基于hnmr的代谢组学联合HPLC-PDA-MS-SPE-NMR研究银杏叶标准化制剂。

Sara Agnolet, Jerzy W Jaroszewski, Robert Verpoorte, Dan Staerk
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引用次数: 71

摘要

银杏商业制剂是由原始叶提取物经过一系列提取和预纯化步骤制备的非常复杂的混合物。其药理活性归因于一些黄酮类苷和独特的萜烯三内酯(TTLs),与神经系统疾病相关的靶标具有很大程度上未表征的药理特征。因此,重要的是补充现有的有针对性的分析方法,以替代技术平台对银杏制剂进行全面和全面的表征。(1)采用高效液相色谱、光电二极管阵列检测、质谱、固相萃取和核磁共振(HPLC-PDA-MS-SPE-NMR)联用技术,对16种市售银杏制剂进行了代谢组学和联用研究。标准化提取物来自丹麦、意大利、瑞典和英国,结果表明:(1)H NMR光谱可以同时评估黄酮类苷和TTLs的含量以及基于丙酮-d中提取、蒸发和重构的非常简单的样品制备程序(6)。意想不到的或不需要的提取物成分也很容易在(1)H NMR光谱中识别出来,这与依赖于紫外线吸收或MS电离性的传统方法形成了对比,通常需要参考标准的可用性。(1)氢核磁共振谱段(宽度为0.02 ppm的桶或桶)的自动化集成提供了基于其H-12共振的ttl的相对分布图。本研究表明(1)基于核磁共振的代谢组学是一种有吸引力的非选择性综合分析银杏提取物的方法。电子补充材料:本文的在线版本(doi:10.1007/s11306-009-0195-x)包含补充材料,授权用户可以使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

H NMR-based metabolomics combined with HPLC-PDA-MS-SPE-NMR for investigation of standardized Ginkgo biloba preparations.

H NMR-based metabolomics combined with HPLC-PDA-MS-SPE-NMR for investigation of standardized Ginkgo biloba preparations.

H NMR-based metabolomics combined with HPLC-PDA-MS-SPE-NMR for investigation of standardized Ginkgo biloba preparations.

H NMR-based metabolomics combined with HPLC-PDA-MS-SPE-NMR for investigation of standardized Ginkgo biloba preparations.

Commercial preparations of Ginkgo biloba are very complex mixtures prepared from raw leaf extracts by a series of extraction and prepurification steps. The pharmacological activity is attributed to a number of flavonoid glycosides and unique terpene trilactones (TTLs), with largely uncharacterized pharmacological profiles on targets involved in neurological disorders. It is therefore important to complement existing targeted analytical methods for analysis of Ginkgo biloba preparations with alternative technology platforms for their comprehensive and global characterization. In this work, (1)H NMR-based metabolomics and hyphenation of high-performance liquid chromatography, photo-diode array detection, mass spectrometry, solid-phase extraction, and nuclear magnetic resonance spectroscopy (HPLC-PDA-MS-SPE-NMR) were used for investigation of 16 commercially available preparations of Ginkgo biloba. The standardized extracts originated from Denmark, Italy, Sweden, and United Kingdom, and the results show that (1)H NMR spectra allow simultaneous assessment of the content as well as identity of flavonoid glycosides and TTLs based on a very simple sample-preparation procedure consisting of extraction, evaporation and reconstitution in acetone-d(6). Unexpected or unwanted extract constituents were also easily identified in the (1)H NMR spectra, which contrasts traditional methods that depend on UV absorption or MS ionizability and usually require availability of reference standards. Automated integration of (1)H NMR spectral segments (buckets or bins of 0.02 ppm width) provides relative distribution plots of TTLs based on their H-12 resonances. The present study shows that (1)H NMR-based metabolomics is an attractive method for non-selective and comprehensive analysis of Ginkgo extracts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11306-009-0195-x) contains supplementary material, which is available to authorized users.

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