Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Toxicology and applied pharmacology 1997-12, Vol.147 (2), p.399-410
Main Authors: 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.
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c465t-b53911328305fe0eff3ab5397e4c3b256aed9a279c9854aa4d30024033341fd13
cites
container_end_page 410
container_issue 2
container_start_page 399
container_title Toxicology and applied pharmacology
container_volume 147
creator 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.
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_16490161</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0041008X97982673</els_id><sourcerecordid>16490161</sourcerecordid><originalsourceid>FETCH-LOGICAL-c465t-b53911328305fe0eff3ab5397e4c3b256aed9a279c9854aa4d30024033341fd13</originalsourceid><addsrcrecordid>eNp1kc1u1DAUhS0EKtPClh2SF4hVM9ix8-NllUKpVAkEg8TOurFvkFESBzspzI536CPwZjwJsWboAomVdc_5fHV1DiHPONtyxspXM8C05UpV2zovqwdkw5kqMyaEeEg2jEmeMVZ_fkxOY_zKGFNS8hNyoqRQlSg25FfjhwkCzO4W6fulH_wIYU8v2ujDNDs_ntNLF-fg2uUwwWjpzv9wxs176jva-GnCQK-g790yJBh7HJ3F87_W9Wj_ddKSBuyQ9B32_RJWmbqRfpwCfFnw98-7S_je455-gDk-IY866CM-Pb5n5NOb17vmbXbz7uq6ubjJjCyLOWsLoTgXeS1Y0SHDrhOQtAqlEW1elIBWQV4po-pCAkgrGMtlikryznJxRl4e9k7Bf1swznpw0aznwYh-iZqXUjFeJnB7AE3wMQbs9BTcsOamOdOpFZ1a0akVnVpZPzw_bl7aAe09fqxh9V8cfYgG-i7AaFy8x3KeFzWrV6w-YLimcOsw6GgcjgatC2hmbb373wV_ABWBq6s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16490161</pqid></control><display><type>article</type><title>Comparative Pulmonary Absorption, Distribution, and Toxicity of Copper Gallium Diselenide, Copper Indium Diselenide, and Cadmium Telluride in Sprague–Dawley Rats</title><source>Elsevier</source><creator>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.</creator><creatorcontrib>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.</creatorcontrib><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><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&amp;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>
fulltext fulltext
identifier ISSN: 0041-008X
ispartof Toxicology and applied pharmacology, 1997-12, Vol.147 (2), p.399-410
issn 0041-008X
1096-0333
language eng
recordid cdi_proquest_miscellaneous_16490161
source Elsevier
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T23%3A21%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Comparative%20Pulmonary%20Absorption,%20Distribution,%20and%20Toxicity%20of%20Copper%20Gallium%20Diselenide,%20Copper%20Indium%20Diselenide,%20and%20Cadmium%20Telluride%20in%20Sprague%E2%80%93Dawley%20Rats&rft.jtitle=Toxicology%20and%20applied%20pharmacology&rft.au=Morgan,%20Daniel%20L.&rft.date=1997-12-01&rft.volume=147&rft.issue=2&rft.spage=399&rft.epage=410&rft.pages=399-410&rft.issn=0041-008X&rft.eissn=1096-0333&rft.coden=TXAPA9&rft_id=info:doi/10.1006/taap.1997.8267&rft_dat=%3Cproquest_cross%3E16490161%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c465t-b53911328305fe0eff3ab5397e4c3b256aed9a279c9854aa4d30024033341fd13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=16490161&rft_id=info:pmid/9439735&rfr_iscdi=true