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采用固相微萃取-同位素稀释质谱联用方法对化妆品中的甲醛进行定量测定。

Quantitative determination of formaldehyde in cosmetics using a combined solid-phase microextraction-isotope dilution mass spectrometry method.

作者信息

Rivero René Thomas, Topiwala Vinod

机构信息

Analytical Lab, Coty Research and Development Center, 410 American Road, Morris Plains, NJ 07950-2451, USA.

出版信息

J Chromatogr A. 2004 Mar 12;1029(1-2):217-22. doi: 10.1016/j.chroma.2003.12.054.

Abstract

Solid-phase microextraction (SPME) in conjunction with isotope dilution mass spectrometry (ID-MS) was employed for the analysis of formaldehyde in cosmetic products. The formaldehyde is derivatized in situ with pentafluorophenyl hydrazine. The formed hydrazone is adsorbed over a poly(dimethylsiloxane)-divinylbenzene-coated fiber and analyzed using gas chromatography-mass spectrometry. The adsorption-time profiles and salting effect were studied. The quantitation was performed by using a stable isotope labeled analogue as an internal standard. The precision, recovery and detection limits were determined with spiked samples. The relative standard deviations from different spiked cosmetic samples were all less than 10% and the recoveries were between 89.00 and 101.23%. The limit of detection was of 0.39 microg/l. Compared with other techniques, the study shown here provides a simple, fast and reliable method for the analysis of formaldehyde in cosmetic products.

摘要

采用固相微萃取(SPME)结合同位素稀释质谱法(ID-MS)对化妆品中的甲醛进行分析。甲醛与五氟苯肼进行原位衍生化。生成的腙吸附在聚(二甲基硅氧烷)-二乙烯基苯涂层纤维上,并采用气相色谱-质谱法进行分析。研究了吸附时间曲线和盐效应。使用稳定同位素标记的类似物作为内标进行定量。通过加标样品测定精密度、回收率和检测限。不同加标化妆品样品的相对标准偏差均小于10%,回收率在89.00%至101.23%之间。检测限为0.39微克/升。与其他技术相比,本文所示研究为化妆品中甲醛的分析提供了一种简单、快速且可靠的方法。

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