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序贯混合三维气相色谱-精确质量质谱联用:一种用于多组分样品高分辨特性分析的新工具。

Sequential Hybrid Three-Dimensional Gas Chromatography with Accurate Mass Spectrometry: A Novel Tool for High-Resolution Characterization of Multicomponent Samples.

机构信息

Australian Centre for Research on Separation Science, School of Natural Sciences , University of Tasmania , Hobart , TAS 7001 , Australia.

Australian Centre for Research on Separation Science, School of Chemistry , Monash University , Wellington Road , Clayton , VIC 3800 , Australia.

出版信息

Anal Chem. 2018 Apr 17;90(8):5264-5271. doi: 10.1021/acs.analchem.8b00142. Epub 2018 Apr 2.

Abstract

A novel sequential three-dimensional gas chromatography-high-resolution time-of-flight mass spectrometry (3D GC-accTOFMS) approach for profiling secondary metabolites in complex plant extracts is described. This integrated system incorporates a nonpolar first-dimension (D) separation step, prior to a microfluidic heart-cut (H/C) of a targeted region(s) to a cryogenic trapping device, directly followed by the rapid reinjection of a trapped solute into a polar second-dimension (D) column for multidimensional separation (GC-GC). For additional separation, the effluent from D can then be modulated according to a comprehensive 2D GC process (GC×GC), using an ionic liquid phase as a third-dimension (D) column, to produce a sequential GC-GC×GC separation. Thus, the unresolved or poorly resolved components, or regions that require further separation, can be precisely selected and rapidly transferred for additional separation on D or D columns, based on the greater separation realized by these steps. The described integrated system can be used in a number of modes, but one useful approach is to target specific classes of compounds for improved resolution. This is demonstrated through the separation and detection of the oxygenated sesquiterpenes in hop ( Humulus lupulus L.) essential oil and agarwood ( Aquilaria malaccensis) oleoresin. Improved resolution and peak capacity were illustrated through the progressive comparison of the tentatively identified components for GC-GC and GC-GC×GC methods. Relative standard deviations of intraday retentions ( t, t, and t) and peak areas of ≤0.01, 0.07, 0.71, and 7.5% were achieved. This analytical approach comprising three GC column selectivities, hyphenated with high-resolution TOFMS detection, should be a valuable adjunct for the improved characterization of complex plant samples, particularly in the area of plant metabolomics.

摘要

一种新型的顺序三维气相色谱-高分辨飞行时间质谱(3D GC-accTOFMS)方法用于分析复杂植物提取物中的次生代谢产物。该集成系统包含非极性的第一维(D)分离步骤,然后对目标区域(s)进行微流控心脏切割(H/C)到低温捕集装置,直接紧随其后的是被捕获的溶质快速重新注入到极性二维(D)柱中进行多维分离(GC-GC)。为了进一步分离,D 的流出物可以根据全面的 2D GC 过程(GC×GC)进行调制,使用离子液体相作为第三维(D)柱,以产生顺序 GC-GC×GC 分离。因此,可以根据这些步骤实现的更大分离,精确选择和快速转移未解决或分离不良的成分或需要进一步分离的区域,以进行 D 或 D 柱上的额外分离。所描述的集成系统可以在多种模式下使用,但一种有用的方法是针对特定类别的化合物进行目标分离,以提高分辨率。这是通过分离和检测啤酒花(Humulus lupulus L.)精油和沉香(Aquilaria malaccensis)香脂中的含氧倍半萜来证明的。通过逐步比较 GC-GC 和 GC-GC×GC 方法中暂定鉴定成分的方法,说明了分辨率和峰容量的提高。日内保留时间( t, t,和 t)和峰面积的相对标准偏差分别为≤0.01、0.07、0.71 和 7.5%。这种分析方法包含三个 GC 柱选择性,与高分辨飞行时间质谱检测联用,对于改善复杂植物样品的表征应该是一个有价值的辅助手段,特别是在植物代谢组学领域。

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