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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Magnetic C-60 nanospheres based solid-phase extraction coupled with isotope dilution gas chromatography-mass spectrometry method for the determination of sixteen polycyclic aromatic hydrocarbons in Chinese herbal medicines
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Magnetic C-60 nanospheres based solid-phase extraction coupled with isotope dilution gas chromatography-mass spectrometry method for the determination of sixteen polycyclic aromatic hydrocarbons in Chinese herbal medicines

机译:基于同位素稀释气相色谱 - 质谱法的基于磁性C-60纳米型固相萃取,用于测定中草药中的十六个多环芳烃 - 质谱法

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摘要

C-60-based magnetic nanospheres were synthesized by coating Fe3O4 nanospheres with silica, then modifying with 3-aminopropyltriethoxysilane as a linker and a C-60 fullerene stationary phase. The morphologies, magnetic properties, infrared absorption and carbon content of magnetic nanospheres were studied by TEM, VSM, FTIR and carbon and sulfur analyzer. The magnetic nanospheres were employed for the magnetic solid-phase extraction (MSPE) of 16 polycyclic aromatic hydrocarbons (PAHs) in nine Chinese herbal medicines. The analyses were conducted by isotope dilution gas chromatography-mass spectrometry. The main parameters influencing the extraction, including extraction solvent, adsorbent amount, and extraction time were optimized. Method validation showed that the limit of detection (LOD) was 0.02-0.11 mu g/kg, and the limit of quantification (LOQ) was 0.07-0.36 mu g/kg. The spiked recoveries rates for 16 PAHs in white peony root were 84.7-107.2%. The relative standard deviation (RSD) was 1.7-8.4%. The established method was further used for the determination 16 PAHs in nine Chinese herbal medicines. Total content of 16 PAHs varied from 73.6 mu g/kg (fructus lycii) to 2172.6 mu g/kg (astragalus root). The results indicate that the pollution of PAHs in Chinese herbal medicines is serious. The established method can effective detect PAHs contamination in Chinese herbal medicines.
机译:通过用二氧化硅涂布Fe3O4纳米球合成C-60基磁性纳米球,然后用3-氨基丙基三乙氧基硅烷改性作为接头和C-60富勒烯固定相。通过TEM,VSM,FTIR和碳和硫分析仪研究了磁性纳米球的形态,磁性,红外吸收和碳含量。磁性纳米球用于九种中草药中16种多环芳烃(PAH)的磁性固相萃取(MSPE)。通过同位素稀释气相色谱 - 质谱法进行分析。优化影响提取的主要参数,包括提取溶剂,吸附量和提取时间。方法验证表明,检测极限(LOD)为0.02-0.11μg/ kg,量化限制(LOQ)为0.07-0.36μg/ kg。白色牡丹根部的16个PAHs的尖刺回收率为84.7-107.2%。相对标准偏差(RSD)为1.7-8.4%。该已建立的方法进一步用于九种中草药中的16个PAH。 16个PAH的总含量从73.6μg/ kg(fructus lycii)不同于2172.6μg/ kg(黄芪根)。结果表明,中草药中PAH的污染严重。建立的方法可以有效地检测中草药中的PAHS污染。

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