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BSI PD ISO/TR 16197:2014

$167.15

Nanotechnologies. Compilation and description of toxicological screening methods for manufactured nanomaterials

Published By Publication Date Number of Pages
BSI 2014 42
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This Technical Report provides a compilation and description of in vitro and in vivo methods that can be useful for the toxicological, including ecotoxicological screening of engineered and manufactured nanomaterials. Toxicological screening tests included in this Technical Report can be used for such purposes as early decision-making in research and product development, rapid feedback on potential toxicological/safety concerns, or for the preliminary assessment of manufactured nanomaterials. This Technical Report is divided between screening assays related to humans and screening assays related to the environment. A screening test is a relatively simple, inexpensive test that can be administered easily and provides an indication of potential adverse outcomes and effects on human health or the environment.

The Technical Report is intended to complement other international efforts that address nanomaterial toxicology by focusing on screening methods suited for preliminary assessment and is not intended to duplicate similar efforts in other international organizations such as the Organization for Economic Cooperation and Development (OECD). If screening provides an early indication of hazard, the guidance will refer to other organizations’ approaches for full-scale toxicological assessment or further tiered studies.

PDF Catalog

PDF Pages PDF Title
6 Foreword
7 Introduction
9 Section sec_1
Section sec_2
Section sec_3
Section sec_3.1
1 Scope
2 Normative references
3 Terms and definitions
10 Section sec_3.2
Section sec_3.3
Section sec_3.4
Section sec_3.5
Section sec_3.6
Section sec_3.7
11 Section sec_3.8
Section sec_3.9
Section sec_3.10
Section sec_4
Section sec_5
Section sec_5.1
4 Symbols (and abbreviated terms)
5 Background
5.1 Role and relevance of toxicological screening for the safety evaluation of manufactured NMs
12 Section sec_5.2
5.2 Toxicological screening as part of tiered approaches to toxicological assessment of manufactured NMs
13 Section sec_5.3
5.3 Discussion of relevant dosing for toxicological screening
14 Section sec_5.4
Section sec_5.5
Section sec_5.6
Table tab_1
5.4 Discussion of the relationship between this Technical Report and ISO/DTR 16196, Compilation and description of sample preparation and dosing methods for manufactured NMs
5.5 Discussion of the relationship between this Technical Report and ISO/TR 13014, Nanotechnologies — Guidance on physico-chemical characterization of engineered nanoscale materials for toxicological assessment
5.6 ​Review of other relevant international activities and published documents
15 Table tab_2
Section sec_6
Section sec_6.1
Section sec_6.2
6 Methods for toxicological screening related to human health
6.1 General
6.2 Positive and negative controls for nanomaterial toxicity testing
16 Section sec_6.3
Section sec_6.3.1
6.3 Relevant methods for in vitro toxicological screening of manufactured NMs
17 Section sec_6.3.2
Section sec_6.3.3
20 Table tab_3
Section sec_6.3.4
Section sec_6.3.4.1
Section sec_6.3.4.2
21 Section sec_6.3.4.3
Section sec_6.3.4.3.1
Section sec_6.3.4.3.2
Section sec_6.3.4.3.3
22 Section sec_6.3.5
Section sec_6.3.5.1
Section sec_6.3.5.2
Section sec_6.3.5.3
Section sec_6.3.5.4
23 Section sec_6.3.6
24 Section sec_6.3.7
Section sec_6.3.7.1
Section sec_6.3.7.2
25 Section sec_6.3.7.3
26 Section sec_6.3.8
Section sec_6.3.9
27 Section sec_6.4
Section sec_6.4.1
Section sec_6.4.2
Section sec_6.4.3
6.4 Relevant methods for in vivo toxicological screening of manufactured NMs
28 Section sec_7
Section sec_7.1
Section sec_7.2
7 Methods for toxicological screening related to the environment
7.1 Introduction
7.2 Environmental fate and distribution
29 Section sec_7.3
Section sec_7.4
7.3 Environmental degradation and transformation
7.4 Environmental biopersistence and bioaccumulation
30 Reference ref_1
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Bibliography
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BSI PD ISO/TR 16197:2014
$167.15