C2C12 mouse myoblast cells, grown in glass vials, were connected to a cryofocusing unit to trap volatile organic compounds (VOCs). The VOCs were eluted from the trap by capacitive discharge into a gas chromatograph with time-of-flight mass spectral capabilities (GC-TOFMS) and were found to include the lipid peroxidation product hexanal. The pro-oxidant cumene hydroperoxide elevated the levels of these lipid peroxidation products, whereas the anti-oxidant butylated hydroxy toluene (BHT) impaired their production. Derivatization of the aldehyde products of lipid peroxidation in the same myoblast cells with pentafluorobenzyl hydroxylamine hydrochloride (PFB) provided evidence for formation of non-volatile products of lipid peroxidation such as malondialdehyde and 4hydroxynonenal.
Similar experiments with the human tracheal epithelial cells, 9-HTE cells treated with Haemophilus influenza bacteria, showed elevated levels of malondialdehyde at 8- hour incubation time intervals giving the initial evidence that the products of lipid peroxidation are formed long before the COX-1 enzyme is activated.
","abstract_html":"<p>C2C12 mouse myoblast cells, grown in glass vials, were connected to a cryofocusing unit to trap volatile organic compounds (VOCs). The VOCs were eluted from the trap by capacitive discharge into a gas chromatograph with time-of-flight mass spectral capabilities (GC-TOFMS) and were found to include the lipid peroxidation product hexanal. The pro-oxidant cumene hydroperoxide elevated the levels of these lipid peroxidation products, whereas the anti-oxidant butylated hydroxy toluene (BHT) impaired their production. Derivatization of the aldehyde products of lipid peroxidation in the same myoblast cells with pentafluorobenzyl hydroxylamine hydrochloride (PFB) provided evidence for formation of non-volatile products of lipid peroxidation such as malondialdehyde and 4hydroxynonenal.</p> <p>Similar experiments with the human tracheal epithelial cells, 9-HTE cells treated with <em>Haemophilus influenza</em> bacteria, showed elevated levels of malondialdehyde at 8- hour incubation time intervals giving the initial evidence that the products of lipid peroxidation are formed long before the COX-1 enzyme is activated.</p>","abstract_has_math":false,"creators":["Lokireddy, Madhavi"],"institution":null,"degree_name":"Master of Science (MS)","degree_level":"Open Access Thesis","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":["Dr. Steven Pernecky","Dr. Heather Holmes","Dr. Hedeel Guy Evans"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2005,"date_issued":"2005-01-01T08:00:00Z","date_published":"2005-01-01T08:00:00Z","updated_at":"2026-07-24T02:16:30Z","subjects":["Mass spectrometry Instruments","Gas chromatography Instruments","Volatile organic compounds","Myoblasts","Peroxidation Measurement","Lipids Measurement","Chemistry"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://commons.emich.edu/theses/113","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Dr. Steven Pernecky","Dr. Heather Holmes","Dr. Hedeel Guy Evans"]},{"key":"dc:creator","label":"Author","values":["Lokireddy, Madhavi"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Open Access Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science (MS)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Mass spectrometry Instruments","Gas chromatography Instruments","Volatile organic compounds","Myoblasts","Peroxidation Measurement","Lipids Measurement","Chemistry"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://commons.emich.edu/theses/113"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["C2C12 mouse myoblast cells, grown in glass vials, were connected to a cryofocusing unit to trap volatile organic compounds (VOCs). The VOCs were eluted from the trap by capacitive discharge into a gas chromatograph with time-of-flight mass spectral capabilities (GC-TOFMS) and were found to include the lipid peroxidation product hexanal. The pro-oxidant cumene hydroperoxide elevated the levels of these lipid peroxidation products, whereas the anti-oxidant butylated hydroxy toluene (BHT) impaired their production. Derivatization of the aldehyde products of lipid peroxidation in the same myoblast cells with pentafluorobenzyl hydroxylamine hydrochloride (PFB) provided evidence for formation of non-volatile products of lipid peroxidation such as malondialdehyde and 4hydroxynonenal.
Similar experiments with the human tracheal epithelial cells, 9-HTE cells treated with Haemophilus influenza bacteria, showed elevated levels of malondialdehyde at 8- hour incubation time intervals giving the initial evidence that the products of lipid peroxidation are formed long before the COX-1 enzyme is activated.
"]},{"key":"dc:title","label":"Title","values":["Measurement of lipid peroxidation in biology models using gas-chromatography-aass spectrometry"]}]}],"canonical_facts":{"dc:contributor":["Dr. Steven Pernecky","Dr. Heather Holmes","Dr. Hedeel Guy Evans"],"dc:creator":["Lokireddy, Madhavi"],"dc:description.abstract":["C2C12 mouse myoblast cells, grown in glass vials, were connected to a cryofocusing unit to trap volatile organic compounds (VOCs). The VOCs were eluted from the trap by capacitive discharge into a gas chromatograph with time-of-flight mass spectral capabilities (GC-TOFMS) and were found to include the lipid peroxidation product hexanal. The pro-oxidant cumene hydroperoxide elevated the levels of these lipid peroxidation products, whereas the anti-oxidant butylated hydroxy toluene (BHT) impaired their production. Derivatization of the aldehyde products of lipid peroxidation in the same myoblast cells with pentafluorobenzyl hydroxylamine hydrochloride (PFB) provided evidence for formation of non-volatile products of lipid peroxidation such as malondialdehyde and 4hydroxynonenal.
Similar experiments with the human tracheal epithelial cells, 9-HTE cells treated with Haemophilus influenza bacteria, showed elevated levels of malondialdehyde at 8- hour incubation time intervals giving the initial evidence that the products of lipid peroxidation are formed long before the COX-1 enzyme is activated.
"],"dc:identifier":["https://commons.emich.edu/theses/113"],"dc:subject":["Mass spectrometry Instruments","Gas chromatography Instruments","Volatile organic compounds","Myoblasts","Peroxidation Measurement","Lipids Measurement","Chemistry"],"dc:title":["Measurement of lipid peroxidation in biology models using gas-chromatography-aass spectrometry"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Open Access Thesis"],"thesis:degree_name":["Master of Science (MS)"]},"updated_at":"2026-07-24T02:16:30Z"}