|Toxicity of perfluorinated carboxylic acids for aquatic organisms.|
|Jump to Full Text|
|PMID: 21217876 Owner: NLM Status: PubMed-not-MEDLINE|
|Toxicity of perfluorinated carboxylic acids with carbon chain C(8) to C(12) were tested with oligochaeta Tubifex tubifex. Toxicity was evaluated as the exposure time ET(50) from onset of damage of the oligochaeta in saturated aqueous solutions. The ET(50) fluctuated between 25 and 257 minutes. No statistically significant difference was found among the C(8), C(9) and C(12) acids (ET(50) between 143 and 257 minutes with large standard deviation). The acids with carbon chain C(10) and C(11) induced the effect significantly quicker (25 to 47 minutes). No acute toxicity measured in the three-minute test was observed in any case.|
|Miloň Tichý; Radka Valigurová; Radomír Cabala; Rut Uzlová; Marián Rucki|
Related Documents :
|6194776 - Concentrations of 5-hydroxyindoleacetic acid and homovanillic acid in the cerebrospinal...
1371076 - Csf amine metabolites in depression.
7813986 - A competitive enzyme-linked immunoassay for domoic acid determination in human body flu...
19426416 - Selection of dialysate and replacement fluids and management of electrolyte and acid-ba...
22430526 - Co adsorption on amorphous silica-alumina: electrostatic or brønsted acidity probe?
6413256 - Effect of fatty acid anilides on the generation of arachidonic acid by human polymorpho...
|Type: Journal Article|
|Title: Interdisciplinary toxicology Volume: 3 ISSN: 1337-9569 ISO Abbreviation: Interdiscip Toxicol Publication Date: 2010 Jun|
|Created Date: 2011-01-10 Completed Date: 2011-07-14 Revised Date: 2013-05-29|
Medline Journal Info:
|Nlm Unique ID: 101528175 Medline TA: Interdiscip Toxicol Country: Slovakia|
|Languages: eng Pagination: 73-5 Citation Subset: -|
|Laboratory of Predictive Toxicology, National Institute of Public Health, Praha, Czech Republic.|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): Interdiscip Toxicol
Journal ID (publisher-id): ITX
Publisher: Slovak Toxicology Society SETOX
Copyright © 2010 Slovak Toxicology Society SETOX
Received Day: 10 Month: 6 Year: 2010
Revision Received Day: 20 Month: 6 Year: 2010
Accepted Day: 21 Month: 6 Year: 2010
Print publication date: Month: 6 Year: 2010
Electronic publication date: Month: 6 Year: 2010
Volume: 3 Issue: 2
First Page: 73 Last Page: 75
PubMed Id: 21217876
Publisher Id: ITX-3-073
|Toxicity of perfluorinated carboxylic acids for aquatic organisms|
1Laboratory of Predictive Toxicology, National Institute of Public Health, Praha, Czech Republic
2Charles University in Prague, Faculty of Science, Department of Analytical Chemistry, Praha, Czech Republic
|Correspondence: Correspondence address: Assoc. Prof. Miloň Tichý, DSc. Laboratory of Predictive Toxicology, National Institute of Public Health, 10042 Praha 10, Czech Republic. E-MAIL: firstname.lastname@example.org
It is impossible to mention all the fluorinated products used nowadays in miscellaneous human activities, whereas naturally occurring ones are more than rare. Moreover, fluorinated derivatives of organic compounds belong to the most stable compounds, badly degradable, easily distributed in various media and matrices over the world. Their unique chemical properties make them important ingredients in various products. The compounds are found as widespread environmental contaminants. The global-scale multispecies mass balance model was used for simulation of the long-term transport of polyfluorinated carboxylic acids containing 8 to 13 carbons (Armitage et al., 2009). Model scenarios estimated their direct emission and indicated that the mass fluxes to the Arctic marine environment associated with oceanic transport were in excess of mass fluxes from indirect sources (atmospheric transport of precursors such as fluorotelomer alcohols and subsequent degradation to perfluorinated carboxylic acids, PFCAs).
Organic fluorinated acids are present in both arctic and antarctic ice or in equatorial waters. The polyfluoroalkyl acids and, in the past, fluoro-chloro methanes or ethanes belong among the most extended ones. The fluoro-halogen alkanes were used in sprays, their ethers as anesthetics, perfluorooctanoic and perfluorooctane sulphonate acids are widely used today in a lot of products as repellents, paper coatings, coatings for leather, upholstery or carpets, in fire fighting foams, pharmaceutics, insecticides, etc., (Alloatti et al., 2008, Houde et al., 2006, Kovarova & Svobodova, 2008).
On the other hand, monofluorinated organic compounds are important in clinical disciplines. Thus e.g. during the last decades, 2-deoxy-2-fluoro-D-glucose has been used to assess glucose uptake in the normal and diseased heart muscle (Hariharan et al., 1995), fluoro-derivatives of benzimidazole-quinoline were found to be inhibitors of the multitargeted receptor tyrosine kinase and on aspiration to be an anticancer drug (Henk et al., 2005), or fluoro-derivatives of 1,4-benzoquinone were used for studying the participation of ubiquinone in bovine heart mitochondrial respiratory chain, among many other products. The introduction of fluorine atoms into biologically active compounds proved to be beneficial. Several antitumor agents of this type can be named, such as fluorouracil, floxuridin, tegafur, getitinib or camptothecin (Alloatti et al., 2008).
And all these compounds eventually end up in our environment.
Generally, acute toxicity of polyfluorinated compounds is low (Kovarova and Svobodova, 2008), yet there is a lack of toxicological data. There is also a lack of data on their physico-chemical properties. Due to discrepancies in measurements performed by different methods, confidence in the existing data is low. Data on physicochemical properties should therefore be used as estimates only (Hertzke et al., 2007). It can be concluded that QA/QC should be carefully considered when generating and interpreting the results of analyses on both toxicological and physicochemical data. Often, uncommon properties of polyfluorinated organic compounds are a result of their structure, which resembles a rigid rod.
The aim of this contribution is a proposal how to estimate the relative toxicity of polyfluorinated compounds. Acute toxicity determination using oligochaeta Tubifex tubifex and the relevant mode of approach have been thoroughly described (Tichy & Rucki, 1996, Tichy et al., 2007; 2008). The duration of action of polyfluorinated organic compounds in oligochaeta Tubifex tubifex was taken as the basis for this consideration.
The perfluorinated acids C8 (95%), C9 (97%), C10 (98%), C11 (95%) and C12 (95%) were obtained from Aldrich (Steilheim, Germany). Always fresh oligochaeta Tubifex tubifex were purchased in a common shop. Manganese chloride (extra pure grade, Merck) was used as a reference compound (Tichy et al., 2007) to check the quality of the test object.
Solutions of C8 to C12 linear perfluorinated acids were prepared and tested at the concentration of 400 µg/ml (from 0.44 × 10–3 mol/l for C12 to 0.58 × 10–3 mol/l for C8), which was close to saturated concentrations. The amount of exactly 0.01 g of acid was weighed and dissolved by 15 ml water in a 25 ml plastic volumetric flask and sonicated 10 min at room temperature (22–24°C). The resulting aqueous acidic solution (pH 3 to 4) was neutralized by titration with a solution of sodium hydroxide (0.1 mol/l) to about pH 7 (checked by pH-meter) and filled up to 25 ml. Neutralization of the solutions was necessary because the low acidity itself could affect the oligochaeta.
ETn is the effective time when n % of individuals from the population exposed shows a recognizable reaction. In our case, ET5, ET50 and ET95 were determined by counting the number of immobilized Tubifex tubifex during the exposure time. Immobilized worms were counted each half hour for five hours of exposure at room temperature (22–24°C). Deformation of bodies of the oligochaeta was observed: they wrinkled, bled and finally the worms were destroyed and broke up into pieces. Thus immobilization could be noticed only with difficulties. Each solution was tested three times in various seasons and always in a triplicate. The experimental data were processed with special computer software (Logistic Method for Determination of LD50 by National Institute of Public Health, Prague) modified for calculation of ET50.
At the concentration of 400 µg/ml, aqueous solutions of perfluorinated aliphatic carboxylic acid are not toxic if the acute toxicity is measured in three minutes with Tubifex tubifex (Tichý et al., 1996; 2007). The three-minute exposure caused no apparent changes of Tubifex tubifex. Thus the solutions of the acids were not acutely toxic for the oligochaeta and the common testing procedure could not be applied.
However, the effect begins to be noticeable after a longer time, in chronic exposure, and the time necessary for induction of observable changes could be taken as a measure of toxicity of the acids. The start of the effect depends on the chain length of the given acid, however with the minimum at C11 acid.
The results are summarized in Table 1, which contains values and confidence intervals (n = 3, α = 0.05) of ET5, ET50 and ET95 for the time necessary to immobilize 5%, 50% and 95%, respectively, of the oligochaeta from the whole population under exposure. The minimum ET50 value appeared with perfluoroundecanoic acid (C11) being comparable with perfluorodecanoic acid (C10).
We applied an uncommon measure of toxicity, ET50, the time necessary for the onset of destruction of the oligochaeta body. The shorter the ET50, the more toxic is a compound considered. We used this measure because no acute toxicity was observed, a fact that corresponded with the generally accepted opinion that perfluorinated carboxylic acids have limited toxicity for aquatic organisms.
Using the ET50 measure, the most toxic of the set of the compounds tested, i.e. linear polyfluorinated carboxylic acids, were perfluorodecanoic (C10) and perfluoroundecanoic (C11) acids. No statistically significant differences between the toxic indices exist among C8, C9 and C12 acids. The C10 and C11 acids form a clear minimum, statistically significantly distinguished, and thus considered the most toxic ones in chronic exposures. Naturally, this conclusion applies only for our laboratory conditions in a closed system (on Petri dishes).
The question arises how does logP(n-octanol–water) of these acids or their salts behave. Unfortunately, even with simpler alcohols and fluorotelomers, it is still an unsolved problem because of the unique behavior of the fluorine substituents in the compounds. As far as the image of perfluorinated acids as rigid rods is true, a bending or a break may exist at C10 and C11. We can thus just speculate that there is some non-linearity at the C10 to C11 carbon chain. The ability to penetrate membranes by this special form of compounds could then be influenced by this fact, although a better penetrating Tubifex surface with a rod is more probable than with anything else. The effect in the oligochaeta starts much sooner with C10 and C11 perfluorinated acids than with shorter or longer carbon chains.
We thank the National Institute of Public Health and the Department of Analytical Chemistry, Faculty of Science, Charles University in Prague for allowing to perform this work in their laboratories and to use their libraries.
Sources funding the project: grant of the Ministry of Education of the Czech Republic no. 2B08075, Projects VZ MSM 0021620857 and RP 14/63 MSMT
|Alloatti D,Giannini G,Cabri W,Lustrati I,Marzi M,Ciacci A,Gallo G,Tinti MO,Marcellini M,Riccioni T,Guglielmi P,Pisano C. Synthesis and biological activity of fluorinated Combrestatin analoguesJ. Med. Chem.Year: 2008512708272118396857|
|Armitage JM,MacLead M,Cousins IT. Comparative assessment of the global fate and transport pathways of long-chain perfluorocarboxylic acids (PFCAs) and perfluorocarboxalates (PFCs) emitted from direct sourcesEnviron. Sci. Technol.Year: 2009435830583619731684|
|Herzke D,Schlabach M,Mariussen E,Uggerud H,Heimstad E. A literature survey on selected chemical compoundsYear: 2007 TA-2238/2007. http://www.sft.no/publikasjoner/2238/ta2238.pdf.|
|Broxterman HJ,Georgopapadakou NH. Anticancer Therapeutics: “Addictive” multi-targeted drugs, new drug combinationsDrug Resistance UpdatesYear: 2005818319716154800|
|Houde M,Martin JW,Letcher RJ,Solomon KR,Muir DCG. Biological monitoring of polyfluoroalkyl substances: A reviewEnvironmental Science & TechnologyYear: 2006403463347316786681|
|Kovarova J,Svobodova Z. Perfluorinated compounds: occurrence and risk – A reviewNeurotoxicol. LettersYear: 200829599608|
|Hariharan R,Bray M,Ganim R,Doenst T,Goodwin GW,Taegtmeyer H. Fundamental limitations of [18F]2-deoxy-2-fluoro-D-glucose for assessing myocardial glucose uptakeCirculationYear: 199591243524447729031|
|Tichý M,Rucki M. An alternative method for determining acute toxicity of chemicals: cessation of movements in Tubifex tubifex wormsPracov LékYear: 199648225230 [in czech].|
|Tichý M,Rucki M,Hanzlíková I,Roth Z. The Tubifex tubifex assay for the determibation of acute toxicityATLAYear: 20073522923717559312|
|Tichý M,Rucki M,Hanzlíková I,Roth Z. Acute toxicity determination by calculation – Tubifex tubifex assay and quantitative structure – activity relationshipsEnviron. Toxicol. Chem.Year: 2008272281228618522479|
|Valigurova R. Thesis: Toxicity determination of salts of perfluorinated organic acids, Charles University in PragueYear: 2008|
Effective time ET50, ET5 and ET95 (mins.). Tubifex tubifex was exposed in neutral aqueous saturated solutions of perfluorinated carboxylic acids (C8–C12).
|Perfluorinated acid||Effective time (min)|
|C7F15COOH||111 (62–141)||274 (240–347)||675 (471–1687)|
|C8F17COOH||155 (106–181)||284 (257–339)||519 (405–972)|
|C9F19COOH||23 (12–32)||59 (47–70)||151 (118–233)|
|C10F21COOH||13 (7–18)||32 (25–39)||74 (56–130)|
|C11F23COOH||13 (7–18)||176 (143–221)||1073 (627–3328)|
values in brackets represent confidence intervals (n = 3, α = 0.05)
Keywords: perfluorinated carboxylic acids, Tubifex tubifex, water pollution, effective exposure time, acute toxicity.
Previous Document: Protective effect of manganese in cadmium-induced hepatic oxidative damage, changes in cadmium distr...
Next Document: Effect of pomiferin administration on kidney ischaemia-reperfusion injury in rats.