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High-throughput and Comprehensive Drug Surveillance Using Multisegment Injection-Capillary Electrophoresis-Mass Spectrometry
Published on: April 23, 2019
Coupling CE with atmospheric pressure photoionization MS for pharmaceutical basic compounds: optimization of
Julie Schappler1, Davy Guillarme, Josiane Prat
1Laboratory of Analytical Pharmaceutical Chemistry, School of Pharmaceutical Sciences, EPGL, University of Geneva, University of Lausanne, Geneva, Switzerland.
This study optimizes atmospheric pressure photoionization (APPI) for capillary electrophoresis-mass spectrometry (CE-MS) analysis. Experimental design successfully enhanced sensitivity for charged species detection in small sample volumes.
Area of Science:
- Analytical Chemistry
- Separation Science
- Mass Spectrometry
Background:
- Capillary electrophoresis coupled with mass spectrometry (CE-MS) is vital for analyzing charged species.
- Electrospray ionization (ESI) is the standard interface for CE-MS due to its ease of use and sensitivity.
- Atmospheric pressure photoionization (APPI) offers an alternative but requires extensive parameter optimization for CE coupling.
Purpose of the Study:
- To systematically optimize APPI source parameters for enhanced CE-MS sensitivity.
- To evaluate the effectiveness of experimental design methodologies in optimizing complex analytical interfaces.
- To achieve high signal-to-noise ratios for sensitive detection of analytes.
Main Methods:
- Utilized a fractional factorial design (FFD) to screen critical APPI source parameters.
- Employed a face-centered central composite design (CCD) for predicting and optimizing sensitivity.
- Evaluated parameters including sheath liquid flow rate, drying gas conditions, nebulizing gas pressure, vaporizer temperature, and capillary voltage.
Main Results:
- Identified key factors significantly influencing CE-MS sensitivity and efficiency using FFD.
- Successfully optimized APPI source parameters through CCD, leading to improved analytical performance.
- Achieved height-to-noise ratios (H/N) of approximately 10 for analytes at 200 ng/mL concentrations.
Conclusions:
- Experimental design methodologies are effective for optimizing APPI-CE-MS interfaces.
- Optimized APPI-CE-MS provides a sensitive and robust method for analyzing charged species.
- This work advances the application of APPI as a viable alternative to ESI for CE-MS.
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