Peña-Velasco Gabriela, Hinojosa-Reyes Laura, Escamilla-Coronado Maricela, Turnes-Palomino Gemma, Palomino-Cabello Carlos, Guzmán-Mar Jorge Luis
Universidad Autónoma de Nuevo León (UANL), Facultad de Ciencias Químicas, Cd. Universitaria, Pedro de Alba S/n, C.P. 66455, San Nicolás de Los Garza, Nuevo León, Mexico.
Universidad Autónoma de Nuevo León (UANL), Facultad de Ciencias Químicas, Cd. Universitaria, Pedro de Alba S/n, C.P. 66455, San Nicolás de Los Garza, Nuevo León, Mexico.
Anal Chim Acta. 2020 Nov 1;1136:157-167. doi: 10.1016/j.aca.2020.09.049. Epub 2020 Sep 26.
A solid-phase extraction methodology using a MIL-101(Fe)/PVDF membrane was proposed as a useful alternative for the simultaneous determination of naproxen, diclofenac, and ibuprofen, three anti-inflammatory drugs (NSAIDs), in wastewater samples by HPLC-CCD analysis. The MIL-101(Fe) was prepared by a rapid microwave-assisted method and supported in a polymeric PVDF membrane. The prepared material was characterized by X-ray diffraction (XRD), nitrogen adsorption-desorption, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and Fourier-transform infrared spectroscopy (FT-IR). The factors that affect the extraction of the NSAIDs using the MIL-101(Fe)/PVDF membrane as the sample volume, the solution pH and the elution solvent were studied in detail. The selected conditions were 50 mL of sample solution at pH 3 and 5 mL of methanol: acetone (30:70, v v) acidified with formic acid at 2% as elution solvent. The analytical method was linear with determination coefficients (r ≥ 0.998) in the calibration ranges from 2 to 100 ng mL for naproxen, 20-200 ng mL for diclofenac, and 100-300 ng mL for ibuprofen. The intra and inter-day precision (repeatability and reproducibility, respectively) of the method (RSD%, n = 5) were lower than 4.8% and 7.1%, respectively. The accuracy reported as recovery percentages ranged from 82 to 118%, and the limits of detection were between 1.8 and 32.3 ng mL. Moreover, MIL-101(Fe)/PVDF membrane exhibited improved adsorption efficiency compared to that of its analog MIL-101(Cr)/PVDF and the pristine PVDF membranes, obtaining in an easy and rapid (60 min) way a low-cost and low-toxic adsorbent with excellent stability, reusability, mechanic resistance, and simple operation which shows excellent performance.
提出了一种使用MIL-101(Fe)/PVDF膜的固相萃取方法,作为通过HPLC-CCD分析同时测定废水中三种抗炎药物(非甾体抗炎药)萘普生、双氯芬酸和布洛芬的有效替代方法。MIL-101(Fe)通过快速微波辅助法制备,并负载在聚合物PVDF膜中。通过X射线衍射(XRD)、氮吸附-脱附、扫描电子显微镜(SEM)、X射线光电子能谱(XPS)和傅里叶变换红外光谱(FT-IR)对制备的材料进行了表征。详细研究了使用MIL-101(Fe)/PVDF膜萃取非甾体抗炎药时的影响因素,如样品体积、溶液pH值和洗脱溶剂。选择的条件为50 mL pH值为3的样品溶液,以及5 mL用2%甲酸酸化的甲醇:丙酮(30:70, v/v)作为洗脱溶剂。该分析方法在萘普生2至100 ng/mL、双氯芬酸20至200 ng/mL、布洛芬100至300 ng/mL的校准范围内呈线性,测定系数(r≥0.998)。该方法的日内和日间精密度(分别为重复性和再现性,RSD%,n = 5)分别低于4.8%和7.1%。以回收率百分比表示的准确度范围为82%至1%,检测限在1.8至32.3 ng/mL之间。此外,与类似的MIL-101(Cr)/PVDF和原始PVDF膜相比,MIL-101(Fe)/PVDF膜表现出更高的吸附效率,以简单快速(60分钟)的方式获得了一种低成本、低毒的吸附剂,具有出色的稳定性、可重复使用性、机械抗性和简单的操作,表现优异。