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Published on: May 24, 2017
Molecular modeling of major tobacco alkaloids in mainstream cigarette smoke
Caren Kurgat1, Joshua Kibet1, Peter Cheplogoi1
1Department of Chemistry, Egerton University, P.O Box 536, Egerton, 20115 Kenya.
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.Graphical abstractSome molecular alkaloids of tobacco the plant.
Insights
Cigarette smoke damages DNA and health. This study details the breakdown of tobacco alkaloids like nicotine, revealing harmful intermediates formed during smoking. Understanding these pathways is crucial for tobacco harm reduction.
Area of Science:
- Chemical research
- Environmental science
- Toxicology
Background:
- Cigarette smoke causes genetic damage and respiratory issues.
- Tobacco alkaloids, including nicotine, are linked to addiction, mental illness, and cancer.
- Limited research exists on the degradation pathways of certain tobacco alkaloids.
Purpose of the Study:
- Investigate the mechanistic degradation of major tobacco alkaloids.
- Determine the energetics and environmental fate of these compounds.
- Identify harmful intermediates formed during cigarette smoking.
Main Methods:
- Gas chromatography-mass spectrometry (GC-MS) for intermediate identification.
- Density Functional Theory (DFT/B3LYP) with a 6-31G basis set for energetic calculations.
- Experimental validation of theoretical predictions.
Main Results:
- Calculated bond dissociation energies for nicotine, β-nicotyrine, and 3,5-dimethyl-1-phenylpyrazole degradation.
- Predicted major by-products: pyridine, 3-methylpyridine, toluene, and benzene.
- Results align with experimental findings on thermal degradation products.
Conclusions:
- π-π interactions significantly stabilize key bonds in tobacco alkaloids.
- Elucidated the energetics of free radical and intermediate formation.
- Identified detrimental intermediates in cigarette smoke relevant to human health.
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