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HPLC法同时测定紫果西番莲叶提取物异荭草素与荭草素的含量 被引量:1

HPLC Determination of Isorientin and Orientin in Passiflora Incamata Extract Simultaneously
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摘要 目的建立紫果西番莲叶提取物中异荭草素和荭草素的含量测定方法。方法采用HPLC法。Inertsil C18色谱柱(4.6mm×250mm,5μm);流动相:水-四氢呋喃-异丙醇-乙腈(87∶8∶2∶3);柱温:30℃,流速:1mL/min;检测波长:360nm。结果异荭草素、荭草素回归方程:Y=2.901×104X-188.1,r=0.999 8;Y=1.824×104X-228.83,r=0.999 5;线性范围分别为0.012~0.602、0.009~0.451mg.mL-1。平均回收率分别为100.09%、98.66%,RSD分别为2.10%、1.81%。结论HPLC法测定紫果西番莲叶提取物中异荭草素和荭草素的含量,专属性强、精密度好、操作简单、准确性高。 Aim To establish a method for detecting isorientin and orientin by HPLC. Methods The chromatographic conditions include the Intersil C18 column and a mobile phase consisting of a trinal aquatic solution , i. e. H2O-tetrahydrofuran-isopropanol-acetonitrile (87: 8: 2:3 ). The flow rate was 1.0mL/min. The detection wave- length was 360nm. The temperature was 30℃. Results The regression equation for isorientin and orientin was:Y = 2.901 × 10^4X - 188.1, ( r = 0.999 8) ; Y = 1. 824 × 10^4X - 228.83 ( r = 0. 999 5 ) respectively ; the linear range was 0.012 -0. 602mg.mL^-1 ,0.009 - 0. 451mg.mL^-1 respectively; the average recovery ( RSD ) was 100.09% (2.10) ,98.66% ( 1.81 ) respectively. Conclusions The method is rapid ,accurate and reliable.
出处 《解放军药学学报》 CAS 2009年第5期443-445,共3页 Pharmaceutical Journal of Chinese People's Liberation Army
基金 广州市科委基础性研究计划项目 No.2005J1-C0352
关键词 紫果西番莲叶 异荭草素 荭草素 含量测定 HPLC passiflora incamata extract isorientin orientin content determination HPLC
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参考文献5

  • 1潘琢,郑穗平.两种西番莲的化学成分及药理活性研究进展[J].现代食品与药品杂志,2007,17(2):5-9. 被引量:29
  • 2周玉娟,谈锋,邓君.西番莲属植物的研究进展[J].中国中药杂志,2008,33(15):1789-1793. 被引量:60
  • 3云南省药材公司.云南中药资源目录[M].北京:科学出版社,1993:366.
  • 4Dhawan K,Dhawan S,Shama A.Passiflora:a review update[J].Journal of Ethnopharmacology,2004,94:1.
  • 5Andrea Raffaelli,Gloriano Moneti,Valentina Mercati,et al.Mass spectrometric characterization of flavonoidas in extracts from passiflora in carnata[J].journal of chromatography A,1997,777:223.

二级参考文献77

  • 1吴均秀.浅谈西番莲及其发展前景[J].广西热作科技,1994(1):43-46. 被引量:15
  • 2陈惠芳.植物药数据库[J].国外医药(植物药分册),2005,20(6):270-273. 被引量:10
  • 3Gavasheli NM,Moniava Ⅱ.Flavonoids from P.incarnata[J].Khimiya Prirodnykh Soedinenii,1974,10:95-96.
  • 4Lutomski J,Segieg E,Szpunar K,et al.Die Bedeutung der Passionsblume in der Heilkunde.Importance of Passion flower in the therapeutics[J].Pharmazie in Unserer Zeit,1981.10:45-49.
  • 5Kamaldeep Dhawan,Sanju Dhawan,Anupam Sharma.Passiflora:a review update[J].Journal of EthnopharmacologY,2004,94:1-23.
  • 6Menghini A,Capuccella M,Mercati V,et al.Flavonoids contents in Passiflora spp[J].Pharmacology ResearchCommunications,1993,27:13-14.
  • 7Poethke VW.,Schwarz C,Gerlach H.Substances of Passiflora incarnata Lin.(Constituents of Passiflora bryonioides)[J].Alkaloids Planta Medica,1970,18:303-314.
  • 8Bennati E.Quantitative determination of harman and harmine in P.incarnata extract[J].Bollettino Chimico Farmaceutico,1971,110:664-669.
  • 9Tsuehiya H,Hayashi H,Sato M,et al.Quantitative analysis of all types of beta-carboline alkaloids in medicinal plants and dried edible plants by.high performance liquid chromatography with selective fluorometric detection[J].Phytochemical Analysis,1999,10:247-253.
  • 10Aoyagi N,Kimura R,Murata T.P.incarnata dry extract.Ⅰ.Isolation of maltol and pharmacological action of maltol and ethyt maltol[J].Chemical and Pharmaceutical Bulletin,1974,22:1008-1013.

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