利用 C18 功能化磁性纳米材料和超临界流体色谱法快速测定人血浆中的丙泊酚。

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Shan-Yan Liang, Xiao-Min Xu, Peng Wang, Ming-Li Ye, Shui-Feng Zhang, Yong-Gang Zhao
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引用次数: 0

摘要

以 N, N-二甲基十八胺为改性剂,合成了新型 C18 功能化磁性纳米材料,即 C18@poly-styrene-divinylbenzene-glycidyl methacrylate-Fe3O4 (C18@PS-DVB-GMA-Fe3O4),该材料有利于去除血液中的磷脂。在超临界流体色谱(SFC)分析异丙酚之前,C18@PS-DVB-GMA-Fe3O4 纳米粒子被用于快速、简便、廉价、有效、坚固和安全(QuEChERS)人血浆分析程序中并进行了评估。在 QuEChERS 程序中,人血浆样品与萃取溶剂和 C18@PS-DVB-GMA-Fe3O4 纳米粒子直接混合,萃取和净化程序同时完成。采用 C18 色谱柱(Thermo Scientific™ Acclaim™ 120, 250 × 4. 6 mm, 5 μm),以百里酚为内标,在 5 分钟内完成 SFC 分离。以超临界二氧化碳为流动相,甲醇为助溶剂,流速为 1.0 mL/min。色谱柱温度为 38°C,检测波长为 275 nm。丙泊酚在 0.5-10 mg/L 浓度范围内线性关系良好(R2=0.9997),检出限为 0.17 mg/L。回收率为76.5%-91.9%,RSD小于7.9%。该方法简便、快速、准确度高、基质效应小,适用于丙泊酚血浆浓度的快速测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fast Determination of Propofol in Human Plasma Using C18-Functionalized Magnetic Nanomaterials Followed by Supercritical Fluid Chromatography.

Novel C18-functionalized magnetic nanomaterials; i.e., C18@poly-styrene-divinylbenzene-glycidyl methacrylate-Fe3O4 (C18@PS-DVB-GMA-Fe3O4) have been synthesized by using N, N-dimethyloctadecylamine as modifying agent, which could be beneficial to remove the blood phospholipids. The C18@PS-DVB-GMA-Fe3O4 nanoparticles have been used and evaluated in the Quick, Easy, Cheap, Effective, Rugged and Safe (QuEChERS) procedure for human plasma prior to the analysis of propofol by supercritical fluid chromatography (SFC). In the QuEChERS procedure, human plasma samples are directly mixed with extraction solvent and C18@PS-DVB-GMA-Fe3O4 nanoparticles, and the extraction and cleanup procedures have been accomplished simultaneously. The SFC separation was performed with a C18 column (Thermo Scientific™ Acclaim™ 120, 250 × 4. 6 mm, 5 μm) within 5 min, using thymol as the internal standard. Supercritical carbon dioxide was used as the mobile phase with methanol as the cosolvent at the flow rate of 1.0 mL/min. The column temperature was 38°C, and detection wavelength was 275 nm. A good linearity was obtained among the propofol concentration range of 0.5-10 mg/L (R2 = 0.9997) with the limit of detection of 0.17 mg/L. Recoveries were in the range of 76.5-91.9%, with RSD less than 7.9%. These results suggested that method is convenient, rapid with high accuracy and little matrix effect, and suitable for rapid determination of propofol plasma concentration.

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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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