Chang Lan-Fang, Jiang Shiuh-Jen, Sahayam A C
Department of Chemistry, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.
J Chromatogr A. 2007 Dec 28;1176(1-2):143-8. doi: 10.1016/j.chroma.2007.10.072. Epub 2007 Oct 30.
A liquid chromatography-inductively coupled plasma mass spectrometric (LC-ICP-MS) method for lead and mercury speciation analysis was described. Sample containing ionic lead and mercury compounds was subjected to liquid chromatographic separation before injection into the direct injection high efficiency nebulizer (DIHEN, 170-AA). The species studied include inorganic lead (Pb(II)), trimethyl lead (trimethyl-Pb), triethyl lead (triethyl-Pb), inorganic mercury (Hg(II)), methyl mercury (methyl-Hg) and ethyl mercury (ethyl-Hg), which were well separated by reversed-phase liquid chromatography with a C18 column as the stationary phase and a pH 2.8 solution of 0.2% (v/v) 2-mercaptoethanol, 1 mg L(-1) ETDA, 174.2 mg L(-1) sodium 1-pentanesulfonate and 12% (v/v) methanol as the mobile phase. The lead and mercury species in biological tissues were quantitatively extracted, into 10 g L(-1) EDTA and 0.2% (v/v) 2-mercaptoethanol solution taken in a closed centrifuge tube and kept on water bath, using microwaves at 65 degrees C for 2 min. The spike recovery of individual lead and mercury species determined by spiking the samples with suitable concentration of lead and mercury mixture standard were between 93% and 99%. The detection limits of the species studied were in the range 0.1-0.3 microg Pb L(-1) and 0.2-0.3 microg Hg L(-1). The procedure has been applied for the speciation analysis of two reference samples namely NRCC DOLT-3 Dogfish Liver and DORM-2 Dogfish Muscle and a swordfish sample obtained locally. The sum of the concentrations of individual species has been compared with the certified values for total lead and mercury to verify the accuracy of the method. The precision between sample replicates was better than 10% with LC-DIHEN-ICP-MS method.
描述了一种用于铅和汞形态分析的液相色谱 - 电感耦合等离子体质谱(LC - ICP - MS)方法。含有离子态铅和汞化合物的样品在注入直接进样高效雾化器(DIHEN,170 - AA)之前先进行液相色谱分离。所研究的形态包括无机铅(Pb(II))、三甲基铅(三甲基 - Pb)、三乙基铅(三乙基 - Pb)、无机汞(Hg(II))、甲基汞(甲基 - Hg)和乙基汞(乙基 - Hg),它们通过以C18柱为固定相,以0.2%(v/v)2 - 巯基乙醇、1 mg L⁻¹乙二胺四乙酸(EDTA)、174.2 mg L⁻¹1 - 戊烷磺酸钠和12%(v/v)甲醇的pH 2.8溶液为流动相的反相液相色谱得到了很好的分离。生物组织中的铅和汞形态在封闭的离心管中定量提取到10 g L⁻¹EDTA和0.2%(v/v)2 - 巯基乙醇溶液中,并在65℃水浴中使用微波处理2分钟。通过向样品中加入合适浓度的铅和汞混合标准溶液来测定各个铅和汞形态的加标回收率,回收率在93%至99%之间。所研究形态的检测限在0.1 - 0.3 μg Pb L⁻¹和0.2 - 0.3 μg Hg L⁻¹范围内。该方法已应用于两个参考样品即NRCC DOLT - 3角鲨鱼肝和DORM - 2角鲨鱼肉以及当地获得的剑鱼样品的形态分析。将各个形态的浓度总和与总铅和汞的认证值进行比较,以验证该方法的准确性。使用LC - DIHEN - ICP - MS方法,样品重复之间的精密度优于10%。