In the current paper, a new strategy for risk assessment of nanomaterials is described, which builds upon previous project outcomes and is developed within the FP7 NANoREG project. NANoREG has the aim to develop, for the long term, new testing strategies adapted to a high number of nanomaterials where many factors can affect their environmental and health impact. In the proposed risk assessment strategy, approaches for (Quantitative) Structure Activity Relationships ((Q)SARs), grouping and read-across are integrated and expanded to guide the user how to prioritise those nanomaterial applications that may lead to high risks for human health. Furthermore, those aspects of exposure, kinetics and hazard assessment that are most likely to be influenced by the nanospecific properties of the material under assessment are identified. These aspects are summarised in six elements, which play a key role in the strategy: exposure potential, dissolution, nanomaterial transformation, accumulation, genotoxicity and immunotoxicity. With the current approach it is possible to identify those situations where the use of nanospecific grouping, read-across and (Q)SAR tools is likely to become feasible in the future, and to point towards the generation of the type of data that is needed for scientific justification, which may lead to regulatory acceptance of nanospecific applications of these tools.

The NanoRelease Food Additive project developed a catalog to identify potential engineered nanomaterials (ENMs) used as ingredients, using various food‐related databases. To avoid ongoing debate on defining the term nanomaterial , NanoRelease did not use any specific definition other than the ingredient is not naturally part of the food chain, and its dimensions are measured in the nanoscale. Potential nanomaterials were categorized based on physical similarity; analysis indicated that the range of ENMs declared as being in the food chain was limited. Much of the catalog's information was obtained from product labeling, likely resulting in both underreporting (inconsistent or absent requirements for labeling) and/or overreporting (inability to validate entries, or the term nano was used, although no ENM material was present). Three categories of ingredients were identified: emulsions, dispersions, and their water‐soluble powdered preparations (including lipid‐based structures); solid encapsulates (solid structures containing an active material); and metallic or other inorganic particles. Although much is known regarding the physical/chemical properties for these ingredient categories, it is critical to understand whether these properties undergo changes following their interaction with food matrices during preparation and storage. It is also important to determine whether free ENMs are likely to be present within the gastrointestinal tract and whether uptake of ENMs may occur in their nanoform physical state. A practical decision‐making scheme was developed to help manage testing requirements.

Nowadays, hundreds of consumer products contain metal and metal oxide nanoparticles (NP); this increases the probability of such particles to be released to natural waters generating a potential risk to human health and the environment. This paper presents the development of efficient carboneous nanofibrous membranes for NP filtration from aqueous solutions. Free‐standing carbon nanofiber (CNF) mats with different fiber size distribution ranging from 126 to 554 nm in diameter were produced by electrospinning of polyacrylonitrile (PAN) precursor solution followed by thermal treatment. Moreover, tetraethoxyorthosilicate was added to provide flexibility and increase the specific surface area of the CNF. The resulting membranes are bendable and mechanically strong enough to withstand filtration under pressure or vacuum. The experimental results of filtration revealed that the fabricated membranes could efficiently reject nanoparticles of different types (Au, Ag, and TiO₂) and size (from 10 to 100 nm in diameter) from aqueous solutions. It is worth mentioning that the removal of Ag NP with diameters as small as 10 nm was close to 100% with an extremely high flux of 47620 L m⁻² h⁻¹ bar⁻¹.