Timothy T. Salomons, David Simon and Richard Oleschuk
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Mass spectrometry analysis is performed utilizing a liquid micro-junction surface sampling probe to extract dried analytes from the surface of the SETs followed by electrospray ionisation. A reverse phase separation of pharmaceutical compounds is “recorded” using the micro-fractionation device followed by “reading” the chromatographic trace with a mass spectrometer 24 hours after the separation was performed/archived, demonstrating a true decoupling of LC, and MS. Additionally, we demonstrate the ability to collect microfractions with sub-one-second integration time, approaching the scan time of a mass spectrometer or UV-Vis detector. 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引用次数: 0
摘要
我们报告了一种用于高效液相色谱-质谱联用技术的微型分馏装置,可将色谱分离过程归档到优化的表面能阱(SET)阵列上。该方法有望显著改变纳升液相色谱-质谱工作流程,实现分离与分析的解耦。SET 的润湿特性可使 HPLC 洗脱液流自发分裂成液滴微馏分。然后对液滴微馏分进行干燥,以便于存档分离的储存和运输。通过结合 SET 的设计、形状、大小和间距,探索了间断脱水阵列参数,以最大限度地提高阵列体积和分辨率。利用液态微结表面取样探针从 SET 表面提取干燥的分析物,然后进行电喷雾离子化,从而进行质谱分析。使用微分馏装置 "记录 "药物化合物的反相分离,然后在分离/存档 24 小时后使用质谱仪 "读取 "色谱跟踪,从而展示了液相色谱和质谱的真正解耦。此外,我们还展示了以亚一秒积分时间收集微馏分的能力,接近质谱仪或紫外可见检测器的扫描时间。随着设备的进一步改进,1 秒以下的微馏分可实现与在线 LC-MS 数据无异的存档色谱图的无缝重建,同时还具有便于存储和运输存档分离物的优点。
Storing liquid chromatographic separations on surface energy traps: decoupling the LC and the mass spectrometer†
We report a micro-fractionation device for high performance liquid chromatography-mass spectrometry to archive chromatographic separations on an array of optimized surface energy traps (SETs). The method has the potential to significantly alter nanoflow LC-MS workflow, decoupling separation and analysis. The wetting characteristics of the SETs cause the HPLC eluent stream to spontaneously split into droplet microfractions. The droplet mirofractions are then dried down to enable facile storage and transport of the archived separation. Discontinuously dewetting array parameters were explored to maximize array volume and resolution using a combination of SET design, shape, size, and spacing. Mass spectrometry analysis is performed utilizing a liquid micro-junction surface sampling probe to extract dried analytes from the surface of the SETs followed by electrospray ionisation. A reverse phase separation of pharmaceutical compounds is “recorded” using the micro-fractionation device followed by “reading” the chromatographic trace with a mass spectrometer 24 hours after the separation was performed/archived, demonstrating a true decoupling of LC, and MS. Additionally, we demonstrate the ability to collect microfractions with sub-one-second integration time, approaching the scan time of a mass spectrometer or UV-Vis detector. With further improvements to the device, sub-1-second micro-fractionation may enable seamless reconstruction of archived chromatograms indistinguishable from online LC-MS data, while also providing the benefits of easy storage and transport of archived separations.