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平面色谱和液相色谱的正交分割用于生物测定基质中生物标志物的质谱分析(NP-HPTLC-UV/vis/FLD-生物测定-RP/IEX-HPLC-UV/vis-ESI-MS)。

Orthogonal Hyphenation of Planar and Liquid Chromatography for Mass Spectrometry of Biomarkers out of the Bioassay Matrix (NP-HPTLC-UV/vis/FLD-Bioassay-RP/IEX-HPLC-UV/vis-ESI-MS).

机构信息

Chair of Food Science, Institute of Nutritional Science, and TransMIT Center for Effect-Directed Analysis, Justus Liebig University Giessen, Heinrich-Buff-Ring 26-32, 35392 Giessen, Germany.

出版信息

Anal Chem. 2020 Jul 7;92(13):9057-9064. doi: 10.1021/acs.analchem.0c01251. Epub 2020 Jun 9.

Abstract

Bioprofiling on the planar chromatogram with in situ biological/enzymatic assays is a powerful bioanalytical screening tool for the nontargeted detection of known and especially unknown/unidentified bioactive compounds directly in multicomponent mixtures (e.g., foods, spices, and botanicals). However, together with the bioactive zone, the adsorbed bioassay medium is eluted into the mass spectrometer (MS) and interfering with evaluation. Another sample track without bioassay has thus been handled in parallel. Hence, for a direct zone elution from the bioautogram, different setups were investigated to reduce the impact of the bioassay medium load. A biocompatible filter, orthogonal reversed-phase/cation-exchange columns (RP/IEX-HPLC), UV/vis detector, and a Rheodyne valve were installed between the zone eluting interface (after normal-phase high-performance thin-layer chromatography-multi-imaging-bioassay, NP-HPTLC-UV/vis/FLD-bioassay) and the MS. For the negative electrospray ionization mode (ESI), an RP-18e-HPLC column and valve switch were exploited. After gradient optimization, the RP-column retarded the eluted polar compounds and split-off the salts of the bioassay medium in the first minutes. This reduced the bioassay load and separated analyte signals thereof. However, most bioassay medium mass signals were predominantly detectable in ESI-MS. Here, the reduction of bioassay matrix signals was achieved by integrating a mixed-mode RP/IEX column. Finally, two different superhyphenations were successfully proven: NP-HPLC-UV/vis/FLD-bioassay-RP-HPLC-UV/vis-ESI-MS with a valve switch and NP-HPLC-UV/vis/FLD-bioassay-RP/IEX-HPLC-UV/vis-ESI-MS with or without it. Although the original bioprofiling (NP-HPTLC-UV/vis/FLD-bioassay) was prolonged from 3 to 13 min per sample, such superhyphenations covering chemistry/biology/mass spectrometry are considered as an efficient nontarget bioanalytical tool for fast evaluation of complex samples.

摘要

在平面色谱图上进行原位生物/酶分析的生物剖析是一种强大的生物分析筛选工具,可用于直接在多组分混合物(例如食品、香料和植物药)中对已知和特别是未知/未识别的生物活性化合物进行非靶向检测。然而,与生物活性区带一起,吸附的生物测定介质被洗脱到质谱仪(MS)中,并干扰了评估。因此,在平行处理了另一条没有生物测定的样品轨道。因此,为了直接从生物自显影图洗脱区带,研究了不同的设置以减少生物测定介质负载的影响。在洗脱界面(在正相高效薄层色谱-多成像-生物测定、NP-HPTLC-UV/vis/FLD-生物测定之后)和 MS 之间安装了生物相容的过滤器、正交反相/阳离子交换柱(RP/IEX-HPLC)、UV/vis 检测器和 Rheodyne 阀。对于负电喷雾电离模式(ESI),利用了 RP-18e-HPLC 柱和阀切换。经过梯度优化,RP 柱延迟了洗脱的极性化合物,并在最初的几分钟内将生物测定介质的盐分离开。这减少了生物测定基质的负载并分离了分析物信号。然而,ESI-MS 中主要检测到大多数生物测定介质的质量信号。在这里,通过整合混合模式 RP/IEX 柱实现了生物测定基质信号的减少。最后,成功证明了两种不同的超链接:带有阀切换的 NP-HPLC-UV/vis/FLD-生物测定-RP-HPLC-UV/vis-ESI-MS 和无或有它的 NP-HPLC-UV/vis/FLD-生物测定-RP/IEX-HPLC-UV/vis-ESI-MS。虽然原始生物剖析(NP-HPTLC-UV/vis/FLD-生物测定)的每个样品耗时从 3 分钟延长到 13 分钟,但这种涵盖化学/生物学/质谱学的超链接被认为是快速评估复杂样品的高效非靶向生物分析工具。

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