Department of Analytical Chemistry, University of Valencia, 46100 Burjassot, Valencia, Spain.
Department of Analytical Chemistry, University of Valencia, 46100 Burjassot, Valencia, Spain.
J Chromatogr A. 2018 Mar 30;1543:34-39. doi: 10.1016/j.chroma.2018.02.031. Epub 2018 Feb 20.
An analytical method for the determination of traces of formaldehyde in cosmetic products containing formaldehyde-releasing preservatives has been developed. The method is based on reversed-phase dispersive liquid-liquid microextraction (RP-DLLME), that allows the extraction of highly polar compounds, followed by liquid chromatography-ultraviolet/visible (LC-UV/vis) determination with post-column derivatization. The variables involved in the RP-DLLME process were studied to provide the best enrichment factors. Under the selected conditions, a mixture of 500 μL of acetonitrile (disperser solvent) and 50 μL of water (extraction solvent) was rapidly injected into 5 mL of toluene sample solution. The extracts were injected into the LC-UV/vis system using phosphate buffer 6 mmol L at pH 2 as mobile phase. After chromatographic separation, the eluate merged with a flow stream of pentane-2,4-dione in ammonium acetate solution as derivatizing reagent and passed throughout a post-column reactor at 85 °C in order to derivatize formaldehyde into 3,5-diacetyl-1,4-dihydrolutidine, according to Hantzsch reaction, which was finally measured spectrophotometrically at 407 nm. The method was successfully validated showing good linearity, an enrichment factor of 86 ± 2, limits of detection and quantification of 0.7 and 2.3 ng mL, respectively, and good repeatability (RSD < 9.2%). Finally, the proposed analytical method was applied to the determination of formaldehyde in different commercial cosmetic samples containing formaldehyde-releasing preservatives, such as bronopol, diazolidinyl urea, imidazolidinyl urea, and DMDM hydantoin, with good relative recovery values (91-113%) thus showing that matrix effects were negligible. The good analytical features of the proposed method besides of its simplicity and affordability, make it useful to carry out the quality control of cosmetic products containing formaldehyde-releasing preservatives.
一种用于测定含有甲醛释放防腐剂的化妆品中痕量甲醛的分析方法已经开发出来。该方法基于反相分散液液微萃取(RP-DLLME),允许萃取高度极性化合物,然后通过液相色谱-紫外/可见(LC-UV/vis)测定,同时进行柱后衍生。研究了 RP-DLLME 过程中的变量,以提供最佳的富集因子。在所选择的条件下,将 500μL 乙腈(分散溶剂)和 50μL 水(萃取溶剂)的混合物快速注入 5mL 甲苯样品溶液中。萃取物用磷酸盐缓冲液 6mmolL 在 pH 2 作为流动相注入 LC-UV/vis 系统。在色谱分离后,洗脱液与戊烷-2,4-二酮在乙酸铵溶液中的流动相合并作为衍生化试剂,并通过后柱反应器在 85°C 下通过,以便根据 Hantzsch 反应将甲醛衍生为 3,5-二乙酰基-1,4-二氢噻吩,最后在 407nm 处分光光度法测量。该方法经过成功验证,表现出良好的线性、86±2 的富集因子、分别为 0.7 和 2.3ngmL 的检出限和定量限,以及良好的重复性(RSD<9.2%)。最后,将所提出的分析方法应用于测定含有甲醛释放防腐剂的不同商业化妆品样品中的甲醛,如溴硝醇、二羟甲基二羟乙内酰脲、咪唑烷基脲和 DMDM 乙内酰脲,具有良好的相对回收率(91-113%),表明基质效应可以忽略不计。该方法具有简单、经济的特点,除了良好的分析性能外,还可用于含有甲醛释放防腐剂的化妆品的质量控制。