Liu Baojun, Yan Lili, Li Qiuyue, Wang Jinfang, Shi Yue
State Food and Drug Administration Review of Health Food Center, Beijing 100070, China.
Wei Sheng Yan Jiu. 2012 Sep;41(5):790-3.
A high performance liquid chromatographic (HPLC) method was developed for the simultaneous determination of 4 furocoumarins, including 8-methoxycoumarin, 5-methoxycoumarin, trioxsalen and imperatorin in cosmetics.
The separation was carried on Diamonsil C18 column (4.6 mm x 250 mm, 5 microm) by gradient elution with methanol-water as mobile phase at a flow rate of 1.0 ml/min and column temperature of 30 degrees C. The analysis of 4 furocoumarins was performed by HPLC with diodearray detector at the wavelength of 248 nm.
Identification of 4 furocoumarins was achieved by retention time, and quantification analysis was performed by the external standard method. The limits of quantitation (LOQ) for 4 furocoumarins were 0.54, 0.52, 0.58 and 0.50 microg/g, respectively. The method showed a good linearity in the range of 0.05-10 microg/ml with correlation coefficients more than 0.999. The mean recoveries at spiked levels were in the range of 89.9%-105.2% with RSDs of 0.20%-1.08%.
The method was accurate and simple, and was suitable for the determination of 4 furocoumarins in cosmetics.
建立一种高效液相色谱(HPLC)法,用于同时测定化妆品中的4种呋喃香豆素,包括8-甲氧基香豆素、5-甲氧基香豆素、三甲沙林和欧前胡素。
采用Diamonsil C18柱(4.6 mm×250 mm,5 µm),以甲醇-水为流动相进行梯度洗脱,流速为1.0 ml/min,柱温为30℃。采用二极管阵列检测器,在波长248 nm处对4种呋喃香豆素进行HPLC分析。
通过保留时间对4种呋喃香豆素进行鉴定,采用外标法进行定量分析。4种呋喃香豆素的定量限(LOQ)分别为0.54、0.52、0.58和0.50 μg/g。该方法在0.05-10 μg/ml范围内线性良好,相关系数大于0.999。加标水平下的平均回收率在89.9%-105.2%之间,相对标准偏差(RSD)为0.20%-1.08%。
该方法准确、简便,适用于化妆品中4种呋喃香豆素的测定。