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Fast Enzymatic Processing of Proteins for MS Detection with a Flow-through Microreactor
Published on: April 6, 2016
The capillary gap sampler, a new microfluidic platform for direct coupling of automated solid-phase microextraction
Sahar Ghiasikhou1, Marcos Fabrício da Silva2, Ying Zhu1,3
1Department of Chemistry and Applied Bioscience, ETH Zürich, HCI E 329 ETH Hönggerberg, 8093, Zurich, Switzerland.
A novel capillary gap sampler automates solid-phase microextraction coupled with mass spectrometry for rapid, site-specific analysis. This technology demonstrates high stability and repeatability for extracting benzodiazepines from plasma.
Area of Science:
- Analytical Chemistry
- Biochemistry
Background:
- Solid-phase microextraction (SPME) coupled with mass spectrometry (MS) is a powerful analytical technique.
- Existing methods can be time-consuming and require larger sample volumes.
Purpose of the Study:
- To introduce a new technology for rapid, automated coupling of SPME and MS.
- To evaluate the performance of a capillary gap sampler for automated SPME and direct analyte delivery to MS.
Main Methods:
- Development and optimization of a capillary gap sampler for automated SPME.
- Coupling the sampler to a mass spectrometer for direct analysis.
- Systematic optimization for stability, reusability, and repeatability.
- Analysis of diazepam, oxazepam, and nordiazepam in human plasma.
Main Results:
- The capillary gap sampler enables quick, automated, and site-specific extraction from low-volume samples.
- High stability, reusability, and repeatability were achieved.
- Successful extraction of benzodiazepines from human plasma with a limit of detection of 0.3 μg/mL.
- A linear dynamic range from 1 to 1000 ng/mL was established for the analytes.
- Relative standard deviation for 20 extractions ranged from 11% to 17%, indicating acceptable repeatability.
Conclusions:
- The capillary gap sampler offers significant advantages for automated SPME-MS analysis.
- The technology is suitable for analyzing benzodiazepines in human plasma within the therapeutic range.
- The method is robust, repeatable, and efficient for trace-level analysis.
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