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Chemical Risk Assessment in Toxicological Perspective

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Abstract

The discipline of toxicology is concerned with the health risks of human exposure to chemicals. According to the Paracelsus’ paradigm toxicology is charged with describing the adverse effects of chemicals in a qualitative sense, and with evaluating them quantitatively by determining how much of a chemical is required to produce a substance specific. Taken together the intrinsic properties of an agent are described (hazard identification) and the amount of the chemical required to produce these (risk characterization) is determined. Since humans or organisms in the environment can be exposed via inhalation, skin contact or oral intake, the concentrations in the different environmental compartments, which result in human or environmental exposure, must be evaluated. Obviously risk characterization comprises the following elements:

  • Hazard identification, i.e. a description of the agent’s toxic potential. Dose–response, including information on the concentration above which the agent induces toxic effects to identify the no observable effect level (NOEL).

  • Exposure assessment, in which the concentration of the agent in the relevant medium and time of exposure are evaluated.

Based in this information difference between the NOEL and human exposure or the risk at a given exposure is determined. Humans may be exposed to chemicals in the air, water, food, or on the skin. From the concentrations of a chemical in these ­different compartments the external daily exposure is estimated. The response to the chemical depends upon duration and route of exposure, the toxicokinetics of the chemical, the dose–response relationship and the susceptibility of the individual. Thus, the precise definition of the terms hazard, exposure, and risk is essential to understand toxicological evaluations (details on data requirements and procedures for risk assessment are given subsequently).

Hazard: this qualitative term represents the intrinsic toxic properties of a ­compound. The expression of hazard depends upon conditions of use and exposure.

Dose: is determined by the concentration of the chemical and the time of exposure.

Risk: is the likelihood of an adverse effect resulting from a given exposure.

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References

  • ACGIH (2008) Threshold Limit Values and Biological Exposure Indices. Signature Publications

    Google Scholar 

  • Angerer, J., Ewers, U., Wilhelm, M. (2007) Human biomonitoring: state of the art. International Journal of Hygiene and Environmental Health 210: 201–228.

    Article  CAS  Google Scholar 

  • Bolt, H.M., Huici-Montagud, A. (2008) Strategy of the scientific committee of occupational exposure limits (SCOEL) in the derivation of occupational exposure limits for carcinogens and mutagens. Archives of Toxicology 82(1): 61–64.

    Article  CAS  Google Scholar 

  • Boogaard, P.J. (2007) Human biomonitoring activities – programmes by industry. International Journal of Hygiene and Environmental Health 210: 259–261.

    Article  Google Scholar 

  • Dorne, J.L.C.M., Renwick, A.G. (2005) The refinement of uncertainty/safety factors in risk assessment by the incorporation of data on toxicokinetic variability in humans. Toxicological Sciences 86: 20–26.

    Article  CAS  Google Scholar 

  • Dunn, W.B., Bailey, N.J., Johnson H.E. (2005) Measuring the Metabolome: Current Analytical Technologies. Analyst, Cambridge.

    Google Scholar 

  • EFSA (2005) Opinion of the scientific committee on a request from EFSA related to a harmonised approach for risk assessment of substances which are both genotoxic and carcinogenic. The EFSA Journal 282: 1–31. http://www.efsa.eu.int/science/sc_commitee/sc_opinions/1201/sc_op_ej282_gentox_summary_en1.pdf

  • EPA (US Environmental Protection Agency; 2005) Guidelines for carcinogen risk assessment EPA/630/P-03/001F. USEPA, Washington, DC.

    Google Scholar 

  • European Communities, Directive 67/548/EEC Annex V Part B. http://ecb.jrc.it/testing-methods/

  • Greim, H., Reuter, U. (2001) Classification of carcinogenic chemicals in the work area by the German MAK Commission: current examples for the new categories. Toxicology 166: 11–23.

    Article  CAS  Google Scholar 

  • Greim, H., Snyder, R. (eds.) (2008) Toxicology and Risk Assessment – A Comprehensive Introduction. Wiley.

    Google Scholar 

  • Greim, H., Ziegler-Skylakakis, K. (2007) Risk assessment for biopersistent granular particles. Inhalation Toxicology 19: 1–6.

    Article  Google Scholar 

  • IARC (International Agency for Research on Cancer). IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. WHO, Lyon.

    Google Scholar 

  • Kroes, R.A.G., Renwick, Feron V., Galli, C.L., Gibney, M., Greim, H., Guy, R. H., Lhuguenot, J.C., van de Sandt, J.J.M. (2007) Application of the threshold of toxicological concern (TTC) to the safety evaluation of cosmetic ingredients. Food Chemicals Toxicology 45: 2533–2562.

    Article  CAS  Google Scholar 

  • Luhe, A., Suter, L., Ruepp, S., Singer, T., Weiser, T., Albertini, S. (2005) Toxicogenomics in the pharmaceutical industry: hollow promises or real benefit? Mutation Research 575: 102–115.

    Article  Google Scholar 

  • Munro, I.C., Renwick, A.G., Danielewska-Nikiel, B. (2008) The threshold of toxicological concern (TTC) in risk assessment. Toxicology Letters 180: 151–156.

    Article  CAS  Google Scholar 

  • Needham, L.L., Calafat, A.M., Barr, D.B. (2007) Uses and issues of biomonitoring. International Journal of Hygiene and Environmental Health 210: 229–238.

    Article  CAS  Google Scholar 

  • OECD, Guidelines for the Testing of Chemicals, Section 4: Health Effects. http://lysander.­sourceoecd. org/vL¼3769318/cL¼31/nw¼1/rpsv/cw/vhosts/oecdjournals/1607310x/v1n3/contp1-1.htm

  • Renwick, A.G. (1993) Data-derived safety factors for the evaluation of food additives and ­environmental contaminants. Food Additives and Contamination 10: 275–305.

    Article  CAS  Google Scholar 

  • Renwick, A.G., Lazarus, N.R. (1998) Human variability and noncancer risk assessment – an analysis­ of the default uncertainty factor. Regulatory Toxicology and Pharmacology 27: 3–20.

    Article  CAS  Google Scholar 

  • SCHER, SCCP, SCENIHR (2008) Risk Assessment Methodologies and Approaches for Mutagenic and Carcinogenic Substances. Health and Consumer Protection Directorate-General, The EU Commission.

    Google Scholar 

  • Swenberg, J.A., Fryar-Tita, E., Jeong, Y.C., Boysen, G., Starr, T. (2008) Biomarkers in toxicology and risk assessment: informing critical dose-response relationships. Chemical Research in Toxicology 21: 253–225.

    Article  Google Scholar 

  • TGD: Technical Guidance Document in support of Commission Directive 93/67/EEC on Risk Assessment for new notified substances, Commission Regulation (EC) No 1488/94 on Risk Assessment for existing substances and Directive 98/8/EC of the European Parliament and of the Council concerning the placing of biocidal products on the market. ecb.jrc.ec.europa.eu/tgd

    Google Scholar 

  • UNECE (United Nations Economic Commission for Europe). Globally harmonized system of classification and labelling of chemicals (GHS) http://www.unece.org/trans/danger/publi/ghs/ghs_rev02/02files_e.html

  • Wetmore, B.A., Merrick, B.A. (2004) Toxicoproteomics: proteomics applied to toxicology and pathology. Toxicologic Pathology 32: 619–642.

    Article  CAS  Google Scholar 

  • WHO (1987) Principles for the Safety Assessment of Food Additives and Contaminants in Food. Environmenal Health Criteria 70. International Programme on Chemical Safety, World Health Organisation, Geneva.

    Google Scholar 

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Correspondence to Helmut Greim .

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Greim, H. (2010). Chemical Risk Assessment in Toxicological Perspective. In: Eriksson, J., Gilek, M., Rudén, C. (eds) Regulating Chemical Risks. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-9428-5_8

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