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Molecular modeling of major tobacco alkaloids in mainstream cigarette smoke
BACKGROUND: Consensus of opinion in literature regarding tobacco research has shown that cigarette smoke can cause irreparable damage to the genetic material, cell injury, and general respiratory landscape. The alkaloid family of tobacco has been implicated is a series of ailments including addictio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947291/ https://www.ncbi.nlm.nih.gov/pubmed/27429644 http://dx.doi.org/10.1186/s13065-016-0189-5 |
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author | Kurgat, Caren Kibet, Joshua Cheplogoi, Peter |
author_facet | Kurgat, Caren Kibet, Joshua Cheplogoi, Peter |
author_sort | Kurgat, Caren |
collection | PubMed |
description | BACKGROUND: Consensus of opinion in literature regarding tobacco research has shown that cigarette smoke can cause irreparable damage to the genetic material, cell injury, and general respiratory landscape. The alkaloid family of tobacco has been implicated is a series of ailments including addiction, mental illnesses, psychological disorders, and cancer. Accordingly, this contribution describes the mechanistic degradation of major tobacco alkaloids including the widely studied nicotine and two other alkaloids which have received little attention in literature. The principal focus is to understand their energetics, their environmental fate, and the formation of intermediates considered harmful to tobacco consumers. METHOD: The intermediate components believed to originate from tobacco alkaloids in mainstream cigarette smoke were determined using as gas-chromatography hyphenated to a mass spectrometer fitted with a mass selective detector (MSD) while the energetics of intermediates were conducted using the density functional theory framework (DFT/B3LYP) using the 6-31G basis set. RESULTS: The density functional theory calculations conducted using B3LYP correlation function established that the scission of the phenyl C–C bond in nicotine and β-nicotyrine, and C–N phenyl bond in 3,5-dimethyl-1-phenylpyrazole were respectively 87.40, 118.24 and 121.38 kcal/mol. The major by-products from the thermal degradation of nicotine, β-nicotyrine and 3,5-dimethyl-1-phenylpyrazole during cigarette smoking are predicted theoretically to be pyridine, 3-methylpyridine, toluene, and benzene. This was found to be consistent with experimental data presented in this work. CONCLUSION: Clearly, the value of the bond dissociation energy was found to be dependent on the π–π interactions which plays a primary role in stabilizing the phenyl C–C in nicotine and β-nicotyrine and the phenyl C–N linkages in 3,5-dimethyl-1-phenylpyrazole. This investigation has elucidated the energetics for the formation of free radicals and intermediates considered detrimental to human health in cigarette smoking. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13065-016-0189-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4947291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-49472912016-07-17 Molecular modeling of major tobacco alkaloids in mainstream cigarette smoke Kurgat, Caren Kibet, Joshua Cheplogoi, Peter Chem Cent J Research Article BACKGROUND: Consensus of opinion in literature regarding tobacco research has shown that cigarette smoke can cause irreparable damage to the genetic material, cell injury, and general respiratory landscape. The alkaloid family of tobacco has been implicated is a series of ailments including addiction, mental illnesses, psychological disorders, and cancer. Accordingly, this contribution describes the mechanistic degradation of major tobacco alkaloids including the widely studied nicotine and two other alkaloids which have received little attention in literature. The principal focus is to understand their energetics, their environmental fate, and the formation of intermediates considered harmful to tobacco consumers. METHOD: The intermediate components believed to originate from tobacco alkaloids in mainstream cigarette smoke were determined using as gas-chromatography hyphenated to a mass spectrometer fitted with a mass selective detector (MSD) while the energetics of intermediates were conducted using the density functional theory framework (DFT/B3LYP) using the 6-31G basis set. RESULTS: The density functional theory calculations conducted using B3LYP correlation function established that the scission of the phenyl C–C bond in nicotine and β-nicotyrine, and C–N phenyl bond in 3,5-dimethyl-1-phenylpyrazole were respectively 87.40, 118.24 and 121.38 kcal/mol. The major by-products from the thermal degradation of nicotine, β-nicotyrine and 3,5-dimethyl-1-phenylpyrazole during cigarette smoking are predicted theoretically to be pyridine, 3-methylpyridine, toluene, and benzene. This was found to be consistent with experimental data presented in this work. CONCLUSION: Clearly, the value of the bond dissociation energy was found to be dependent on the π–π interactions which plays a primary role in stabilizing the phenyl C–C in nicotine and β-nicotyrine and the phenyl C–N linkages in 3,5-dimethyl-1-phenylpyrazole. This investigation has elucidated the energetics for the formation of free radicals and intermediates considered detrimental to human health in cigarette smoking. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13065-016-0189-5) contains supplementary material, which is available to authorized users. Springer International Publishing 2016-07-15 /pmc/articles/PMC4947291/ /pubmed/27429644 http://dx.doi.org/10.1186/s13065-016-0189-5 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kurgat, Caren Kibet, Joshua Cheplogoi, Peter Molecular modeling of major tobacco alkaloids in mainstream cigarette smoke |
title | Molecular modeling of major tobacco alkaloids in mainstream cigarette smoke |
title_full | Molecular modeling of major tobacco alkaloids in mainstream cigarette smoke |
title_fullStr | Molecular modeling of major tobacco alkaloids in mainstream cigarette smoke |
title_full_unstemmed | Molecular modeling of major tobacco alkaloids in mainstream cigarette smoke |
title_short | Molecular modeling of major tobacco alkaloids in mainstream cigarette smoke |
title_sort | molecular modeling of major tobacco alkaloids in mainstream cigarette smoke |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947291/ https://www.ncbi.nlm.nih.gov/pubmed/27429644 http://dx.doi.org/10.1186/s13065-016-0189-5 |
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