sp-ICP-MS and HR–CS–GFAAS as useful available techniques for the size characterization and speciation of ionic and nanoparticular zinc in cosmetic and pharmaceutical samples

• Published in: Talanta (Oxford) 2024-02, Vol.268, p.125360-125360, Article 125360
• Main Authors: García-Mesa, J.C., Morales-Benítez, I., Montoro-Leal, P., López Guerrero, M.M., Vereda Alonso, E.I.
• Format: Article
• Language: English
• Subjects: antibiotics; atomic absorption spectrometry; nanoparticles; octoxynol; pharmaceutical industry; solar radiation; solubilization; sonication; surfactants; toxicity; transmission electron microscopy; wet digestion method; zinc; zinc oxide
• ISSN: 0039-9140; 1873-3573
• DOI: 10.1016/j.talanta.2023.125360

The use of zinc oxide nanoparticles (ZnO NPs) in cosmetic and pharmaceutical industry has been increased in recent years due to their good properties as solar radiation filters and antibacterial agent. According to the literature, the potential toxicity of these NPs could be size-dependent and the amount of solubilized metal. This work investigates new reliable and straightforward methodologies that enables the determination of ZnO NPs, discriminating them from ionic zinc in cosmetic samples. Two different techniques of analysis have been applied in this study: high-resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS-GFAAS), and "single particle" inductively coupled plasma mass spectrometry (sp-ICP-MS). Triton X-100 has been used as a surfactant for the formation of homogeneous and stable slurries which allowed the determination of the concentration and sizes of ZnO NPs and Zn2+ in baby creams, eyeshadows, and lotions. A central composite design (CCD) was performed for the two techniques to optimize the concentration of Triton X-100 and sonication time. For validation purpose, the results of Zn2+ and ZnO NPs contents achieved by HR-CS-GFAAS were compared with the total Zn content obtained by acid digestion of the samples. A size comparison of the ZnO NPs was also carried out with the data obtained through the two methodologies and validated with transmission electron microscopy (TEM). In the case of TEM analysis, two different media were tried to study possible agglomerates and interactions between the particles and the matrix.