Determination of polychlorinated biphenyls in marine fish samples by gas chromatography tandem mass spectrometry (GC-MS/MS)

Quynh Pham Thi Diem, Mai Pham Thi Ngoc, Anh Hoang Quoc, Thuy Le Minh, Huong Nguyen Thi, Hoa Vu Khanh, H. Do Thi Thu, Xuyen Nguyen Thi, Hung Nguyen Xuan, Binh Chu Dinh, Nam Vu Duc
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Abstract

Polychlorinated biphenyls (PCBs) are a typical group of persistent organic pollutants (POPs), which have been listed under Annex A (Elimination) and Annex C (Unintentional production) of the Stockholm Convention. In this study, a gas chromatography tandem mass spectrometry method was developed and applied to analyze concentrations of 28 PCB congeners in some Vietnamese marine fish samples. PCBs in fish samples were ultrasonically extracted with an acetone/n-hexane (1/1, v/v) mixture. The extracts were cleaned up by using multilayer silica gel columns with dichloromethane/n-hexane (1/1, v/v) as elution solvent. PCBs were separated on a DB-5MS column and quantified by using a triple quadrupole mass spectrometer. The MS detector was operated in positive electron impact ionization (EI) mode and selected reaction monitoring (SRM) mode. Calibration curves of 28 PCBs exhibited good linearity (R2 ≥ 0.9998). Instrument detection limits (IDLs) and method detection limits (MDLs) ranged from 0.08 to 0.023 ng/mL and from 0.07 to 1.84 ng/g, respectively. Recoveries of 28 PCBs native and 7 labeled standards in matrix-spike samples ranged from 62.3 to 88.1% and from 75.5 to 91.9%, satisfying criteria proposed by AOAC (recovery 60-115% for 10-100 ppb levels). The validated method was applied to analyze 10 marine fish samples, showing levels of ∑28PCBs from 17 to 851 (mean 230) ng/g lipid. The sum of 6in-PCBs (PCB-28; -52; -101; -138; -153; -180) based on wet weight (w/w) ranged from 1.24 to 3.15 ng/g, which is lower than the maximum level recommended by The European Union (75 ng/g (w/w). Congeners PCB-126 and PCB-169 were not detected in marine fish samples.
气相色谱-串联质谱法(GC-MS/MS)测定海鱼样品中的多氯联苯
多氯联苯是一类典型的持久性有机污染物,已列入《斯德哥尔摩公约》附件a(消除)和附件C(无意产生)。本研究建立了气相色谱串联质谱法,并应用于分析越南部分海鱼样品中28种多氯联苯同系物的浓度。用丙酮/正己烷(1/1,v/v)混合物超声提取鱼类样品中的多氯联苯。以二氯甲烷/正己烷(1/1,v/v)为洗脱溶剂,采用多层硅胶柱对萃取物进行净化。采用DB-5MS色谱柱分离多氯联苯,采用三重四极杆质谱仪定量。质谱仪在正电子冲击电离(EI)模式和选择性反应监测(SRM)模式下工作。28种pcb的校准曲线线性良好(R2≥0.9998)。仪器检出限(IDLs)为0.08 ~ 0.023 ng/mL,方法检出限(MDLs)为0.07 ~ 1.84 ng/g。28种多氯联苯的天然标准和7种标记标准在基质峰样中的回收率分别为62.3 ~ 88.1%和75.5 ~ 91.9%,满足AOAC提出的标准(10-100 ppb水平的回收率为60 ~ 115%)。将验证的方法应用于10份海鱼样品的分析,结果显示∑28PCBs含量在17 ~ 851(平均230)ng/g脂质范围内。6 - in- pcb之和(PCB-28;-52;-101;-138;-153;-180),湿重(w/w)范围为1.24 ~ 3.15 ng/g,低于欧盟推荐的最大限值(75 ng/g (w/w))。同系物多氯联苯126和多氯联苯169未在海鱼样本中检测到。
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