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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >LC-MS/MS determination and urinary excretion study of seven alkaloids in healthy Chinese volunteers after oral administration of Shuanghua Baihe tablets
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LC-MS/MS determination and urinary excretion study of seven alkaloids in healthy Chinese volunteers after oral administration of Shuanghua Baihe tablets

机译:口服双花百和片对健康中国志愿者的7种生物碱的LC-MS / MS测定和尿排泄研究

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An LC-MS/MS method was developed and validated for the simultaneous determination of magnoflorine, berberrubine, jatrorrhizine, coptisine, epiberberine, palmatine and berberine in human urine. The sample preparation procedure involved the four-fold dilution of the urine samples with acetonitrile/water (1:3, v/v). The chromatographic separation was achieved on a Hedera ODS-2 column under gradient elution at a flow rate of 0.4 mL/min with acetonitrile and water containing 0.5% formic acid as the mobile phase. The mass detection was performed in the positive mode. Calibration curves of the seven alkaloids showed good linearity (correlation coefficients > 0.9973) over their concentration ranges. To meet the requirements of urinary excretion study for each alkaloid in human, the lower limit of quantification was set at different values from 0.05063 ng/mL to 2.034 ng/mL for the seven alkaloids, respectively. The intraand inter-batch precision and accuracy were all within +/- 15%. No matrix effect was observed for the analytes. The validated method was applied to the excretion study for the seven alkaloids in healthy Chinese volunteers after oral administration of Shuanghua Baihe tablets. The average 72 h cumulative urinary excretion of magnoflorine, berberrubine, jatrorrhizine, coptisine, epiberberine, palmatine and berberine accounted for 1.81%, 0.27%, 0.29%, 0.046%, 0.027%, 0.010% and 0.021% of the respective administered dose. (c) 2015 Elsevier B.V. All rights reserved.
机译:建立了LC-MS / MS方法,并验证了该方法可同时测定人尿中的厚朴花碱,小,红花,香根草碱,黄连,黄连素,棕榈碱和小and碱。样品制备程序涉及用乙腈/水(1:3,v / v)将尿液样品稀释四倍。在Hedera ODS-2色谱柱上以0.4 mL / min的流速,以乙腈和含0.5%甲酸的水为流动相,进行色谱分离。质量检测以阳性模式进行。七个生物碱的校准曲线在其浓度范围内均显示出良好的线性(相关系数> 0.9973)。为了满足人体中每种生物碱的尿排泄研究要求,将这七个生物碱的定量下限分别设置为0.05063 ng / mL至2.034 ng / mL。批内和批间的精度和准确性均在+/- 15%之内。对于分析物未观察到基质效应。将经验证的方法用于双华白鹤片口服后健康中国志愿者体内7种生物碱的排泄研究。厚朴素,小ber红素,麻风果碱,黄连,黄连素,小palm碱,小at碱和小ber碱的平均72 h累积尿排出量分别占给药剂量的1.81%,0.27%,0.29%,0.046%,0.027%,0.010%和0.021%。 (c)2015 Elsevier B.V.保留所有权利。

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