Vaping Additives Affect Lateral Organization and Functionality of Lung Surfactant Model Systems

dc.contributor.advisorPrenner, Elmar J.
dc.contributor.authorVan Bavel, Nicolas
dc.contributor.committeememberAnikovskiy, Max
dc.contributor.committeememberLoebenberg, Raimar
dc.date2022-11
dc.date.accessioned2022-08-04T18:55:38Z
dc.date.available2022-08-04T18:55:38Z
dc.date.issued2022-07-28
dc.description.abstractRecent use of THC-based vapes has led to an outbreak of respiratory health issues. While the pathology is unresolved, common symptoms point to dysfunction of the lung surfactant (LS). This is a lipid-protein monofilm situated at the air-water interface in alveolar sacs, which acts to lower surface tension, preventing lung collapse during respiration. Inhaled substances that reach the alveoli will encounter LS. Certain vape additives have been identified as potential causative agents, these being tetrahydrocannabinol and cannabidiol, commonly found in THC products, as well as vitamin E and its derivative vitamin E acetate. The lipophilic nature of these additives may allow them to partition into the monofilm, wherein they could interact with lipids to disrupt proper function. The aim of this thesis was to use model surfactants to better understand the interactions between vaping additives and the primary lipid components of lung surfactant. These films were made up of phosphatidylcholines, phosphatidylglycerols, and cholesterol. Additionally, the clinical surfactant BLES was also used and compared to the model systems. BLES is used in surfactant replacement therapy, making it a good physiological counterpart to the simple model films studied. Surface activity of the films were measured using a Langmuir-Blodgett trough which allowed for compression and expansion of the films, mimicking respiration. Changes to the lateral organization of the films was conducted with Brewster angle microscopy. Visualization of BLES was also carried out with atomic force microscopy, which allowed for higher resolution images of the surfactant’s molecular architecture. Vape additives were found to destabilize domain formations in most systems, often accompanied by fluidization of the film. The effects on BLES provided a unique insight into the mechanistic action of additive induced surfactant dysfunction. Crucial multilayer structures that form on the surface of the film during compression were abolished in the presence of vitamin E acetate, reducing the surfactants ability to maintain a low surface tension. The Langmuir-Blodgett trough has demonstrated to be useful for studying in vitro interactions between lipids and vape additives. With further optimization, this method may be used to predict in vivo effects of vape additives.en_US
dc.identifier.citationVan Bavel, N. (2022). Vaping Additives Affect Lateral Organization and Functionality of Lung Surfactant Model Systems (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca.en_US
dc.identifier.urihttp://hdl.handle.net/1880/114913
dc.identifier.urihttps://dx.doi.org/10.11575/PRISM/39962
dc.language.isoengen_US
dc.publisher.facultyScienceen_US
dc.publisher.institutionUniversity of Calgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.en_US
dc.subjectVaping additivesen_US
dc.subjectLung surfactanten_US
dc.subject.classificationBiophysicsen_US
dc.titleVaping Additives Affect Lateral Organization and Functionality of Lung Surfactant Model Systemsen_US
dc.typemaster thesisen_US
thesis.degree.disciplineBiological Sciencesen_US
thesis.degree.grantorUniversity of Calgaryen_US
thesis.degree.nameMaster of Science (MSc)en_US
ucalgary.item.requestcopytrueen_US
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