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EU Regulation of Nanobiocides: Challenges in Implementing the Biocidal Product Regulation (BPR)
The Biocidal Products Regulation (BPR) contains several provisions for nanomaterials (NMs) and is the first regulation in the European Union to require specific testing and risk assessment for the NM form of a biocidal substance as a part of the information requirements. Ecotoxicological data are on...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302488/ https://www.ncbi.nlm.nih.gov/pubmed/28344290 http://dx.doi.org/10.3390/nano6020033 |
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author | Brinch, Anna Hansen, Steffen Foss Hartmann, Nanna B. Baun, Anders |
author_facet | Brinch, Anna Hansen, Steffen Foss Hartmann, Nanna B. Baun, Anders |
author_sort | Brinch, Anna |
collection | PubMed |
description | The Biocidal Products Regulation (BPR) contains several provisions for nanomaterials (NMs) and is the first regulation in the European Union to require specific testing and risk assessment for the NM form of a biocidal substance as a part of the information requirements. Ecotoxicological data are one of the pillars of the information requirements in the BPR, but there are currently no standard test guidelines for the ecotoxicity testing of NMs. The overall objective of this work was to investigate the implications of the introduction of nano-specific testing requirements in the BPR and to explore how these might be fulfilled in the case of copper oxide nanoparticles. While there is information and data available in the open literature that could be used to fulfill the BPR information requirements, most of the studies do not take the Organisation for Economic Co-operation and Development’s nanospecific test guidelines into consideration. This makes it difficult for companies as well as regulators to fulfill the BPR information requirements for nanomaterials. In order to enable a nanospecific risk assessment, best practices need to be developed regarding stock suspension preparation and characterization, exposure suspensions preparation, and for conducting ecotoxicological test. |
format | Online Article Text |
id | pubmed-5302488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-53024882017-03-21 EU Regulation of Nanobiocides: Challenges in Implementing the Biocidal Product Regulation (BPR) Brinch, Anna Hansen, Steffen Foss Hartmann, Nanna B. Baun, Anders Nanomaterials (Basel) Article The Biocidal Products Regulation (BPR) contains several provisions for nanomaterials (NMs) and is the first regulation in the European Union to require specific testing and risk assessment for the NM form of a biocidal substance as a part of the information requirements. Ecotoxicological data are one of the pillars of the information requirements in the BPR, but there are currently no standard test guidelines for the ecotoxicity testing of NMs. The overall objective of this work was to investigate the implications of the introduction of nano-specific testing requirements in the BPR and to explore how these might be fulfilled in the case of copper oxide nanoparticles. While there is information and data available in the open literature that could be used to fulfill the BPR information requirements, most of the studies do not take the Organisation for Economic Co-operation and Development’s nanospecific test guidelines into consideration. This makes it difficult for companies as well as regulators to fulfill the BPR information requirements for nanomaterials. In order to enable a nanospecific risk assessment, best practices need to be developed regarding stock suspension preparation and characterization, exposure suspensions preparation, and for conducting ecotoxicological test. MDPI 2016-02-16 /pmc/articles/PMC5302488/ /pubmed/28344290 http://dx.doi.org/10.3390/nano6020033 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Brinch, Anna Hansen, Steffen Foss Hartmann, Nanna B. Baun, Anders EU Regulation of Nanobiocides: Challenges in Implementing the Biocidal Product Regulation (BPR) |
title | EU Regulation of Nanobiocides: Challenges in Implementing the Biocidal Product Regulation (BPR) |
title_full | EU Regulation of Nanobiocides: Challenges in Implementing the Biocidal Product Regulation (BPR) |
title_fullStr | EU Regulation of Nanobiocides: Challenges in Implementing the Biocidal Product Regulation (BPR) |
title_full_unstemmed | EU Regulation of Nanobiocides: Challenges in Implementing the Biocidal Product Regulation (BPR) |
title_short | EU Regulation of Nanobiocides: Challenges in Implementing the Biocidal Product Regulation (BPR) |
title_sort | eu regulation of nanobiocides: challenges in implementing the biocidal product regulation (bpr) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302488/ https://www.ncbi.nlm.nih.gov/pubmed/28344290 http://dx.doi.org/10.3390/nano6020033 |
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