4.6 Article

Determination of 18 Intact Glucosinolates in Brassicaceae Vegetables by UHPLC-MS/MS: Comparing Tissue Disruption Methods for Sample Preparation

期刊

MOLECULES
卷 27, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27010231

关键词

intact glucosinolates; Brassicaceae vegetables; triple quadrupole mass spectrometry; tissue disruption

资金

  1. Collaborative Innovation Center of Beijing Academy of Agriculture and Forestry Sciences [KJCX201915]
  2. Youth Scientific Research Funds of Beijing Academy of Agriculture and Forestry Sciences [QNJJ201914]
  3. Innovation and Capacity-building Project of Beijing Academy of Agriculture and Forestry Sciences [KJCX20200213]
  4. China Postdoctoral Science Foundation [2021M700494]

向作者/读者索取更多资源

The study compared and optimized three tissue disruption methods for sample preparation, revealing limitations in processing intact GSLs in different plant tissues under the same microwave conditions, yet achieving good recoveries through methanol extraction. It emphasized the necessity of heating extraction when extracting GSLs from frozen-fresh samples.
Glucosinolates (GSLs) are important precursor compounds with anticancer activities in Brassicaceae vegetables and are readily hydrolyzed by myrosinase. Given the diversity of these species, establishing an accurate and universal method to quantify intact GSLs in different plant tissues is necessary. Here, we compared and optimized three tissue disruption methods for sample preparation. After microwave treatment for 90 s, 13 GSLs in homogenized Chinese cabbage samples were recovered at 73-124%. However, a limitation of this method was that different tissues could not be processed under the same microwave conditions. Regarding universality, GSLs in Brassicaceae vegetables could be extracted from freeze-dried sample powder with 70% methanol (v/v) or frozen-fresh sample powder with 80% methanol (v/v). Moreover, heating extraction is necessary for GSLs extracted from frozen-fresh sample powder. Average recoveries of the two optimized methods were 74-119% with relative standard deviations <= 15%, with the limits of quantification 5.72-17.40 nmol/g dry weight and 0.80-1.43 nmol/g fresh weight, respectively. Notably, the method for analyzing intact GSLs was more efficient than that for desulfo-GSLs regarding operational complexity, detection speed and quantification accuracy. The developed method was applied to identify the characteristic GSLs in 15 Brassicaceae vegetables, providing a foundation for further research on GSLs.

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