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Optimized selection of liquid chromatography conditions for wide range analysis of natural compounds

机译:优化选择自然化合物广泛分析的液相色谱条件

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Plant secondary metabolites are an almost unlimited reservoir of potential bioactive compounds. In view of the wide chemical space covered by natural compounds, their comprehensive analysis requires multiple and complementary approaches. In this study, numerous chromatographic conditions were tested for the analysis of a set of 120 representative natural compounds covering a wide polarity range (18 log P units). The experiments were performed on 59 different conditions involving 29 RPLC and HILIC dedicated stationary phases, as well as more exotic mixed mode columns. The best RPLC and HILIC conditions were determined using Derringer's desirability functions, based on various criteria (i.e. retention, peak shape, distribution of compounds during the gradient...). After this first selection, only the most promising conditions were kept (19 in RPLC and 11 in HILIC). The selectivity complementarity among each chromatographic mode was assessed by principal component analysis (PCA) and hierarchical cluster analysis (HCA). In RPLC, a pentabromobenzyl (PBrBz) stationary phase was identified as particularly versatile and could constitute an elegant first intention screening column. Two additional conditions allowed to extend the range of natural compounds space that can be analyzed, while offering better selectivity for basic analytes (hybrid silica graft with C8 moiety operated at pH 9 (Hyb C8)) and acidic compounds (positively charged hybrid silica graft with pentafluorophenyl moiety (Hyb+ PFPh). Although less generic in terms of amenable compounds, an ion exchange/RP mixed mode stationary phase (MM TriP1) offered notably enhanced retention of more polar analytes under RPLC conditions. With these four conditions, 89% of the natural substances were detected by LC MS with acceptable retentions and peak shapes. In HILIC, four acceptable and complementary conditions were also highlighted. Both Syncro-Z (zwitterionic HILIC phase) and Diol columns were found to offer balanced retention and selectivity for most of the polar compounds (log D-PH3 < 1.0). These two columns could be advantageously complemented by hybrid Amide column operated at pH 3 and Amino stationary phase at pH 5, to further enhance both retention and selectivity of polar basic and acidic species, respectively. (C) 2017 Elsevier B.V. All rights reserved.
机译:植物次级代谢物是一种几乎无限的潜在生物活性化合物的储层。鉴于天然化合物覆盖的宽化学空间,它们的综合分析需要多种和互补的方法。在该研究中,测试了许多色谱条件,用于分析覆盖宽极性范围(18个LOG P单位)的一组120个代表性天然化合物。在59种不同的条件下进行实验,涉及29个RPLC和HILIC专用固定阶段,以及更加异种混合模式柱。基于各种标准(即保持,峰值形状,化合物在梯度期间的化合物的分布)确定最佳的RPLC和HILIC条件是使用Derringer的期望功能确定的。在第一次选择之后,只有最有希望的条件才存(RPLC和HILIC中的11个)。通过主成分分析(PCA)和分层聚类分析(HCA)评估每种色谱模式之间的选择性互补性。在RPLC中,鉴定了五溴苄基(PBRBZ)固定相特别通用,可以构成优雅的第一意图筛选柱。允许两种额外的条件延长可以分析的天然化合物空间的范围,同时为基本分析物提供更好的选择性(杂合二氧化硅接枝在pH 9(HYB C8))和酸性化合物(带正电荷的杂交硅胶移植物中)五氟苯基部分(Hyb + PFPH)。尽管在可允许化合物方面的较少通用,但是离子交换/ RP混合模式固定相(MM TRIP1)在RPLC条件下,显着提高了更多极性分析物的保留。有这四种条件,其中89% LC MS检测天然物质,具有可接受的留下和峰形状。在HILIC,还突出了四种可接受的和互补的条件。发现Syncro-Z(两性离子相位)和二醇塔为大多数情况提供平衡的保留和选择性。极性化合物(log d-ph3 <1.0)。这两列可以有利地通过在pH3和氨基静止P处操作的杂种酰胺柱互补在pH5处散列,进一步增强极性碱性和酸性物质的保留和选择性。 (c)2017年Elsevier B.V.保留所有权利。

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