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Determination and Pharmacokinetic Study of Gentiopicroside, Geniposide, Baicalin, and Swertiamarin in Chinese Herbal Formulae after Oral Administration in Rats by LC-MS/MS

机译:LC-MS / MS法测定大鼠口服中药制剂中龙胆苦甙,Gen子苷,黄ical苷和苦味marin素的含量及其药代动力学研究

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A sensitive and efficient liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed for the simultaneous determination of gentiopicroside, geniposide, baicalin, and swertiamarin in rat plasma. To avoid the stress caused by restraint or anesthesia, a freely moving rat model was used to investigate the pharmacokinetics of herbal medicine after the administration of a traditional Chinese herbal prescription of Long-Dan-Xie-Gan-Tang (10 g/kg, p.o.). Analytes were separated by a C18 column with a gradient system of methanol-water containing 1 mM ammonium acetate with 0.1% formic acid. The linear ranges were 10-500 ng/mL for gentiopicroside, geniposide, and baicalin, and 5-250 ng/mL for swertiamarin in biological samples. The intra-and inter-day precision (relative standard deviation) ranged from 0.9% to 11.4% and 0.3% to 14.4%, respectively. The accuracy (relative error) was from -6.3% to 10.1% at all quality control levels. The analytical system provided adequate matrix effect and recovery with good precision and accuracy. The pharmacokinetic data demonstrated that the area under concentration-time curve (AUC) values of gentiopicroside, geniposide, baicalin, and swertiamarin were 1417 +/- 83.8, 302 +/- 25.8, 753 +/- 86.2, and 2.5 +/- 0.1 min mu g/mL. The pharmacokinetic profiles provide constructive information for the dosage regimen of herbal medicine and also contribute to elucidate the absorption mechanism in herbal applications and pharmacological experiments.
机译:建立了灵敏而高效的液相色谱-串联质谱(LC-MS / MS)方法,用于同时测定大鼠血浆中龙胆苦苷,子苷,黄ical苷和swertiamarin的含量。为避免束缚或麻醉引起的压力,使用了自由移动的大鼠模型,研究了中药龙胆泻肝汤(10 g / kg,口服)的中药药代动力学。 )。通过C18色谱柱,用含有1 mM乙酸铵和0.1%甲酸的甲醇-水梯度系统分离分析物。生物样品中龙胆苦苷,子苷和黄ical苷的线性范围为10-500 ng / mL,而苦参素的线性范围为5-250 ng / mL。日内和日间精度(相对标准偏差)分别为0.9%至11.4%和0.3%至14.4%。在所有质量控制水平下,准确度(相对误差)为-6.3%至10.1%。该分析系统提供了足够的基质效果和良好的精密度和准确度。药代动力学数据表明龙胆苦苷,子苷,黄ical苷和swertiamarin的浓度-时间曲线(AUC)值分别为1417 +/- 83.8、302 +/- 25.8、753 +/- 86.2和2.5 +/- 0.1最小μg / mL。药代动力学概况为草药的给药方案提供了建设性的信息,也有助于阐明草药应用和药理实验中的吸收机制。

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