Schaumlöffel Dirk, Ruiz Encinar Jorge, Łobiński Ryszard
Group of Bio-Inorganic Analytical Chemistry, CNRS UMR 5034, Hélioparc, 2, Av. Pr. Angot, F-64053 Pau, France.
Anal Chem. 2003 Dec 15;75(24):6837-42. doi: 10.1021/ac034819h.
A sheathless interface based on a total consumption micronebulizer operating at flow rates in the range 0.5-7.5 microL min(-1) was developed between capillary HPLC and ICPMS. It allowed the efficient nebulization and transport into the plasma of mobile phases containing up to 100% organic solvent without either cooling the spray chamber or oxygen addition. The coupled system was applied to selenopeptide mapping in a protein fraction isolated from a selenized yeast extract. The detection limits were 150 (80Se) and 200 fg (82Se) for a quadrupole instrument with and without a collision cell, respectively, which is a factor 100-150 less than that reported elsewhere for HPLC-ICPMS. The minimal peak broadening ( approximately 5 s at the half-height) allowed baseline resolution of a mixture containing more than 30 selenopeptides, many of which could not be separated using the conventional HPLC-ICPMS coupling.
在毛细管高效液相色谱(HPLC)和电感耦合等离子体质谱(ICPMS)之间开发了一种基于全消耗微雾化器的无鞘接口,该微雾化器在0.5 - 7.5微升/分钟的流速范围内运行。它能够在不冷却喷雾室或添加氧气的情况下,对含有高达100%有机溶剂的流动相进行高效雾化并传输到等离子体中。该联用系统应用于从富硒酵母提取物中分离出的蛋白质组分中的硒肽图谱分析。对于带和不带碰撞池的四极杆仪器,检测限分别为150(80Se)和200飞克(82Se),这比其他地方报道的HPLC - ICPMS检测限低100 - 150倍。最小的峰展宽(半高宽约5秒)使得包含30多种硒肽的混合物能够实现基线分离,其中许多硒肽使用传统的HPLC - ICPMS联用无法分离。