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Mutagenicity testing of diethylene glycol monobutyl ether.
The mutagenic potential of diethylene glycol monobutyl ether (diEGBE) was examined with a Tier I battery of in vitro assays followed by a Tier II in vivo Drosophila sex-linked recessive lethal assay. The in vitro battery consisted of: the Salmonella mutagenicity test, the L5178Y mouse lymphoma test,...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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1984
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1568284/ https://www.ncbi.nlm.nih.gov/pubmed/6389113 |
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author | Thompson, E D Coppinger, W J Valencia, R Iavicoli, J |
author_facet | Thompson, E D Coppinger, W J Valencia, R Iavicoli, J |
author_sort | Thompson, E D |
collection | PubMed |
description | The mutagenic potential of diethylene glycol monobutyl ether (diEGBE) was examined with a Tier I battery of in vitro assays followed by a Tier II in vivo Drosophila sex-linked recessive lethal assay. The in vitro battery consisted of: the Salmonella mutagenicity test, the L5178Y mouse lymphoma test, a cytogenetics assay using Chinese hamster ovary cells and the unscheduled DNA synthesis (UDS) assay in rat hepatocytes. Results of the Salmonella mutagenicity test, the cytogenetics test, and the rat hepatocyte assay were negative at concentrations up to 20 microL/plate, 7.92 microL/mL, and 4.4 microL/mL, respectively. Toxicity was clearly demonstrated at all high doses. A weak, but dose-related increase in the mutation frequency (4-fold increase over the solvent control at 5.6 microL/mL with 12% survival) was obtained in the L5178Y lymphoma test in the absence of metabolic activation. Results of the mouse lymphoma assay were negative in the presence of the S-9 activation system. The significance of the mouse lymphoma assay were negative in the presence of the S-9 activation system. The significance of the mouse lymphoma assay results were assessed by performing the Tier II sex-linked recessive lethal assay in Drosophila in which the target tissue is maturing germinal cells. Both feeding (11,000 ppm for 3 days) and injection (0.3 microL of approximately 14,000 ppm solution) routes of administration were employed in the Drosophila assay. Approximately 11,000 individual crosses with an equal number of negative controls were performed for each route of administration. diEGBE produced no increase in recessive lethals under these conditions.(ABSTRACT TRUNCATED AT 250 WORDS) |
format | Text |
id | pubmed-1568284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1984 |
record_format | MEDLINE/PubMed |
spelling | pubmed-15682842006-09-18 Mutagenicity testing of diethylene glycol monobutyl ether. Thompson, E D Coppinger, W J Valencia, R Iavicoli, J Environ Health Perspect Research Article The mutagenic potential of diethylene glycol monobutyl ether (diEGBE) was examined with a Tier I battery of in vitro assays followed by a Tier II in vivo Drosophila sex-linked recessive lethal assay. The in vitro battery consisted of: the Salmonella mutagenicity test, the L5178Y mouse lymphoma test, a cytogenetics assay using Chinese hamster ovary cells and the unscheduled DNA synthesis (UDS) assay in rat hepatocytes. Results of the Salmonella mutagenicity test, the cytogenetics test, and the rat hepatocyte assay were negative at concentrations up to 20 microL/plate, 7.92 microL/mL, and 4.4 microL/mL, respectively. Toxicity was clearly demonstrated at all high doses. A weak, but dose-related increase in the mutation frequency (4-fold increase over the solvent control at 5.6 microL/mL with 12% survival) was obtained in the L5178Y lymphoma test in the absence of metabolic activation. Results of the mouse lymphoma assay were negative in the presence of the S-9 activation system. The significance of the mouse lymphoma assay were negative in the presence of the S-9 activation system. The significance of the mouse lymphoma assay results were assessed by performing the Tier II sex-linked recessive lethal assay in Drosophila in which the target tissue is maturing germinal cells. Both feeding (11,000 ppm for 3 days) and injection (0.3 microL of approximately 14,000 ppm solution) routes of administration were employed in the Drosophila assay. Approximately 11,000 individual crosses with an equal number of negative controls were performed for each route of administration. diEGBE produced no increase in recessive lethals under these conditions.(ABSTRACT TRUNCATED AT 250 WORDS) 1984-08 /pmc/articles/PMC1568284/ /pubmed/6389113 Text en |
spellingShingle | Research Article Thompson, E D Coppinger, W J Valencia, R Iavicoli, J Mutagenicity testing of diethylene glycol monobutyl ether. |
title | Mutagenicity testing of diethylene glycol monobutyl ether. |
title_full | Mutagenicity testing of diethylene glycol monobutyl ether. |
title_fullStr | Mutagenicity testing of diethylene glycol monobutyl ether. |
title_full_unstemmed | Mutagenicity testing of diethylene glycol monobutyl ether. |
title_short | Mutagenicity testing of diethylene glycol monobutyl ether. |
title_sort | mutagenicity testing of diethylene glycol monobutyl ether. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1568284/ https://www.ncbi.nlm.nih.gov/pubmed/6389113 |
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