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高效液相色谱法测定化妆品中艾地苯醌和辅酶Q10

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建立高效液相色谱法测定化妆品中艾地苯醌和辅酶Q10的含量.样品经无水乙醇超声提取,用Waters XBridge C18色谱柱(250 mm×4.6 mm,5 μm)分离.以无水乙醇-水作为流动相进行梯度洗脱,流量为1.0 mL/min,柱温为40℃,检测波长为275 nm,以色谱峰面积外标法定量.艾地苯醌和辅酶Q10的质量浓度在0.5~100 mg/L范围内与色谱峰面积具有良好的线性关系,线性相关系数均为0.999 9.艾地苯醌和辅酶Q10的方法检出限分别为0.11、0.41 mg/kg,定量限分别为0.37、1.35 mg/kg.爽肤水、乳液、面霜和凝胶4种基质3个浓度水平的加标平均回收率为94.7%~102.6%,测定结果的相对标准偏差为0.3%~2.8%(n=6).该方法操作简便,适用于化妆品中艾地苯醌和辅酶Q10的测定.
Determination of idebenone and coenzyme Q10 in cosmetics by high performance liquid chromatography
A method for determining the content of idebenone and coenzyme Q10 in cosmetics by high performance liquid chromatography was established.The samples were ultrasonically extracted with anhydrous ethanol and separated using a Waters XBridge C18 column(250 mm×4.6 mm,5 μm).Gradient elution was performed with anhydrous ethanol-water as the mobile phase at a flow rate of 1.0 mL/min,with column temperature of 40℃and detection wavelength of 275 nm.Quantitative analysis was conducted using the external standard method based on chromatographic peak areas.The mass concentrations of idebenone and coenzyme Q10 had a good linear relationship with the chromatographic peak area in the range of 0.5-100 mg/L,the correlation coefficients were all 0.999 9.The detection limits of idebenone and coenzyme Q10 was 0.11,0.41 mg/kg,respectively,and the quantification limits was 0.37,1.35 mg/kg,respectively.The average recoveries of the four matrices(toner,lotion,cream and gel)at three concentration levels were 94.7%-102.6%,and the relative standard deviations of the determination results was 0.3%-2.8%(n=6).This method is simple and convenient to operate,making it suitable for the determination of idebenone and coenzyme Q10 in cosmetics.

cosmeticshigh performance liquid chromatographyidebenonecoenzyme Q10

王继双、李莉、张隆龙、王海燕

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中国食品药品检定研究院,国家药品监督管理局化妆品研究与评价重点实验室,北京 100050

化妆品 高效液相色谱法 艾地苯醌 辅酶Q10

2025

化学分析计量
中国兵器工业集团第五三研究所(国防科技工业应用化学一级计量站)

化学分析计量

影响因子:0.444
ISSN:1008-6145
年,卷(期):2025.34(1)