Department of Food Safety and Food Quality, Faculty of Bioscience Engineering, Ghent University, Belgium; Department of Industrial Engineering and Technology, University College West Flanders, Kortrijk, Belgium; Department of Crop Protection, Faculty of Bioscience Engineering, Ghent University, Belgium.
Department of Industrial Engineering and Technology, University College West Flanders, Kortrijk, Belgium; Department of Industrial Biological Science, Faculty of Bioscience Engineering, Ghent University, Belgium.
J Chromatogr A. 2014 Jan 3;1323:39-48. doi: 10.1016/j.chroma.2013.10.077. Epub 2013 Nov 7.
In this paper, a strategy for the detection and structural elucidation of flavonoid glycosides from a complex matrix in a single chromatographic run using U(H)PLC-ESI-IMS-HDMS/MS(E) is presented. This system operates using alternative low and high energy voltages that is able to perform the task of conventional MS/MS in a data-independent way without re-injection of the sample, which saves analytical time. Also, ion mobility separation (IMS) was employed as an additional separation technique for compounds that are co-eluting after U(H)PLC separation. First, the fragmentation of flavonoid standards were analyzed and criteria was set for structural elucidation of flavonoids in a plant extract. Based on retention times, UV spectra, exact mass, and MS fragment characteristics, such as abundances of daughter ions and the presence of radical ions (Y0-H), a total 19 flavonoid glycosides, of which 8 non-acylated and 11 acylated, were detected and structurally characterized in a cauliflower waste extract. Kaempferol and quercetin were the main aglycones detected while sinapic and ferulic acid were the main phenolic acids. C-glycosides were also found although their structure could not be elucidated. The proposed method can be used as a rapid screening test for flavonoid identification and for routine analysis of plant extracts, such as these derived from cauliflower waste. The study also confirms that agroindustrial wastes, such as cauliflower leaves, could be seen as a valuable source of different bioactive phenolic compounds.
本文提出了一种在单次色谱运行中从复杂基质中检测和结构解析类黄酮糖苷的策略,该策略使用 U(H)PLC-ESI-IMS-HDMS/MS(E)。该系统使用交替的低能和高能电压运行,能够以数据非依赖的方式执行传统 MS/MS 的任务,而无需重新注入样品,从而节省了分析时间。此外,离子迁移谱(IMS)被用作在 U(H)PLC 分离后共洗脱化合物的附加分离技术。首先,分析了类黄酮标准品的碎片,并为植物提取物中类黄酮的结构解析设定了标准。基于保留时间、紫外光谱、精确质量以及 MS 碎片特征,例如子离子的丰度和自由基离子(Y0-H)的存在,总共检测到 19 种类黄酮糖苷,其中 8 种非酰化和 11 种酰化,在花椰菜废物提取物中进行了结构鉴定。山奈酚和槲皮素是检测到的主要苷元,而咖啡酸和阿魏酸是主要的酚酸。虽然它们的结构无法阐明,但也发现了 C-糖苷。该方法可用于类黄酮鉴定的快速筛选测试以及植物提取物的常规分析,如花椰菜废物提取物。该研究还证实,农业工业废物,如花椰菜叶,可被视为不同生物活性酚类化合物的有价值来源。