Skip to main navigation Skip to search Skip to main content

Biocompatible SPME coupled to GC/MS for analysis of xenobiotics in blood plasma

  • University of Toledo

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

This work proposes a new method for biomonitoring studies focused on the screening and quantification of xenobiotics in blood-derived samples. The performance of a polydimethylsiloxane/divinylbenzene/polydimethylsiloxane (PDMS/DVB/PDMS) biocompatible extraction phase was investigated for extraction of pesticides and pharmaceuticals from plasma samples via direct immersion solid-phase microextraction (SPME) prior to gas chromatography-mass spectrometry. Under the optimum extraction settings, which included an attentive optimization of the fiber rinsing conditions, the microextraction device was able to endure 100 consecutive extractions from undiluted and diluted plasma with an overall reproducibility up to 28% for all the analytes tested, except chlorpyrifos-methyl. Optimized conditions were used to validate a quantitative method using matrix-matched calibration with isotopically labeled internal standard correction. Accuracy and precision values obtained for analysis of bovine plasma were within 96–132% and 0.05–5.82% respectively. LLOQs for all the analytes were at 1 µg L−1 and LDR ranged within 1–100 µg L−1. The applicability of this method to plasma from different species (human, rat, rabbit) was also investigated. This work represents the first step toward broader use of the biocompatible PDMS/DVB/PDMS extraction phases for analysis of multiclass xenobiotics in plasma and other complex biofluids.

Original languageEnglish
Article number123308
JournalJournal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences
Volume1203
DOIs
StatePublished - Jul 1 2022

Keywords

  • Biocompatibility
  • Gas chromatography-mass spectrometry
  • Solid phase microextraction
  • Xenobiotics

Fingerprint

Dive into the research topics of 'Biocompatible SPME coupled to GC/MS for analysis of xenobiotics in blood plasma'. Together they form a unique fingerprint.

Cite this