Related Experiment Video
Updated: Jun 21, 2026

Testing of Nanoparticle Release from a Composite Containing Nanomaterial Using a Chamber System
Published on: November 22, 2016
The status of in vitro toxicity studies in the risk assessment of nanomaterials
Margriet Vdz Park1, Daniëlle Pk Lankveld, Henk van Loveren
1Laboratory for Health Protection Research, National Institute for Public Health & the Environment (RIVM), Bilthoven, The Netherlands. margriet.park@rivm.nl
Abstract:
Nanotechnology applications already on the market or in development promise great benefits for humans as well as the environment. Simultaneously, the pressure to advance the development of fast methods for evaluating the potential risks of increased human exposure to nanomaterials is augmented. One way forward would be to enhance the role of in vitro toxicity studies in risk assessment procedures of nanomaterials. However, to maximize the use of in vitro assays for this purpose, their values and limitations need to be revealed. Even in risk assessment frameworks for regular chemicals, in vitro studies play a minor role. A comparative analysis of published in vitro data with nanomaterials demonstrates that there are a number of issues that need resolving before in vitro studies can play a role in the risk assessment of nanomaterials.
Related Concept Videos
Toxicity Testing in Animals
Mutagenicity and Carcinogenicity
In Vitro Drug Release Testing: Overview, Development and Validation

