Chen Jie, Xu Juan, Xiong Lihua
Technology Center of Guangdong Entry-Exit Inspection and Quarantine Bureau, Guangzhou 510623, China.
Se Pu. 2011 May;29(5):454-7. doi: 10.3724/sp.j.1123.2011.00454.
A novel method for the simultaneous determination of imperatorin and isoimperatorin in cosmetics by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed. The imperatorin and isoimperatorin were extracted by methanol. The analytes were separated on a C18 column using 10 mmol/L ammonium acetate/ methanol-5 mmol/L ammonium acetate aqueous solution (80:20, v/v) as mobile phase, and then detected by HPLC-MS/MS using multiple reaction monitoring (MRM) mode. The good linearities (r > 0.999) were achieved for the target compounds over the range of 0.25-20 microg/L. The limits of quantification (LOQs) were 0.5 mg/kg. The recoveries for the imperatorin and isoimperatorin varied from 82.2% to 105% and 80.0% to 103% with the relative standard deviations ranging from 2.7% to 4.9% and 1.8% to 4.6% respectively in the range of 0.50-10.0 mg/kg. The method can meet the requirements for the simultaneous determination of imperatorin and isoimperatorin in cosmetics.
建立了一种采用高效液相色谱 - 串联质谱法(HPLC-MS/MS)同时测定化妆品中欧前胡素和异欧前胡素的新方法。欧前胡素和异欧前胡素用甲醇提取。分析物在C18柱上分离,以10 mmol/L醋酸铵/甲醇 - 5 mmol/L醋酸铵水溶液(80:20,v/v)为流动相,然后采用多反应监测(MRM)模式通过HPLC-MS/MS进行检测。目标化合物在0.25 - 20 μg/L范围内具有良好的线性关系(r > 0.999)。定量限(LOQs)为0.5 mg/kg。在0.50 - 10.0 mg/kg范围内,欧前胡素和异欧前胡素的回收率分别为82.2%至105%和80.0%至103%,相对标准偏差分别为2.7%至4.9%和1.8%至4.6%。该方法能够满足化妆品中欧前胡素和异欧前胡素同时测定的要求。