The Development of a Rapid, Cost-Effective, and Green Analytical Method for Mercury Speciation.
Patrícia Cristina Costa LadeiraCaroline Cristine AugustoBruno Alves RochaJairo Lisboa RodriguesGiovanna de Fátima Moreno AguiarBruno Lemos BatistaPublished in: Toxics (2024)
Mercury is a naturally occurring metal found in various inorganic and organic forms within the environment. Due to its high toxicity, there is global concern regarding human exposure to this element. The combination of high-performance liquid chromatography and inductively coupled plasma mass spectrometry (HPLC-ICP-MS) is commonly used to analyze the different forms of mercury in a sample due to its high sensitivity and ability to selectively detect mercury. However, the traditional HPLC-ICP-MS methods are often criticized for their lengthy analysis times. In this study, we have refined the conventional approach by transitioning to ultra-high performance liquid chromatography coupled with inductively coupled plasma mass spectrometry (UHPLC-ICP-MS). This modification has resulted in significant reductions in runtime as well as reagent and argon usage, thereby offering a more rapid, environmentally friendly, and cost-effective method. We successfully adapted an HPLC-ICP-MS method to UHPLC-ICP-MS, achieving the analysis of Hg 2+ and MeHg + within 1 min with a mobile phase consumption of only 0.5 mL and a sample volume of 5.0 µL; this is a major advance compared to HPLC analysis with run times generally between 5 and 10 min. The method's performance was assessed by analyzing muscle and liver tissue samples (serving as reference material) from fish, demonstrating the versatility of the method in relation to different complex matrices.
Keyphrases
- mass spectrometry
- high performance liquid chromatography
- ms ms
- tandem mass spectrometry
- liquid chromatography
- ultra high performance liquid chromatography
- simultaneous determination
- solid phase extraction
- high resolution mass spectrometry
- gas chromatography
- capillary electrophoresis
- high resolution
- multiple sclerosis
- endothelial cells
- skeletal muscle