Republication or reproduction of this report or its storage and/or dissemination by electronic means is permitted without the need for formal IUPAC permission on condition that an acknowledgment Endocrine disruptors in the environment (IUPAC Technical Report)Abstract: Many chemical substances of natural or anthropogenic origin are suspected or known to be endocrine disruptors, which can influence the endocrine system of life. This observation has led to increased interest on the part of the public and the media, as well as to a steep rise of research activities in the scientific community. New papers and results are presented so fast that it is impossible to give a complete review of this emerging research field. Therefore, this paper tries to give insight into some topics of the great scope of endocrine disruptors in the environment. To get a general idea of the biochemical and biological background, some parts of the endocrine systems of mammalians and nonmammalians are explained. The sections that follow describe important mechanisms of endocrine disruption such as interactions with hormone receptors. Test strategies for anthropogenic chemicals on various organisms are critically reviewed with respect to their problems and gaps concerning endocrine disruptors. The main emphasis of the paper is on the chemical substances suspected or known to be endocrine disruptors. To get a better comprehension of their behavior in the environment, physicochemical data such as water solubility or K ow , as well as information about their use and/or function are reviewed and compared. The main routes of exposure for most chemicals are shortly described, and data about concentrations in the environment (soil/sediment, water) are detailed.
National governments introduced residue limits and guideline levels for pesticide residues in water when policies were implemented to minimize the contamination of ground and surface waters. Initially, the main attention was given to drinking water.Regulatory limits for pesticide residues in waters should have the following characteristics: definition of the type of water, definition of the residue, a suitable analytical method for the residues, and explanation for the basis for each limit.Limits may be derived by applying a safety factor to a no-effect-level, or from levels occurring when good practices are followed and also passing a safety assessment, or from the detection limit of an analytical method, or directly by legislative decision.The basis for limits and guideline values issued by WHO, Australia, the United States, New Zealand, Japan, Canada, European Union, and Taiwan is described, and examples of the limits are provided. Limits have been most commonly developed for drinking water, but values have also been proposed for environmental waters, effluent waters, irrigation waters, and livestock drinking waters. The contamination of ground water is of concern because it may be used as drinking water and act as a source of contamination for surface waters. Most commonly, drinking water standards have been applied to ground water.The same terminology may have different meanings in different systems. For example, guideline value (GV) in WHO means a value calculated from a toxicology parameter, whereas in Australia, a GV is at or about the analytical limit of determination or a maximum level that might occur if good practices are followed. In New Zealand, the GV is the concentration where aesthetic significance is influenced.The Australian health value (HV) is conceptually the same as the WHO GV. The New Zealand maximum acceptable value (MAV) and the Canadian maximum acceptable concentration (MAC) are also conceptually the same as the WHO GV.Each of the possible ways of defining the residues has its merits. A residue limit in water expressed as the sum of parent and toxicologically relevant transformation products makes sense where it is derived from the acceptable daily intake (ADI). For monitoring purposes, where it is best to keep the residue definition as simple as possible for the sake of practical enforcement and economy, theparent or a marker residue is preferable. It is also possible for parent and degradation products (hydrolysis and photolysis products and metabolites) to become physically separated as the water moves through soil strata, which suggests that separate limits should be set for parent and important degradation products.The Commission has made 12 recommendations for regulatory limits for pesticide residues in water. The recommendations will act as a checklist for authorities introducing or revising limits or guidelines for pesticide residues in water.
The degradation of uniformly 14C-labeled isomers (a, y , and P) of hexachlorocyclohexane (HCH), added separately to a mineral salts medium as a sole source of carbon, by a soil bacterium, Pseudomonas sp., under aerobic conditions was studied. During aerobic degradation, about 10-12% of the 14C in a-and y-HCH was accounted for as 14C02 as compared to 5% from P-HCH. Most of the 14C in a-and y-HCH accumulated as water-soluble products, while formation of water-soluble products from P-HCH was negligible. Almost all of the 14C in the three isomers of HCH was accounted for in different fractions (Con, chloroform-diethyl ether, water phase) following bacterial degradation under aerobic conditions. GC-MS analysis of P-HCH residues in the chloroformdiethyl ether extract suggested the formation of pentachlorocyclohexanol and tetrachlorocyclohexanediol as products of aerobic metabolism of P-HCH.
For lindane degradation, a cell suspension of Clostridium rectum strain S-17 demands the addition of substrates such as leucine, alanine, pyruvate, a leucine-proline mixture, and molecular hydrogen. In the presence of leucine-proline mixture, lindane decomposed in parallel with isovaleric acid formation, and both lindane degradation and isovaleric acid formation were inhibited by monoiodoacetic acid, suggesting a close relation between lindane degradation and the Stickland reaction. Lindane was degraded by cell-free extracts of C. rectum in the presence of dithiothreitol (DTT). Radiogaschromatograms of n-hexane soluble metabolites from [14C] lindane showed the presence of monochlorobenzene and gamma-3,4,5,6-tetrachlorocyclohexene. Leucine, NADH, and NADPH were somewhat less active than DTT for lindane degradation in cell-free extracts. Reductive dechlorination seemed the major route of lindane degradation in cell-free extracts as well as in the intact cells of C. rectum.
Republication or reproduction of this report or its storage and/or dissemination by electronic means is permitted without the need for formal IUPAC permission on condition that an acknowledgement, with full reference to thesource along with use of the copyright symbol 0, the name IUPAC and the year ofpublication are prominently visible. Publication of a translation into another language is subject to the additional condition of prior approval from the relevant IUPAC National Adhering Organization.Brought to you by | Abstract: Most synthetic agrochemicals with chiral structures are marketed as racemates even though the desired biological activity may be derived from only one enantiopure isomer. However some synthetic agrochemicals such as pyrethroid insecticides, aryloxypropanoate herbicides and triazole fungicides are marketed as the most biologically active enantiopure isomer. Numerous reports describing the relative biological actitivites, preparations and analyses of enantiopure agrochemicals are available. Some examples of how different enantiomers in racemates are selectively metabolized have also been reported. When agrochemicals have chiral structures, efforts should be made to define the mode of action, elucidate metabolic pathways and to define the human and environmental toxicity of each enantiopure isomer. If there are large differences in the biological activities of individual enantiomers in racemates, it is desirable to develop and use only the enantiopure isomer with the highest sought-after biological activities. 2008 0 1997 IUPAC Brought to you by | University of Birmingham Authenticated Download Date | 6/3/15 2:32 PM
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.