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    <titleInfo>
      <title>Can aquatic distribution of human pharmaceuticals be related to pharmacological data?</title>
    </titleInfo>
    <name type="personnal">
      <namePart type="family">Williams</namePart>
      <namePart type="given">M.</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
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    <name type="personnal">
      <namePart type="family">Saison</namePart>
      <namePart type="given">Carine L. A.</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
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    <name type="personnal">
      <namePart type="family">Williams</namePart>
      <namePart type="given">D. B.</namePart>
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        <roleTerm type="text">auteur</roleTerm>
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    <name type="personnal">
      <namePart type="family">Kookana</namePart>
      <namePart type="given">R. S.</namePart>
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      <languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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    <abstract>The recognition of pharmaceuticals as significant environmental contaminants has only been a recent phenomenon. Therefore there is a paucity of data relating to the fate and effects of pharmaceuticals once they enter an aquatic receiving system. The amount of work that needs to be done in terms of risk assessment for pharmaceuticals required by regulatory agencies is substantial. This paper has determined the environmental partitioning coefficient (K-d) of 13 diverse human pharmaceuticals in three model systems of differing combinations of solid phases and solutions. The K-d values were then compared with distribution values of the pharmaceuticals in the human body determined from pharmacological studies. This was done to assess the functional relationship between Kd and distribution values in the human body (VD). Kd values ranged from 3 to 2450 L kg(-1). Regression coefficients ranged from r(2) = 0.62-0.72, indicating that VD values are a useful indicator for the Kd values of the tested pharmaceuticals within the batch sorption systems. The relationship between K-d and V-D should therefore be further explored to determine whether this relationship can be applied to a broader range of pharmaceuticals in more diverse environmental systems. Exploiting available human pharmacological data in such a way would be of great benefit in prioritising human pharmaceuticals as environmental contaminants in the risk assessment process.</abstract>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <subject>
      <topic>pharmacokinetics</topic>
      <topic>fate</topic>
      <topic>batch sorption</topic>
      <topic>partitioning coefficient</topic>
      <topic>volume of distribution</topic>
      <topic>risk assessment</topic>
    </subject>
    <classification authority="local">020</classification>
    <classification authority="local">038</classification>
    <relatedItem type="host">
      <titleInfo>
        <title>Chemosphere</title>
      </titleInfo>
      <part>
        <detail type="volume">
          <number>65</number>
        </detail>
        <detail type="volume">
          <number>11</number>
        </detail>
        <extent unit="pages">
          <list> 2253-2259</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>2006</dateIssued>
      </originInfo>
      <identifier type="issn">0045-6535</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010037756</identifier>
    <identifier type="doi">10.1016/j.chemosphere.2006.05.036</identifier>
    <identifier type="issn">0045-6535</identifier>
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    <accessCondition type="restriction access" displayLabel="Accès réservé">Accès réservé (Intranet de l'IRD)</accessCondition>
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      <recordContentSource>IRD - Base Horizon / Pleins textes</recordContentSource>
      <recordCreationDate encoding="w3cdtf">2007-03-01</recordCreationDate>
      <recordChangeDate encoding="w3cdtf">2017-08-23</recordChangeDate>
      <recordIdentifier>fdi:010037756</recordIdentifier>
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        <languageTerm authority="iso639-2b">fre</languageTerm>
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