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Chemical and pharmacological standardization of herbal extracts

机译:草药提取物的化学和药理学标准化

摘要

One of the aspects of the present invention relates to a method of obtaining a reproducible extraction process for use as a standard process for extracting a pharmacologically active mixture of chemical components from a plant, the method comprising: (a) extracting a plurality of pharmacologically active mixtures of chemical components from the plant in a plurality of different extraction processes to obtain a plurality of extracts; (b) obtaining a biological fingerprint of the pharmacological activity of each extract from step (a) by conducting at least two in vitro and at least two in vivo pharmacological tests on each extract, wherein each of the tests is known to correlate with effective treatment of a medical condition in a patient; (c) choosing one of the plurality of extracts which displays the best pharmacological activity in step (b); (d) repeating, at least once, the extraction process used to produce the chosen extract of step (c) to produce at least one test extract; (e) (1) obtaining chemical fingerprints of the chosen extract and the at least one test extract by distinguishing the identity and amount, relative to each other, of the chemical components in the pharmacologically active mixture of each extract, and (2) repeating said step (b) using the at least one test extract; and (f) comparing the chemical fingerprints and the biological fingerprints of the chosen extract and the at least one test extract.
机译:本发明的一个方面涉及一种获得可再现的提取方法的方法,该方法用作从植物中提取化学成分的药理活性混合物的标准方法,该方法包括:(a)提取多种药理活性来自植物的化学成分的混合物在多种不同的提取过程中获得多种提取物; (b)通过对每种提取物进行至少两次体外和至少两次体内药理试验,从步骤(a)获得每种萃取物的药理活性的生物学指纹,其中已知每种试验与有效治疗相关患者的医疗状况; (c)在步骤(b)中选择表现出最佳药理活性的多种提取物中的一种; (d)至少重复一次用于产生步骤(c)的所选提取物的提取过程,以产生至少一种测试提取物; (e)(1)通过区分每种提取物的药理活性混合物中化学成分的同一性和相对量,获得所选提取物和至少一种测试提取物的化学指纹,以及(2)重复所述步骤(b)使用至少一种测试提取物; (f)比较所选提取物和至少一种测试提取物的化学指纹和生物学指纹。

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