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A headache for water treatment.


Acetaminophen is turned into at least two toxic compounds by chlorination chlorination Public health Addition of chlorinated compounds to drinking water as disinfectants. Cf Ozonation.  treatment, researchers report in the 15 January 2006 issue of Environmental Science & Technology, raising concerns about the fate of this and other pharmaceuticals that end up in water supplies. Acetaminophen is one of the most widely used over-the-counter painkillers in the world--in the United States alone, some 37,000 metric tons are produced each year, says coauthor Mary Bedner, a research chemist at the National Institute of Standards and Technology National Institute of Standards and Technology, governmental agency within the U.S. Dept. of Commerce with the mission of "working with industry to develop and apply technology, measurements, and standards" in the national interest. . "Some of this is reaching the environment," she says, "but no one really knows what happens to it or what effect it might ultimately have on ecosystems or people."

Reports of acetaminophen in European rivers have appeared since the 1990s, and in the 15 March 2002 issue of Environmental Science & Technology a USGS USGS United States Geological Survey (US Department of the Interior)  team reported detecting it in nearly a quarter of the water bodies it sampled. "It gets there through wastewater [i.e., via human excretion] and in some cases through poor disposal practices," says Nick Voulvoulis, a senior lecturer in natural sciences at Imperial College London History
Imperial College was founded in 1907, with the merger of the City and Guilds College, the Royal School of Mines and the Royal College of Science (all of which had been founded between 1845 and 1878) with these entities continuing to exist as "constituent colleges".
. Only 22% of Britons and just 1.4% of Americans return unwanted medicines to pharmacies, says Voulvoulis. More than 35% of U.S. nonreturners flush unused drugs down the toilet, while most British drugs end up in landfills, from which they can leach into water bodies.

Concerned that acetaminophen's structure renders it likely to react with chlorine, Bedner and colleague William MacCrehan used reversed-phase liquid chromatography to follow its interaction with the chlorinating agent hypochlorite hypochlorite /hy·po·chlo·rite/ (-klor´it) any salt of hypochlorous acid; used as a medicinal agent with disinfectant action, particularly as a diluted solution of sodium hypochlorite. . Under simulated treatment conditions in samples of distilled water and wastewater, 11 new compounds were formed from acetaminophen within an hour, the time the reactants would likely be in contact at any plant. Among them were 1,4-benzoquinone (a mutagen mutagen: see mutation.
mutagen

Any agent capable of altering a cell's genetic makeup by changing the structure of the hereditary material, DNA. Many forms of electromagnetic radiation (e.g.
) and N-acetyl-p-benzoquinone imine imine (i-men´) an organic compound containing an imino group; in a substituted imine, a nonacyl group replaces the imino hydrogen.

im·ine
n.
 (a hepatotoxicant also produced during acetaminophen metabolism that is responsible for overdose deaths). Together, these compounds represented the fate of nearly 27% of the original drug concentration.

"Fortunately, these are unstable compounds, especially in the presence of sulfite sulfite /sul·fite/ (sul´fit) any salt of sulfurous acid.

sul·fite
n.
A salt or ester of sulfurous acid.
, which is sometimes used to dechlorinate treated water, so they are unlikely to persist long in the environment," Bedner says. "However, they could accumulate where treated wastewater is returned to rivers, and the effects of resupply re·sup·ply  
tr.v. re·sup·plied, re·sup·ply·ing, re·sup·plies
To provide with fresh supplies, as of weapons and ammunition.



re
 over long periods are unknown." The results also raise the question of what other drug-derived toxicants are out there, she says.

"This work shows we need to know much more about the fate of the drugs that contaminate our water supplies," says Damia Barcelo, a professor of environmental chemistry at Barcelona's Centre for Research and Development. "We also have to look for what they turn into. Searching only for the original compounds themselves will not reveal all the dangers these contaminants may pose."
COPYRIGHT 2006 National Institute of Environmental Health Sciences
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Title Annotation:Pharmaceuticals
Author:Burton, Adrian
Publication:Environmental Health Perspectives
Date:May 1, 2006
Words:454
Previous Article:Score for the environment.(The Beat)
Next Article:Genetic basis of UVB sensitivity.(Cancer)



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