Bogan D P, O'Kennedy R
School of Biological Sciences, Dublin City University, Ireland.
J Chromatogr B Biomed Appl. 1996 Nov 15;686(2):267-73. doi: 10.1016/s0378-4347(96)00234-4.
A HPLC method was developed for the determination of the metabolites of coumarin and 7-hydroxycoumarin in plasma and serum. Separation was based on gradient elution of 7-hydroxycoumarin glucuronide, 7-hydroxycoumarin, coumarin and finally 4-hydroxycoumarin (which is used as an internal standard). Standards, prepared in plasma or serum, and samples were treated with trichloroacetic acid, mixed and centrifuged. The supernatant was removed and analyzed by reversed-phase high-performance liquid chromatography on a C18 column. The limit of detection was 50 ng/ml for 7-hydroxycoumarin and 200 ng/ml for coumarin and 7-hydroxycoumarin glucuronide. The linear range was 0.5-100 micrograms/ml for each of the analytes. The percentage relative standard deviation about the mean measured concentrations were all below 10%. There was no statistical difference between the standard curves prepared in plasma or serum. The method developed was applied to the determination of each of the three compounds in serum, after the administration of 7-hydroxycoumarin, and in plasma after the administration of coumarin. The concentrations of total 7-hydroxycoumarin in the serum samples were also determined by another HPLC method and the results were compared. There was no statistical difference between the results determined.
建立了一种高效液相色谱法,用于测定血浆和血清中香豆素及7-羟基香豆素的代谢产物。分离基于7-羟基香豆素葡萄糖醛酸苷、7-羟基香豆素、香豆素,最后是4-羟基香豆素(用作内标)的梯度洗脱。在血浆或血清中制备的标准品和样品用三氯乙酸处理,混合并离心。去除上清液,在C18柱上通过反相高效液相色谱法进行分析。7-羟基香豆素的检测限为50 ng/ml,香豆素和7-羟基香豆素葡萄糖醛酸苷的检测限为200 ng/ml。每种分析物的线性范围为0.5-100微克/毫升。所测浓度平均值的相对标准偏差百分比均低于10%。在血浆或血清中制备的标准曲线之间无统计学差异。所建立的方法应用于7-羟基香豆素给药后血清中三种化合物的测定,以及香豆素给药后血浆中三种化合物 的测定。还通过另一种高效液相色谱法测定了血清样品中总7-羟基香豆素浓度,并对结果进行了比较。所测结果之间无统计学差异。