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首页> 外文期刊>Analytical methods >Organic solvent-free matrix solid phase dispersion (MSPD) for determination of synthetic colorants in chilli powder by high-performance liquid chromatography (HPLC-UV)
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Organic solvent-free matrix solid phase dispersion (MSPD) for determination of synthetic colorants in chilli powder by high-performance liquid chromatography (HPLC-UV)

机译:高效液相色谱法(HPLC-UV)用于测定辣椒粉中合成色素的无有机溶剂基质固相分散体(MSPD)

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摘要

A green and simple organic solvent-free matrix solid phase dispersion (MSPD) was developed and applied to the extraction of four synthetic colorants (amaranth, sunset yellow, allura red and erythrosine) in chilli samples. High-performance liquid chromatography (HPLC) coupled with ultraviolet (UV) detection was used for the separation and determination of the analytes. The chromatographic separation was performed on a Phenomenex Luna C18 (2) 100A column in a gradient using methanol/water as the mobile phase at a flow rate of 0.8 mL mina?’1 and 35 ?°C of temperature. Factors such as the type of dispersant, the ratio of sample to dispersant, and the type, volume, pH value and ionic strength of elution solvent were investigated. Under the optimum experimental conditions, the linearities for determining the analytes were in the range of 30a€“2000 ng ga?’1 for amaranth and erythrosine, 20a€“2000 ng ga?’1 for sunset yellow and allura erythrosine. Limits of detection ranged between 8.6 and 13.5 ng ga?’1. No organic solvents were used in the extraction procedure, and 4 mL water directly eluted the analytes. Thus, the method avoided environmental pollution of organic solvents and removed multi-step procedures in the sample pretreatment and has potential to be applied using a simple instrument presented in most analytical laboratories.
机译:开发了一种绿色且简单的无有机溶剂基质固相分散体(MSPD),并将其用于辣椒样品中四种合成着色剂(ama色,日落黄,阿鲁拉红和赤藓红)的提取。高效液相色谱(HPLC)结合紫外(UV)检测用于分离和测定分析物。色谱分离在Phenomenex Luna C18(2)100A色谱柱上进行,使用甲醇/水作为流动相,在0.8 mL min-1和35°C的流速下进行梯度洗脱。研究了分散剂的类型,样品与分散剂的比例以及洗脱溶剂的类型,体积,pH值和离子强度等因素。在最佳实验条件下,determining菜和赤藓红的分析物线性测定范围为30a€2000 ng ga-1,日落黄和艳红赤藓酸的测定范围为20a€2000 ng ga-1。检测限介于8.6和13.5 ng ga?’1之间。萃取过程中不使用有机溶剂,而4 mL水则直接洗脱了分析物。因此,该方法避免了有机溶剂的环境污染,并消除了样品预处理中的多步骤程序,并且具有使用大多数分析实验室中提供的简单仪器进行应用的潜力。

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