Hines Cynthia J, Yau Alice Y, Zuniga Michelle M, Wells J Raymond, Nilsen Hopf Nancy B, Camann David E
National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention, 4776 Columbia Pkwy, R-14, Cincinnati, OH 45226, USA.
J Environ Monit. 2010 Feb;12(2):491-9. doi: 10.1039/b913700a. Epub 2009 Oct 28.
Phthalates are used as plasticizers in many industrial and consumer products. Urinary biomonitoring has shown widespread human exposure to phthalates, with workers having especially high exposures. Phthalates can be present in workplace air as either aerosols or vapors depending on source materials, vapor pressure, and processing temperatures. We sought to develop a dual-phase air sampling method for 6 phthalates, dimethyl phthalate (DMP), diethyl phthalate (DEP), di-n-butyl phthalate (DBP), benzyl butyl phthalate (BzBP), di(2-ethylhexyl) phthalate (DEHP), and di-n-octyl phthalate (DnOP), adaptable to aerosol inlets with known particle collection characteristics. Collection media consisted of a quartz fiber filter and XAD-2 resin. Limit of detection (LOD) and limit of quantification (LOQ) were determined for each phthalate. Phthalate recoveries were evaluated at 3x, 10x and 30x the LOQ, and after storage at -21 degrees C and 21 degrees C. Media were Soxhlet extracted in 10% diethyl ether in hexanes along with an extraction surrogate, di-n-pentyl phthalate-d(4). Gas chromatography/mass spectrometry was performed to quantify the phthalate diesters using di(2-ethylhexyl) phthalate-d(4) as an internal standard. Estimated LODs were 1 microg per sample (BzBP, DEHP, and DnOP), 2 microg per sample (DMP and DBP), and 5 microg per sample (DEP). Mean recoveries under static conditions were 85-104% for DBP, BzBP, DEHP, and DnOP; but <70% for DMP and DEP at 3x and 10x the LOQ. After air was pulled through spiked samples, DMP and DEP recoveries improved to 74-81%. After storage for 62 days, phthalate recovery was better at -21 degrees C than at 21 degrees C. Method accuracy was best for DBP, BzBP, DEHP, and DnOP (range 11-18%), and less so for DMP (28%) and DEP (29%).
邻苯二甲酸盐在许多工业和消费品中用作增塑剂。尿液生物监测表明人类广泛接触邻苯二甲酸盐,其中工人的接触程度尤其高。根据源材料、蒸气压和加工温度,邻苯二甲酸盐在工作场所空气中可能以气溶胶或蒸气的形式存在。我们试图开发一种针对6种邻苯二甲酸盐(邻苯二甲酸二甲酯(DMP)、邻苯二甲酸二乙酯(DEP)、邻苯二甲酸二正丁酯(DBP)、邻苯二甲酸苄基丁酯(BzBP)、邻苯二甲酸二(2-乙基己基)酯(DEHP)和邻苯二甲酸二正辛酯(DnOP))的双相空气采样方法,该方法适用于具有已知颗粒收集特性的气溶胶入口。收集介质由石英纤维滤膜和XAD-2树脂组成。测定了每种邻苯二甲酸盐的检测限(LOD)和定量限(LOQ)。在LOQ的3倍、10倍和30倍浓度下,以及在-21℃和21℃储存后,评估了邻苯二甲酸盐的回收率。介质用10%乙醚的己烷溶液进行索氏提取,并加入提取替代物邻苯二甲酸二正戊酯-d(4)。使用邻苯二甲酸二(2-乙基己基)酯-d(4)作为内标,通过气相色谱/质谱法对邻苯二甲酸二酯进行定量。估计的检测限为每个样品1微克(BzBP、DEHP和DnOP)、每个样品2微克(DMP和DBP)和每个样品5微克(DEP)。在静态条件下,DBP、BzBP、DEHP和DnOP的平均回收率为85-104%;但在LOQ的3倍和10倍浓度下,DMP和DEP的回收率<70%。空气通过加标样品后,DMP和DEP的回收率提高到74-81%。储存62天后,邻苯二甲酸盐在-21℃下的回收率比在21℃下更好。该方法对DBP、BzBP、DEHP和DnOP的准确度最佳(范围为11-18%),对DMP(28%)和DEP(29%)的准确度稍低。