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Trace determination of chlorpheniramine in human plasma using magnetic dispersive solid-phase extraction based on a graphene oxide/Fe3O4@polythionine nanocomposite combined with high-performance liquid chromatography

机译:基于石墨烯氧化物/ Fe3O4的磁性色散固相萃取痕量用磁性色散固相萃取法测定人血浆中氯苯那甲胺氨基胺。高性能液相色谱法与高效液相色谱法

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摘要

Graphene oxide/Fe3O4@polythionine (GO/Fe3O4@PTh) nanocomposite was fabricated as a new and promising sorbent for magnetic dispersive solid-phase extraction (MDSPE) and high-performance liquid chromatography-ultraviolent detection (HPLC) of chlorpheniramine in human plasma. To fabricate the sorbent, thionine was polymerized on the surface of magnetic GO via an oxidative polymerization in order to produce polythionine as a surface modifier and obtain reasonable extraction yield. The characteristics of the sorbent were studied with transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), energy-dispersive X-ray analysis (EDX), vibrating sample magnetometry (VSM) and Fourier transform-infrared (FT-IR) spectroscopy. The calibration curve revealed linearity in the range of 2.0-550.0 ng mL(-1) with a regression coefficient corresponding to 0.995. Limits of detection (LOD, S/N - 3) and quantification (LOQ, S/N - 10) were 0.4 and 2.0 ng mL(-1), respectively. A desired recovery range of 87.9-96.4% and acceptable intra-day (4.1-5.0%) and inter-day (4.9-5.6%) precision as well as remarkable sample clean up showed the good efficiency of the method. To investigate the practical suitability of the proposed method, it was applied for the determination of chlorpheniramine in human plasma after oral administration of the drug while some pharmacokinetic data were achieved. This technique proved to be reliable and green for screening purposes.
机译:将石墨烯(GO / Fe3O4 @ PTH)纳米复合材料制成了用于磁性色散固相萃取(MDSPE)和高性能液相色谱 - 紫外线中的新的和有前途的吸附剂。为了制造吸附剂,通过氧化聚合在磁性的表面上聚合噻嗪,以产生聚硫氨酸作为表面改性剂并获得合理的提取产率。用透射电子显微镜(TEM),扫描电子显微镜(SEM),X射线衍射(XRD),能量分散X射线分析(EDX),振动样品磁体(VSM)和傅里叶变换进行研究了吸附剂的特性-Infared(FT-IR)光谱。校准曲线显示出2.0-550.0 ng ml(-1)范围内的线性度,回归系数对应于0.995。检测限(LOD,S / N-3)和定量(LOQ,S / N-10)分别为0.4和2.0ng mL(-1)。所需的恢复范围为87.9-96.4%,可接受的白天(4.1-5.0%)和日内(4.9-5.6%)精度以及显着的样品清洁显示了该方法的良好效率。为了研究所提出的方法的实用适用性,在口服药物施用后,应用了在口服施用后的人血浆中氯苯那胺的测定。实现了一些药代动力学数据。该技术证明是可靠的和绿色,用于筛选目的。

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  • 来源
    《RSC Advances》 |2017年第84期|共9页
  • 作者单位

    Islamic Azad Univ Fac Sci Dept Appl Chem South Tehran Branch POB 1777613651 Tehran Iran;

    Islamic Azad Univ Fac Sci Dept Appl Chem South Tehran Branch POB 1777613651 Tehran Iran;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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