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Analysis of a series of chlorogenic acid isomers using differential ion mobility and tandem mass spectrometry

化学 串联质谱法 质谱法 离子迁移光谱法 串联 绿原酸 离子 差速器(机械装置) 系列(地层学) 色谱法 离子迁移谱-质谱 分析化学(期刊) 选择性反应监测 有机化学 航空航天工程 工程类 古生物学 生物
作者
Jamie L. Willems,Mona M. Khamis,Waleed Mohammed‐Saeid,Randy W. Purves,George S. Katselis,Nicholas H. Low,Anas El‐Aneed
出处
期刊:Analytica Chimica Acta [Elsevier BV]
卷期号:933: 164-174 被引量:134
标识
DOI:10.1016/j.aca.2016.05.041
摘要

Chlorogenic acids are among the most abundant phenolics found in the human diet. Of these, the mono-caffeoylquinic acids are the predominant phenolics found in fruits, such as apples and pears, and products derived from them. In this research, a comprehensive study of the electrospray ionization (ESI) tandem mass spectrometric (MS/MS) dissociation behavior of the three most common mono-caffeoylquinic acids, namely 5-O-caffeoylquinic acid (5-CQA), 3-O-caffeoylquinic acid (3-CQA) and 4-O-caffeoylquinic acid (4-CQA), were determined using both positive and negative ionization. All proposed structures of the observed product ions were confirmed with second-generation MS(3) experiments. Similarities and differences between the dissociation pathways in the positive and negative ion modes are discussed, confirming the proposed structures and the established MS/MS fingerprints. MS/MS dissociation was primarily driven via the cleavage of the ester bond linking the quinic acid moiety to the caffeic acid moiety within tested molecules. Despite being structural isomers with the same m/z values and dissociation behaviors, the MS/MS data in the negative ion mode was able to differentiate the three isomers based on ion intensity for the major product ions, observed at m/z 191, 179 and 173. This differentiation was consistent among various MS instruments. In addition, ESI coupled with high-field asymmetric waveform ion mobility spectrometry-mass spectrometry (ESI-FAIMS-MS) was employed for the separation of these compounds for the first time. By combining MS/MS data and differential ion mobility, a method for the separation and identification of mono-caffeoylquinic in apple/pear juice samples was developed with a run time of less than 1 min. It is envisaged that this methodology could be used to identify pure juices based on their chlorogenic acid profile (i.e., metabolomics), and could also be used to detect juice-to-juice adulteration (e.g., apple juice addition to pear juice).
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