期刊名称:药物分析杂志 主管单位:中国科学技术协会 主办单位:中国药学会承办:中国食品药品检定研究院 主编:金少鸿 地址:北京天坛西里2号 邮政编码:100050 电话:010-67012819,67058427 电子邮箱:ywfx@nifdc.org.cn 国际标准刊号:ISSN 0254-1793 国内统一刊号:CN 11-2224/R 邮发代号:2-237
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高效液相色谱法同时测定化妆品中17种美白成分
Simultaneous determination of seventeen kinds of whitening ingredients in cosmetics by high performance liquid chromatography
分类号:R917
出版年·卷·期(页码):2019,39 (9):1643-1650
DOI:
10.16155/j.0254-1793.2017.01.01
-----摘要:-------------------------------------------------------------------------------------------
目的:建立高效液相色谱法(HPLC)同时测定化妆品中17种美白成分。方法:样品经50%甲醇溶液提取、过滤后,进行HPLC分析。采用Agilent
ZORBAX Eclipse XDB-C18色谱柱(4.6 mm×250 mm,5 μm),流动相为甲醇-0.02
mol·L-1磷酸二氢钾溶液,梯度洗脱,二极管阵列检测器多波长分析,熊果苷、氢醌、烟酰胺、间苯二酚、杜鹃醇、4-丁基间苯二酚、苯乙基间苯二酚和四氢木兰醇的检测波长为230
nm,抗坏血酸磷酸酯镁、抗坏血酸葡糖苷、烟酸、3-O-乙基抗坏血酸、4-甲氧基水杨酸钾、鞣花酸和甘草酸二钾的检测波长为254
nm,曲酸和苯酚的检测波长为270 nm。结果:17种成分分离度良好,峰面积与质量浓度在2~50
μg·mL-1范围内呈良好的线性关系(r>0.999),霜类、乳液类、水剂类3种化妆品基质中17种美白成分的回收率良好,3个添加水平分别为0.025%、0.05%和0.25%,平均回收率(n=6)为86.9%~104.3%,RSD为0.51%~3.7%;稳定性良好,17种成分在24
h内保持稳定,RSD在0.12%~0.73%之间,检测下限在0.000
5%~0.005%之间。50批样品中检出7种美白成分,抗坏血酸磷酸酯镁、抗坏血酸葡糖苷、烟酸、熊果苷、烟酰胺、3-O-乙基抗坏血酸、甘草酸二钾的含量分别为0.021%~0.095%、0.018%~0.025%、0.019%~0.024%、0.028%~3.5%、0.027%~3.9%、0.034%~2.8%、0.023%~1.6%。结论:该方法经方法学验证,可同时测定化妆品中17种美白成分的含量。
-----英文摘要:---------------------------------------------------------------------------------------
Objective:To establish a quantitative method for simultaneous
determination of 17 kinds of whitening ingredient in cosmetics by high
performance liquid chromatography(HPLC). Methods:Samples were extracted
by 50% methanol solution and filtered,then separated on a Agilent ZORBAX Eclipse
XDB-C18 column(4.6 mm×250 mm,5 μm) and detected at different
wavelength. The mobile phase was methanol and 0.02 mol·L-1 monopotassium phosphate solution with gradient elution. Diode array
detector(DAD) was used with the wavelength of 230 nm for
arbutin,hydroquinone,nicotinamide,resorcinol,rhododendrol,4-butylresorcinol,phenylethyl
resorcinol and tetrahydromagnolitol,and 254 nm for magnesium ascorbyl
phosphate,ascorbyl glucoside,nicotinic acid,3-O-ethyl ascorbic
acid,potassium methoxysalicylate,ellagic acid and dipotassium glycyrrhizate,and
270 nm for kojic acid and phenol. Results:The seventeen constituents were
well separated.The linear range was 2-50
μg·mL-1(r>0.999).The recoveries(spiked at 0.025%,0.05% and
0.25%,respectively) in 3 different types of cosmetic ranged from 86.9% to
104.3%,and the RSD range was 0.51% to 3.7%.The results of the stability tests
were satisfactory and the seventeen constituents remained stable in 24 hours
with all RSDs were between 0.12% and 0.73%.The lower limit of detection of the
17 whitening ingredients were in the range of 0.000 5%-0.005%. The contents of
magnesium ascorbyl phosphate、ascorbyl glucoside、nicotinic
acid、arbutin、nicotinamide、3-O-ethyl ascorbic acid and dipotassium
glycyrrhizate in 50 batches of samples were
0.021%-0.095%,0.018%-0.025%,0.019%-0.024%,0.028%-3.5%,0.027%-3.9%,0.034%-2.8%,0.023%-1.6%,respectively.
Conclusion:It is proved by methodology validation that the established
method can be utilized for simultaneous determination of seventeen kinds of
whitening ingredients in cosmetics.
-----参考文献:---------------------------------------------------------------------------------------
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