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Comparison of solid phase micro-extraction headspace GC/FID and headspace GC/MSD for analysis of aromatic solvents in urine

机译:固相微萃取顶空GC / FID和顶空GC / MSD的比较分析尿液中的芳族溶剂

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Detection limit of toluene by SPME HS GC/FID was 6.8 μg/L, which enabled micro-scale analysis of organic solvent in urine. Linear range of each organic solvent was 10-400 μg/L, with fair correlation constant from 0.992 to 0.999. The detection sensitivity was 4 times better than HS GC/MSD(SIM mode). Accuracy was confirmed using commercial reference material containing 200 mg/L organic solvent, with about 90% accuracy. Toluene in urine was detected from 45 samples from workplace in the range of 20 - 324 μg/L. The data produced by SPME HS GC/FID method showed good relationship with hippuric acid in urine by GC/FID method. Analytical method for micro analysis of organic solvent in urine was investigated and showed good sensitivity and linearity for biological monitoring of organic solvent.
机译:SPME HS GC / FID的甲苯检测极限为6.8μg/ L,这使能尿液中有机溶剂的微观分析。每种有机溶剂的线性范围为10-400μg/ L,具有比0.992至0.999的公平相关性。检测灵敏度比HS GC / MSD(SIM模式)好4倍。使用含有200mg / L有机溶剂的商业参考材料确认精度,精度约为90%。从20-324μg/升的工作场所的45个样品中检测尿脂的甲苯。 SPME HS GC / FIT方法产生的数据显示GC / FIF法与尿液中的尿酸中的良好关系。研究了尿液中有机溶剂微分析的分析方法,呈现出有机溶剂生物监测的良好敏感性和线性性。

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