在液相色谱-串联质谱法之前,基于涂在网状物上的共价有机框架从血浆中进行薄膜微萃取阿哌沙班。

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography B Pub Date : 2024-09-20 DOI:10.1016/j.jchromb.2024.124302
Aysan Changizi Kecheklou , Mohammad Reza Afshar Mogaddam , Saeed Mohammad Sorouraddin , Mir Ali Farajzadeh , Ali Akbar Fathi
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引用次数: 0

摘要

本研究合成了一种新型共价有机框架,并将其作为薄膜微萃取的涂层,用于从血浆样品中萃取阿哌沙班。该涂层通过浸泡在氢氟酸溶液中应用于改性网状物上。然后使用液相色谱-串联质谱法对提取的药物进行分析。通过将共价有机框架的高比表面积和选择性与创新的薄膜微萃取方法和灵敏的分析系统相结合,实现了一种高效的分析方法。将涂有共价有机框架的网状物作为吸收剂浸入生物样品中,对目标分析物进行预浓缩和提取。随后,进行一定时间的超声处理。之后,使用乙腈作为洗脱溶剂对提取的分析物进行解吸。通过采用 "一次一个参数 "的策略,对所建议技术的有效参数进行了优化,并选出了最佳条件。通过整合所开发的方法,在以下方面取得了显著成果:低检出限和定量限(分别为 0.17 和 0.56 µg/L)、宽线性范围(0.05-250 µg/L)、日内和日间精确度(相对标准偏差≤14%)以及令人满意的提取回收率(在血浆和去离子水中分别为 53% 和 54%)。因此,可以得出结论:该技术在生物样本中的应用具有高效性和可靠性。
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Thin film microextraction of apixaban from plasma based on the covalent organic framework coated on a mesh prior to liquid chromatography-tandem mass spectrometry
In this research, a new covalent organic framework was synthesized and utilized as a coating in thin film microextraction for the extraction of apixaban from plasma samples. This coating was applied to the mesh modified through immersion in a HF solution. The extracted drug was then analyzed using liquid chromatography-tandem mass spectrometry. By combining the high specific surface area and selectivity of the covalent organic framework, along with integrating the innovative thin film microextraction method and a sensitive analysis system, an efficient analytical approach was achieved. The target analyte was preconcentrated and extracted by immersing of the covalent organic framework-coated mesh as an absorbent into the biological sample. Subsequently, a sonication process was conducted for a specific duration. Following this, the extracted analyte was desorbed using acetonitrile as the elution solvent. The effective parameters of the proposed technique were optimized by using “one-parameter-at-a-time” strategy and the optimal conditions were selected. By integrating the developed method notable achievements were made in the terms of low limits of detection and quantification (0.17 and 0.56 µg/L, respectively), a wide linear range (0.05–250 µg/L), intra- and inter day precisions (with relative standard deviations of ≤14 %), as well as satisfactory extraction recoveries (53 % and 54 % in plasma and deionized water, respectively). Hence, it can be concluded that the introduced technique exhibits high efficiency and reliability when applied to biological samples.
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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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