Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.714918
Title: Lung-targeted receptor occupancy by drug inhalation : an experimental and computational evaluation
Author: Boger, Elin
Awarding Body: University of Warwick
Current Institution: University of Warwick
Date of Award: 2016
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
Inhalation is attractive for treating respiratory diseases since it offers an opportunity to achieve lung-selectivity, i.e. high local and low systemic levels of unbound drug. Nevertheless, evaluation and prediction of the former is challenging for reasons including: 1) the unbound blood concentration cannot be assumed to reflect the free lung target site exposure after inhalation, 2) it is not possible directly measure unbound drug concentrations locally in the lung, and 3) pulmonary drug disposition is known to be a complex interplay between numerous processes. This thesis therefore aims to increase the understanding of how different drug- and formulation-specific properties relate to the free target site exposure to inhaled drug. This was done by: 1) developing and subsequently applying an experimental methodology for measuring pulmonary and systemic occupancy of a receptor targeted by inhaled drugs, and 2) developing a rat physiologically-based pharmacokinetic (PBPK) model, which mechanistically describes underlying processes of pulmonary drug disposition. Experimental studies provided data on the time-course of the PK and receptor occupancy after intravenous (IV) and inhaled drug delivery of fluticasone propionate (FP). The binding kinetics parameters, which were estimated from data generated after IV-dosing, were used as input parameters to the developed model together with other properties specific to FP. The model accurately described the PK and receptor binding for several IV-doses. Predictions were consistent with the observations from inhalation studies, confirming that FP has a dissolution rate-limited absorption and highlighting that drug in solid state does not contribute to receptor binding. As the model is mechanistic, it can assess how different drug- and formulation-specific properties, or combinations thereof, give rise to lung-selectivity. Specific findings include lung-selectivity possibly being unattainable in well-perfused lung regions and that slow drug-receptor dissociation can provide lung-selectivity. Hence, the model lends itself to guiding the design of inhaled compounds and formulations.
Supervisor: Not available Sponsor: European Commission
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.714918  DOI: Not available
Keywords: RC Internal medicine
Share: