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液相色谱串联质谱法测定化妆品中酸性红73和溶剂红1的含量

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建立同时测定化妆品中酸性红 73 和溶剂红 1 含量的液相色谱串联质谱(LC-MS)检测方法.试样经四氢呋喃、氨水溶液或水、氯化钠超声分散提取后加入甲醇,再超声离心,经 0.22 μm的滤膜过滤,然后进行检测,采用电喷雾离子源正离子(ESI+)多反应监测(MRM)模式测定,保留时间和相对离子对丰度定性,外标法定量.结果表明,样品中酸性红73和溶剂红1在2.0~1 000.0 μg/L呈线性关系,线性相关系数大于0.999;检出限为 0.034 mg/kg,定量限为0.100 mg/kg;平均回收率为73.1%~112.8%,相对标准偏差(RSD)为 1.23%~6.09%(n=6).该方法操作简便、准确、灵敏度高、回收率和重复性好,适合于化妆品中酸性红73和溶剂红1的测定.
Determination of Constituents Acid Red 73 and Solvent Red 1 in Cosmetics by LC-MS
A method for the simultaneous determination of acid red 73 and solvent red 1 in cosmetics by liquid chromatography-tandem mass spectrometry(LC-MS)was developed.The sample was extracted by ultrasonic dispersion of tetrahydrofuran,ammonia or water and sodium chloride,then methanol was added.After ultrasonic centrifugation,the sample was filtered by 0.22 μm filter membrane,and the solution was detected by the electrospray ion source positive ion(ESI+)multi reaction monitoring(MRM)model.The retention time and relative ion pair abundance were used for qualitative analysis,while the external standard method was used for quantitative analysis.The results showed that there was a linear relationship within the range of 2.0-1 000.0 μg/L,with a linear correlation coefficient greater than 0.999.The limits of detection for the two components were 0.034 mg/kg and the limits of quantitation were 0.100 mg/kg.The average recoveries of the two components were 73.1%-112.8%,and the relative standard deviations(RSD)were 1.23%-6.09%(n=6).The method is simple,accurate,highly sensitive,with good recovery and repeatability,and is suitable for the determination of acid red 73 and solvent red 1 in cosmetics.

cosmeticsacid red 73solvent red 1liquid chromatography-tandem mass spectrometry(LC-MS)external standard method

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上海香料研究所有限公司,上海 200232

化妆品 酸性红73 溶剂红1 液相色谱串联质谱法 外标法

2024

香料香精化妆品
上海香料研究所

香料香精化妆品

CSTPCD
影响因子:0.341
ISSN:1000-4475
年,卷(期):2024.(1)
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