کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1195247 964302 2009 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Capillary Electrophoresis-Atmospheric Pressure Chemical Ionization-Mass Spectrometry Using an Orthogonal Interface: Set-Up and System Parameters
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Capillary Electrophoresis-Atmospheric Pressure Chemical Ionization-Mass Spectrometry Using an Orthogonal Interface: Set-Up and System Parameters
چکیده انگلیسی

The feasibility of atmospheric pressure chemical ionization (APCI) as an alternative ionization technique for capillary electrophoresis-mass spectrometry (CE-MS) was investigated using a grounded sheath-flow CE-MS sprayer and an orthogonal APCI source. Infusion experiments indicated that highest analyte signals were achieved when the sprayer tip was in close vicinity of the vaporizer entrance. The APCI-MS set-up enabled detection of basic, neutral, and acidic compounds, whereas apolar and ionic compounds could not be detected. In the positive ion mode, analytes could be detected in the entire transfer voltage range (0–5 kV), whereas highest signal intensities were observed when the corona discharge current was between 1000 and 2000 nA. In the negative ion mode, the transfer voltage typically was 500 V and the optimum corona discharge current was 6000 nA. Analyte signals were raised with increasing nebulizing gas pressure, but the pressure was limited to 25 psi to avoid siphoning and current drops. Signal intensities appeared to be optimal and constant over a wide range of sheath liquid flow rate (5–25 μL/min) and vaporizer temperature (200–350 °C). APCI-MS signals were unaffected by the composition of the background electrolyte (BGE), even when it contained sodium phosphate and sodium dodecyl sulfate (SDS). Consequently, BGE composition, sheath-liquid flow rate, and vaporizer temperature can be optimized with respect to the CE separation without affecting the APCI-MS response. The analysis of a mixture of basic compounds and a steroid using volatile and nonvolatile BGEs further demonstrates the feasibility of CE-APCI-MS. Detection limits (S/N = 3) were 1.6–10 μM injected concentrations.

Graphical AbstractCoupling of CE with APCI-MS is achieved using an orthogonal ion source with only minor modifications.Figure optionsDownload high-quality image (80 K)Download as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of the American Society for Mass Spectrometry - Volume 20, Issue 7, July 2009, Pages 1311–1318
نویسندگان
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