Direct Coupling of Bio-SPME to Liquid Electron Ionization-MS/MS via a Modified Microfluidic Open Interface.
Priscilla Rocío-BautistaGiorgio FamigliniVeronica TermopoliPierangela PalmaEmir NazdrajićJanusz PawliszynAchille CappielloPublished in: Journal of the American Society for Mass Spectrometry (2020)
We present a modified microfluidic open interface (MOI) for the direct coupling of Bio-SPME to a liquid electron ionization-tandem mass spectrometry (LEI-MS/MS) system as a sensitive technique that can directly analyze biological samples without the need for sample cleanup or chromatographic separations as well as without measurable matrix effects (ME). We selected fentanyl as test compound. The method uses a C18 Bio-SPME fiber by direct immersion (DI) in urine and plasma and the subsequent quick desorption (1 min) in a flow-isolated volume (2.5 μL) filled with an internal standard-acetonitrile solution. The sample is then transferred to an EI source of a triple-quadrupole mass spectrometer via a LEI interface at a nanoscale flow rate. The desorption and analysis procedure requires less than 10 min. Up to 150 samples can be analyzed without observing a performance decline, with fentanyl quantitation at microgram-per-liter levels. The method workflow is extremely dependable, relatively fast, sustainable, and leads to reproducible results that enable the high-throughput screening of various biological samples.
Keyphrases
- tandem mass spectrometry
- gas chromatography
- ultra high performance liquid chromatography
- high performance liquid chromatography
- ms ms
- simultaneous determination
- liquid chromatography
- liquid chromatography tandem mass spectrometry
- solid phase extraction
- mass spectrometry
- high resolution
- minimally invasive
- high resolution mass spectrometry
- high throughput
- circulating tumor cells
- single cell
- ionic liquid
- room temperature
- staphylococcus aureus
- label free
- cystic fibrosis
- electronic health record
- escherichia coli
- electron transfer