Suppr超能文献

使用磁性纳米粒子修饰的多壁碳纳米管结合表面活性剂增强荧光光谱法的分散微固相萃取用于灵敏测定生物样品中的洛美沙星和氧氟沙星。

Dispersive micro-solid phase extraction using magnetic nanoparticle modified multi-walled carbon nanotubes coupled with surfactant-enhanced spectrofluorimetry for sensitive determination of lomefloxacin and ofloxacin from biological samples.

作者信息

Amoli-Diva Mitra, Pourghazi Kamyar, Hajjaran Somayeh

机构信息

Department of Physics, Sharif University of Technology, P.O. Box 11365-9161, Tehran, Iran; Department of Chemistry, Payame Noor University (PNU), P.O. Box 19395-3697, Tehran, Iran.

Novel Medical Technologies Department, Darou Pakhsh Pharmaceutical Mfg. Co., Tehran, Iran.

出版信息

Mater Sci Eng C Mater Biol Appl. 2016 Mar;60:30-36. doi: 10.1016/j.msec.2015.11.013. Epub 2015 Nov 10.

Abstract

A dispersive micro-solid-phase extraction (D-μ-SPE) procedure coupled with surfactant-enhanced spectrofluorimetric detection was developed for determination of ofloxacin and lomefloxacin from biological and environmental samples. The D-μ-SPE procedure was performed using magnetic Fe3O4 nanoparticle grafted multi-walled carbon nanotube as an efficient adsorbent. The main factors affecting the signal enhancement (including surfactant concentration and pH) and extraction efficiency (including pH, extraction time, sample volume, amount of magnetic adsorbent, and desorption conditions) were investigated in detail. Under the optimized conditions, the calibration curves were linear (R(2)˃0.9995) over the concentration range of 50-450 ng mL(-1) with detection limits (LOD) of 12 and 15 ng mL(-1) for ofloxacin and lomefloxacin respectively. The relative standard deviation (RSD %) of 1.9 and 2.1% (C=100 ng mL(-1), n=5) and the enrichment factor of 192 and 188 were achieved for ofloxacin and lomefloxacin respectively. Finally, the method was successfully applied to the extraction and preconcentration of these drugs in biological (plasma and urine) samples.

摘要

建立了一种分散微固相萃取(D-μ-SPE)与表面活性剂增强荧光光谱检测相结合的方法,用于测定生物和环境样品中的氧氟沙星和洛美沙星。采用磁性Fe3O4纳米粒子接枝多壁碳纳米管作为高效吸附剂进行D-μ-SPE操作。详细研究了影响信号增强的主要因素(包括表面活性剂浓度和pH值)和萃取效率(包括pH值、萃取时间、样品体积、磁性吸附剂用量和解吸条件)。在优化条件下,校准曲线在50-450 ng mL(-1)浓度范围内呈线性(R(2)>0.9995),氧氟沙星和洛美沙星的检测限(LOD)分别为12和15 ng mL(-1)。氧氟沙星和洛美沙星的相对标准偏差(RSD%)分别为1.9%和2.1%(C=100 ng mL(-1),n=5),富集因子分别为192和188。最后,该方法成功应用于生物(血浆和尿液)样品中这些药物的萃取和预富集。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验