Department of Analytical Chemistry, Faculty of Chemistry, University of Valencia, Dr Moliner 50, 46100, Burjassot, Valencia, Spain.
Mikrochim Acta. 2019 Nov 11;186(12):759. doi: 10.1007/s00604-019-3923-6.
A (glycidyl methacrylate)-co-(ethylene glycol dimethacrylate) polymer (poly(GMA-co-EDMA)) was functionalized with metal-organic frameworks (MOF) and used as a sorbent for solid-phase extraction (SPE). The polymeric sorbent was prepared in-situ by photopolymerization in a previously wall-modified spin column, and then modified with an amino-modified MOF of type NH-MIL-101(Cr). The sorbents were used for the extraction of nonsteroidal anti-inflammatory drugs (NSAIDs) from human urine samples. The sorbent was compared with the parent monolith and embedded approach, where the MOF particles are admixed in the polymerization mixture before the in-situ polymerization in the modified spin column. SPE is performed by percolating the sample solutions in a centrifuge, which streamlines the SPE steps. The hybrid composites were characterized by scanning electron microscopy and nitrogen intrusion porosimetry. Three NSAIDs (ketoprofen, flurbiprofen, and ibuprofen) were tested. They were eluted from the sorbent with acidified water-acetonitrile mixtures and subsequently analyzed by reversed-phase HPLC with UV detection. The detection limits varied in the range from 0.1 to 7 μg·L, and the precisions (relative standard deviation) were <14% in all the cases. The recoveries were between 71.0 and 78.0% in spiked urine samples. Graphical abstractA hybrid monolith modified with amino-modified MOF [named NH-MIL-101(Cr)] in wall-modified spin columns was prepared. The resulting micro-extraction device was applied to the extraction and preconcentration of non-steroidal anti-inflammatory drugs.
一种(甲基丙烯酸缩水甘油酯)-共-(乙二醇二甲基丙烯酸酯)聚合物(聚(GMA-co-EDMA))被功能化的金属-有机骨架(MOF)并用作固相萃取(SPE)的吸附剂。聚合物吸附剂通过在预先壁修饰的螺旋柱中进行光聚合原位制备,然后用氨基修饰的 MOF NH-MIL-101(Cr)进行修饰。吸附剂用于从人尿样中提取非甾体抗炎药(NSAIDs)。将吸附剂与母体整体柱和嵌入方法进行了比较,其中在改性螺旋柱中进行原位聚合之前,将 MOF 颗粒混入聚合混合物中。SPE 通过在离心机中渗滤样品溶液来进行,这简化了 SPE 步骤。通过扫描电子显微镜和氮侵入孔隙率法对混合复合材料进行了表征。测试了三种 NSAIDs(酮洛芬、氟比洛芬和布洛芬)。它们用酸化的水-乙腈混合物从吸附剂中洗脱出来,然后用反相 HPLC 与紫外检测进行分析。检测限在 0.1 到 7 μg·L 的范围内变化,所有情况下的精密度(相对标准偏差)均小于 14%。在加标尿样中的回收率在 71.0%到 78.0%之间。