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1.
Arch Toxicol ; 92(1): 121-141, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29273819

RESUMO

Development and market introduction of new nanomaterials trigger the need for an adequate risk assessment of such products alongside suitable risk communication measures. Current application of classical and new nanomaterials is analyzed in context of regulatory requirements and standardization for chemicals, food and consumer products. The challenges of nanomaterial characterization as the main bottleneck of risk assessment and regulation are presented. In some areas, e.g., quantification of nanomaterials within complex matrices, the establishment and adaptation of analytical techniques such as laser ablation inductively coupled plasma mass spectrometry and others are potentially suited to meet the requirements. As an example, we here provide an approach for the reliable characterization of human exposure to nanomaterials resulting from food packaging. Furthermore, results of nanomaterial toxicity and ecotoxicity testing are discussed, with concluding key criteria such as solubility and fiber rigidity as important parameters to be considered in material development and regulation. Although an analysis of the public opinion has revealed a distinguished rating depending on the particular field of application, a rather positive perception of nanotechnology could be ascertained for the German public in general. An improvement of material characterization in both toxicological testing as well as end-product control was concluded as being the main obstacle to ensure not only safe use of materials, but also wide acceptance of this and any novel technology in the general public.


Assuntos
Exposição Ambiental/análise , Nanoestruturas/análise , Nanoestruturas/toxicidade , Medição de Risco/métodos , Administração Oral , Animais , Desinfetantes , Ecotoxicologia/métodos , Exposição Ambiental/efeitos adversos , Embalagem de Alimentos , Alemanha , Humanos , Indústrias/métodos , Exposição por Inalação/efeitos adversos , Exposição por Inalação/análise , Legislação sobre Alimentos , Nanoestruturas/administração & dosagem , Nanoestruturas/normas , Opinião Pública
2.
Arch Toxicol ; 87(12): 2249-62, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23779146

RESUMO

In light of the broad spectrum of products containing nanosilver, the harmfulness of nanosilver to human health and the environment was intensively discussed at a conference held in February 2012 at the BfR. The conference agenda covered the aspects of analytics of nanosilver materials, human exposure and toxicology as well as effects on microorganisms and the environment. The discussion recovered major gaps related to commonly agreed guidelines for sample preparation and central analytical techniques. In particular, the characterization of the nanoparticles in complex matrices was regarded as a challenge which might become a pitfall for further innovation and application. Historical and anecdotal records of colloidal silver have been sometimes taken as empirical proof for the general low toxicity of nanosilver. Yet as reported herein, a growing number of animal studies following modern performance standards of toxicity testing have been carried out recently revealing well-characterized adverse effects on different routes of exposure in addition to argyria. Furthermore, recent approaches in exposure assessment were reported. However, consumer exposure scenarios are only starting to be developed and reliable exposure data are still rare. It was further widely agreed on the workshop that the use of silver may lead to the selection of silver resistant bacteria. With respect to its environmental behavior, it was suggested that nanosilver released to wastewater may have negligible ecotoxicological effects. Finally, the presentations and discussion on risk assessment and regulation of nanosilver applications gave insights into different approaches of risk assessment of nanomaterials to be performed under the various regulatory frameworks.


Assuntos
Nanopartículas Metálicas/efeitos adversos , Compostos de Prata/efeitos adversos , Compostos de Prata/análise , Animais , Qualidade de Produtos para o Consumidor , Resistência a Medicamentos , Exposição Ambiental , União Europeia , Humanos , Legislação de Medicamentos , Nanopartículas Metálicas/toxicidade , Nanoestruturas , Medição de Risco , Compostos de Prata/toxicidade , Testes de Toxicidade
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