Hommerson Paul, Khan Amjad M, Bristow Tony, Niessen Wilfried, de Jong Gerhardus J, Somsen Govert W
Department of Biomedical Analysis, Utrecht University, P.O. Box 80082, 3508 TB Utrecht, The Netherlands.
Anal Chem. 2007 Jul 15;79(14):5351-7. doi: 10.1021/ac070426x. Epub 2007 Jun 13.
In a previous study on capillary electrophoresis-atmospheric pressure photoionization mass spectrometry (CE-APPI-MS), it was observed that the formation of gas-phase ions does not always proceed through photon-induced mechanisms (Hommerson, P.; Khan, A. M.; De Jong, G. J.; Somsen, G. W. Electrophoresis 2007, 28, 1444-1453). That is, analyte signals were observed when the VUV excitation source was switched off. The aim of the present study was to further explore this photon-independent ionization (PII) process. Parameters such as MS capillary voltage, compound nature, background electrolyte (BGE) composition, and presence of dopants were studied using a CE-APPI-MS setup. Infusion experiments showed a relatively low MS capillary voltage of approximately 600 V to be the main prerequisite for PII. Quaternary ammonium compounds showed strong responses in PII-MS but could not be observed in dopant-assisted APPI. Basic amines could be ionized by both photoionization (PI) and PII, whereas neutral compounds (steroids) could only be observed using PI. Nonvolatile BGEs appeared to cause substantial ionization suppression in PII, while PI signals remained largely unaffected. Selection of the proper interface and MS settings allowed PI and PII to proceed simultaneously, which broadened the range of compounds that could be analyzed in a single CE-APPI-MS run. Based on the observed characteristics, it is concluded that PII most probably occurs by a liquid-phase ionization mechanism, which appears to arise in the APPI source when specific conditions are selected.
在先前一项关于毛细管电泳-大气压光电离质谱(CE-APPI-MS)的研究中,观察到气相离子的形成并非总是通过光子诱导机制进行(霍默森,P.;汗,A. M.;德容,G. J.;索姆森,G. W.《电泳》2007年,28卷,1444 - 1453页)。也就是说,当真空紫外(VUV)激发源关闭时,仍能观察到分析物信号。本研究的目的是进一步探索这种与光子无关的电离(PII)过程。使用CE-APPI-MS装置研究了诸如质谱毛细管电压、化合物性质、背景电解质(BGE)组成和掺杂剂的存在等参数。进样实验表明,约600 V的相对较低的质谱毛细管电压是PII的主要先决条件。季铵化合物在PII-MS中显示出强烈响应,但在掺杂剂辅助的APPI中未观察到。碱性胺类既可以通过光电离(PI)也可以通过PII电离,而中性化合物(类固醇)只能通过PI观察到。非挥发性BGEs似乎在PII中导致显著的电离抑制,而PI信号基本不受影响。选择合适的接口和质谱设置可使PI和PII同时进行,这拓宽了在单次CE-APPI-MS运行中可分析的化合物范围。基于观察到的特征,得出结论:PII很可能通过液相电离机制发生,当选择特定条件时,这种机制似乎在APPI源中出现。