黄熙,陈可冀,任平,李军昌,马红艳.高效液相色谱直接测定沸水浴处理人血清中冠心Ⅱ号来源的阿魏酸[J].中国中西医结合杂志,1999,(2):71-74 |
高效液相色谱直接测定沸水浴处理人血清中冠心Ⅱ号来源的阿魏酸 |
Direct Determination of Serum Content of Ferulic Acid Treated with Boiling Water by HPLC in Vonlunteers after Oral Administration of Coronary Heart No. Ⅱ Decoction |
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DOI: |
中文关键词: 冠心Ⅱ号 阿魏酸 血药浓度测定 水浴法 高效液相色谱 |
英文关键词:Coronary Heart No Ⅱ ferulic acid blood drug concentration detection water bath high performance liquid chromatography |
基金项目:国家自然科学基金,博士后基金 |
作者 | 单位 | 黄熙 | Huang Xi, Chen Keji, Ren Ping, et al Xiyuan Hospital, China Academy of TCM ,Beijing (100091 | 陈可冀 | Huang Xi, Chen Keji, Ren Ping, et al Xiyuan Hospital, China Academy of TCM ,Beijing (100091 | 任平 | Huang Xi, Chen Keji, Ren Ping, et al Xiyuan Hospital, China Academy of TCM ,Beijing (100091 | 李军昌 | Huang Xi, Chen Keji, Ren Ping, et al Xiyuan Hospital, China Academy of TCM ,Beijing (100091 | 马红艳 | Huang Xi, Chen Keji, Ren Ping, et al Xiyuan Hospital, China Academy of TCM ,Beijing (100091 |
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中文摘要: |
目的:探讨建立健康人口服冠心Ⅱ号后吸收入血清成分的临床药动学(PK)研究的新方法。方法:用高效液相色谱(HPLC)直接测定5名健康人服冠心Ⅱ号后经沸水浴处理过的血清样品中的阿魏酸(FA)。分别用二维、三维HPLC和紫外分光光度法定性FA后,FA用内标(香豆精)法定量。结果:甲醇∶乙酸∶水(38∶03∶617)为流动相,C18(ODS2)柱(150mm×46mm,5μm)为固定相时,FA的最低检测限6ng(N/S=3);沸水浴10min的最低检测血清浓度是202μg/L,线性范围337~21568μg/L,r=09993;方法平均回收率(9359±236)%,日间及日内精密度RSD值均<844%。结论:与乙睛法比较,本法灵敏、快速、简便、精确、专一、价廉、无毒和重复性好。 |
英文摘要: |
Objective: To develop a new method for clinical pharmacokinetic detection of chemical component of Coronary Heart NO. Ⅱ in serum after oral administration in healthy person. Methods: Content of ferulic acid (FA) in serum ,which had been treated with boiling water bath, was determined directly by high performance liquid chromotography (HPLC) and spectrophotometer. After qualitative detection performed by using Bi and tri dimensional HPLC and ultraviolet spectrophotometer, the quantitative detection was determined with the internal standard (coumarin). Results: When eluted by mobile phase of a mixture of methanol, acetic acid and water (38∶0.3∶61.7 in ratio), and stationary phase of C 18 (ODS 2), column (150mm×4.6mm, 5μm), the minimal detectable limit of free methanol FA was 6 ng (N/S=3), and the minimal detectable serum FA concentration, after 10 min of boiling water bath, was 20.2 μg/L, with a linearity of 33.7~2156.8 μg/L, r=0.9993. The mean recovery of serum FA was (93.59±2.36) μg/L. The RSD within day and day to day were all less than 8.44%. Conclusion: In comparing with sample Preparation of acetonitrile, this method is simple, rapid, sensitive, cheap, accurate, specific, reproducible and no toxic. |
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