BIOLOGICAL MONITORING OF OCCUPATIONAL EXPOSURE TO TOLUENE DIISOCYANATE - MEASUREMENT OF TOLUENEDIAMINE IN HYDROLYZED URINE AND PLASMA BY GAS CHROMATOGRAPHY-MASS SPECTROMETRY

Citation
P. Persson et al., BIOLOGICAL MONITORING OF OCCUPATIONAL EXPOSURE TO TOLUENE DIISOCYANATE - MEASUREMENT OF TOLUENEDIAMINE IN HYDROLYZED URINE AND PLASMA BY GAS CHROMATOGRAPHY-MASS SPECTROMETRY, British Journal of Industrial Medicine, 50(12), 1993, pp. 1111-1118
Citations number
22
Categorie Soggetti
Public, Environmental & Occupation Heath
ISSN journal
00071072
Volume
50
Issue
12
Year of publication
1993
Pages
1111 - 1118
Database
ISI
SICI code
0007-1072(1993)50:12<1111:BMOOET>2.0.ZU;2-#
Abstract
Exposure to toluene diisocyanate (TDI) was studied during 48 hours and biological samples from nine subjects were taken in a factory produci ng flexible polyurethane (PUR) foam. Five PUR workers, two white colla r workers, and two volunteers were studied. The concentrations of TDI in air were determined by high performance liquid chromatography with the 9-(N-methyl-aminomethyl)-anthracene reagent. Urine and plasma samp les were collected and the TDI related amines, 2,4-toluenediamine (2,4 -TDA) and 2,6-toluenediamine (2,6-TDA), were determined (after hydroly sis) as pentafluoropropionic anhydride (PFPA) derivatives by capillary gas chromatography-mass spectrometry (CC-MS) with selected ion monito ring (SIM) in the negative chemical ionisation mode. The concentration of TDI in air was 1%-10% of the Swedish threshold limit value (TLV) o f 40 mu g/m(3). The ratio between 2,4-TDI and 2,6-TDI varied in the ai r samples in the range of 60%:40%-5%:95%. Calibration plots for human urine spiked with 2,6-TDA and 2,4-TDA in the range of 0.2-12 mu g/1 we re produced on eight different occasions during five weeks. The SDS of the calibration plot slopes (n = 8) were less than 4%. Urine and bloo d samples were taken on six occasions for eight of the studied subject s and on four occasions for one subject during a two day period. The f ive male PUR workers showed the highest average urinary elimination ra te of TDA. Two PUR workers and the two white collar workers had an eli mination rate of 20-70 ng on average for the sum of 2,6-TDA and 2,4-TD A per hour and three PUR workers had an average of 100-300 ng TDA per hour. The elimination rate curves for all the studied subjects had a l inear relation with exposure to TDI.The concentrations of 2,4-TDA and 2,6-TDA in plasma for the PUR factory employees were virtually stable. No relation between the elimination rates of TDA in urine and plasma concentrations of TDA was found. The five PUR workers showed plasma co ncentrations of the sum of 2,4-TDA and 2,6-TDA in the range 1-8 ng per ml. The two white collar workers, present only on occasions in the fa ctory, had 0.2-1 ng TDA per mi plasma. The two volunteers showed an in creasing concentration of TDA in plasma with time. At the end of the s tudy their plasma concentrations were 0.6 ng/ml and 0.2 ng/ml plasma. Three subjects had the same concentration of the two TDA isomers in pl asma, two subjects had about double, and two subjects had 12 times hig her concentrations of 2,6-TDA than 2,4-TDA. The presented study indica tes that it is possible to monitor exposure to TDI by monitoring plasm a concentrations of TDA.