Division of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Helsinki, P.O. Box 56, FIN-00014 Viikinkaari 5 E, Finland.
Anal Chem. 2013 Jun 18;85(12):5715-9. doi: 10.1021/ac4002673. Epub 2013 May 28.
We present a capillary photoionization (CPI) method for mass spectrometric (MS) analysis of liquid and gaseous samples. CPI utilizes a heated transfer capillary with a vacuum ultraviolet transparent MgF2 window, through which vacuum UV light (10 eV) from an external source enters the capillary. The liquid or gaseous sample, together with dopant, is introduced directly into the heated transfer capillary between the atmosphere and the vacuum of the MS. Since the sample is vaporized and photoionized inside the capillary, ion transmission is maximized, resulting in good overall sensitivity for nonpolar and polar compounds. As in atmospheric pressure photoionization, ionization in CPI occurs either by proton transfer or by charge exchange reactions. The feasibility of CPI was demonstrated with selected nonpolar and polar compounds. A particular advantage of CPI is that it enables the analysis of nonvolatile and nonpolar compounds in liquid samples with high ionization efficiency. This is not possible with existing capillary ionization methods. The performance of CPI as an interface between GC and MS and its applicability for the analysis of steroids in biological samples are also demonstrated. The GC-CPI-MS method shows good chromatographic resolution, linearity (R(2) > 0.993), limits of detection (LOD) in the range of 2-6 pg/mL and repeatability of injection with relative standard deviations of 4-15%.
我们提出了一种毛细管光电离(CPI)方法,用于液体和气体样品的质谱(MS)分析。CPI 利用带有真空紫外透明 MgF2 窗口的加热传输毛细管,外部光源的真空紫外光(10 eV)通过该窗口进入毛细管。液体或气体样品与掺杂剂一起直接引入加热的传输毛细管中,该毛细管位于大气压和 MS 真空之间。由于样品在毛细管内被蒸发和光电离,因此离子传输最大化,从而实现了非极性和极性化合物的良好整体灵敏度。与大气压光电离一样,CPI 中的电离通过质子转移或电荷交换反应发生。通过选择非极性和极性化合物证明了 CPI 的可行性。CPI 的一个特殊优点是它能够以高的电离效率分析液体样品中的非挥发性和非极性化合物。这是现有毛细管电离方法不可能实现的。还展示了 CPI 作为 GC 和 MS 之间的接口的性能及其在生物样品中类固醇分析中的应用。GC-CPI-MS 方法显示出良好的色谱分辨率、线性(R(2)> 0.993)、检测限(LOD)范围为 2-6 pg/mL 以及进样重复性,相对标准偏差为 4-15%。