CAS Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China; University of Chinese Academy of Sciences, Beijing 100049, China.
CAS Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China.
Anal Chim Acta. 2019 Oct 31;1078:78-89. doi: 10.1016/j.aca.2019.06.022. Epub 2019 Jun 11.
Based on a one-step combustion fabrication approach, a novel magnetic porous carbon (MPC) was fabricated using filter paper as porous carbon source and iron salts as magnetic precursors. The textural properties of the MPC were characterized by transmission electron microscopy (TEM), Fourier transform infrared spectrometry (FT-IR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), vibration sample magnetometer (VSM) and nitrogen absorption-desorption isotherms. The as-prepared MPC possessed a high specific surface area, a microstructure comprised of mesopores and strong magnetic response. It was employed as a magnetic solid-phase extraction (MSPE) adsorbent for the determination of three non-steroidal anti-inflammatory drugs (NSAIDs) in environmental water and biological samples coupled with high performance liquid chromatography (HPLC). The main parameters affecting extraction efficiency were investigated in detail and a satisfactory performance was obtained under the optimal conditions. The calibration curves were linear over the concentration ranging from 1 to 1200 μg L for ketoprofen (KET) and 2-1200 μg L for naproxen (NAP) and diclofenac (DCF) with determination coefficients (R) between 0.9995 and 0.9997. The limits of detection (LODs) were in the range of 0.2-0.4 μg L. The intra- and inter-day relative standard deviations (RSDs) were less than 4.03% and 8.72%, respectively. The recoveries ranged from 84.67% to 113.73% with RSDs less than 7.76%. The satisfactory results confirmed the great potential of the novel MPC adsorbent for the extraction of NSAIDs from complex sample matrices.
基于一步燃烧法制备了一种新型磁性多孔碳(MPC),以滤纸为多孔碳源,铁盐为磁性前体。采用透射电子显微镜(TEM)、傅里叶变换红外光谱(FT-IR)、X 射线光电子能谱(XPS)、X 射线衍射(XRD)、振动样品磁强计(VSM)和氮吸附-解吸等温线对 MPC 的结构特性进行了表征。所制备的 MPC 具有高比表面积、由中孔组成的微观结构和强磁响应。它被用作磁性固相萃取(MSPE)吸附剂,用于与高效液相色谱(HPLC)耦合,测定环境水样和生物样品中的三种非甾体抗炎药(NSAIDs)。详细研究了影响萃取效率的主要参数,并在最佳条件下获得了令人满意的性能。在 1-1200 μg/L 范围内,对于酮洛芬(KET)和 2-1200 μg/L 范围内,对于萘普生(NAP)和双氯芬酸(DCF),校准曲线均呈线性,相关系数(R)在 0.9995 至 0.9997 之间。检出限(LODs)在 0.2-0.4 μg/L 范围内。日内和日间相对标准偏差(RSD)分别小于 4.03%和 8.72%。回收率在 84.67%-113.73%之间,RSD 小于 7.76%。满意的结果证实了新型 MPC 吸附剂从复杂样品基质中萃取 NSAIDs 的巨大潜力。