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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Octadecyl functionalized core-shell magnetic silica nanoparticle as a powerful nanocomposite sorbent to extract urinary volatile organic metabolites
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Octadecyl functionalized core-shell magnetic silica nanoparticle as a powerful nanocomposite sorbent to extract urinary volatile organic metabolites

机译:十八烷基官能化的核壳磁性二氧化硅纳米粒子,作为一种强大的纳米复合吸附剂,可提取尿液中的挥发性有机代谢物

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In this present study, magnetic Fe3O4@SiO2 nanoparticles (MNPs) functionalized with octadecyl groups (Fe3O4@SiO2-C-18 NPs) were synthesized, characterized and employed, for the first time, as powerful nanosorbent to extract endogenous volatile organic metabolites (EVOMs) namely, hexanal, heptanal, decanal, benzaldehyde, 4-heptanone, 5-methyl-2-furfural and phenol, described as potential biomarkers of cancer, from human urine. By using co-precipitation, surface modification methods, the carbon-ferromagnetic nanocomposite was synthesized and characterized by infrared spectrum (IR) and transmission electron microscopy (TEM). By coupling with gas chromatography-mass spectrometry (GC-qMS), a reliable, sensitive and cost-effective method was validated. To test the extraction efficiency of the carbon-ferromagnetic nanocomposite toward urinary EVOMs experimental variables affecting the extraction performance,including nanosorbent amount, adsorption time, elution time, and nature of elution solvent, were investigated in detail. The extraction process was performed by dispersing Fe3O4@SiO2-C18 NPs into working solution containing targeted VOMs, and into urine samples, and then eluted with an adequate organic solvent. The eluate was collected, concentrated and analyzed by GC-qMS. Under the optimized conditions, the LODs and LOQs achieved were in the range of 9.7-57.3 and 32.4-190.9 ng/mL, respectively. Calibration curves were linear (r(2) >= 0.988) over the concentration ranges from 0.25 to 250 ng/mL. In addition, a satisfying reproducibility was achieved by evaluating the intra- and inter-day precisions with relative standard deviations (RSDs) less than 3 and 11%, respectively. The method also afforded satisfactory results in terms of the matrix effect (72.8-96.1%) and recoveries (accuracy) higher than 75.1% for most of the studied EVOMs. The Fe3O4@SiO2-Cis NPs-based sorbent extraction combined with GC-qMS revealed that the new nanosorbent had a strong ability to retain the target metabolites providing a new, reliable and high throughput strategy for isolation of targeted EVOMs in human urine, suggesting their potential to be applied in other EVOMs. (C) 2015 Elsevier B.V. All rights reserved.
机译:在本研究中,首次合成,表征和表征了十八烷基官能化的磁性Fe3O4 @ SiO2纳米颗粒(Fe3O4 @ SiO2-C-18 NPs),并作为强大的纳米吸附剂用于提取内源性挥发性有机代谢物(EVOM) ),即人尿中所描述的潜在潜在癌症标志物,己醛,庚醛,癸醛,苯甲醛,4-庚酮,5-甲基-2-糠醛和苯酚。通过共沉淀,表面改性的方法,合成了碳铁磁性纳米复合材料,并通过红外光谱(IR)和透射电子显微镜(TEM)表征。通过与气相色谱-质谱联用(GC-qMS),验证了一种可靠,灵敏且具有成本效益的方法。为了测试碳铁磁性纳米复合物对尿液EVOM的萃取效率,详细研究了影响萃取性能的实验变量,包括纳米吸附剂的量,吸附时间,洗脱时间和洗脱溶剂的性质。通过将Fe3O4 @ SiO2-C18 NP分散到含有目标VOM的工作溶液中和尿液样品中,然后用适当的有机溶剂洗脱来进行提取。收集洗脱液,浓缩并通过GC-qMS分析。在优化的条件下,获得的LOD和LOQ分别为9.7-57.3和32.4-190.9 ng / mL。在0.25至250 ng / mL的浓度范围内,校准曲线是线性的(r(2)> = 0.988)。此外,通过评估日内和日间精度的相对标准偏差(RSD)分别小于3%和11%,可以实现令人满意的重现性。对于大多数研究的EVOM,该方法在基质效应(72.8-96.1%)和回收率(准确性)高于75.1%方面也提供了令人满意的结果。 Fe3O4 @ SiO2-Cis基于NPs的吸附剂提取物与GC-qMS的结合表明,这种新型纳米吸附剂具有强大的保留目标代谢物的能力,为分离人尿中的目标EVOM提供了新的,可靠的且高通量的策略,表明在其他EVOM中应用的潜力。 (C)2015 Elsevier B.V.保留所有权利。

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