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Relative bioavailability of gastrodin and parishin from extract and powder of Gastrodiae rhizoma in rat

机译:天麻根提取物和粉末中天麻素和堂蛋白的相对生物利用度在大鼠中

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摘要

A rapid, sensitive and reliable UHPLC-ESI-MS/MS method was developed for simultaneous determination of gastrodin and parishin in rat plasma. The LLOQ of the two analytes were 1.00 x 10(-1) and 8.30 x 10(-5) mu g/mL, respectively. The intra-day and inter-day precision were all less than 10% of the relative standard deviation (RSD), whilst the accuracy were all within +/- 15% of the relative error (RE). The proposed method was successfully applied for pharmacokinetics study on the two analytes in rats after oral administration of Gastrodiae rhizoma (GR) extract and powder at low, medium and high dosages. Blood samples were collected from the suborbital vein at predetermined time points and were precipitated using methanol. Chromatographic separations were carried out on a Kinetex XB-C18 column (2.1 mm x 150 mm, 1.7 mu m) with a gradient mobile phase of acetonitrile-water with 0.1% formic acid as a modifier. The pharmacokinetic parameters of the two analytes in rats were obtained and the relative bioavailability of gastrodin and parishin in two formulations were calculated. The results indicated that higher bioavailability was obtained when low dosage of GR powder was used, whereas, higher bioavailability values were obtained when medium and high dosages of GR extract were used. (C) 2014 Published by Elsevier B.V.
机译:建立了一种快速,灵敏,可靠的UHPLC-ESI-MS / MS方法,用于同时测定大鼠血浆中的天麻素和教区蛋白。两种分析物的LLOQ分别为1.00 x 10(-1)和8.30 x 10(-5)μg / mL。日内和日间精度均小于相对标准偏差(RSD)的10%,而精度均在相对误差(RE)+/- 15%之内。所建议的方法成功地以低,中,高剂量口服天麻提取物和粉末后,在大鼠中的两种分析物上进行了药代动力学研究。在预定的时间点从眼眶下静脉收集血样,并使用甲醇沉淀。色谱分离是在Kinetex XB-C18色谱柱(2.1 mm x 150 mm,1.7μm)上进行的,其中乙腈-水的梯度流动相含0.1%的甲酸作为改性剂。获得了两种分析物在大鼠中的药代动力学参数,并计算了两种制剂中天麻素和parishin的相对生物利用度。结果表明,当使用低剂量的GR粉末时,可获得较高的生物利用度,而当使用中等剂量和高剂量的GR提取物时,可获得较高的生物利用度。 (C)2014由Elsevier B.V.发布

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