...
首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Sol-gel-derived magnetic SiO2/TiO2 nanocomposite reinforced hollow fiber-solid phase microextraction for enrichment of non-steroidal anti-inflammatory drugs from human hair prior to high performance liquid chromatography
【24h】

Sol-gel-derived magnetic SiO2/TiO2 nanocomposite reinforced hollow fiber-solid phase microextraction for enrichment of non-steroidal anti-inflammatory drugs from human hair prior to high performance liquid chromatography

机译:溶胶凝胶衍生的磁性SiO2 / TiO2纳米复合增强中空纤维固相微萃取技术,可在高效液相色谱之前从人发中富集非甾体类抗炎药

获取原文
获取原文并翻译 | 示例
           

摘要

Hollow fiber-solid phase micro-extraction (HF-SPME) technique containing sol-gel-derived Fe3O4/SiO2/TiO2 core-double shell nanocomposite as a novel high efficiency sorbent, coupled with high performance liquid chromatography was used to extraction and determination of six non-steroidal anti-inflammatory drugs; acetylsalicylic acid, naproxen, piroxicam, diclofenac, indomethacin and mefenamic acid, in hair samples. First, magnetite nanoparticles (Fe3O4-NPs) were synthesized by chemical co-precipitation of Fe(II) and Fe(III) ions (where the ratio of Fe(II) to Fe(III) is 1:2 and a non-oxidizing environment), in alkaline medium to produce magnetite particles. Subsequently, surface of Fe3O4-NPs was modified with SiO2 and TiO2 using layer-by-layer chemical technique. A core-shell structure of Fe3O4/SiO2/TiO2 composite was prepared by coating magnetite core particles with silica and titania layers. In the proposed method, NSAIDs were extracted by the synthesized nanocomposite and analyzed by HPLC. The parameters affecting the efficiency of magnetic nanoparticle (MNPs) assisted HF-SPME were investigated and optimized. The method validation was included and satisfying results with high pre-concentration factors (405 up to 2450) were obtained. It owes large surface area and porosity of the nano-adsorbent. Under the optimal conditions, the method detection limits (S/N = 3) were in the range of 0.01-0.10 mu g ml(-1) and the limits of quantification (S/N = 10) between 0.04 and 0.30 mu g ml(-1). Relative standard deviations were 3.09-6.61%. Eventually, the method was successfully applied to human hair after administration of NSAIDs. (C) 2014 Elsevier B.V. All rights reserved.
机译:以溶胶-凝胶法制备的Fe3O4 / SiO2 / TiO2核-双壳纳米复合材料为新型高效吸附剂的空心纤维固相微萃取(HF-SPME)技术与高效液相色谱法联用进行了萃取和测定。六种非甾体抗炎药;头发样本中的乙酰水杨酸,萘普生,吡罗昔康,双氯芬酸,消炎痛和甲芬那酸。首先,通过化学共沉淀Fe(II)和Fe(III)离子(其中Fe(II)与Fe(III)的比例为1:2,并且具有非氧化性)合成磁铁矿纳米颗粒(Fe3O4-NPs)环境),在碱性介质中产生磁铁矿颗粒。随后,采用逐层化学技术,用SiO2和TiO2修饰Fe3O4-NPs的表面。 Fe3O4 / SiO2 / TiO2复合材料的核-壳结构是通过在磁铁矿核颗粒上覆盖二氧化硅和二氧化钛层而制备的。在所提出的方法中,通过合成的纳米复合材料提取NSAIDs并通过HPLC进行分析。研究和优化了影响磁性纳米颗粒(MNPs)辅助HF-SPME效率的参数。包括了方法验证,并获得了高预浓缩因子(405至2450)的满意结果。它具有较大的表面积和纳米吸附剂的孔隙率。在最佳条件下,方法检出限(S / N = 3)在0.01-0.10μg ml(-1)范围内,定量限(S / N = 10)在0.04至0.30μgml ml之间(-1)。相对标准偏差为3.09-6.61%。最终,该方法在施用NSAID后成功应用于人的头发。 (C)2014 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
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