Safety assessment of cosmetic products containing nanomaterials. Current research trends and challenges

Elisa Roda, Raffaella Butera, Teresa Coccini, Luigi Manzo

Research output: Contribution to journalArticle

Abstract

Nanomaterials (NMs) may exert biological effects that differ from their macroscale counterparts. The combination of small particle size, large surface area, and ability to generate reactive oxygen species has been demonstrated to be a key factor in induction of cell injury following exposure to certain engineered NMs. Nanostructure can be associated with modification of biological properties and toxicological effects of ingredients used in cosmetics. However, the issue is controversial. Contrasting results have been obtained with widely used agents such as TiO2 and ZnO. From a regulatory perspective, there are two major uncertainties that impact on safety assessment strategies for nanotechnology-derived products. The first is as to whether nano-sized particles have to be considered new chemicals, or whether the use of existing materials at the nano-level should be considered a "new use" of an existing chemical. Addressing this question is of crucial importance to define adequate strategies and establish whether NM-tailored testing methods should be added to conventional toxicity testing protocols to comply with regulatory demand. A second issue is whether the classical toxicity testing methods and strategies that are currently used in the hazard evaluation of macroscale chemicals are adequate when applied to NMs. NMs used in cosmetics can be divided into two groups: labile nanoparticles which disintegrate upon application to skin into their molecular components (e.g. liposomes microemulsions, nanoemulsions) and insoluble nanoparticles such as TiO2, fullerenes and quantum dots. It is currently believed that while conventional risk assessment methodologies may be adequate for labile nanoparticles, specific toxicological and physicochemical parameters must be investigated to establish safety characteristics of insoluble particles. At the present time, the production and commercialisation of manufactured NMs do not trigger additional safety testing. However, the European regulation of chemical substances (REACH), which effectively shifts responsibility from authorities to industry to assess safety of chemical substances, is likely to represent a significant challenge in resolving the conflict between progress and protection of cosmetics containing NMs.

Original languageEnglish
Pages (from-to)27-39
Number of pages13
JournalJournal of Applied Cosmetology
Volume29
Issue number1
Publication statusPublished - Jan 2011

    Fingerprint

Keywords

  • Cosmetics
  • Nanomaterials
  • Risk assessment
  • Toxicological evaluation

ASJC Scopus subject areas

  • Dermatology

Cite this