Simultaneous determination of N-hydroxymethyl- N-methylformamide, N-methylformamide and N-acetyl- S-( N-methylcarbamoyl)cystein in urine samples from workers exposed to N,N-dimethylformamide by liquid chromatography–tandem mass spectrometry

Abstract

N-Hydroxymethyl- N-methylformamide (HMMF) and N-methylformamide (NMF) in urine samples from workers exposed to N,N-dimethylformamide (DMF) cannot be distinguished by a gas chromatographic method because HMMF is converted to NMF at the injection port of gas chromatography (GC). Total NMF (HMMF + NMF) has been measured instead. Also, the determination of N-acetyl- S-( N-methylcarbamoyl)cystein (AMCC), which is supposed to be related to the toxicity of DMF, needs multiple treatments to convert to a volatile compound before GC analysis. There is no previous report of a simultaneous determination of three major metabolites of DMF in urine. The aim of this study is to develop a simple and selective method for the determination of DMF metabolite in urine. By using a liquid chromatography–tandem mass spectrometry, we can directly distinguish these three major metabolites of DMF in a single run. The diluted urine samples were analyzed on Capcell Pak MF SG80 column with the mobile phase of methanol in 2 mM formic acid (10:90, v/v). The analytes were detected by an electrospray ionization tandem mass spectrometry in the multiple-reaction-monitoring mode. The standard curves were linear ( r > 0.999) over the concentration ranges of 0.004–8 μg/mL. The precision and accuracy of quality control samples for inter-batch ( n = 6) analyses were in the range of 1.3–9.8% and 94.7–116.8, respectively. The sum of each HMMF and NMF concentration determined by LC-MS/MS method shows high correlation ( r = 0.9927 with the slope of 1.0415, p < 0.0001) with NMF included HMMF concentration determined by GC method for 13 urine samples taken from workers exposed to DMF. The excretion ratio of HMMF:NMF:AMCC is approximately 4:1:1 in molar concentration.