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作 者:陈玉平[1] 石任兵[1] 刘斌[1] 孙建宁[1] 王永炎[2]
机构地区:[1]北京中医药大学中药学院,北京100102 [2]中国中医科学院
出 处:《北京中医药大学学报》2007年第3期191-195,共5页Journal of Beijing University of Traditional Chinese Medicine
基 金:北京市教委产学研重点项目
摘 要:目的建立血浆中清脑宣窍方有效部位中栀子苷、人参皂苷Rg1、Rb1及三七皂苷R1的HPLC血药浓度测定方法。方法血浆样品用C18固相柱萃取,以亥茅酚苷为内标,选用Agilent Eclipse XDB—C18色谱柱(4.6mm×250mm,5um),流动相为乙腈-水二元梯度洗脱,柱温为30℃;流速为1.0mL/min;检测波长为203nm。结果各成分的最低检测浓度(S/N〉3)在0.2~0.9mg/L之间,平均回收率均在90%以上,日内、日间精密度及稳定性的RSD均小于10%。结论该方法简便、准确。可作为清脑宣窍方血药浓度定量分析方法。Objective To establish a method for determinating the concentration of geniposide, ginsenoside Rg1 , ginsenoside RbI and notoginsenoside R1 in the effective fraction of Qingnaoxuanqiao Formula in beagle dog plasma by HPLC. Method Plasma samples were extracted by Cls solid phase column. Sec-o-glucosylhamaudol was taken as internal standard. Agilent Eclipse XDB-Clschromatography column (4.6 mm × 250 mm, 5 um) was applied. The gradient mobile phase was HCN-H2O system with column temperature 30 ℃ and flow rate 1.0 mL/min. The detecting wavelength was 203 nm. Results The limited concentrations of each component were between 0.2 -0.9 mg/L; the average recoveries were all above 90%; RSDs of intra- day and inter- days accuracies and stability were all below 10%. Conclusion The method is simple and accurate, and can be used as the quantitative analysis method for the 4 components in the effective fraction of Qingnaoxuanqiao Formula in plasma .
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