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采用基于溶胶-凝胶的金属有机骨架涂层固相萃取法萃取人血浆和水样中非甾体抗炎药。

Solid-phase extraction of non-steroidal anti-inflammatory drugs in human plasma and water samples using sol-gel-based metal-organic framework coating.

机构信息

Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, Mashhad 9177948974, Iran.

Department of Chemical and Process Engineering, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia (UKM), Bangi, Selangor 43600, Malaysia.

出版信息

J Chromatogr A. 2021 Jul 5;1648:462168. doi: 10.1016/j.chroma.2021.462168. Epub 2021 May 2.

Abstract

In this research, the Cu-based metal-organic framework (MOF-199) was fabricated and coated on the stainless steel mesh as substrates through sol-gel procedure. Then the coated substrates were placed in a small column known as solid-phase extraction cartridge. The SPE based coated stainless steel mesh coupled with high-performance liquid chromatography-UV detector (HPLC-UV) was used for the fast extraction, and quantification of non-steroidal anti-inflammatory drugs (NSAIDs) from human plasma and water samples. To find optimum extraction conditions, the impacts of effective parameters on analytical performance like sample pH, sample volume, type, and volume of desorption solvent were optimized. At the optimized conditions, calibration graphs of analytes were linear in the concentration range of 0.03-300 ng mL for water samples, and 0.1-200 ng mL for plasma samples. The correlation coefficients were in the range of 0.9938 to 0.9989. Also, the limits of detection (LODs) were from 0.01 to 0.02 ng mL for water samples and 0.03 to 0.1 ng mL for plasma samples. The cartridge repeatability was studied at different values, and the relative standard deviations (RSDs%) were achieved between 3.5 and 5.1%. Consequently, this procedure was successfully used in the extraction and detection of NSAIDs in real water and plasma samples with relative recoveries ranged from 93.6 to 99.6%.

摘要

在这项研究中,通过溶胶-凝胶法制备了铜基金属有机骨架(MOF-199)并将其涂覆在不锈钢网上作为基底。然后,将涂覆的基底放置在称为固相萃取柱的小柱中。基于固相萃取的涂覆不锈钢网与高效液相色谱-紫外检测器(HPLC-UV)结合使用,用于快速提取和定量人血浆和水样中的非甾体抗炎药(NSAIDs)。为了找到最佳的提取条件,研究了样品 pH 值、样品体积、洗脱溶剂的类型和体积等有效参数对分析性能的影响。在优化条件下,水样品中分析物的校准曲线在 0.03-300ng/mL 浓度范围内呈线性,血浆样品在 0.1-200ng/mL 浓度范围内呈线性。相关系数在 0.9938 到 0.9989 之间。此外,水样品的检测限(LOD)在 0.01-0.02ng/mL 之间,血浆样品的检测限在 0.03-0.1ng/mL 之间。在不同值下研究了卡匣的重复性,相对标准偏差(RSD%)在 3.5%至 5.1%之间。因此,该方法成功地用于真实水和血浆样品中非甾体抗炎药的提取和检测,相对回收率在 93.6%至 99.6%之间。

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