调谐单四极杆质量检测器与超临界流体色谱联用的参数,用于合成卡西酮的对映体分离

Natalie Paškanová , Petra Hlavatá , Bronislav Jurásek , Martin Kuchař , Michal Kohout
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引用次数: 0

摘要

在上一篇论文中,我们介绍了一种利用 SFC-ESI-MS 和反补溶剂梯度在手性齐聚物离子交换器上对对映体分离卡西酮的新方法。反梯度使我们能够在提高质谱响应的同时稳定电喷雾离子化。在本研究中,我们对之前优化的 SFC-ESI-MS 方法进行了微调,并将其效率与默认的 ESI-MS 方法进行了比较。为了提高分析物的检测能力,我们设计了一系列复杂的实验,对以下三个参数的所有组合进行了评估:锥体电压(5 至 27 V)、探针温度(250 至 550 °C)和用于正电离的毛细管电压(0.3 至 1.5 kV)。优化之后,还测试了进入 ESI 离子源之前引入的各种比例的补充溶剂(甲醇/水/甲酸)。尽管进行了如此全面的测试,但调整后的 ESI-MS 参数与默认参数的测试结果并无明显差异。同样,最合适的补充溶剂成分是最初使用的 90/10/0.1(v/v/v)比例。这些结果加强了我们上一篇论文的研究结果,在该论文中,我们优化了补充溶剂的流速,并显示了其对 ESI-MS 响应的重大影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tuning parameters of single quadrupole mass detector hyphenated to supercritical fluid chromatography for enantioseparation of synthetic cathinones

Tuning parameters of single quadrupole mass detector hyphenated to supercritical fluid chromatography for enantioseparation of synthetic cathinones

In our previous paper, we introduced a new method for the enantioseparation of cathinones on chiral zwitterion ion exchangers by SFC-ESI-MS with an inverse make-up solvent gradient. The inverse gradient enabled us to stabilize electrospray ionization while simultaneously increasing MS response. In this study, we fine-tuned our previously optimized SFC-ESI-MS method and compared its efficiency with that of the default ESI-MS method. To enhance analyte detection, we designed a complex series of experiments in which all combinations of the following three parameters were evaluated: cone voltage (5 to 27 V), probe temperature (250 to 550 °C) and capillary voltage for positive ionization (0.3 to 1.5 kV). After optimization, various ratios of the make-up solvent (methanol/water/formic acid) introduced before entering the ESI ion source were also tested. Despite this comprehensive testing regime, there were no significant differences between the results obtained for the tuned and default ESI-MS parameters. Similarly, the most suitable make-up solvent composition was the originally used ratio of 90/10/0.1 (v/v/v). These results reinforce the findings of our previous paper, in which we optimized the make-up solvent flow rate and showed its significant impact on ESI-MS response.

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来源期刊
Journal of chromatography open
Journal of chromatography open Analytical Chemistry
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