Bureau de recherches géologiques et minières (French Geological Survey), Laboratory Division, 3 avenue Claude Guillemin, 45060, Orléans Cedex 02, France,
Anal Bioanal Chem. 2014 Feb;406(4):1181-91. doi: 10.1007/s00216-013-7248-8. Epub 2013 Aug 2.
Laboratory experimentation is essential for our understanding of the fate and behaviour of pollutants. Many analytical techniques exist, but they all have disadvantages either in terms of sensitivity or of selectivity. The number of samples that can be analysed, the low volume of samples available during the experiment and the need to identify different degradates are all obstacles that new techniques are able to overcome. The work presented here summarizes progress in the field of metrology as concerns online solid phase extraction technology coupled with liquid chromatography followed by tandem mass spectrometry detection. Recently developed analytical techniques were validated for both 18 pesticides and their degradates and 17 pharmaceuticals and their degradates. Limits of quantification from 20 to 70 ng L(-1) for pharmaceuticals and from 15 to 25 ng L(-1) for pesticides and metabolites have been obtained, with linearity range up to 1 μg L(-1). The limits of quantification of a few nanograms per litre, the possibility of working on less than 1 mL of sample and the simultaneous quantification of the target products and their transformation products are all advantages that are demonstrated by two environmental applications. The first application concerns the evaluation of ecotoxicological effects of pesticides on aquatic organisms exposed in mesocosms. The second application aims to determine the adsorption constants of pharmaceutical molecules on soils and river sediments. For both applications, the robustness, range of linearity and limit of quantification of the developed analytical methods satisfy the requirements for laboratory experiments conducted under controlled conditions. Specific constraints generated by this type of experiment (adding CaCl2 for the adsorption study and filtration of the water coming from the mesocosms) were not found to limit the use of online SPE. These two preliminary studies show that new experimental fields are possible thanks to online solid phase extraction coupled with liquid chromatography.
实验室实验对于我们理解污染物的归宿和行为至关重要。虽然存在许多分析技术,但它们在灵敏度或选择性方面都存在缺点。可分析的样品数量、实验过程中可用的小样品量以及需要识别不同降解产物,这些都是新技术能够克服的障碍。这里介绍的工作总结了在线固相萃取技术与液相色谱串联质谱检测联用领域的计量学进展。最近开发的分析技术已对 18 种农药及其降解产物和 17 种药物及其降解产物进行了验证。药物的定量限为 20-70ng/L,农药及其代谢物的定量限为 15-25ng/L,线性范围高达 1μg/L。每升数纳克的定量限、能够处理少于 1mL 样品的能力以及同时定量目标产物及其转化产物的能力,这些都是通过两个环境应用实例所展示的优势。第一个应用涉及在中宇宙系统中评估农药对水生生物的生态毒理学影响。第二个应用旨在确定药物分子在土壤和河流沉积物上的吸附常数。对于这两种应用,所开发的分析方法的稳健性、线性范围和定量限都满足了在受控条件下进行实验室实验的要求。这种实验类型产生的特定限制(对于吸附研究添加 CaCl2 和过滤从中宇宙系统出来的水)并未限制在线 SPE 的使用。这两项初步研究表明,在线固相萃取与液相色谱相结合为新的实验领域开辟了可能。