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高效液相色谱-带电气溶胶检测法采用反相梯度对鼠李糖脂生物表面活性剂进行定量分析。

High performance liquid chromatography-charged aerosol detection applying an inverse gradient for quantification of rhamnolipid biosurfactants.

作者信息

Behrens Beate, Baune Matthias, Jungkeit Janek, Tiso Till, Blank Lars M, Hayen Heiko

机构信息

Institute of Inorganic and Analytical Chemistry, University of Münster, Corrensstr. 30, 48149 Münster, Germany.

Department of Food Chemistry, Faculty of Mathematics and Natural Sciences, University of Wuppertal, Gaussstr. 20, 42119 Wuppertal, Germany.

出版信息

J Chromatogr A. 2016 Jul 15;1455:125-132. doi: 10.1016/j.chroma.2016.05.079. Epub 2016 May 25.

Abstract

A method using high performance liquid chromatography coupled to charged-aerosol detection (HPLC-CAD) was developed for the quantification of rhamnolipid biosurfactants. Qualitative sample composition was determined by liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). The relative quantification of different derivatives of rhamnolipids including di-rhamnolipids, mono-rhamnolipids, and their precursors 3-(3-hydroxyalkanoyloxy)alkanoic acids (HAAs) differed for two compared LC-MS instruments and revealed instrument dependent responses. Our here reported HPLC-CAD method provides uniform response. An inverse gradient was applied for the absolute quantification of rhamnolipid congeners to account for the detector's dependency on the solvent composition. The CAD produces a uniform response not only for the analytes but also for structurally different (nonvolatile) compounds. It was demonstrated that n-dodecyl-β-d-maltoside or deoxycholic acid can be used as alternative standards. The method of HPLC-ultra violet (UV) detection after a derivatization of rhamnolipids and HAAs to their corresponding phenacyl esters confirmed the obtained results but required additional, laborious sample preparation steps. Sensitivity determined as limit of detection and limit of quantification for four mono-rhamnolipids was in the range of 0.3-1.0 and 1.2-2.0μg/mL, respectively, for HPLC-CAD and 0.4 and 1.5μg/mL, respectively, for HPLC-UV. Linearity for HPLC-CAD was at least 0.996 (R(2)) in the calibrated range of about 1-200μg/mL. Hence, the here presented HPLC-CAD method allows absolute quantification of rhamnolipids and derivatives.

摘要

开发了一种使用高效液相色谱-电荷气溶胶检测(HPLC-CAD)的方法来定量鼠李糖脂生物表面活性剂。通过液相色谱-串联质谱(LC-MS/MS)确定样品的定性组成。对于两台比较的LC-MS仪器,鼠李糖脂不同衍生物(包括二鼠李糖脂、单鼠李糖脂及其前体3-(3-羟基链烷酰氧基)链烷酸(HAAs))的相对定量有所不同,并显示出仪器依赖性响应。我们在此报道的HPLC-CAD方法提供了一致的响应。采用反梯度对鼠李糖脂同系物进行绝对定量,以考虑检测器对溶剂组成的依赖性。CAD不仅对分析物,而且对结构不同的(非挥发性)化合物都产生一致的响应。结果表明,正十二烷基-β-D-麦芽糖苷或脱氧胆酸可用作替代标准品。将鼠李糖脂和HAAs衍生为相应的苯甲酰酯后进行HPLC-紫外(UV)检测的方法证实了所得结果,但需要额外的、繁琐的样品制备步骤。对于四种单鼠李糖脂,HPLC-CAD的检测限和定量限分别为0.3-1.0μg/mL和1.2-2.0μg/mL,HPLC-UV的检测限和定量限分别为0.4μg/mL和1.5μg/mL。HPLC-CAD在约1-200μg/mL的校准范围内线性至少为0.996(R(2))。因此,本文提出的HPLC-CAD方法可对鼠李糖脂及其衍生物进行绝对定量。

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