制工艺。最佳炮炙工艺为:取甘草6份,加水煎煮3次,每次30分钟,合并滤液,浓缩至远志量的2.5倍体积,加入净远志100份,140℃浸润90分钟,取出,100℃烘干;根据20批中试实测结果,制定了制远志专属性的质量标准,暂定制远志中远志皂苷元(C_(30)H_(45)O_6Cl)不得少于0.30%,甘草酸(C_(42)H_(62)O_(16))不得少于0.03%。本研究为制远志工艺规范化提供了相应的技术参数和质量控制指标。
     3.采用指纹图谱技术结合变异系数法,对制远志和生远志、远志-甘草(100:6)及蜜远志进行了比较分析,三种规格及配伍具有23个共有色谱峰;制远志的变异最大,其变异与2个色谱峰(CV>2.02)关系密切。
To establish the evaluating index and method of principal component for quality control in Polygala tenuifolia Willd,Our article analyzed the wild Polygala tenuifolia、cultivated Polygala tenuifolia、commercial PolygaIa tenuifolia and the Processed Radix Polygalae by HPLC fingerprint、Statistica and content mensuration.The results are almost consistent with chronically using.Then,seven ranks of Polygala tenuifolia samples from Ping Yao of Shanxi were analyzed by HPLC with gradient elution. Clustering method and Principal Component Analysis(PCA)were processed according to the peak area.We owned the evaluating equation.This method confirms the conclusion that Polygala tenuifolia has many effective components,demonstrating that it can be used for the quality evaluation and development of new resource of POlygala tenuifolia.
     Besides,one orthogonal test was employed to determine the effects of the three factors.The content of senegenin(C_(30)H_(45)O_6Cl)and glycyrrhizic acid(C_(42)H_(62)O_(16))were determined by HPLC.The best decoction techinics was satifued with some conditions as follows:Adding 100mL water to Glycytthizae,its baking time was 30min,baking three times.The best preparative technics was satisfied with some conditions as follows:Adding 2.5 multiple Radix Glycytthizae-water to Radix Polygalae,its baking time was 90min.baking temperature was 140℃,and drying temperature was 100℃. This research is meaningful to standardization of stir-bake with Radix Glycytthizae on Radix Polygalae.Furthermore,we had constituted a special standard for Processed Radix Polygalae.
     HPLC fingerprint and Coefficient of Variance were used to analysis Radix Polygalae and Processed Radix Polygalae.The result showed that the Processed Radix Polygalae was the most variation.
引文
[1]中国药材公司,中国测绘科学研究院编.中国药材资源地图集[M].科学出版社.1995:48.
    [2]姜勇,屠鹏飞.远志的化学成分研究(Ⅰ)[J].中草药.2002,33(10):874-877.
    [3]姜勇,屠鹏飞.远志的化学成分研究(Ⅱ)[J].中国中药杂志.2004,29(8):751-753.
    [4]姜勇,刘蕾,屠鹏飞,远志的化学成分研究(Ⅲ)[J].中国天然药物,2003,1(9):142-145.
    [5]王玉萍,杨峻山,张聿梅等.远志的化学成分研究[J].中草药,2005,36(9):1291-1293.
    [6]李萍,闫明,李平亚.远志化学成分的分离与鉴定[J].中国药物化学杂志,2005,15(1):35-38.
    [7]Ikeya Yukinobu,Sugama Ko,Okuda Minoru,et al.Two xanthones from Polygala tenuifolia[J].Phytochemistry,1991,30(6):2061-2065.
    [8]Fujita T,Liu DY,Ueda S,et al.Xanthones from Polygala tenuifolia[J].Phytoch emistry,1992,31(11):3997-4000.
    [9]Ito H,Taniguchi H,Kita T,et al.Xanthones and acinnamic acid derivatives from Polygala tenuifolia[J].Phytochemistry,1977,16(10):1614-1616.
    [10]Miyase T,Ueno A.Sucrose derivative from Polygala tenuifolia[J].Shoyakugaku Zasshi,1993,47(3):267-278.
    [11]Ikeya Y,Sugama K,Okada M,et al.Four new phenolic glycosides from Polygala Tenuifolia Willd[J].Chem Pham Bull.1991,39(10):2600-2605.
    [12]Mao S L,Liao S X,Wu J H,et al.Studies on chemical constituents of Polygala arillata Buch-Ham[J].Acta Phama Sin,1996,31(2):118-121.
    [13]Anne-Claire,Tomofumi Miyamoto,et al.Triterpene Saponins from Four Species of the Polygalaceae Family[J].HELVETICA CHIMICA ACTA.2005,88:2986-2995.
    [14]DENG Shi-ming,YANG Xian-hui,et al.New Xanthones from Polygala crot alarioides[J].CHEM.RES,CHINESE U.2006,22(3):400-402.
    [15]金宝渊,朴政一.远志生物碱成分的研究[J].中国中药杂志.1993,18(11):675-677.
    [16]沈行良,Witt MR Dekermendjian K et al.从远志中分离鉴定出1种多巴胺受体活性化合物[J].海南医学院学报.2004,10(3):133-135.
    [17]孙晓飞,时素琴,杨国红.远志脂肪油的成分分析[J].中药材.2000,23(1):35-37.
    [18]WeiDong Zhang,TingZhao Li,et al.A new cerebroside from Polygala japonica.Firorerapia.2006,77:336-337.
    [19]彭汶铎.四种远志皂苷的镇咳和祛痰作用[J].中国药学杂志.1998,3(8):491.
    [20]彭汶铎.四种远志皂苷的镇咳和祛痰作用[J].中国药学杂志.1998,3(8):491.
    [21]聂淑琴.远志中前体药物的筛选[J].国外医药·中医中药分册.1996,18(6):39-44.
    [22]郑良朴.远志-石菖蒲水煎合剂对U_半乳糖导致小鼠衰老作用的实验研究[J].福建中医药.2002,33(4):35-36.
    [23]陈勤.远志皂对淀粉样肽鹅膏蕈氨酸引起的胆碱能系统功能降低的影响[J].药学学报.2002,37(12):913-917.
    [24]饭冢进.远志的脑保护活性成分[J].国外医学·中医药学分册,1995,17(5):29.
    [25]彭汶铎.远志皂苷的降压作用及机制[J].中国药理学报.1995,17(5):29-32.
    [26]彭汶铎.远志皂苷H对离体平滑肌与心脏的作用[J].中国药学杂志.1999,34(4):241-243.
    [27]杨学东.植物中酮类成分及药理研究进展[J].天然产物的研究与开发.2000,123(5):90-93.
    [28]朱玉琢.中草药对实验性小鼠雄性生殖细胞遗传物质损伤的保护作用[J].吉林大学学报(医学版).2003,29(3):258-259.
    [29]刘德祥.102种中药水溶性提取物的抗诱变性筛选[J].中国中药杂 志.1990,15(10):41-46.[30]马俊英,苏木.15种中草药水提液体外对HL-60,Yac-1,K562,1929的细胞毒作用[J].天津医药.1990,1:41-42.
    [31]刘晓义.远志的炮制沿革及现代研究.基层中药杂志.1996,10(2):17.
    [32]李明贵.远志不同炮制方法的分析[J].海峡药学.2005,27(5):80-81.
    [33]李光巍,杨吉奎,沈秀英等.远志的炮炙研究[J].黑龙江中医药.1994,5:42.
    [34]李希,谢守德.远志不同工艺的研究[J].四川中医.2002,20(3):19-20.
    [35]姜勇等.远志研究进展[J].中草药.2001,32(8):759.
    [36]彭汶泽.远志皂苷的降压作用及其机制[J].中国药理学报.1999,20(7):639-642.
    [37]刘慧茹,唐家福,肖辉.甘草制远志不同炮制品远志皂苷的HPLC法测定[J].中国中医药科技,2000,7(4):235.
    [38]国家中医药管理局<中华本草>编委会.中华本草[M].上海:上海科学出版社,1998:1096.
    [39]王建.郭娟.刘贤武等.生远志及与甘草不同配伍比例对小鼠胃肠运动的影响.中药药理与临床.2002,18(5):27.
    [40]王建.郭娟.武云.远志不同炮制品对胃肠运动及消化功能能得影响.中药药理与临床.2006,22(3、4):120-122.
    [41]姜勇,张娜崔振等.远志药材的HPLC指纹图谱[J].药学学报.2006,41(2):179-183.
    [41]孙磊,王玉蓉.星点设计-效应面法优选远志的提取工艺[J].中成药.2006,28(3):328-331.
    [42]刘友平,万德光,鄢丹等.大孔吸附树脂纯化远志皂苷工艺研究[J].中国实验方剂学杂志.2004,10(6):3-6.
    [43]孙文基,沙振方,向红红.远志及其制剂中远志皂苷元的薄层扫描法测定[J].中成药.1990,12(5):15-16.
    [44]刘友平,万德光,黄荣,等.薄层扫描法测定远志中远志皂苷元的含量[J].中草药.2000,3l(7):512-514.
    [45]刘友平,万德光,刘涛,等.分光光度法测定不同产地远志总皂苷的含量[J].成都中医药大学学报.2000,23(2):46-47.
    [46]杨国红,孙晓飞.反相高效液相色谱法测定远志中远志皂苷元的含量[J].药物分析杂志.2001,21(4):260-263.
    [47]刘友平,万德光,宋英.HPLC法测定远志中去羟基远志皂苷元含量[J].中草药.2001,32(9):786-787.
    [48]周玉新.现代中药鉴定技术[M].北京:化学工业出版社.2004.
    [49]蔡宝昌,刘训红主编.常用中药材HPLC指纹图谱测定技术[M].北京:化学工业出版社,2005.
    [50]Wagner.H,Norman Farnsworth.Economic and Medicinal Plant Research [J],1995,5:253-231.
    [51]孙振球主编.医学统计学[M].北京:人民卫生出版社.2006.
    [52]江苏新医学院.中药大词典[M].上海:上海科学技术出版社.1985,(上册):1028-1030.
    [53]江苏新医学院.中药大词典.上海:上海科学技术出版社.1985,(上册):1028-1030.
    [54]陈承,裴宗元,陈师文编.增广太平惠民和剂局方[M].2002:411-412.
    [55]Wang.ss,Koji KOZUKA,Ken-ini SAITO etc.Pharmacological properties of galenical preparations(Ⅹ Ⅶ):Active compounds in blood and bile of rats after oral administrations of extracts of Polygalae Radix[J].Journal of Traditional Medicinen 11,44-49,1994.
    [56]Wang ss,Koji KOZUKA,Ken-ini SAITO,etc.Pharmacological properties of galenical preparations(Ⅹ Ⅶ):Pharmacokinetics of active compounds of Polygalae Radix[J].Journal of Traditional Medicinen 11,168-175,1994.
    [57]Wang ss,Ken-ini SAITO,Eiji OWADA,etc.Pharrnacological properties of galenical preparations(Ⅹ Ⅹ):Acreening of natural prodrugs in Polygalae Radix[J].Journal of Traditional Medicinen 12,102-108,1995.
    [58]杨学东.植物中酮类成分及药理研究进展[J].天然产物的研究与开发.2000,123(5):90-93.
    [59]朱玉琢.中草药对实验性小鼠雄性生殖细胞遗传物质损伤的保护作用[J].吉林大学学报(医学版).2003,29(3):258-259.
    [60]刘德祥.102种中药水溶性提取物的抗诱变性筛选[J].中国中药杂志.1990,15(10):41-46.
    [61]马俊英,苏木.15种中草药水提液体外对HL-60,Yac-1,K562,1929的细胞毒作用[J].天津医药.1990,1:41-42.
    [62]刘晓义.远志的炮制沿革及现代研究.基层中药杂志.1996,10(2):17.
    [63]李明贵.远志不同炮制方法的分析[J].海峡药学.2005,27(5):80-81.
    [64]李光巍,杨吉奎,沈秀英等.远志的炮炙研究[J].黑龙江中医药.1994,5:42.

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