Department of Chemistry, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Food Science College, Shenyang Agricultural University, Shenyang 110866, China.
Anal Chem. 2023 Apr 25;95(16):6718-6724. doi: 10.1021/acs.analchem.3c00508. Epub 2023 Apr 11.
Solid-phase microextraction (SPME) is a simple and effective sample-preparation technique for the analysis of complex samples. However, sample matrices containing high concentrations of nonpolar substances or spiked analytes in free form can cause swelling, saturation, and/or competition phenomena in the coating material. This results in a displacement effect wherein polar analytes with low affinities for the solid coating material are displaced by nonpolar substances in the matrix or spiked analytes with a high affinity. Therefore, the quantitative analysis of polar analytes can be challenging, as the displacement effect causes non-linearity in the calibration curves. This paper presents a comprehensive investigation of the conditions under which the displacement effect occurs and how it influences the quantitative analysis of polar analytes. To remedy this issue, a sequential SPME strategy using two SPME blades with different selectivities is applied. SPME blades offer a large surface area and coating volume─and thus, greater extraction capacity─which may mitigate the displacement effect. In addition, the biocompatible coatings on the SPME blades are comprised of small amounts of sorbent particles embedded by a polyacrylonitrile (PAN) binder, which allows them to be directly immersed into complex matrixes such as biological and food samples, as the PAN acts as a barrier that prevents the adsorption of large macromolecules (e.g., cells and proteins). As such, a C18/PAN-coated blade was applied for the first extraction step, which significantly decreased the concentrations of nonpolar compounds in the sample. In the second step, a hydrophilic-lipophilic balanced (HLB)/PAN-coated blade was employed to extract the polar analytes and any remaining nonpolar analytes. The proposed sequential SPME strategy successfully enabled the quantitative determination of polar and nonpolar drugs of abuse with log values ranging from 0.16 to 4.98 in biological matrices while also providing good linearities.
固相微萃取 (SPME) 是一种简单有效的样品制备技术,可用于分析复杂样品。然而,含有高浓度非极性物质或游离形式加标分析物的样品基质可能会导致涂层材料发生溶胀、饱和和/或竞争现象。这会导致置换效应,其中对固体涂层材料亲和力低的极性分析物会被基质中的非极性物质或具有高亲和力的加标分析物置换。因此,极性分析物的定量分析具有挑战性,因为置换效应会导致校准曲线呈非线性。本文全面研究了置换效应发生的条件以及它如何影响极性分析物的定量分析。为了解决这个问题,采用了两种具有不同选择性的 SPME 刀片的顺序 SPME 策略。SPME 刀片具有较大的表面积和涂层体积,因此具有更大的萃取能力,这可能会减轻置换效应。此外,SPME 刀片上的生物相容性涂层由少量嵌入聚丙烯腈 (PAN) 粘合剂的吸附剂颗粒组成,这允许它们直接浸入复杂基质中,如生物和食品样品,因为 PAN 充当阻止大分子(如细胞和蛋白质)吸附的屏障。因此,在第一个萃取步骤中使用了 C18/PAN 涂层刀片,这显著降低了样品中非极性化合物的浓度。在第二步中,采用亲水亲脂平衡 (HLB)/PAN 涂层刀片来萃取极性分析物和任何残留的非极性分析物。所提出的顺序 SPME 策略成功地实现了在生物基质中对数 值范围为 0.16 至 4.98 的极性和非极性滥用药物的定量测定,同时还提供了良好的线性度。