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Pharmaceuticals bioaccumulation

DOSS, because of its use in foods and pharmaceuticals, was the target of numerous studies concerning toxicity, bioaccumulation, and reproduction as well as gastroenterological issues, so it can be concluded that DOSS is one of the best examined surfactants in the sulfosuccinates. [Pg.535]

Historically, organic environmental pollutants were hydrophobic, often persistent, neutral compounds. As a consequence, these substances were readily sorbed by particles and soluble in lipids. In modern times, efforts have been made to make xenobiotics more hydrophilic - often by including ionisable substituents. Presumably, these functional groups would render the compound less bioaccumulative. In particular, many pesticides and pharmaceuticals contain acidic or basic functions. However, studies on the fate and effect of organic environmental pollutants focus mainly on the neutral species [1], In the past, uptake into cells and sorption to biological membranes were often assumed to be only dependent on the neutral species. More recent studies that are reviewed in this chapter show that the ionic organic species play a role both for toxic effects and sorption of compounds to membranes. [Pg.207]

The Swedish Classification Scheme initiated in 2005 by the Swedish Association of Pharmacy Industries (LIF), the Swedish Medical Products Agency, Apoteket (National Corporation of Swedish Pharmacies), the Swedish Association of Local Authorities and Regions and the Stockholm County Council, take in account Persistence, Bioaccumulation and Toxicity (PBT) characteristics of pharmaceutical products. This voluntary scheme looks at the environmental hazard and the associated risk of pharmaceutical products. The environmental risk is calculated based on the ratio PEC/PNEC according to the EMEA guideline [17,124, 127]. The obtained information is only available on the website www.fss.se, since due to European restrictions it is not possible to include warning labels on the packaging of medications [17]. [Pg.233]

Mercury is mined predominantly as HgS in cinnabar ore and is then converted commercially to a variety of chemical forms. Key industrial and commercial applications of mercury are found in the electrolytic production of chlorine and caustic soda the manufacture of electrical equipment, thermometers, and other instruments fluorescent lamps dental amalgam and artisanal gold production. Use in pharmaceuticals and in biocides has declined substantially in recent years, but occasional use in antiseptics and folk medicines is still encountered. Thimerosal, an organomercurial preservative that is metabolized in part to ethylmercury, has been removed from almost all the vaccines in which it was formerly present. Environmental exposure to mercury from the burning of fossil fuels, or the bioaccumulation of methylmercury in fish, remains a concern in some regions of the world. Low-level exposure to mercury released from dental amalgam fillings occurs, but systemic toxicity from this source has not been established. [Pg.1235]

If the pharmaceutical fulfills the criteria for PBT (Persistent, Bioaccumulative and Toxic) and/or vPvB (very Persistent and very Bioaccumulative), the following phrase is added The substance fulfills the EU criteria for PBT/vPvB classification. [Pg.89]

A chemical structure can be used to predict its interaction with environmental media and biological systems. Even simple physical chemistry can accurately predict the persistent and bioaccumulative properties of certain types of chemical [86]. Equally, certain hazardous properties can be qualitatively predicted by comparing a molecular structure with similar substances with known hazard profiles [87], Many developments have been achieved using actual computational techniques (e.g., QSAR) to quantitatively evaluate the toxic properties of substances, particularly pharmaceuticals (see [88, 89]). [Pg.26]

Apart from their pharmaceutical applications, the organic arsenicals are also used as herbicides. The main compounds are monosodium methanarsonate (MSMA) and hydroxydimethylarsine oxide (cacodylic acid). The relatively wide use of these agents is one of the main reasons for concern about their potential hazard to public health. Additionally, bioaccumulation of organic arsenicals in aquatic organisms such as seaweeds, freshwater algae and Crustacea plays a major role in the evaluation of the toxicity of these materials. Consequently, human exposure to organic arsenicals due to the combination of environmental and therapeutic applications is the main cause of the variety of toxic manifestations of these compounds. [Pg.719]

Wastewater from pharmaceutical industries producing these therapeutics may allow introduction of these endocrine disruptors into the ecosystem if proper filtration is not employed. Moreover, the conjugated products excreted in urine and feces from individuals receiving these pharmaceuticals also can be introduced into the wastewater supply. There are few published results regarding bioaccumulation and biotransformation of estrogen-like pharmaceutics released into the ecosystem. [Pg.1069]

Synonyms Pentachloro(trichloroethenyl)-benzene Chemical/Pharmaceutical/Other Class Octachlorostyrene is a persistent, bioaccumulative, halogenated aromatic compound. Related compounds include other chlorinated styrenes that... [Pg.1872]

Highly hpid-soluble active pharmaceutical substances may have the ability to bioaccumulate in the fat tissue of animals. Animals higher in the food chain are most susceptible. They eat animals that in turn have eaten other organisms that may have accumulated the substance. A top predator may hence be exposed to higher concentrations of the substance once again the risk has increased. Active pharmaceutical substances are classified in regard to bioaccumulation based on standard laboratory tests. [Pg.830]

The prescribing guide Pass also provides, in addition to information on environmental risk, information on whether a certain pharmaceutical substance is persistent or biodegradable, and whether it can bioaccumulate in aquatic organisms. [Pg.835]

Potential to bioaccumulate in aquatic organisms Certain pharmaceuticals are exempted from classification as for various reasons they are considered not to cause any environmental effect. This is in line with the EU s environmental risk assessment guidelines for medicinal products (see Sect. 38.2.2.2). [Pg.835]


See other pages where Pharmaceuticals bioaccumulation is mentioned: [Pg.212]    [Pg.229]    [Pg.181]    [Pg.48]    [Pg.72]    [Pg.231]    [Pg.479]    [Pg.189]    [Pg.208]    [Pg.24]    [Pg.39]    [Pg.255]    [Pg.435]    [Pg.87]    [Pg.94]    [Pg.18]    [Pg.76]    [Pg.58]    [Pg.478]    [Pg.33]    [Pg.223]    [Pg.1845]    [Pg.126]    [Pg.189]   
See also in sourсe #XX -- [ Pg.86 , Pg.87 ]




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Bioaccumulation

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