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超高效超临界流体色谱与大气压化学电离高分辨率质谱联用:第1部分。天然非极性化合物分析的联用参数研究。

Hyphenation of ultra high performance supercritical fluid chromatography with atmospheric pressure chemical ionisation high resolution mass spectrometry: Part 1. Study of the coupling parameters for the analysis of natural non-polar compounds.

作者信息

Duval Johanna, Colas Cyril, Pecher Virginie, Poujol Marion, Tranchant Jean-François, Lesellier Eric

机构信息

Univ. Orléans, CNRS, ICOA, UMR 7311, F-45067 Orléans, France.

Univ. Orléans, CNRS, ICOA, UMR 7311, F-45067 Orléans, France; CNRS, CBM, UPR 4301, Univ. Orléans, F-45071 Orléans, France.

出版信息

J Chromatogr A. 2017 Aug 4;1509:132-140. doi: 10.1016/j.chroma.2017.06.016. Epub 2017 Jun 8.

DOI:10.1016/j.chroma.2017.06.016
PMID:28619592
Abstract

An analytical method based on Ultra-High-Performance Supercritical Fluid Chromatography (UHPSFC) coupled with Atmospheric Pressure Chemical Ionization - High-resolution mass spectrometry (APCI-Q-TOF-HRMS) was developed for compounds screening from oily samples. The hyphenation was made using a commercial UHPLC device coupled to a CO pump in order to perform the chromatographic analysis. An adaptation of the injection system for compressible fluids was accomplished for this coupling: this modification of the injection sequence was achieved to prevent unusual variations of the injected volume related to the use of a compressible fluid. UHPSFC-HRMS hyphenation was optimized to enhance the response of the varied compounds from a seed extract (anthraquinones, free fatty acids, diacylglycerols, hydroxylated triacylglycerols and triacylglycerols). No split was used prior to the APCI ionization source, allowing introducing all the compounds in the spectrometer, ensuring a better sensitivity for minor compounds. The effects of a mechanical make-up (T-piece) added before this ionization source was discussed in terms of standard deviation of response, response intensity and fragmentation percentage. The location of the T-piece with regards to the backpressure regulator (BPR), the flow rate and the nature of the make-up solvent were studied. Results show that the effects of the studied parameters depend on the nature of the compounds, whereas the make-up addition favours the robustness of the mass response (quantitative aspect).

摘要

开发了一种基于超高效超临界流体色谱(UHPSFC)与大气压化学电离-高分辨率质谱(APCI-Q-TOF-HRMS)联用的分析方法,用于从油性样品中筛选化合物。联用是通过将商用UHPLC设备与CO泵连接来进行色谱分析实现的。针对这种联用,对可压缩流体的进样系统进行了改进:通过改变进样顺序来防止因使用可压缩流体而导致进样体积出现异常变化。对UHPSFC-HRMS联用进行了优化,以增强种子提取物中多种化合物(蒽醌、游离脂肪酸、二酰基甘油、羟基化三酰基甘油和三酰基甘油)的响应。在APCI电离源之前未使用分流,从而可将所有化合物引入质谱仪,确保对痕量化合物具有更高的灵敏度。从响应的标准偏差、响应强度和碎片百分比方面讨论了在该电离源之前添加机械补充装置(T型接头)的影响。研究了T型接头相对于背压调节器(BPR)的位置、补充溶剂的流速和性质。结果表明,所研究参数的影响取决于化合物的性质,而补充装置的添加有利于提高质谱响应的稳健性(定量方面)。

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