首页> 美国卫生研究院文献>Molecules >A Compositive Strategy to Study the Pharmacokinetics of TCMs: Taking Coptidis Rhizoma and Coptidis Rhizoma-Glycyrrhizae Radix et Rhizoma as Examples
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A Compositive Strategy to Study the Pharmacokinetics of TCMs: Taking Coptidis Rhizoma and Coptidis Rhizoma-Glycyrrhizae Radix et Rhizoma as Examples

机译:研究中药药代动力学的综合策略:以黄连甘草-甘草为例

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摘要

Pharmacokinetic studies are crucial for elucidating the effective constituents and formula compatibility of traditional Chinese medicines (TCMs). However, studies have usually been limited to single dosages and detection of systemic blood concentrations. To obtain comprehensive pharmacokinetic information, here we propose a multi-dosage and multi-sampling (blood from portal vein or systemic circulation, and liver) strategy to comparatively study the pharmacokinetics of multi-form TCMs, i.e., pure constituents, TCMs, or TCM formula extracts. Based on this strategy, we studied the pharmacokinetics of pure berberine, berberine in Coptidis Rhizoma (CRE), and berberine in Coptidis Rhizoma-Glycyrrhizae Radix et Rhizoma extracts (CR-GRE). After simple calculation and comparison of the obtained area under the curve (AUC) values, the results revealed the drastically different pharmacokinetic properties of pure berberine compared to CRE and CR-GRE. The results contribute to explaining the pharmacological loss of berberine activity after purification and the compatibility of the CR-GR drug pair. The results also innovatively showed that it was intestinal absorption that differentiated the pharmacokinetics of CRE and pure berberine, and CRE and CR-GRE. In conclusion, we propose a composite strategy to comparatively study the pharmacokinetics of TCMs, which could provide sufficient information to obtain a comprehensive view, before follow-up mechanism-of-action studies.
机译:药代动力学研究对于阐明中药(TCM)的有效成分和配方相容性至关重要。但是,研究通常仅限于单剂量和全身血药浓度的检测。为了获得全面的药代动力学信息,在此我们提出一种多剂量和多采样(门静脉或全身循环血液和肝脏的血液)策略,以比较研究多种形式的中药的药代动力学,即纯成分,中药或中药配方提取物。基于此策略,我们研究了纯黄连素,黄连中黄连素的药代动力学(CRE)和黄连中甘草黄连提取物(CR-GRE)中的小ber碱的药代动力学。经过简单的计算并比较了曲线下的面积(AUC)值,结果表明与CRE和CR-GRE相比,纯小ine碱的药代动力学特性完全不同。结果有助于解释纯化后小ber碱活性的药理学损失以及CR-GR药物对的相容性。该结果还创新性地表明,肠吸收是区别CRE和纯小ber碱以及CRE和CR-GRE的药代动力学的原因。总之,我们提出了一种复合策略来比较研究中药的药代动力学,它可以为后续的作用机理研究提供足够的信息以获得全面的观点。

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