Mercury is considered one of the most toxic elements for plants and animals. Nevertheless, in the Middle East, Asia and Latin America, whitening creams containing mercury are being manufactured and purchased, despite their obvious health risks. Due to the mass distribution of these products, this can be considered a global public health issue. In Mexico, these products are widely available in pharmacies, beauty aid and health stores. They are used for their skin lightening effects. The aim of this work was to analyze the mercury content in some cosmetic whitening creams using the cold vapor technique coupled with atomic absorption spectrometry (CV-AAS). A total of 16 skin-lightening creams from the local market were investigated. No warning information was noted on the packaging. In 10 of the samples, no mercury was detected. The mercury content in six of the samples varied between 878 and 36,000 ppm, despite the fact that the U.S. Food and Drug Administration (FDA) has determined that the limit for mercury in creams should be less than 1 ppm. Skin creams containing mercury are still available and commonly used in Mexico and many developing countries, and their contents are poorly controlled.

A multicommuted system has been developed for lead (Pb) isolation, pre-concentration and determination using an atomic fluorescence spectrometer as the detector. The lab-on-valve (LOV) technique allows automatic separation and pre-concentration of lead by means of solid phase extraction. The Pb resin was conditioned with nitric acid (1 mol L⁻¹) and the analyte was eluted with 1.3 mol L⁻¹ glycine solution. Chemical and flow variables affecting the extraction/pre-concentration of Pb²⁺ were investigated by a multivariate approach. First, screening of the independent variables and their interactions was carried out by a two level full factorial design (2^k). Then, a face centered central composite design was performed in order to find the optimal values of the significant variables. Because a wide range of sample volumes can be loaded on the microcolumn (1–100 mL), a mass calibration curve was obtained in order to quantify Pb in sample batches with a wide variability in lead concentration. Under optimal conditions, the limit of detection and the quantification limit were 0.004 and 0.014 ng of Pb²⁺, respectively. The linear response range was 0.014–20 ng of Pb²⁺. The repeatability, expressed as relative standard deviation (RSD), is 2.4% for 4 μg L⁻¹ Pb²⁺ (n = 10). A small amount (0.6 g) of Pb resin is enough to fill the microcolumn of the LOV device. The durability of the resin reached 154 injections. The injection frequency permitted between a sample frequency of 1–10 h⁻¹ depending on the sample pre-concentration volume. This method was validated using certified reference materials such as SRM-1400 (bone ash), SRM-2976 (mussel tissue) and BCR-610 (groundwater), and the results obtained showed good agreement with the certified values. The proposed LOV system was successfully applied to different samples of environmental and biological interest (water, fish and human teeth) with satisfactory recoveries, between 90–110%. The proposed system has some advantages such as minimization of sample handling, sensitivity, good precision, reduction of reagent volumes, high durability of the column and the versatility achieved by a variety of managed sample volumes.