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源于自然的药物发现:自动化高质量样品制备

Drug discovery from nature: automated high-quality sample preparation.

作者信息

Thiericke R

机构信息

Hans-Knöll-Institute for Natural Products Research, Beutenbergstrasse 11, Jena D-07745, Germany.

出版信息

J Autom Methods Manag Chem. 2000;22(5):149-57. doi: 10.1155/S1463924600000249.

DOI:10.1155/S1463924600000249
PMID:18924703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2562846/
Abstract

Secondary metabolites from plants, animals and microorganisms have been proven to be an outstanding source for new and innovative drugs and show a striking structural diversity that supplements chemically synthesized compounds or libraries in drug discovery programs. Unfortunately, extracts from natural sources are usually complex mixtures of compounds: often generated in time consuming and for the most part manual processes. As quality and quantity of the provided samples play a pivotal role in the success of high-throughput screening programs this poses serious problems. In order to make samples of natural origin competitive with synthetic compound libraries, we devised a novel, automated sample preparation procedure based on solid-phase extraction (SPE). By making use of a modified Zymark RapidTrace SPE workstation an easy-to-handle and effective fractionation method has been developed which allows the generation of high quality samples from natural origin, fulfilling the requirements of an integration into high-throughput screening programs.

摘要

植物、动物和微生物产生的次生代谢产物已被证明是新型创新药物的重要来源,其结构多样性显著,可补充药物研发项目中化学合成的化合物或文库。不幸的是,天然来源的提取物通常是复杂的化合物混合物,往往通过耗时且大多为手工的过程产生。由于所提供样品的质量和数量在高通量筛选项目的成功中起着关键作用,这就带来了严重问题。为了使天然来源的样品能与合成化合物文库竞争,我们设计了一种基于固相萃取(SPE)的新型自动化样品制备程序。通过使用改良的Zymark RapidTrace SPE工作站,开发出了一种易于操作且有效的分馏方法,该方法能够从天然来源生成高质量样品,满足整合到高通量筛选项目中的要求。