Advances in Derivatization Techniques Enabled by DABCO for Novichok Agent Analysis in Biofluids Using LC-MS.
Akinori YamaguchiHajime MiyaguchiPublished in: Analytical chemistry (2023)
The characterization of Novichoks (NVs), a new group of nerve agents that have been implicated in two recent poisonings, has not been extensively conducted. Here, we present a novel method for analyzing NV hydrolysates using liquid chromatography-tandem mass spectrometry (LC-MS/MS) enabled by pentafluorobenzyl (PFB) derivatization followed by reaction with 1,4-diazabicyclo[2.2.2]octane (DABCO). This approach enabled efficient, simultaneous screening of six NV hydrolysates, with 1-2 orders improvement in the limit of detection in relation to that achieved through previous methods. A straightforward pretreatment using DABCO and filtration was employed for biological samples, mitigating instrument damage and allowing LC-MS/MS after a reaction with highly hydrophobic PFB bromide (PFBBr). In addition, the use of pralidoxime (PAM) significantly enhanced the detection of NV hydrolysates from NV-surrogate-spiked serum. While PAM is not a proven NV antidote, its effectiveness as an analytical reagent to aid in the detection of NV hydrolysates was demonstrated for the first time. Understanding the proposed mechanism of DABCO-mediated derivatization reagent removal in this research could broaden the range of compounds amenable to derivatization LC, thereby enhancing the capabilities of conventional derivatization techniques.
Keyphrases
- liquid chromatography tandem mass spectrometry
- simultaneous determination
- ms ms
- solid phase extraction
- high performance liquid chromatography
- liquid chromatography
- gas chromatography mass spectrometry
- tandem mass spectrometry
- loop mediated isothermal amplification
- ultra high performance liquid chromatography
- gas chromatography
- label free
- real time pcr
- mass spectrometry
- randomized controlled trial
- systematic review
- oxidative stress
- high resolution mass spectrometry
- data analysis