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Dietary supplements and related products: a brief summary.

机译:膳食补充剂和相关产品:简短摘要。

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摘要

We were gratified by the interest expressed in publishing a large number of presentations from the NIDA organized Workshop on "Natureceuticals (Natural Products), Nutraceuticals, Herbal Botanicals, Psychoactives: Drug Discovery and Drug-Drug Interactions". The number of manuscripts received necessitated two volumes of proceedings. In this brief summary of the second volume, we present an introduction to the roles of organizations such as National Center for Complementary and Alternate Medicine and Office of Dietary Supplements, both at the National Institutes of Health, and the Food and Drug Administration. These agencies are involved in research and regulation of dietary supplements and related products. Next, a brief summary of each of the fifteen articles is provided. The first four articles are related to regulatory and standardization aspects: issues related to botanicals (Khan); USP and dietary supplements (Srinivasan); dietary supplement reference materials (Sander et al.); and proposed cGMPs and the scientific basis behind the proposed regulations by FDA (Melethil). The next three articles relate to the methodologies employed in research: LC/MS for the pharmacokinetic analysis polyphenols from dietary supplements (Barnes et al.); proteomic analysis of grape seed extract (Kim et al.); and a nematode model, C. elegans, in Alzheimer's and ginkgo biloba extract for mechanistic studies; another model, a hepatocyte tissue culture model for drug herbal interaction, is reviewed later and presented by Venkataramanan. The next four chapters are on specific dietary supplements: green tea and the polyphenolic catechins (Zaveri); curcumin (Maheswari et al.); tocotrienols (alpha-tocotrienol, Sen and Roy), gamma-tocotrienol (Sree Kumar et al.). This topic is followed by drug interaction studies: in vitro and in vivo assessment methodologies (Venkataramanan); flavonoid-drug interactions (Morris); MDR and CYP3A4-mediated drug-herb interaction (Pal and Mitra); and evidence-based examination of drug-herb interaction (Chavez and Chavez).
机译:我们很高兴看到有兴趣发表NIDA组织的关于“天然药物(天然产品),营养食品,草药植物,精神活性剂:药物发现和药物与药物相互作用”的专题演讲。收到的手稿数量需要两卷本。在第二卷的简短摘要中,我们介绍了国立卫生研究院和食品药品管理局等国家补充和替代医学中心和膳食补充剂办公室等组织的作用。这些机构参与膳食补充剂和相关产品的研究和监管。接下来,提供了这十五篇文章的简要摘要。前四篇文章涉及法规和标准化方面:与植物药相关的问题(汗); USP和膳食补充剂(Srinivasan);膳食补充剂参考材料(Sander等);以及拟议的cGMP和FDA(Melethil)拟议法规背后的科学依据。接下来的三篇文章与研究中使用的方法有关:LC / MS用于膳食补充剂中多酚的药代动力学分析(Barnes等人);葡萄籽提取物的蛋白质组学分析(Kim等);以及用于机制研究的阿尔茨海默氏病和银杏叶提取物中的线虫模型秀丽隐杆线虫;另一个模型,即用于药物草药相互作用的肝细胞组织培养模型,将在稍后进行审查,并由Venkataramanan提出。接下来的四章介绍特定的膳食补充剂:绿茶和多酚儿茶素(Zaveri);姜黄素(Maheswari等);生育三烯酚(α-生育三烯酚,Sen和Roy),γ-生育三烯酚(Sree Kumar等)。该主题之后是药物相互作用研究:体外和体内评估方法(Venkataramanan);黄酮类药物相互作用(莫里斯); MDR和CYP3A4介导的药草相互作用(Pal和Mitra);以及基于证据的药草相互作用研究(查韦斯和查韦斯)。

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