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首页> 外文期刊>Journal of liquid chromatography and related technologies >The determination of the level, source, and risk of polycyclic aromatic hydrocarbon content in traditional Chinese medicines using a QuEChERS based extraction and HPLC-UV-FLD analysis
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The determination of the level, source, and risk of polycyclic aromatic hydrocarbon content in traditional Chinese medicines using a QuEChERS based extraction and HPLC-UV-FLD analysis

机译:使用基于QueCher的提取和HPLC-UV-FLD分析,测定中药中多环芳烃含量的水平,源和风险

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摘要

A rapid and highly sensitive modified QuEChERS method was combined with high performance liquid chromatography-ultraviolet fluorescence detection (HPLC-UV-FLD) to determine and evaluate sixteen polycyclic aromatic hydrocarbons (PAHs) in 74 traditional Chinese medicines (TCMs). A sample-based QuEChERS method pretreatment technology was used to improve sensitivity and selectivity through decolorization and purification in five different medicinal parts of plant TCMs. The limits of detection (LODs) ranged from 0.03 to 0.60μg/kg in dry TCMs. All linearity coefficients (r2) for PAHs exceeded 0.999 within the linear range from 0.1 to 1000ng/mL The spiked recoveries in five matrices were within the range 84.1-98.8%. The relative standard deviations (RSDs) ranged from 1.2% to 8.3%. Spiked recovery tests were done in five parts of dry matrices to conclusively validate the accuracy of the method. The total PAHs ranged from 1.4 to 156.0μg/kg. Among the 16 PAHs, the detection rate of pyrene (Pyr) was generally the highest (33.3-66.7%), and the carcinogenic risk of benzo(a)anthracene (BaA) was as high as 14.2-61.1%. The characteristic ratio analysis indicated that petroleum, coal, and biomass combustion were primary sources of PAHs in TCMs. The health risk of TCMs was evaluated using the carcinogenic toxicity contribution rate analysis.
机译:采用高效液相色谱-紫外荧光检测法(HPLC-UV-FLD),对74种中药中的16种多环芳烃(PAHs)进行了快速、高灵敏度的改良QuEChERS法测定和评价。采用基于样品的QuEChERS法预处理技术,通过对植物中药的五个不同药用部位进行脱色和纯化,提高灵敏度和选择性。干中药的检测限(LOD)范围为0.03至0.60μg/kg。在0.1至1000ng/mL的线性范围内,多环芳烃的所有线性系数(r2)均超过0.999。五种基质中的加标回收率在84.1-98.8%范围内。相对标准偏差(RSD)范围为1.2%至8.3%。在五部分干燥基质中进行加标回收试验,以最终验证该方法的准确性。多环芳烃总量为1.4~156.0μg/kg。在16种多环芳烃中,芘(Pyr)的检出率最高(33.3-66.7%),苯并(a)蒽(BaA)的致癌风险高达14.2-61.1%。特征比值分析表明,石油、煤炭和生物质燃烧是中药中多环芳烃的主要来源。采用致癌毒性贡献率分析评估中药的健康风险。

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