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Comparative Pulmonary Absorption, Distribution, and Toxicity of Copper Gallium Diselenide, Copper Indium Diselenide, and Cadmium Telluride in Sprague–Dawley Rats
Copper gallium diselenide (CGS), copper indium diselenide (CIS), and cadmium telluride (CdTe) are novel compounds used in the photovoltaic and semiconductor industries. This study was conducted to characterize the relative toxicities of these compounds and to evaluate the pulmonary absorption and di...
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Published in: | Toxicology and applied pharmacology 1997-12, Vol.147 (2), p.399-410 |
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description | Copper gallium diselenide (CGS), copper indium diselenide (CIS), and cadmium telluride (CdTe) are novel compounds used in the photovoltaic and semiconductor industries. This study was conducted to characterize the relative toxicities of these compounds and to evaluate the pulmonary absorption and distribution after intratracheal instillation. Female Sprague–Dawley rats were administered a single equimolar dose (70 m
m) of CGS (21 mg/kg), CIS (24 mg/kg), CdTe (17 mg/kg), or saline by intratracheal instillation. Bronchoalveolar lavage fluid (BALF) protein, fibronectin, inflammatory cells, lung hydroxyproline, and tissue distribution were measured 1, 3, 7, 14, and 28 days after instillation. Relative lung weights were significantly increased in CIS- and CdTe-treated rats at most time points. Inflammatory lesions in the lungs consisting of an influx of macrophages, lymphocytes, and PMNs were most severe in CdTe-treated rats, intermediate in CIS-treated rats, and minimal in rats receiving CGS. Hyperplasia of alveolar type 2 cells was present in CIS- and CdTe-treated rats and was greatest in CdTe-treated rats. Pulmonary interstitial fibrosis was observed in CdTe-treated rats at all time points. All three compounds caused marked increases in total BALF cell numbers, with the greatest increase observed in CIS-treated rats. BALF protein, fibronectin, and lung hydroxyproline were significantly increased in all treated animals and were highest in CdTe-treated animals. There was no apparent pulmonary absorption or tissue distribution of CGS. Indium levels increased in extrapulmonary tissues of CIS-treated rats, although Cu and Se levels remained unchanged. CdTe was absorbed from the lung to a greater extent than CGS and CIS. Cd and Te levels decreased in the lung and increased in extrapulmonary tissues. Of these compounds CdTe presents the greatest potential health risk because it causes severe pulmonary inflammation and fibrosis and because it is readily absorbed from the lung may potentially cause extrapulmonary toxicity. |
doi_str_mv | 10.1006/taap.1997.8267 |
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m) of CGS (21 mg/kg), CIS (24 mg/kg), CdTe (17 mg/kg), or saline by intratracheal instillation. Bronchoalveolar lavage fluid (BALF) protein, fibronectin, inflammatory cells, lung hydroxyproline, and tissue distribution were measured 1, 3, 7, 14, and 28 days after instillation. Relative lung weights were significantly increased in CIS- and CdTe-treated rats at most time points. Inflammatory lesions in the lungs consisting of an influx of macrophages, lymphocytes, and PMNs were most severe in CdTe-treated rats, intermediate in CIS-treated rats, and minimal in rats receiving CGS. Hyperplasia of alveolar type 2 cells was present in CIS- and CdTe-treated rats and was greatest in CdTe-treated rats. Pulmonary interstitial fibrosis was observed in CdTe-treated rats at all time points. All three compounds caused marked increases in total BALF cell numbers, with the greatest increase observed in CIS-treated rats. BALF protein, fibronectin, and lung hydroxyproline were significantly increased in all treated animals and were highest in CdTe-treated animals. There was no apparent pulmonary absorption or tissue distribution of CGS. Indium levels increased in extrapulmonary tissues of CIS-treated rats, although Cu and Se levels remained unchanged. CdTe was absorbed from the lung to a greater extent than CGS and CIS. Cd and Te levels decreased in the lung and increased in extrapulmonary tissues. Of these compounds CdTe presents the greatest potential health risk because it causes severe pulmonary inflammation and fibrosis and because it is readily absorbed from the lung may potentially cause extrapulmonary toxicity.</description><identifier>ISSN: 0041-008X</identifier><identifier>EISSN: 1096-0333</identifier><identifier>DOI: 10.1006/taap.1997.8267</identifier><identifier>PMID: 9439735</identifier><identifier>CODEN: TXAPA9</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Absorption ; Animals ; Biological and medical sciences ; Body Weight - drug effects ; Bronchoalveolar Lavage Fluid - chemistry ; Bronchoalveolar Lavage Fluid - cytology ; Cadmium Compounds - metabolism ; Cadmium Compounds - toxicity ; Chemical and industrial products toxicology. Toxic occupational diseases ; Copper - metabolism ; Copper - toxicity ; Female ; Fibronectins - chemistry ; Gallium - metabolism ; Gallium - toxicity ; Hydroxyproline - metabolism ; Indium - metabolism ; Indium - toxicity ; Kidney - drug effects ; Kidney - pathology ; Lung - drug effects ; Lung - metabolism ; Lung - pathology ; Medical sciences ; Metals and various inorganic compounds ; Organ Size - drug effects ; Rats ; Rats, Sprague-Dawley ; Selenium - metabolism ; Selenium - toxicity ; Spleen - drug effects ; Spleen - pathology ; Tellurium - metabolism ; Tellurium - toxicity ; Toxicology</subject><ispartof>Toxicology and applied pharmacology, 1997-12, Vol.147 (2), p.399-410</ispartof><rights>1997 Academic Press</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-b53911328305fe0eff3ab5397e4c3b256aed9a279c9854aa4d30024033341fd13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2125808$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9439735$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morgan, Daniel L.</creatorcontrib><creatorcontrib>Shines, Cassandra J.</creatorcontrib><creatorcontrib>Jeter, Shawn P.</creatorcontrib><creatorcontrib>Blazka, Mark E.</creatorcontrib><creatorcontrib>Elwell, Michael R.</creatorcontrib><creatorcontrib>Wilson, Ralph E.</creatorcontrib><creatorcontrib>Ward, Sandra M.</creatorcontrib><creatorcontrib>Price, Herman C.</creatorcontrib><creatorcontrib>Moskowitz, Paul D.</creatorcontrib><title>Comparative Pulmonary Absorption, Distribution, and Toxicity of Copper Gallium Diselenide, Copper Indium Diselenide, and Cadmium Telluride in Sprague–Dawley Rats</title><title>Toxicology and applied pharmacology</title><addtitle>Toxicol Appl Pharmacol</addtitle><description>Copper gallium diselenide (CGS), copper indium diselenide (CIS), and cadmium telluride (CdTe) are novel compounds used in the photovoltaic and semiconductor industries. This study was conducted to characterize the relative toxicities of these compounds and to evaluate the pulmonary absorption and distribution after intratracheal instillation. Female Sprague–Dawley rats were administered a single equimolar dose (70 m
m) of CGS (21 mg/kg), CIS (24 mg/kg), CdTe (17 mg/kg), or saline by intratracheal instillation. Bronchoalveolar lavage fluid (BALF) protein, fibronectin, inflammatory cells, lung hydroxyproline, and tissue distribution were measured 1, 3, 7, 14, and 28 days after instillation. Relative lung weights were significantly increased in CIS- and CdTe-treated rats at most time points. Inflammatory lesions in the lungs consisting of an influx of macrophages, lymphocytes, and PMNs were most severe in CdTe-treated rats, intermediate in CIS-treated rats, and minimal in rats receiving CGS. Hyperplasia of alveolar type 2 cells was present in CIS- and CdTe-treated rats and was greatest in CdTe-treated rats. Pulmonary interstitial fibrosis was observed in CdTe-treated rats at all time points. All three compounds caused marked increases in total BALF cell numbers, with the greatest increase observed in CIS-treated rats. BALF protein, fibronectin, and lung hydroxyproline were significantly increased in all treated animals and were highest in CdTe-treated animals. There was no apparent pulmonary absorption or tissue distribution of CGS. Indium levels increased in extrapulmonary tissues of CIS-treated rats, although Cu and Se levels remained unchanged. CdTe was absorbed from the lung to a greater extent than CGS and CIS. Cd and Te levels decreased in the lung and increased in extrapulmonary tissues. Of these compounds CdTe presents the greatest potential health risk because it causes severe pulmonary inflammation and fibrosis and because it is readily absorbed from the lung may potentially cause extrapulmonary toxicity.</description><subject>Absorption</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Bronchoalveolar Lavage Fluid - chemistry</subject><subject>Bronchoalveolar Lavage Fluid - cytology</subject><subject>Cadmium Compounds - metabolism</subject><subject>Cadmium Compounds - toxicity</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Copper - metabolism</subject><subject>Copper - toxicity</subject><subject>Female</subject><subject>Fibronectins - chemistry</subject><subject>Gallium - metabolism</subject><subject>Gallium - toxicity</subject><subject>Hydroxyproline - metabolism</subject><subject>Indium - metabolism</subject><subject>Indium - toxicity</subject><subject>Kidney - drug effects</subject><subject>Kidney - pathology</subject><subject>Lung - drug effects</subject><subject>Lung - metabolism</subject><subject>Lung - pathology</subject><subject>Medical sciences</subject><subject>Metals and various inorganic compounds</subject><subject>Organ Size - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Selenium - metabolism</subject><subject>Selenium - toxicity</subject><subject>Spleen - drug effects</subject><subject>Spleen - pathology</subject><subject>Tellurium - metabolism</subject><subject>Tellurium - toxicity</subject><subject>Toxicology</subject><issn>0041-008X</issn><issn>1096-0333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNp1kc1u1DAUhS0EKtPClh2SF4hVM9ix8-NllUKpVAkEg8TOurFvkFESBzspzI536CPwZjwJsWboAomVdc_5fHV1DiHPONtyxspXM8C05UpV2zovqwdkw5kqMyaEeEg2jEmeMVZ_fkxOY_zKGFNS8hNyoqRQlSg25FfjhwkCzO4W6fulH_wIYU8v2ujDNDs_ntNLF-fg2uUwwWjpzv9wxs176jva-GnCQK-g790yJBh7HJ3F87_W9Wj_ddKSBuyQ9B32_RJWmbqRfpwCfFnw98-7S_je455-gDk-IY866CM-Pb5n5NOb17vmbXbz7uq6ubjJjCyLOWsLoTgXeS1Y0SHDrhOQtAqlEW1elIBWQV4po-pCAkgrGMtlikryznJxRl4e9k7Bf1swznpw0aznwYh-iZqXUjFeJnB7AE3wMQbs9BTcsOamOdOpFZ1a0akVnVpZPzw_bl7aAe09fqxh9V8cfYgG-i7AaFy8x3KeFzWrV6w-YLimcOsw6GgcjgatC2hmbb373wV_ABWBq6s</recordid><startdate>19971201</startdate><enddate>19971201</enddate><creator>Morgan, Daniel L.</creator><creator>Shines, Cassandra J.</creator><creator>Jeter, Shawn P.</creator><creator>Blazka, Mark E.</creator><creator>Elwell, Michael R.</creator><creator>Wilson, Ralph E.</creator><creator>Ward, Sandra M.</creator><creator>Price, Herman C.</creator><creator>Moskowitz, Paul D.</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>19971201</creationdate><title>Comparative Pulmonary Absorption, Distribution, and Toxicity of Copper Gallium Diselenide, Copper Indium Diselenide, and Cadmium Telluride in Sprague–Dawley Rats</title><author>Morgan, Daniel L. ; Shines, Cassandra J. ; Jeter, Shawn P. ; Blazka, Mark E. ; Elwell, Michael R. ; Wilson, Ralph E. ; Ward, Sandra M. ; Price, Herman C. ; Moskowitz, Paul D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-b53911328305fe0eff3ab5397e4c3b256aed9a279c9854aa4d30024033341fd13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Absorption</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Bronchoalveolar Lavage Fluid - chemistry</topic><topic>Bronchoalveolar Lavage Fluid - cytology</topic><topic>Cadmium Compounds - metabolism</topic><topic>Cadmium Compounds - toxicity</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Copper - metabolism</topic><topic>Copper - toxicity</topic><topic>Female</topic><topic>Fibronectins - chemistry</topic><topic>Gallium - metabolism</topic><topic>Gallium - toxicity</topic><topic>Hydroxyproline - metabolism</topic><topic>Indium - metabolism</topic><topic>Indium - toxicity</topic><topic>Kidney - drug effects</topic><topic>Kidney - pathology</topic><topic>Lung - drug effects</topic><topic>Lung - metabolism</topic><topic>Lung - pathology</topic><topic>Medical sciences</topic><topic>Metals and various inorganic compounds</topic><topic>Organ Size - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Selenium - metabolism</topic><topic>Selenium - toxicity</topic><topic>Spleen - drug effects</topic><topic>Spleen - pathology</topic><topic>Tellurium - metabolism</topic><topic>Tellurium - toxicity</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morgan, Daniel L.</creatorcontrib><creatorcontrib>Shines, Cassandra J.</creatorcontrib><creatorcontrib>Jeter, Shawn P.</creatorcontrib><creatorcontrib>Blazka, Mark E.</creatorcontrib><creatorcontrib>Elwell, Michael R.</creatorcontrib><creatorcontrib>Wilson, Ralph E.</creatorcontrib><creatorcontrib>Ward, Sandra M.</creatorcontrib><creatorcontrib>Price, Herman C.</creatorcontrib><creatorcontrib>Moskowitz, Paul D.</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>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>Morgan, Daniel L.</au><au>Shines, Cassandra J.</au><au>Jeter, Shawn P.</au><au>Blazka, Mark E.</au><au>Elwell, Michael R.</au><au>Wilson, Ralph E.</au><au>Ward, Sandra M.</au><au>Price, Herman C.</au><au>Moskowitz, Paul D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Pulmonary Absorption, Distribution, and Toxicity of Copper Gallium Diselenide, Copper Indium Diselenide, and Cadmium Telluride in Sprague–Dawley Rats</atitle><jtitle>Toxicology and applied pharmacology</jtitle><addtitle>Toxicol Appl Pharmacol</addtitle><date>1997-12-01</date><risdate>1997</risdate><volume>147</volume><issue>2</issue><spage>399</spage><epage>410</epage><pages>399-410</pages><issn>0041-008X</issn><eissn>1096-0333</eissn><coden>TXAPA9</coden><abstract>Copper gallium diselenide (CGS), copper indium diselenide (CIS), and cadmium telluride (CdTe) are novel compounds used in the photovoltaic and semiconductor industries. This study was conducted to characterize the relative toxicities of these compounds and to evaluate the pulmonary absorption and distribution after intratracheal instillation. Female Sprague–Dawley rats were administered a single equimolar dose (70 m
m) of CGS (21 mg/kg), CIS (24 mg/kg), CdTe (17 mg/kg), or saline by intratracheal instillation. Bronchoalveolar lavage fluid (BALF) protein, fibronectin, inflammatory cells, lung hydroxyproline, and tissue distribution were measured 1, 3, 7, 14, and 28 days after instillation. Relative lung weights were significantly increased in CIS- and CdTe-treated rats at most time points. Inflammatory lesions in the lungs consisting of an influx of macrophages, lymphocytes, and PMNs were most severe in CdTe-treated rats, intermediate in CIS-treated rats, and minimal in rats receiving CGS. Hyperplasia of alveolar type 2 cells was present in CIS- and CdTe-treated rats and was greatest in CdTe-treated rats. Pulmonary interstitial fibrosis was observed in CdTe-treated rats at all time points. All three compounds caused marked increases in total BALF cell numbers, with the greatest increase observed in CIS-treated rats. BALF protein, fibronectin, and lung hydroxyproline were significantly increased in all treated animals and were highest in CdTe-treated animals. There was no apparent pulmonary absorption or tissue distribution of CGS. Indium levels increased in extrapulmonary tissues of CIS-treated rats, although Cu and Se levels remained unchanged. CdTe was absorbed from the lung to a greater extent than CGS and CIS. Cd and Te levels decreased in the lung and increased in extrapulmonary tissues. Of these compounds CdTe presents the greatest potential health risk because it causes severe pulmonary inflammation and fibrosis and because it is readily absorbed from the lung may potentially cause extrapulmonary toxicity.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>9439735</pmid><doi>10.1006/taap.1997.8267</doi><tpages>12</tpages></addata></record> |
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subjects | Absorption Animals Biological and medical sciences Body Weight - drug effects Bronchoalveolar Lavage Fluid - chemistry Bronchoalveolar Lavage Fluid - cytology Cadmium Compounds - metabolism Cadmium Compounds - toxicity Chemical and industrial products toxicology. Toxic occupational diseases Copper - metabolism Copper - toxicity Female Fibronectins - chemistry Gallium - metabolism Gallium - toxicity Hydroxyproline - metabolism Indium - metabolism Indium - toxicity Kidney - drug effects Kidney - pathology Lung - drug effects Lung - metabolism Lung - pathology Medical sciences Metals and various inorganic compounds Organ Size - drug effects Rats Rats, Sprague-Dawley Selenium - metabolism Selenium - toxicity Spleen - drug effects Spleen - pathology Tellurium - metabolism Tellurium - toxicity Toxicology |
title | Comparative Pulmonary Absorption, Distribution, and Toxicity of Copper Gallium Diselenide, Copper Indium Diselenide, and Cadmium Telluride in Sprague–Dawley Rats |
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