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Human Ingestion of Chromium (VI) in Drinking Water: Pharmacokinetics Following Repeated Exposure
Regulatory agencies have established safe drinking water concentrations for hexavalent chromium [Cr(VI)] based in part on the presumed capability of human gastric juices to rapidly reduce Cr(VI) to nontoxic trivalent chromium [Cr(III)] prior to systemic absorption. This study examines dose-related p...
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Published in: | Toxicology and applied pharmacology 1997-01, Vol.142 (1), p.151-159 |
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container_title | Toxicology and applied pharmacology |
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description | Regulatory agencies have established safe drinking water concentrations for hexavalent chromium [Cr(VI)] based in part on the presumed capability of human gastric juices to rapidly reduce Cr(VI) to nontoxic trivalent chromium [Cr(III)] prior to systemic absorption. This study examines dose-related pharmacokinetics in humans following repeated oral exposure to Cr(VI) in drinking water. In particular, we sought to examine whether plausible drinking water exposures to Cr(VI) caused a sustained increase in red blood cell chromium levels, a specific marker for systemic uptake of Cr(VI). Adult male volunteers ingested a liter (in three volumes of 333 ml, at approximate 6-hr intervals) of deionized water containing Cr(VI) concentrations ranging from 0.1 to 10.0 mg/liter. Samples of urine, plasma, and red blood cells were collected and analyzed for chromium. A dose-related increase in urinary chromium excretion was observed in all volunteers. Red blood cell and plasma chromium concentrations became elevated in certain individuals at the highest doses. The RBC chromium profiles suggest that the ingested Cr(VI) was reduced to Cr(III) before entering the bloodstream, since the chromium concentration in the RBCs dropped rapidly postexposure. These findings suggest that the human gastrointestinal tract has the capacity to reduce ingested Cr(VI) following ingestion of up to 1 liter of water containing 10.0 mg/liter of Cr(VI), which is consistent with USEPA's position that the Cr(VI) drinking water standard of 0.10 mg Cr(VI)/liter is below the reductive capacity of the stomach. |
doi_str_mv | 10.1006/taap.1996.7993 |
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This study examines dose-related pharmacokinetics in humans following repeated oral exposure to Cr(VI) in drinking water. In particular, we sought to examine whether plausible drinking water exposures to Cr(VI) caused a sustained increase in red blood cell chromium levels, a specific marker for systemic uptake of Cr(VI). Adult male volunteers ingested a liter (in three volumes of 333 ml, at approximate 6-hr intervals) of deionized water containing Cr(VI) concentrations ranging from 0.1 to 10.0 mg/liter. Samples of urine, plasma, and red blood cells were collected and analyzed for chromium. A dose-related increase in urinary chromium excretion was observed in all volunteers. Red blood cell and plasma chromium concentrations became elevated in certain individuals at the highest doses. The RBC chromium profiles suggest that the ingested Cr(VI) was reduced to Cr(III) before entering the bloodstream, since the chromium concentration in the RBCs dropped rapidly postexposure. These findings suggest that the human gastrointestinal tract has the capacity to reduce ingested Cr(VI) following ingestion of up to 1 liter of water containing 10.0 mg/liter of Cr(VI), which is consistent with USEPA's position that the Cr(VI) drinking water standard of 0.10 mg Cr(VI)/liter is below the reductive capacity of the stomach.</description><identifier>ISSN: 0041-008X</identifier><identifier>EISSN: 1096-0333</identifier><identifier>DOI: 10.1006/taap.1996.7993</identifier><identifier>PMID: 9007044</identifier><identifier>CODEN: TXAPA9</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Administration, Oral ; Adult ; Biological and medical sciences ; Biotransformation ; Chemical and industrial products toxicology. Toxic occupational diseases ; Chromates - administration & dosage ; Chromates - pharmacokinetics ; Chromium - administration & dosage ; Chromium - blood ; Chromium - pharmacokinetics ; Chromium - urine ; Digestive System - metabolism ; Erythrocytes - chemistry ; Humans ; Male ; Medical sciences ; Metals and various inorganic compounds ; Middle Aged ; Oxidation-Reduction ; Potassium Compounds - administration & dosage ; Potassium Compounds - pharmacokinetics ; Toxicology ; Water Pollutants, Chemical - administration & dosage ; Water Pollutants, Chemical - blood ; Water Pollutants, Chemical - pharmacokinetics ; Water Pollutants, Chemical - urine</subject><ispartof>Toxicology and applied pharmacology, 1997-01, Vol.142 (1), p.151-159</ispartof><rights>1997 Academic Press</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-acffcac3c4c6f2a4189bb4dc5d27dd0b8a52159ee8a51f2e34b4fbeaf2ee49b23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27902,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2555787$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9007044$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Finley, Brent L.</creatorcontrib><creatorcontrib>Kerger, Brent D.</creatorcontrib><creatorcontrib>Katona, Melanie W.</creatorcontrib><creatorcontrib>Gargas, Michael L.</creatorcontrib><creatorcontrib>Corbett, Gwen C.</creatorcontrib><creatorcontrib>Paustenbach, Dennis J.</creatorcontrib><title>Human Ingestion of Chromium (VI) in Drinking Water: Pharmacokinetics Following Repeated Exposure</title><title>Toxicology and applied pharmacology</title><addtitle>Toxicol Appl Pharmacol</addtitle><description>Regulatory agencies have established safe drinking water concentrations for hexavalent chromium [Cr(VI)] based in part on the presumed capability of human gastric juices to rapidly reduce Cr(VI) to nontoxic trivalent chromium [Cr(III)] prior to systemic absorption. This study examines dose-related pharmacokinetics in humans following repeated oral exposure to Cr(VI) in drinking water. In particular, we sought to examine whether plausible drinking water exposures to Cr(VI) caused a sustained increase in red blood cell chromium levels, a specific marker for systemic uptake of Cr(VI). Adult male volunteers ingested a liter (in three volumes of 333 ml, at approximate 6-hr intervals) of deionized water containing Cr(VI) concentrations ranging from 0.1 to 10.0 mg/liter. Samples of urine, plasma, and red blood cells were collected and analyzed for chromium. A dose-related increase in urinary chromium excretion was observed in all volunteers. Red blood cell and plasma chromium concentrations became elevated in certain individuals at the highest doses. The RBC chromium profiles suggest that the ingested Cr(VI) was reduced to Cr(III) before entering the bloodstream, since the chromium concentration in the RBCs dropped rapidly postexposure. These findings suggest that the human gastrointestinal tract has the capacity to reduce ingested Cr(VI) following ingestion of up to 1 liter of water containing 10.0 mg/liter of Cr(VI), which is consistent with USEPA's position that the Cr(VI) drinking water standard of 0.10 mg Cr(VI)/liter is below the reductive capacity of the stomach.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Biotransformation</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Chromates - administration & dosage</subject><subject>Chromates - pharmacokinetics</subject><subject>Chromium - administration & dosage</subject><subject>Chromium - blood</subject><subject>Chromium - pharmacokinetics</subject><subject>Chromium - urine</subject><subject>Digestive System - metabolism</subject><subject>Erythrocytes - chemistry</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metals and various inorganic compounds</subject><subject>Middle Aged</subject><subject>Oxidation-Reduction</subject><subject>Potassium Compounds - administration & dosage</subject><subject>Potassium Compounds - pharmacokinetics</subject><subject>Toxicology</subject><subject>Water Pollutants, Chemical - administration & dosage</subject><subject>Water Pollutants, Chemical - blood</subject><subject>Water Pollutants, Chemical - pharmacokinetics</subject><subject>Water Pollutants, Chemical - urine</subject><issn>0041-008X</issn><issn>1096-0333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNp1kE1v1DAQQC0EKtvClRuSD6iCQ5Zx7Gxibmhp6UqVihBfN-M449aQ2KmdFPj3ONpVbz3NaObNaOYR8oLBmgFs3k5aj2sm5WZdS8kfkRUDuSmAc_6YrAAEKwCaH0_JcUq_AEAKwY7IkQSoQYgV-XkxD9rTnb_GNLngabB0exPD4OaBvv62e0Odpx-i87-dv6bf9YTxHf10o-OgTcg1nJxJ9Dz0ffizEJ9xxAx19OzvGNIc8Rl5YnWf8PkhnpCv52dfthfF5dXH3fb9ZWG4lFOhjbVGG26E2dhSC9bIthWdqbqy7jpoG12VrJKIOWG2RC5aYVvUOUUh25KfkNP93jGG2zk_owaXDPa99hjmpPIwL6FewPUeNDGkFNGqMbpBx3-KgVqUqkWpWpSqRWkeeHnYPLcDdvf4wWHuvzr0dTK6t1F749I9VlZVVTd1xpo9htnCncOoknHoDXYuoplUF9xDF_wHxxKUDg</recordid><startdate>199701</startdate><enddate>199701</enddate><creator>Finley, Brent L.</creator><creator>Kerger, Brent D.</creator><creator>Katona, Melanie W.</creator><creator>Gargas, Michael L.</creator><creator>Corbett, Gwen C.</creator><creator>Paustenbach, Dennis J.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T2</scope><scope>7TV</scope><scope>7U1</scope><scope>7U2</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>199701</creationdate><title>Human Ingestion of Chromium (VI) in Drinking Water: Pharmacokinetics Following Repeated Exposure</title><author>Finley, Brent L. ; Kerger, Brent D. ; Katona, Melanie W. ; Gargas, Michael L. ; Corbett, Gwen C. ; Paustenbach, Dennis J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-acffcac3c4c6f2a4189bb4dc5d27dd0b8a52159ee8a51f2e34b4fbeaf2ee49b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Biotransformation</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Chromates - administration & dosage</topic><topic>Chromates - pharmacokinetics</topic><topic>Chromium - administration & dosage</topic><topic>Chromium - blood</topic><topic>Chromium - pharmacokinetics</topic><topic>Chromium - urine</topic><topic>Digestive System - metabolism</topic><topic>Erythrocytes - chemistry</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metals and various inorganic compounds</topic><topic>Middle Aged</topic><topic>Oxidation-Reduction</topic><topic>Potassium Compounds - administration & dosage</topic><topic>Potassium Compounds - pharmacokinetics</topic><topic>Toxicology</topic><topic>Water Pollutants, Chemical - administration & dosage</topic><topic>Water Pollutants, Chemical - blood</topic><topic>Water Pollutants, Chemical - pharmacokinetics</topic><topic>Water Pollutants, Chemical - urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Finley, Brent L.</creatorcontrib><creatorcontrib>Kerger, Brent D.</creatorcontrib><creatorcontrib>Katona, Melanie W.</creatorcontrib><creatorcontrib>Gargas, Michael L.</creatorcontrib><creatorcontrib>Corbett, Gwen C.</creatorcontrib><creatorcontrib>Paustenbach, Dennis J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Pollution Abstracts</collection><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicology and applied pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Finley, Brent L.</au><au>Kerger, Brent D.</au><au>Katona, Melanie W.</au><au>Gargas, Michael L.</au><au>Corbett, Gwen C.</au><au>Paustenbach, Dennis J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human Ingestion of Chromium (VI) in Drinking Water: Pharmacokinetics Following Repeated Exposure</atitle><jtitle>Toxicology and applied pharmacology</jtitle><addtitle>Toxicol Appl Pharmacol</addtitle><date>1997-01</date><risdate>1997</risdate><volume>142</volume><issue>1</issue><spage>151</spage><epage>159</epage><pages>151-159</pages><issn>0041-008X</issn><eissn>1096-0333</eissn><coden>TXAPA9</coden><abstract>Regulatory agencies have established safe drinking water concentrations for hexavalent chromium [Cr(VI)] based in part on the presumed capability of human gastric juices to rapidly reduce Cr(VI) to nontoxic trivalent chromium [Cr(III)] prior to systemic absorption. This study examines dose-related pharmacokinetics in humans following repeated oral exposure to Cr(VI) in drinking water. In particular, we sought to examine whether plausible drinking water exposures to Cr(VI) caused a sustained increase in red blood cell chromium levels, a specific marker for systemic uptake of Cr(VI). Adult male volunteers ingested a liter (in three volumes of 333 ml, at approximate 6-hr intervals) of deionized water containing Cr(VI) concentrations ranging from 0.1 to 10.0 mg/liter. Samples of urine, plasma, and red blood cells were collected and analyzed for chromium. A dose-related increase in urinary chromium excretion was observed in all volunteers. Red blood cell and plasma chromium concentrations became elevated in certain individuals at the highest doses. The RBC chromium profiles suggest that the ingested Cr(VI) was reduced to Cr(III) before entering the bloodstream, since the chromium concentration in the RBCs dropped rapidly postexposure. These findings suggest that the human gastrointestinal tract has the capacity to reduce ingested Cr(VI) following ingestion of up to 1 liter of water containing 10.0 mg/liter of Cr(VI), which is consistent with USEPA's position that the Cr(VI) drinking water standard of 0.10 mg Cr(VI)/liter is below the reductive capacity of the stomach.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>9007044</pmid><doi>10.1006/taap.1996.7993</doi><tpages>9</tpages></addata></record> |
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subjects | Administration, Oral Adult Biological and medical sciences Biotransformation Chemical and industrial products toxicology. Toxic occupational diseases Chromates - administration & dosage Chromates - pharmacokinetics Chromium - administration & dosage Chromium - blood Chromium - pharmacokinetics Chromium - urine Digestive System - metabolism Erythrocytes - chemistry Humans Male Medical sciences Metals and various inorganic compounds Middle Aged Oxidation-Reduction Potassium Compounds - administration & dosage Potassium Compounds - pharmacokinetics Toxicology Water Pollutants, Chemical - administration & dosage Water Pollutants, Chemical - blood Water Pollutants, Chemical - pharmacokinetics Water Pollutants, Chemical - urine |
title | Human Ingestion of Chromium (VI) in Drinking Water: Pharmacokinetics Following Repeated Exposure |
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