Corneal opacity, hydration and endothelial morphology in the bovine cornea opacity and permeability assay using reduced treatment times
The purpose of this study was to determine whether the standard bovine cornea opacity and permeability (BCOP) assay exposure time of 10 minutes overestimates the ocular irritancy of chemical substances. Corneas were subjected to BCOP protocol following 30-second and 1-minute exposures to irritants....
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Veröffentlicht in: | Toxicology in vitro 2000-08, Vol.14 (4), p.379-386 |
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description | The purpose of this study was to determine whether the standard bovine cornea opacity and permeability (BCOP) assay exposure time of 10 minutes overestimates the ocular irritancy of chemical substances. Corneas were subjected to BCOP protocol following 30-second and 1-minute exposures to irritants. Corneal opacity and hydration (mg H
2O/mg cornea) were then measured and compared to data obtained after 10 minute irritant treatments. For most test substances corneal opacity and hydration were lower following reduced exposure times. It is suggested that using shorter exposure times in BCOP protocol may be more predictive of human response to ocular irritants, since irritants are usually in brief contact with the ocular surface during accidental exposure. A second purpose of this study was to examine effects of irritants on the corneal endothelium. Corneas were treated according to BCOP protocol following exposure to irritants for 1 or 10 minutes. The endothelium was stained with Alizarin Red and trypan blue, and examined using light microscopy. Severe irritants, such as NaOH and trichloroacetic acid, cause endothelial cell death. It was also determined that simply mounting the cornea in the BCOP assay holders caused damage to 20% of the endothelial cells. Because the endothelium is essential for normal corneal transparency and hydration, it is suggested that examination of the endothelium be added to the BCOP assay and that optimization of the assay will require modification of the cornea holders. |
doi_str_mv | 10.1016/S0887-2333(00)00029-1 |
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2O/mg cornea) were then measured and compared to data obtained after 10 minute irritant treatments. For most test substances corneal opacity and hydration were lower following reduced exposure times. It is suggested that using shorter exposure times in BCOP protocol may be more predictive of human response to ocular irritants, since irritants are usually in brief contact with the ocular surface during accidental exposure. A second purpose of this study was to examine effects of irritants on the corneal endothelium. Corneas were treated according to BCOP protocol following exposure to irritants for 1 or 10 minutes. The endothelium was stained with Alizarin Red and trypan blue, and examined using light microscopy. Severe irritants, such as NaOH and trichloroacetic acid, cause endothelial cell death. It was also determined that simply mounting the cornea in the BCOP assay holders caused damage to 20% of the endothelial cells. Because the endothelium is essential for normal corneal transparency and hydration, it is suggested that examination of the endothelium be added to the BCOP assay and that optimization of the assay will require modification of the cornea holders.</description><identifier>ISSN: 0887-2333</identifier><identifier>EISSN: 1879-3177</identifier><identifier>DOI: 10.1016/S0887-2333(00)00029-1</identifier><identifier>PMID: 10906444</identifier><identifier>CODEN: TIVIEQ</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Anthraquinones ; Biological and medical sciences ; Body Water - metabolism ; bovine cornea opacity and permeable assay ; bovine corneal opacity and permeability assay ; Cattle ; Cell Death - drug effects ; Chemical and industrial products toxicology. Toxic occupational diseases ; Coloring Agents ; cornea, corneal endothelium ; Corneal Opacity - chemically induced ; Corneal Opacity - metabolism ; Corneal Opacity - pathology ; corneal stroma ; Endothelium, Corneal - drug effects ; Endothelium, Corneal - metabolism ; Endothelium, Corneal - pathology ; Irritants - toxicity ; Medical sciences ; Permeability - drug effects ; Sodium Hydroxide - toxicity ; Staining and Labeling ; Time Factors ; Toxicology ; Trichloroacetic Acid - toxicity ; Trypan Blue ; Various organic compounds</subject><ispartof>Toxicology in vitro, 2000-08, Vol.14 (4), p.379-386</ispartof><rights>2000 Elsevier Science Ltd</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-dd1755faa5ce14e438059291b4d51bacbc2703144f1d11a6efa9bbb68520cc9a3</citedby><cites>FETCH-LOGICAL-c421t-dd1755faa5ce14e438059291b4d51bacbc2703144f1d11a6efa9bbb68520cc9a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0887-2333(00)00029-1$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1419401$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10906444$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ubels, J.L</creatorcontrib><creatorcontrib>Pruis, R.M</creatorcontrib><creatorcontrib>Sybesma, J.T</creatorcontrib><creatorcontrib>Casterton, P.L</creatorcontrib><title>Corneal opacity, hydration and endothelial morphology in the bovine cornea opacity and permeability assay using reduced treatment times</title><title>Toxicology in vitro</title><addtitle>Toxicol In Vitro</addtitle><description>The purpose of this study was to determine whether the standard bovine cornea opacity and permeability (BCOP) assay exposure time of 10 minutes overestimates the ocular irritancy of chemical substances. Corneas were subjected to BCOP protocol following 30-second and 1-minute exposures to irritants. Corneal opacity and hydration (mg H
2O/mg cornea) were then measured and compared to data obtained after 10 minute irritant treatments. For most test substances corneal opacity and hydration were lower following reduced exposure times. It is suggested that using shorter exposure times in BCOP protocol may be more predictive of human response to ocular irritants, since irritants are usually in brief contact with the ocular surface during accidental exposure. A second purpose of this study was to examine effects of irritants on the corneal endothelium. Corneas were treated according to BCOP protocol following exposure to irritants for 1 or 10 minutes. The endothelium was stained with Alizarin Red and trypan blue, and examined using light microscopy. Severe irritants, such as NaOH and trichloroacetic acid, cause endothelial cell death. It was also determined that simply mounting the cornea in the BCOP assay holders caused damage to 20% of the endothelial cells. Because the endothelium is essential for normal corneal transparency and hydration, it is suggested that examination of the endothelium be added to the BCOP assay and that optimization of the assay will require modification of the cornea holders.</description><subject>Animals</subject><subject>Anthraquinones</subject><subject>Biological and medical sciences</subject><subject>Body Water - metabolism</subject><subject>bovine cornea opacity and permeable assay</subject><subject>bovine corneal opacity and permeability assay</subject><subject>Cattle</subject><subject>Cell Death - drug effects</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Coloring Agents</subject><subject>cornea, corneal endothelium</subject><subject>Corneal Opacity - chemically induced</subject><subject>Corneal Opacity - metabolism</subject><subject>Corneal Opacity - pathology</subject><subject>corneal stroma</subject><subject>Endothelium, Corneal - drug effects</subject><subject>Endothelium, Corneal - metabolism</subject><subject>Endothelium, Corneal - pathology</subject><subject>Irritants - toxicity</subject><subject>Medical sciences</subject><subject>Permeability - drug effects</subject><subject>Sodium Hydroxide - toxicity</subject><subject>Staining and Labeling</subject><subject>Time Factors</subject><subject>Toxicology</subject><subject>Trichloroacetic Acid - toxicity</subject><subject>Trypan Blue</subject><subject>Various organic compounds</subject><issn>0887-2333</issn><issn>1879-3177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuLFTEQhYMozp3Rn6BkITKCranu9CMrkYsvGHChrkM6qZ4b6U7aJD3Qv8C_bW7f62PnqqD4zqniHEKeAHsFDJrXX1jXtUVZVdU1Yy8YY6Uo4B7ZQdeKooK2vU92f5ALchnj9wzVXckekgtggjWc8x35uffBoRqpn5W2aX1JD6sJKlnvqHKGojM-HXC0GZl8mA9-9LcrtY7mLe39nXVI9ebx22LTzRgmVL0dt0WMaqVLtO6WBjSLRkNTQJUmdIkmO2F8RB4Maoz4-DyvyLf3777uPxY3nz982r-9KTQvIRXGQFvXg1K1RuDIq47VohTQc1NDr3Svy5ZVwPkABkA1OCjR933T1SXTWqjqijw_-c7B_1gwJjnZqHEclUO_RJntm5oJkcH6BOrgYww4yDnYSYVVApPHBuTWgDzGKxmTWwMSsu7p-cDST2j-UZ0iz8CzM6CiVuMQlNM2_uU4CM6OPm9OGOY07iwGGbVFl6OzAXWSxtv_fPILjIKlqg</recordid><startdate>20000801</startdate><enddate>20000801</enddate><creator>Ubels, J.L</creator><creator>Pruis, R.M</creator><creator>Sybesma, J.T</creator><creator>Casterton, P.L</creator><general>Elsevier Ltd</general><general>Elsevier Science</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>20000801</creationdate><title>Corneal opacity, hydration and endothelial morphology in the bovine cornea opacity and permeability assay using reduced treatment times</title><author>Ubels, J.L ; Pruis, R.M ; Sybesma, J.T ; Casterton, P.L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-dd1755faa5ce14e438059291b4d51bacbc2703144f1d11a6efa9bbb68520cc9a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Anthraquinones</topic><topic>Biological and medical sciences</topic><topic>Body Water - metabolism</topic><topic>bovine cornea opacity and permeable assay</topic><topic>bovine corneal opacity and permeability assay</topic><topic>Cattle</topic><topic>Cell Death - drug effects</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Coloring Agents</topic><topic>cornea, corneal endothelium</topic><topic>Corneal Opacity - chemically induced</topic><topic>Corneal Opacity - metabolism</topic><topic>Corneal Opacity - pathology</topic><topic>corneal stroma</topic><topic>Endothelium, Corneal - drug effects</topic><topic>Endothelium, Corneal - metabolism</topic><topic>Endothelium, Corneal - pathology</topic><topic>Irritants - toxicity</topic><topic>Medical sciences</topic><topic>Permeability - drug effects</topic><topic>Sodium Hydroxide - toxicity</topic><topic>Staining and Labeling</topic><topic>Time Factors</topic><topic>Toxicology</topic><topic>Trichloroacetic Acid - toxicity</topic><topic>Trypan Blue</topic><topic>Various organic compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ubels, J.L</creatorcontrib><creatorcontrib>Pruis, R.M</creatorcontrib><creatorcontrib>Sybesma, J.T</creatorcontrib><creatorcontrib>Casterton, P.L</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 in vitro</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ubels, J.L</au><au>Pruis, R.M</au><au>Sybesma, J.T</au><au>Casterton, P.L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Corneal opacity, hydration and endothelial morphology in the bovine cornea opacity and permeability assay using reduced treatment times</atitle><jtitle>Toxicology in vitro</jtitle><addtitle>Toxicol In Vitro</addtitle><date>2000-08-01</date><risdate>2000</risdate><volume>14</volume><issue>4</issue><spage>379</spage><epage>386</epage><pages>379-386</pages><issn>0887-2333</issn><eissn>1879-3177</eissn><coden>TIVIEQ</coden><abstract>The purpose of this study was to determine whether the standard bovine cornea opacity and permeability (BCOP) assay exposure time of 10 minutes overestimates the ocular irritancy of chemical substances. Corneas were subjected to BCOP protocol following 30-second and 1-minute exposures to irritants. Corneal opacity and hydration (mg H
2O/mg cornea) were then measured and compared to data obtained after 10 minute irritant treatments. For most test substances corneal opacity and hydration were lower following reduced exposure times. It is suggested that using shorter exposure times in BCOP protocol may be more predictive of human response to ocular irritants, since irritants are usually in brief contact with the ocular surface during accidental exposure. A second purpose of this study was to examine effects of irritants on the corneal endothelium. Corneas were treated according to BCOP protocol following exposure to irritants for 1 or 10 minutes. The endothelium was stained with Alizarin Red and trypan blue, and examined using light microscopy. Severe irritants, such as NaOH and trichloroacetic acid, cause endothelial cell death. It was also determined that simply mounting the cornea in the BCOP assay holders caused damage to 20% of the endothelial cells. Because the endothelium is essential for normal corneal transparency and hydration, it is suggested that examination of the endothelium be added to the BCOP assay and that optimization of the assay will require modification of the cornea holders.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>10906444</pmid><doi>10.1016/S0887-2333(00)00029-1</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Anthraquinones Biological and medical sciences Body Water - metabolism bovine cornea opacity and permeable assay bovine corneal opacity and permeability assay Cattle Cell Death - drug effects Chemical and industrial products toxicology. Toxic occupational diseases Coloring Agents cornea, corneal endothelium Corneal Opacity - chemically induced Corneal Opacity - metabolism Corneal Opacity - pathology corneal stroma Endothelium, Corneal - drug effects Endothelium, Corneal - metabolism Endothelium, Corneal - pathology Irritants - toxicity Medical sciences Permeability - drug effects Sodium Hydroxide - toxicity Staining and Labeling Time Factors Toxicology Trichloroacetic Acid - toxicity Trypan Blue Various organic compounds |
title | Corneal opacity, hydration and endothelial morphology in the bovine cornea opacity and permeability assay using reduced treatment times |
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