首页> 美国卫生研究院文献>Acta Pharmaceutica Sinica. B >Study on pharmacokinetics and tissue distribution of the isocorydine derivative (AICD) in rats by HPLC-DAD method
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Study on pharmacokinetics and tissue distribution of the isocorydine derivative (AICD) in rats by HPLC-DAD method

机译:HPLC-DAD法研究异碘衍生物(AICD)在大鼠体内的药动学和组织分布

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摘要

A simple and effective high-performance liquid chromatography with diode-array detection method coupled with a liquid-liquid extraction pretreatment has been developed for determining the pharmacokinetics and tissue distribution of a novel structurally modified derivative (8-acetamino-isocorydine) of isocorydine. According to the in vivo experiments data calculations by DAS 2.0 software, a two-compartment metabolic model was suitable for describing the pharmacokinetic of 8-acetamino-isocorydine in rats. 8-Acetamino-isocorydine was absorbed well after oral administration, and the absolute bioavailability was 76.5%. The half-life of 8-acetamino-isocorydine after intravenous and oral administration was 2.2 h and 2.0 h, respectively. In vivo, 8-acetamino-isocorydine was highly distributed in the lungs, kidney and liver; however, relatively little entered the brain, suggesting that 8-acetamino-isocorydine could not easily pass through the blood brain barrier. Our work describes the first characterization of the pharmacokinetic parameters and tissue distribution of 8-acetamino-isocorydine. The acquired data will provide useful information for the in vivo pharmacology of 8-acetamino-isocorydine, and can be applied to new drug research.
机译:开发了一种简单有效的高效液相色谱-二极管阵列检测方法,结合液-液萃取预处理技术,用于测定异is鱼碱的新型结构修饰衍生物(8-对乙酰氨基-异亮氨酸)的药代动力学和组织分布。根据DAS 2.0软件进行的体内实验数据计算,两室代谢模型适用于描述8-乙酰氨基-异亮氨酸在大鼠体内的药代动力学。口服后8-乙酰氨基-异亮氨酸吸收良好,绝对生物利用度为76.5%。静脉和口服给药后8-乙酰氨基-异亮氨酸的半衰期分别为2.2小时和2.0小时。在体内,8-乙酰氨基-异亮氨酸在肺,肾和肝脏中高度分布。但是,进入大脑的相对较少,这表明8-对乙酰氨基-异亮氨酸不能轻易通过血脑屏障。我们的工作描述了8-对乙酰氨基-异亮氨酸的药代动力学参数和组织分布的首次表征。所获得的数据将为8-乙酰氨基-异亮氨酸的体内药理学提供有用的信息,并可用于新药研究。

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