首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >HPLC method for the determination and pharmacokinetic studies of four triterpenoids in rat plasma after oral administration of Ganoderma lucidum extract.
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HPLC method for the determination and pharmacokinetic studies of four triterpenoids in rat plasma after oral administration of Ganoderma lucidum extract.

机译:口服灵芝提取物后,HPLC法测定大鼠血浆中四种三萜的含量并进行药代动力学研究。

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摘要

Four major triterpenoids (ganoderic acids C(2), B, K and H) in rat plasma after oral administration of G. lucidum extract were analyzed quantitatively by high-performance liquid chromatography (HPLC). Plasma samples taken from rats were acidified with hydrochloric acid and extracted with dichloromethane-ethyl acetate (90:10). The chromatographic separation was achieved on an Agilent Zorbax SB-C(18) column (250 x 4.6 mm, 5 microm) at 35 degrees C, with a linear gradient of acetonitrile and 0.03% aqueous phosphoric acid (v/v), at a flow rate of 1.0 mL/min. The four triterpenoids and internal standard (hydrocortisone) were detected at a wavelength 252 nm. All calibration curves showed good linearity (r(2) > 0.99) within test ranges. The relative deviation of this method was less than 10% for intra- and inter-day assays, and the accuracy ranged from 89 to 108%. The extract recovery for the four triterpenoids and internal standard ranged from 95 to 67%, and the QC samples were found to be stable according to the results of the stability study. This is the first report on determination of the major triterpenoids in rat plasma after oral administration of G. lucidum extract and the results provided a firm basis for clarifying the pharmacological effect of G. lucidum and evaluating the clinical applications of this medicinal fungus.
机译:口服灵芝提取物后大鼠血浆中的四种主要三萜类化合物(灵芝酸C(2),B,K和H)通过高效液相色谱(HPLC)进行定量分析。用盐酸酸化取自大鼠的血浆样品,并用二氯甲烷-乙酸乙酯(90∶10)萃取。色谱分离是在35°C的Agilent Zorbax SB-C(18)色谱柱(250 x 4.6 mm,5微米)上进行的,乙腈和0.03%磷酸水溶液(v / v)的线性梯度为流速为1.0 mL / min。在波长252 nm处检测到了四个三萜类化合物和内标(氢化可的松)。所有校准曲线在测试范围内均显示出良好的线性(r(2)> 0.99)。对于日内和日间分析,此方法的相对偏差小于10%,准确度范围为89%至108%。四种三萜类化合物和内标物的提取物回收率在95%到67%之间,并且根据稳定性研究的结果发现QC样品是稳定的。这是关于口服灵芝提取物后测定大鼠血浆中主要三萜类化合物的首次报道,该结果为阐明灵芝的药理作用和评估该药用真菌的临床应用提供了坚实的基础。

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