Trace Element, Spectroscopy and Speciation Group (GETEE), Strategic Grouping in Materials (AEMAT), Department of Analytical Chemistry, Nutrition and Bromatology, Faculty of Chemistry, Universidade de Santiago de Compostela, Avenida das Ciencias, s/n., 15782, Santiago de Compostela, Spain.
Trace Element, Spectroscopy and Speciation Group (GETEE), Strategic Grouping in Materials (AEMAT), Department of Analytical Chemistry, Nutrition and Bromatology, Faculty of Chemistry, Universidade de Santiago de Compostela, Avenida das Ciencias, s/n., 15782, Santiago de Compostela, Spain.
Talanta. 2021 Mar 1;224:121841. doi: 10.1016/j.talanta.2020.121841. Epub 2020 Oct 31.
In contrast to most of essential and heavy metals, mercury levels in seaweed are very low, and pre-concentration methods are required for an adequate total mercury determination and mercury speciation in this foodstuff. An ionic imprinted polymer-based solid phase extraction (on column) pre-concentration procedure has been optimized for mercury species enrichment before liquid chromatography hyphenated with inductively coupled plasma mass spectrometry determination. The polymer has been synthesized by the precipitation polymerization method and using a ternary pre-polymerization mixture containing the template (methylmercury), a non-vinylated monomer (phenobarbital), and a vinylated monomer (methacrylic acid). Factors affecting the adsorption/desorption of Hg species (extract pH, loading and elution flow rates, volume of eluent, etc.), and parameters such as breakthrough volume and reusability, were fully studied. Mercury species were first isolated from seaweed by ultrasound assisted extraction using a 0.1% (v/v) HCl, 0.12% (w/v) l-cysteine, 0.1% (v/v) mercaptoethanol solution. Under optimized conditions, the limits of detection were 0.007 and 0.02 μg kg dw for methylmercury and Hg(II), respectively. The pre-concentration factor (volume of 10 mL of seaweed extract) was 50. Repeatability and reproducibility of the method were satisfactory with relative standard deviations lower than 16%. The proposed methodology was finally applied for the selective pre-concentration and determination of methylmercury and Hg (II) in a BCR-463 certified reference material and in several edible seaweeds.
与大多数必需和重金属相比,海藻中的汞含量非常低,因此需要预浓缩方法来充分测定这种食品中的总汞和汞形态。本研究采用基于离子印迹聚合物的固相萃取(柱上)预浓缩程序,在与电感耦合等离子体质谱联用的高效液相色谱之前对汞形态进行富集。该聚合物通过沉淀聚合方法合成,使用含有模板(甲基汞)、非乙烯基化单体(苯巴比妥)和乙烯基化单体(甲基丙烯酸)的三元预聚合混合物。充分研究了影响 Hg 形态吸附/解吸的因素(提取 pH 值、负载和洗脱流速、洗脱液体积等)以及穿透体积和可重复使用性等参数。首先通过使用 0.1%(v/v)HCl、0.12%(w/v)l-半胱氨酸和 0.1%(v/v)巯基乙醇溶液的超声辅助提取,从海藻中分离出汞形态。在优化条件下,甲基汞和 Hg(II)的检出限分别为 0.007 和 0.02μg kg dw。预浓缩因子(10mL 海藻提取物的体积)为 50。该方法的重复性和再现性令人满意,相对标准偏差低于 16%。最后将该方法应用于 BCR-463 认证参考物质和几种食用海藻中甲基汞和 Hg(II)的选择性预浓缩和测定。