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气相色谱-质谱法研究白芷中 8 种香豆素类成分在大鼠体内的药代动力学。

Pharmacokinetic study of eight coumarins of Radix Angelicae Dahuricae in rats by gas chromatography-mass spectrometry.

机构信息

School of Medicine, Xi'an Jiaotong University, Xi'an 710061, China.

出版信息

Fitoterapia. 2013 Sep;89:250-6. doi: 10.1016/j.fitote.2013.06.007. Epub 2013 Jun 14.

DOI:10.1016/j.fitote.2013.06.007
PMID:23774663
Abstract

A sensitive, specific gas chromatography-mass spectrometry (GC-MS) method was established for the quantitative determination of eight coumarins of Radix Angelicae Dahuricae including coumarin, isopsoralen, psoralen, xanthotoxin, bergapten, osthole, imperatorin and oxypeucedanin in rat plasma. Nitrendipine was used as the internal standard (IS). The plasma samples were extracted by acetonitrile. GC separation was accomplished on a DB-5MS column with temperature programmed from 160°C (17 min) to 190°C (10 min) at the rate of 20°C/min, then to 240°C (5 min) at 20°C/min, and finally to 280°C (14 min) at 20°C/min. The detection was performed on a quadrupole mass spectrometer detector operated by full-scan mode (m/z 50-500). The lower limit of quantitation was 5-10 ng/mL for eight coumarins, and the linear range was 5-1000 ng/mL for the coumarins (R(2)>0.9990). All the validation data were within the required limits. After oral administration, the plasma concentration-time curves showed that the time for maximum concentration (Tmax) was 1.29 for coumarin, 1.83 for isopsoralen, 1.93 for psoralen, 1.30 for xanthotoxin, 2.04 for bergapten, 0.64 for osthole, 1.41 for imperatorin and 0.51 h for oxypeucedanin. The plasma concentration of the eight coumarins was low, with a mean maximum plasma concentration (Cmax) <6.41 μg/mL. Pharmacokinetic data analysis showed that the eight coumarins had different pharmacokinetic characteristics after oral administration. The method was successfully applied to pharmacokinetic studies of eight coumarins after oral administration in rats.

摘要

建立了一种灵敏、特异的气相色谱-质谱(GC-MS)法,用于定量测定大鼠血浆中 8 种白芷香豆素,包括香豆素、异补骨脂素、补骨脂素、花椒毒素、佛手柑内酯、蛇床子素、欧前胡素和氧化前胡素。硝苯地平作为内标(IS)。血浆样品用乙腈提取。GC 分离在 DB-5MS 柱上进行,程序升温从 160°C(17 min)到 190°C(10 min),升温速率为 20°C/min,然后以 20°C/min 升温至 240°C(5 min),最后以 20°C/min 升温至 280°C(14 min)。检测采用全扫描模式(m/z 50-500)的四极杆质谱仪检测器进行。8 种香豆素的定量下限为 5-10 ng/mL,线性范围为 5-1000 ng/mL(R²>0.9990)。所有验证数据均在要求范围内。口服给药后,血浆浓度-时间曲线显示香豆素的最大浓度时间(Tmax)为 1.29,异补骨脂素为 1.83,补骨脂素为 1.93,花椒毒素为 1.30,佛手柑内酯为 2.04,蛇床子素为 0.64,欧前胡素为 1.41,氧化前胡素为 0.51 h。8 种香豆素的血浆浓度较低,平均最大血浆浓度(Cmax)<6.41 μg/mL。药代动力学数据分析表明,8 种香豆素口服后具有不同的药代动力学特征。该方法成功应用于大鼠口服 8 种香豆素后的药代动力学研究。

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