目的 建立同时测定人参首乌胶囊中8种人参皂苷类成分含量的高效液相色谱-蒸发光散射器检测法。方法 UltimateC18(4.6 mm×250 mm,5 μm)色谱柱,流动相为乙腈-水,梯度洗脱,流速1.0 mL·min-1,蒸发光散射检测器漂移管温度100 ℃,气体流量2.5 L·min-1,增益2。结果 人参皂苷Rg1、Re、Rb1、Rc、Rb2、Rb3、Rd、20(S)-Rg3分别在0.483~12.1、0.444~11.1、0.502~12.6、0.490~12.3 、0.455~23.2、0.464~11.6、0.264~13.2和0.244~12.2 μg内成良好的线性关系(r > 0.999 5),平均加样回收率分别为101.9%、104.5%、98.3%、97.9%、97.8%、101.2%、100.6%和99.0%。结论 该方法简便、准确、分离效果好,无干扰,可用于人参首乌胶囊的质量评价。
Abstract
To develop an HPLC-ELSD method for simultaneous determination of the contents of eight ginsenosides in Renshenshouwu capsules(traditional Chinese medicines). METHODS The analysis was performed on an Ultimate C18 column(4.6 mm× 250 mm,5 μm) eluted with mobile phase consisting of acetonitrile and water in gradient mode at a flow rate of 1.0 mL·min-1. The column temperature was set at 30 ℃. The ELSD drift tube temperature was set at 100 ℃,and the gas flow rate was set at 2.5 L·min-1. RESULTS Good linearity(r>0.999 5) was obtained in the range of 0.483-12.1 μg,0.444-11.1 μg,0.502-12.6 μg,0.490-12.3 μg,0.455-23.2 μg,0.464-11.6 μg,0.264-13.2 μg and 0.244-12.2 μg for ginsenoside Rg1,ginsenoside Re,ginsenoside Rb1,ginsenoside Rc,ginsenoside Rb2,ginsenoside Rb3,ginsenoside Rd and 20(S)- ginsenoside Rg3,respectively. The average recoveries of the eight compounds were 101.9%,104.5%,98.3%,97.9%,97.8%,101.2%,100.6% and 99.0 %,respectively. CONCLUSION The method is reliable,simple,precise, and can be used for the quality control of Renshenshouwu capsules.
关键词
人参首乌胶囊 /
人参皂苷 /
高效液相色谱-蒸发光散射器检测法 /
含量测定
{{custom_keyword}} /
Key words
Renshenshouwu capsules /
ginsenoside /
HPLC-ELSD /
assay
{{custom_keyword}} /
中图分类号:
R284
{{custom_clc.code}}
({{custom_clc.text}})
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1] Ch. P(2010)Vol Ⅰ(中国药典. 一部). 2010:439.[2] WANG L,ZHAO C J,WANG S H. Quantitative determination of ginseng saponing in Junchun le capsule by colormetric method . Chin Pharm J(中国药学杂志),1995,30(6):364-365.[3] XU X Y,ZHENG Y M,FU S Q,et al. Determination of twelve ginsenosides in Panax ginseng by HPLC . China J Chin Mater Med(中国中药杂志),2011,36(11):1463-1465.[4] ZHENG Y L,YANG C H,BAO J C,et al. Determination of ginsengnosides in dry Radix quinguefolii and Red Radix quinguefolii By RP-HPLC . Chin Pharm J(中国药学杂志),2006,41(9):1494-1496.[5] YANG X Q,ZHUO K J,CHEN J. Separation and determination of ginsenoside Rg1,ginsenoside Re and ginsenoside Rb1 in Radix et Rhizoma Ginseng by RRLC . Chin J Pharm Anal(药物分析杂志),2008,28(7):1144-1146.[6] HUANG Y W,WANG J H,JACQUELINE J,et al. Determination of total main ginsenosides contents in american ginseng and Chinese ginseng using near infrared spectroscopy . Chin J Anal Chem(分析化学),2011,39(3):377-381.[7] QIAN M, JIE Y, XIU M C, et al. Target separation of a new anti-tumor saponin and metabo- lic profiling of leaves of Panax notoginseng by liquid chromatography with eletrospray ionization quadrupole time-of-flight mass spectrometry. J Pharm Biomed Anal, 2012,59(5):67-77.[8] ZHANG H J,CAI X J,CHENG Y Y. Differentiation and authentication of saponin extracts from Panax ginseng,Panax quinquefolius and Panax notoginseng by HPLC/ESI-MSn[J]. Chin Pharm J(中国药学杂志),2006,41(5):391-394.[9] TOH D F,NEW L S,KOH H L,et al. Ultra-high performance liquid chromate- graphy/time-of-flight mass spectrometry (UHPLC/TOFMS) for time-dependent profiling of raw and steamed Panax notoginseng. J Pharm Biomed Anal,2010,52(11):43-50. BAI S S, LI J G, ZHE M F, et al. Simultaneous quantification of 19 ginsenosides in black ginseng developed from Panax ginseng by HPLC-ELSD. J Pharm Biomed Anal,2009,50(1):15-22. SU N K, YOUNG W H, HEUNGSOP S, et al. Simultaneous quantification of 14 ginsenosides in Panax ginseng C.A. Meyer(Korean red ginseng)by HPLC-ELSD and its application to quality control . J Pharm Biomed Anal,2007(45):164-170.
{{custom_fnGroup.title_cn}}
脚注
{{custom_fn.content}}
基金
国家“重大新药创制”科技重大专项资助项目(2012ZX09103-101-057);国家自然科学基金资助项目(21175031,20905019)
{{custom_fund}}