首页> 外文期刊>Analytical methods >Sensitive spectrophotometric determination of fluoxetine from urine samples using charge transfer complex formation after solid phase extraction by magnetic multiwalled carbon nanotubes
【24h】

Sensitive spectrophotometric determination of fluoxetine from urine samples using charge transfer complex formation after solid phase extraction by magnetic multiwalled carbon nanotubes

机译:磁性多壁碳纳米管固相萃取后,通过电荷转移配合物形成灵敏分光光度法测定尿液中的氟西汀

获取原文
           

摘要

In this study, magnetic multiwalled carbon nanotubes (MWCNTs/Fe3O4) were prepared by assembling magnetic nanoparticles onto the acid-treated multiwalled carbon nanotubes, and because of their excellent adsorption capability, the MWCNTs/Fe3O4 nanocomposites were used as the adsorbent in a magnetic solid phase extraction procedure (MSPE) to extract fluoxetine from human urine samples. A spectrophotometric detection was performed by the drug reaction with a ?€-acceptor reagent, 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) in nonaqueous media via the formation of a charge transfer complex and by coupling MSPE with visible detection, and a reliable, sensitive and cost-effective method for the determination of trace amounts of fluoxetine was developed. The main factors affecting extraction efficiency and complex formation, including the pH of the sample solution, extraction and desorption time, desorption conditions, sample volume, amount of magnetic adsorbent, DDQ volume and complexation time, were investigated. Under the optimized conditions, the calibration curve was linear (R2 a‰¥ 0.9995) over the concentration range of 0.15 to 2.5 ??g mLa?’1 with an LOD and LOQ of 0.06 and 0.19 ??g mLa?’1, respectively. The relative standard deviation (RSD%) of 2.6% (n = 6) for 1 ??g mLa?’1 and the enrichment factor of 48 was achieved. The method was successfully applied to the extraction and preconcentration of fluoxetine from human urine samples.
机译:在这项研究中,磁性多壁碳纳米管(MWCNTs / Fe3O4)是通过将磁性纳米颗粒组装到酸处理过的多壁碳纳米管上而制备的,由于其出色的吸附能力,MWCNTs / Fe3O4纳米复合材料被用作磁性固体中的吸附剂。相萃取程序(MSPE)从人尿液样本中提取氟西汀。通过在非水介质中与β-受体试剂2,3-二氯-5,6-二氰基苯并醌(DDQ)的药物反应,通过电荷转移配合物的形成,以及将MSPE与可见光检测偶联,进行分光光度检测。并开发了一种可靠,灵敏且具有成本效益的方法来测定痕量氟西汀。研究了影响萃取效率和络合物形成的主要因素,包括样品溶液的pH,萃取和脱附时间,脱附条件,样品量,磁性吸附剂的量,DDQ量和络合时间。在最佳条件下,浓度曲线在0.15至2.5?g mLa?'1的浓度范围内是线性的(R2 a?¥ 0.9995),LOD和LOQ分别为0.06和0.19?g mLa?'1。 。 1 ?? g mLa?’1的相对标准偏差(RSD%)为2.6%(n = 6),富集系数为48。该方法已成功应用于人尿液中氟西汀的提取和预浓缩。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号