陈静, 简龙海, 毛北萍, 袁晓倩, 郑荣. 高效液相色谱法定量测定化妆品中聚氨丙基双胍[J]. 上海预防医学, 2021, 33(4): 349-354. DOI: 10.19428/j.cnki.sjpm.2021.20220
引用本文: 陈静, 简龙海, 毛北萍, 袁晓倩, 郑荣. 高效液相色谱法定量测定化妆品中聚氨丙基双胍[J]. 上海预防医学, 2021, 33(4): 349-354. DOI: 10.19428/j.cnki.sjpm.2021.20220
CHEN Jing, JIAN Long-hai, MAO Bei-ping, YUAN Xiao-qian, ZHENG Rong. Determination of polyaminopropyl biguanide in cosmetics by high performance liquid chromatography[J]. Shanghai Journal of Preventive Medicine, 2021, 33(4): 349-354. DOI: 10.19428/j.cnki.sjpm.2021.20220
Citation: CHEN Jing, JIAN Long-hai, MAO Bei-ping, YUAN Xiao-qian, ZHENG Rong. Determination of polyaminopropyl biguanide in cosmetics by high performance liquid chromatography[J]. Shanghai Journal of Preventive Medicine, 2021, 33(4): 349-354. DOI: 10.19428/j.cnki.sjpm.2021.20220

高效液相色谱法定量测定化妆品中聚氨丙基双胍

Determination of polyaminopropyl biguanide in cosmetics by high performance liquid chromatography

  • 摘要:
    目的建立化妆品中聚氨丙基双胍(PAPB)的高效液相色谱(HPLC)定量测定方法。
    方法不同基质类型的化妆品样品经超声提取,提取液经高速离心处理,其上清液经正己烷除脂,0.22 μm微孔滤膜过滤后取续滤液进样,采用Agilent Zorbax SB⁃C18柱(5 μm,4.6 mm×250 mm)反相色谱柱,以0.02 mol/L乙酸铵(pH=4.8):甲醇(60∶40)等度洗脱,采用HPLC⁃二极管阵列检测器(DAD)对51批市售化妆品中的PAPB进行定性定量测定。
    结果方法的相对标准偏差在1.2%~4.4%(n=6)之间;回收率在97.5%~106.5%之间;在5~1 000 μg/mL的浓度范围内呈良好线性关系,r=0.999 62,方法的检出限为15 mg/kg。51批市售化妆品中有1批卸妆水PAPB为阳性,其与标准品紫外光谱扫描图比对,光谱匹配结果一致。
    结论建立了化妆品中PAPB的高效液相色谱测定方法,该方法定量准确,可用于实际样品的检测。

     

    Abstract:
    ObjectiveTo establish a high performance liquid chromatographic(HPLC) quantitative method for the determination of polyaminopropyl biguanide(PAPB) in cosmetics.
    MethodsDifferent forms of cosmetic samples were prepared by ultrasonic extraction and followed by high speed centrifugation of the extraction solution. The supernatant was degreased by hexane, and then was filtered by 0.22 μm millipore filter. The continued filtrate was taken for analysis. An Agilent reversed phase column, Zorbax SB-C18(5 μm,4.6 mm×250 mm)was used with 0.02 mol/L ammonium acetate buffer (pH=4.8) : methanol (60∶40) as the mobile phase under the condition of isocratic elution. Diode array detection method was used for PAPB determination. Qualitative and quantitative determination of PAPB was conducted in 51 batches of commercially available cosmetics.
    ResultsThe relative standard deviations (RSD) were in the range of 1.2 %-4.4 %(n=6); the recoveries were in the range of 97.5 %-106.5 %.The method showed a good linearity within the concentration range of 5-1 000 μg/mL with correlation coefficient of 0.999 62; The detection limit was 15 mg/kg. In 51 batches of commercially available cosmetics. One batch of makeup remover showed positive resullt, which was consistent with the UV spectrum of the standard.
    ConclusionWe have established a HPLC method for accurate quantification of PAPB. It can be used for analyzing the cosmetics products.

     

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