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Updated: Jan 20, 2026

Whole-body Mass Spectrometry Imaging by Infrared Matrix-assisted Laser Desorption Electrospray Ionization IR-MALDESI
Published on: March 24, 2016
Rapid quantification of acetaminophen in plasma using solid-phase microextraction coupled with thermal desorption
Jentaie Shiea1,2, Suhail Muzaffar Bhat1, Hung Su1
1Department of Chemistry, National Sun Yat-Sen University, Kaohsiung, Taiwan.
A novel Solid-Phase Microextraction coupled with Thermal Desorption Electrospray Ionization Tandem Mass Spectrometry (SPME-TD-ESI-MS/MS) method enables rapid acetaminophen quantification in plasma. This technique provides accurate pharmacokinetic profiling with minimal sample preparation.
Area of Science:
- Analytical Chemistry
- Pharmacokinetics
- Mass Spectrometry
Background:
- Development of rapid and accurate analytical methods is crucial for pharmacokinetics (PK) studies.
- Traditional methods for drug quantification in plasma can be time-consuming.
Purpose of the Study:
- To propose and evaluate a novel Solid-Phase Microextraction coupled with Thermal Desorption Electrospray Ionization Tandem Mass Spectrometry (SPME-TD-ESI-MS/MS) method.
- To enable rapid quantification of acetaminophen in plasma samples for PK studies.
Main Methods:
- Direct immersion SPME using fused-silica fibers coated with a polyacrylate polymer.
- Acetaminophen absorbed on SPME fibers was desorbed and detected by TD-ESI-MS/MS.
- Matrix-matching calibration and linear regression analysis for quantification.
Main Results:
- The SPME-TD-ESI-MS/MS method achieved a lower limit of quantitation of 100 ng/mL within a 10-min SPME time.
- Analysis time per sample was less than 30 seconds.
- Quantification results showed good agreement with conventional LC/MS/MS methods.
Conclusions:
- The proposed SPME-TD-ESI-MS/MS method allows for rapid and accurate quantification of acetaminophen in plasma.
- The method is suitable for complete PK profiling of acetaminophen.
- Optimization of extraction parameters can further reduce analysis time.
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