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Synchronized Survey Scan Approach Allows for Efficient Discrimination of Isomeric and Isobaric Compounds during LC-MS/MS Analyses

机译:同步测量扫描方法允许在LC-MS / MS分析期间有效地辨别异构和异脂化合物

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Liquid chromatography-mass spectrometry- (LC-MS-) based multiple reaction monitoring (MRM) methods have been used to detect and quantify metabolites for years. These approaches rely on the monitoring of various fragmentation pathways of multiple precursors and the subsequent corresponding product ions. However, MRM methods are incapable of confidently discriminating between isomeric and isobaric molecules and, as such, the development of methods capable of overcoming this challenge has become imperative. Due to increasing scanning rates of recent MS instruments, it is now possible to operate MS instruments both in the static and dynamic modes. One such method is known as synchronized survey scan (SSS), which is capable of acquiring a product ion scan (PIS) during MRM analysis. The current study shows, for the first time, the use of SSS-based PIS approach as a feasible identification feature of MRM. To achieve the above, five positional isomers of dicaffeoylquinic acids (diCQAs) were studied with the aid of SSS-based PIS method. Here, the MRM transitions were automatically optimized using a 3,5-diCQA isomer by monitoring fragmentation transitions common to all five isomers. Using the mixture of these isomers, fragmentation spectra of the five isomers achieved with SSS-based PIS were used to identify each isomer based on previously published hierarchical fragmentation keys. The optimized method was also used to detect and distinguish between diCQA components found in Bidens pilosa and their isobaric counterparts found in Moringa oleifera plants. Thus, the method was shown to distinguish (by differences in fragmentation patterns) between diCQA and their isobars, caffeoylquinic acid (CQA) glycosides. In conclusion, SSS allowed the detection and discrimination of isomeric and isobaric compounds in a single chromatographic run by producing a PIS spectrum, triggered in the automatic MS/MS synchronized survey scan mode.
机译:基于液相色谱 - 质谱 - (LC-MS-)的多重反应监测(MRM)方法已被用于检测和量化代谢物多年。这些方法依赖于监测多种前体和随后的相应产物离子的各种碎片途径。然而,MRM方法无法自信地歧视异构和异甲分子之间,因此,能够克服这一挑战的方法的发展已经是势在必行的。由于近期MS仪器的扫描率的增加,现在可以在静态和动态模式下操作MS仪器。一种这样的方法称为同步调查扫描(SSS),其能够在MRM分析期间获取产品离子扫描(PIS)。目前的研究表明,首次使用基于SSS的PIS方法作为MRM的可行识别特征。为达到以上,借助于基于SSS的PIS方法研究了二聚氰酰喹啉酸(DICQAs)的五种位置异构体。这里,通过监测所有五个异构体共同的碎片转变,使用3,5-DICQA异构体自动优化MRM转变。使用这些异构体的混合物,使用基于SSS的PIS实现的五个异构体的碎片光谱来鉴定基于先前公开的分级碎片键的每个异构体。该优化方法还用于检测和区分Bidens Pilosa中发现的DICQA组分及其在Moringa Oleifera植物中发现的病态对应物。因此,显示该方法以区分DICQA及其等离物质之间的碳酸甘油酸(CQA)糖苷之间的(通过碎片模式差异)。总之,SSS通过在自动MS / MS同步调查扫描模式中触发,通过产生PIS光谱,允许SSS在单个色谱过程中检测和辨别单个色谱法中的异构体和等离性化合物。

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