Schindlegger Yvonne, Oburger Eva, Gruber Barbara, Schenkeveld Walter D C, Kraemer Stephan M, Puschenreiter Markus, Koellensperger Gunda, Hann Stephan
Department of Chemistry, University of Natural Resources and Life Sciences-BOKU Vienna, Vienna, Austria.
Electrophoresis. 2014 May;35(9):1375-85. doi: 10.1002/elps.201300551. Epub 2014 Mar 10.
For the first time the phytosiderophore 2'-deoxymugineic acid (DMA) could be accurately quantified by LC-MS/MS in plant and soil related samples. For this purpose a novel chromatographic method employing porous graphitic carbon as stationary phase combined with ESI-MS/MS detection in selected reaction monitoring was developed. Isotope dilution was implemented by using in-house synthesized DMA as external calibrant and ¹³C₄-labeled DMA as internal standard (concentration levels of standards 0.1-80 μM, determination coefficient of linear regression R² > 0.9995). Sample preparation involved acidification of the samples in order to obtain complete dissociation of metal-DMA complexes. Excellent matrix related LOD and LOQ depending on different experimental setups were obtained in the range of 3-34 nM and 11-113 nM, respectively. Standard addition experiments and the implementation of the internal ¹³C₄-DMA standard proved the accuracy of the quantification strategy even in complex matrices such as soil solution. The repeatability of the method, including sample preparation, expressed as short- and long term precision was below 4 and 5% RSD, respectively. Finally, application in the context of plant and soil research to samples from rhizosphere sampling via micro suction cups, from soil solutions and soil adsorption/extraction studies revealed a DMA concentration range from 0.1 to 235 μM.
首次能够通过液相色谱-串联质谱法(LC-MS/MS)对植物和土壤相关样品中的植物铁载体2'-脱氧麦根酸(DMA)进行准确定量。为此,开发了一种新型色谱方法,该方法采用多孔石墨化碳作为固定相,并结合选择反应监测中的电喷雾电离串联质谱检测。通过使用内部合成的DMA作为外部校准物和¹³C₄标记的DMA作为内标来实现同位素稀释(标准品浓度水平为0.1 - 80 μM,线性回归的决定系数R²> 0.9995)。样品制备包括对样品进行酸化,以实现金属-DMA络合物的完全解离。根据不同的实验设置,分别在3 - 34 nM和11 - 113 nM范围内获得了与基质相关的出色检测限(LOD)和定量限(LOQ)。标准加入实验以及内部¹³C₄-DMA标准品的应用证明了即使在土壤溶液等复杂基质中,定量策略的准确性。该方法的重复性,包括样品制备,以短期和长期精密度表示,相对标准偏差(RSD)分别低于4%和5%。最后,在植物和土壤研究背景下,对通过微吸杯从根际采样、土壤溶液和土壤吸附/萃取研究中获得的样品进行应用,结果显示DMA浓度范围为0.1至235 μM。