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Determination of illegal dyes in Salvia miltiorrhiza Bunge by matrix solid phase dispersion and ultrafast liquid chromatography

机译:基质固相分散和超快液相色谱法测定丹参中的非法染料

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A simple, rapid and effective extraction method based on matrix solid phase dispersion (MSPD) and ultrafast liquid chromatographic (UFLC) was developed and validated for the simultaneous cleaning-up and quantitative extraction of illegal dyes (Sudan Ia€“IV) from the roots of Salvia miltiorrhiza Bunge. The experiment parameters, such as dispersing sorbent, the ratio of sorbenta€“sample, washing solvent and elution solvent were evaluated to find the optimal MSPD conditions. The optimal conditions were 0.5 g of Salvia miltiorrhiza Bunge, 1.0 g of silica gel as dispersing sorbent, a volume of 10 mL of water as the washing solvent and 4 mL of acetonitrilea€“methanol (9:1, v/v) as the elution solvent. Under these conditions good linearity for all the Sudan dyes ranged from 0.10 ??g ga?’1 to 10 ??g ga?’1 (r2 a‰¥ 0.9992). The recoveries at three spiked levels (0.1, 1.0, 5.0 ??g ga?’1) were between 80.6% and 96.1% with relative deviations (RSDs) ranging from 2.3% to 8.6%. The limits of detection ranged between 0.013 and 0.024 ??g ga?’1 which were twenty times lower than the values required by European regulations. This method has potential to be applied for the determination of illegal dyes in complicated traditional Chinese herb materials.
机译:开发了一种基于基质固相分散(MSPD)和超快液相色谱(UFLC)的简单,快速且有效的提取方法,并验证了来自根源的同时清洁和定量提取非法染料(苏丹IA€“IV)俄罗斯米尔蒂希萨山山雀。评价试验参数,例如分散吸附剂,Sorbenta€“样品,洗涤溶剂和洗脱溶剂的比例以找到最佳的MSPD条件。最佳条件为0.5g丹参米蒂氏蛋白,1.0g硅胶作为分散吸附剂,作为洗涤溶剂的量为10毫升,4ml乙腈€“甲醇(9:1,v / v)为洗脱溶剂。在这些条件下,所有苏丹染料的良好线性范围为0.10≤1至10 ?? G Ga?1(R2 a¥0.9992)。三个尖刺水平的回收率(0.1,1.0,5.0 ?? g ga-1)在80.6%和96.1%之间,相对偏差(RSD)范围为2.3%至8.6%。检测限范围为0.013和0.024?1,比欧洲法规所需的值低2次。该方法具有潜力可用于测定复杂的传统中草药材料中的非法染料。

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