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Electrospray ionization tandem mass spectrometry (ESI-MS/MS) analysis of urinary metabolites of 1,1,2,2-tetrachloroethylene using an automated SPE sample preparation system.
Cheever-KL; Marlow-KL; Butler-MA; Toraason-MA; DeBord-DG
Toxicologist 2000 Mar; 54(1):207
1,1,2,2-Tetrachloroethylene [Perchloroethylene] (PERC, CAS 127-18-4), used extensively as a dry cleaning agent and in industrial degreasing processes, has been reported to increase the incidence of liver tumors in mice or of nephrotoxicity and renal tumors in male rats. Bioactivation of PERC is reported to occur by two pathways, oxidation by CYP2E1 and glutathione S-conjugation. Trichloroacetic acid (TCA, CAS 76-03-9) and dichloroacetic acid (DCA, CAS 79-43-6) are reported urinary metabolites of PERC oxidation wherease the glutathione conjugate, S-(1,2,2-trichlorovinyl) -L-glutathione (TCVG) is further cleaved to S-(1,2,2-trichlorovinyl)-L-cysteine (TCVC). A potential biomonitoring method was developed to measure urinary levels of TCA, DCA, TCVC and N-ac-TCVC. Stable isotope-labeled analogs of TCVC and N-ac-TCVC were prepared (Bartles and Miner, 1989) and deuterated DCA was purchased as internal standards. A BenchMate II robotic workstation was used to automate sample preparation. PERC metabolites (>90% recovery) were analyzed using a ThermoQuest Finnegan LCQ tandem mass spectrometer. Chromatographic standards TCVC and N-ac-TCVC were synthesized as above. Compounds of interest were eluted within 12 min and detected using ESI-MS/MS in multiple segments, initially in the negative ion mode for detection of TCA and DCA, and subsequently in the position ion mode for TCVC and N-ac-TCVC. Urine samples from rats exposed to 100, 500, or 1000 mg/kg PERC contained detectable amounts of PERC metabolites in urine over a 48-hr period. The LOD per injection was 30 fmol for TCVC, 800 fmol for N-ac-TCVC, 10 pmol for DCA, and 75 pmol for TCA. This procedure appears to offer significant advantages over typical extraction and derivatization methods for the same compounds by GC-MS. Thus, PERC internal dose for various exposures can be rapidly quantified using metabolites in a single assay using an automated sample preparation system.
Ionization; Mass-spectrometry; Metabolites; Sampling; Sampling-methods; Liver-tumors; Liver-cancer; Liver-disorders; Laboratory-animals; Animal-studies; Animals; Pulmonary-system-disorders; Respiratory-system-disorders; Bioactivation; Chromatographic-analysis; Urinalysis; Exposure-levels; Exposure-assessment
127-18-4; 76-03-9; 79-43-6
Issue of Publication
The Toxicologist. Society of Toxicology 39th Annual Meeting, March 19-23, 2000, Philadelphia, Pennsylvania
Page last reviewed: April 12, 2019
Content source: National Institute for Occupational Safety and Health Education and Information Division