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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 …
引用本文:黄熙,陈可冀. 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 …[J]. 中国中西医结合杂志, 1999, 19(2): 71-74
作者姓名:黄熙  陈可冀
作者单位:中国中医研究院西苑医院
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研究的新方法。方法:用高效液相色谱直接测定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。分别用二维,三维HPLC和紫外分光光度法定性FA后,FA用内标法定量。结果;甲醇:乙酸:水为流动相,C、8柱为固定相时,FA的最低检测限6ng;沸水浴10min5的最低检测血清浓度是20.2μg/L,线性范围33.7-2156.8μg/L,

关 键 词:冠心Ⅱ号  阿魏酸  血药浓度  水浴法  高效液相色谱

Direct determination of serum content of ferulic acid treated with boiling water in HPLC in volunteers after oral Administration of Coronary Heart No. II decoction]
X Huang,K Chen,P Ren. Direct determination of serum content of ferulic acid treated with boiling water in HPLC in volunteers after oral Administration of Coronary Heart No. II decoction][J]. Chinese journal of integrated traditional and Western medicine, 1999, 19(2): 71-74
Authors:X Huang  K Chen  P Ren
Affiliation:Xiyuan Hospital, China Academy of TCM, Beijing (100091).
Abstract: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 C18(ODS2), column (150 mm x 4.6 mm, 5 microns), 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 micrograms/L, with a linearity of 33.7-2156.8 micrograms/L, r = 0.9993. The mean recovery of serum FA was (93.59 +/- 2.36) micrograms/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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