Nanomaterials - substances smaller than 100 nanometers in size - have been added in recent years to an increasing numbers of consumer products used in day-to-day life; in food packaging, medical devices, pharmaceuticals, cosmetics, odor-resistant textiles and household appliances. The extensive application of nanomaterials in a wide range of products for human use poses a potential for toxicity risk to human health and the environment. Such adverse effects of nanomaterials on human health have triggered the development of a new scientific discipline known as “nanotoxicity” – the study of the toxicity of nanomaterials.
Nanotoxicity: From
in vivo
and
in vitro
Models to Health Risks
provides up-to-date state-of-the-art information presented by recognized experts in this emerging new field in toxicology. It discusses the safety evaluation of nanomaterials in foods, drugs, medical devices, cosmetics and other regulated products and its use in risk analysis for potential regulatory use. Topics covered include:
biomarkers for nanotoxicity assessment
nanotoxicity assessment by gene expression analysis
models for nanotoxicity testing
mechanisms of nanotoxicity
pharmakokinetics of nanomaterials
nanotoxicity of foods including food processing, food packaging and food safety
nanotoxicity of drugs including drug development and drug delivery
nanotoxicity of cosmetics and consumer products
health and environmental impact of nanotoxicity
safety evaluation of nanomaterials
regulatory impact of nanomaterials
is a valuable authoritative source of information for readers from a wide range of disciplines such as toxicology, pharmacology, drug toxicity and food and environmental sciences. The book will be useful to the research community in academia, industry, hospitals and government, as well as to government regulators and risk assessors of foods, drugs and environmental and agricultural products.