A Novel LC-MS Based Targeted Metabolomic Approach to Study the Biomarkers of Food Intake

被引:11
作者
Tang, Yao [1 ]
Zhu, Yingdong [1 ]
Sang, Shengmin [1 ]
机构
[1] North Carolina Agr & Tech State Univ, Lab Funct Foods & Human Hlth, Ctr Excellence Postharvest Technol, North Carolina Res Campus,500 Laureate Way, Kannapolis, NC 28081 USA
基金
美国农业部;
关键词
dietary metabolite database; food intake biomarkers; paired mass distance networking; targeted metabolomics; whole grain wheat metabolites; DIETARY; IDENTIFICATION; PLASMA; URINE; BENZOXAZINOIDS; CONSUMPTION; WHEAT; ACID;
D O I
10.1002/mnfr.202000615
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Scope In this work, an integrated strategy is developed for rapid discovery, precise identification, and automated quantification for the biomarkers of food intake (BFIs) for specific food exposure using an ultra-high-pressure liquid chromatography-high-resolution mass spectrometry (MS) based targeted metabolomics approach. Methods and results Using whole grain (WG) wheat intake as an example, the combination of paired mass distance networking and parallel reaction monitoring analysis is applied to selectively extract and identify WG metabolites in human urine samples. As a result, a total of 76 wheat phytochemical-derived metabolites, including 17 alkylresorcinol metabolites, 20 benzoxazinoid derivatives, and 39 phenolic acid metabolites are identified. Subsequently, a MS spectral database consisting of the identified metabolites is created by mzVault. The characteristics of identified metabolites from the database are incorporated into the TraceFinder software to establish a quantification platform. Using a standardized urine sample, the authors are able to simultaneously quantify both free and conjugated (sulfate and glucuronide) WG wheat metabolites in real samples without further enzymatic hydrolysis, which is validated by using authentic standards to quantify these metabolites. Conclusion This novel strategy opens the window to study the biomarkers of specific food intake and make it feasible to validate the BFIs in large-scale human studies.
引用
收藏
页数:13
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