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Determination of chloropropanols in foods by one-step extraction and derivatization using pressurized liquid extraction and gas chromatography-mass spectrometry

机译:一步法萃取和衍生化-加压液相萃取-气相色谱-质谱法测定食品中的氯丙醇

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摘要

3-Chloropropane-1,2-diol (3-MCPD) and 1,3-dichloro-2-propanol (1,3-DCP) were determined for the first time in bakery foods using pressurized liquid extraction (PLE) combined with in situ derivatization and GC-MS analysis. This one-step protocol uses N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) as silylation reagent. Initially, screening experimental design was applied to evaluate the effects of the variables potentially affecting the extraction process, namely extraction time (min) and temperature (°C), number of cycles, dispersant reagent (diatomaceous earth in powder form and as particulate matter with high pore volume Extrelut NT) and percent of flush ethyl acetate volume (%). To reduce the time of analysis and improve the sensitivity, derivatization of the compounds was performed in the cell extraction. Conditions, such as the volume of BSTFA, temperature and time for the in situ derivatization of analytes using PLE, were optimized by a screening design followed to a Doehlert response surface design. The effect of the in-cell dispersants/adsorbents with diatomaceous earth, Florisil and sodium sulfate anhydrous was investigated using a Box-Behnken design. Using the final best conditions, 1g of sample dispersed with 0.1g of sodium sulfate anhydrous and 2.5g diatomaceous earth was extracted with ethyl acetate. 1g of Florisil, as clean-up adsorbent, and 70μL of BSTFA were used for 3min at 70°C. Under the optimum conditions, the calibration curves showed good linearity (R2>0.9994) and precision (relative standard deviation, RSD≤2.4%) within the tested ranges. The limits of quantification for 1,3-DCP and 3-MCDP, 1.6 and 1.7μgkg~(-1), respectively, are far below the established limits in the European and American legislations. The accuracy, precision, linearity, and limits of quantification provided make this analytical method suitable for routine control. The method was applied to the analysis of several toasted bread, snacks, cookies and cereal samples, none of which contained chloropropanols at concentrations above the legislation levels.
机译:首次使用加压液体萃取(PLE)结合面包渣中的焙烤食品确定了3-氯丙烷-1,2-二醇(3-MCPD)和1,3-二氯-2-丙醇(1,3-DCP)原位衍生化和GC-MS分析。此一步协议使用N,O-双(三甲基甲硅烷基)三氟乙酰胺(BSTFA)作为甲硅烷基化试剂。最初,采用筛选实验设计来评估可能影响萃取过程的变量的影响,即萃取时间(min)和温度(°C),循环次数,分散剂(粉末形式的硅藻土和作为颗粒物的硅藻土)。高孔体积(Extrelut NT)和冲洗乙酸乙酯体积百分比(%)。为了减少分析时间并提高灵敏度,在细胞提取中对化合物进行了衍生化处理。通过筛选设计和随后的Doehlert响应面设计,可以优化条件,例如BSTFA的体积,使用PLE原位衍生分析物的温度和时间。使用Box-Behnken设计研究了细胞内分散剂/吸附剂与硅藻土,Florisil和无水硫酸钠的关系。在最终的最佳条件下,用乙酸乙酯萃取1g分散有0.1g无水硫酸钠和2.5g硅藻土的样品。在70°C下3分钟使用1g Florisil作为清洁吸附剂和70μLBSTFA。在最佳条件下,校准曲线在测试范围内显示出良好的线性(R2> 0.9994)和精度(相对标准偏差,RSD≤2.4%)。 1,3-DCP和3-MCDP的定量限分别为1.6和1.7μgkg〜(-1),远低于欧洲和美国立法规定的限度。所提供的准确性,精密度,线性和定量极限使这种分析方法适用于常规控制。该方法用于分析几种烤面包,零食,饼干和谷物样品,这些样品均不含高于标准水平的氯丙醇。

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