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Genotoxicity of 2-Nitrofluoranthene in Human Lymphoblastoid Cells In Vitro

dc.contributor.advisorTomkins, Darrell
dc.contributor.authorBurgar-Suligoj, Tanya
dc.contributor.departmentBiologyen_US
dc.date.accessioned2018-06-27T18:17:31Z
dc.date.available2018-06-27T18:17:31Z
dc.date.issued1996-06
dc.description.abstractA micronucleus assay was developed using HSC-3TO, a human continuous lymphoblastoid cell line (LCL) and cytochalasin B (Cyt-B) to block cytokinesis. Mitomycin C (MMC), a chemotherapeutic agent and an inducer of micronuclei in various human cell types, was used as a positive control. MMC induced micronuclei in HSC-3TO at levels over six times that of control cells when cells were treated with the D₅₀ dose (i.e., the dose of MMC which was toxic to 50% of treated cells). It was found that harvest time was a very important variable and that a harvest time of 108 hours was optimal. 2-Nitrofluoranthene (2-NFA), a nitrated polycyclic aromatic hydrocarbon, the most abundant nitroarene found in the particulate organic matter fraction of ambient air and a potent direct-acting mutagen in the Ames Salmonella assay, was tested using the established CBMN assay protocol. Doses (20, 200 and 2000 ng/mL 2-NFA) were chosen based on the estimated yearly total body exposure and did not produce elevated levels of micronuclei at a dose of 100 times the estimated yearly total body exposure.en_US
dc.description.degreeMaster of Science (MS)en_US
dc.description.degreetypeThesisen_US
dc.identifier.urihttp://hdl.handle.net/11375/23143
dc.language.isoenen_US
dc.subjectgeneen_US
dc.subjectnitrofluorantheneen_US
dc.subjecthumanen_US
dc.subjectlymphoblastoiden_US
dc.subjectin vitroen_US
dc.titleGenotoxicity of 2-Nitrofluoranthene in Human Lymphoblastoid Cells In Vitroen_US
dc.typeThesisen_US

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