The zinc oxide is an inorganic compound whose safe use is linked to its particle size distribution.
On the one hand, there are zinc oxide microparticles, often referred to as “non-nano”. With a size on the order of a micrometre, they are too large to pass through the skin barrier. They remain on the surface of the epidermis, creating a physical shield that reflects UV rays. Their main drawback is aesthetic: they leave an opaque white film, which limits their cosmetic acceptability.
On the other hand, zinc oxide nanoparticles, with a size of less than 100 nanometres, have revolutionised mineral sun care. Their small size makes it possible to create transparent and much more fluid formulations. However, this also raises toxicological questions, as some fear that particles this fine could cross the skin barrier and enter the bloodstream.
According to a report by ANSES, the French Agency for Food, Environmental and Occupational Health & Safety, while the effectiveness of the skin barrier is real, it is not absolute. Various studies have shown that the passage of nanoparticles through the layers of the epidermis is possible, particularly when the skin is damaged (irritation, micro-cuts, sunburn), but sometimes also on intact skin.
The repeated use of these products increases the duration of direct contact with the outermost skin layers, making the assessment of this penetration complex. Some studies highlight that numerous parameters intrinsic to nanoparticles, such as their shape, their tendency to agglomerate, or their surface electric charge, influence their ability to infiltrate more or less deeply. This scientific uncertainty regarding the depth of penetration of nanoparticles strengthens the need for vigilance.
To assess the potential hazardousness of ZnO nanoparticles, researchers carried out in-depth experiments, notably on human glial cells—support cells of the nervous system—and on zebrafish embryos, a model frequently used in biology. The study first shows that ZnO nanoparticles exhibit a substantial capacity for cellular uptake. Using flow cytometry, the scientists observed that the entry of the particles into glial cells is “dose-dependent”: the higher the concentration and the longer the exposure time, assessed up to 48 hours in the study, the more the particles accumulate inside the cells. In contrast, zinc sulphate, a non-nanoscale form, showed no such internalisation, demonstrating that it is specifically the “nano” structure that facilitates cellular intrusion.