dc.contributor.author Terakosolphan, W.
dc.contributor.author Lexmond, A. J.
dc.contributor.author Keir, S.
dc.contributor.author Page, C. P.
dc.contributor.author Forbes, B.
dc.date.accessioned 2025-06-14T01:51:36Z
dc.date.available 2025-06-14T01:51:36Z
dc.date.issued 2018-02-21
dc.description.abstract Inhaled adenosine receptor agonists induce bronchoconstriction and inflammation in asthma and are used as bronchial challenge agents for the diagnosis of asthma and in respiratory drug development. Recently developed dry powder aerosols of adenosine have several advantages over nebulised adenosine 5'-monophosphate (AMP) as bronchial challenge agents. However, reverse translation of this bronchial challenge technique to pre-clinical drug development is limited by the difficulty of administering powder aerosols to animals. The aim of the current study was to develop methods for delivering powder aerosols of adenosine receptor agonists to sensitised guinea pigs (as a model of allergic asthma) and evaluate their effect as challenge agents for the measurement of airway responsiveness. The PreciseInhale system delivered micronised AMP and adenosine powders, with mass median aerodynamic diameters of 1.81 and 3.21 μm and deposition fractions of 31 and 48% in the lungs, respectively. Bronchoconstrictor responses in passively sensitised, anaesthetised, spontaneously breathing guinea pigs were compared to responses to nebulised and intravenously administered AMP and adenosine. AMP- and adenosine-induced bronchoconstriction following all routes of administration with the magnitude of response ranking intravenous > dry powder > nebulisation, probably reflecting differences in exposure to the adenosine agonists delivered by the different routes. In conclusion, the PreciseInhale system delivered AMP and adenosine dry powder aerosols accurately into the lungs, suggesting this method can be used to investigate drug effects on airway responsiveness.
dc.description.epage 769
dc.description.spage 760
dc.description.volume 8
dc.identifier.doi 10.1007/s13346-018-0490-z
dc.identifier.handle 11370/4ce12c1b-a272-40fa-8024-96ba003f7e62
dc.identifier.issn 2190-393X
dc.identifier.issn 2190-3948
dc.identifier.openaire doi_dedup___
dc.identifier.pmc PMC5937854
dc.identifier.pmid 29468423
dc.identifier.uri https://trapdev.rcub.bg.ac.rs/handle/123456789/318342
dc.openaire.affiliation King's College London
dc.openaire.collaboration 1
dc.publisher Springer Science and Business Media LLC
dc.rights OPEN
dc.rights.license CC BY
dc.source Drug Delivery and Translational Research
dc.subject Male
dc.subject Adenosine 5′-monophosphate
dc.subject INHALATION EXPOSURES
dc.subject Adenosine
dc.subject Bronchoconstriction
dc.subject Guinea Pigs
dc.subject 610
dc.subject Drug development
dc.subject Adenosine 5 '-monophosphate
dc.subject Drug development Dry powder inhalation
dc.subject RESPONSIVENESS
dc.subject Purinergic P1 Receptor Agonists
dc.subject Respiratory Hypersensitivity
dc.subject Animals
dc.subject Particle Size
dc.subject Lung
dc.subject Aerosols
dc.subject Nebulizers and Vaporizers
dc.subject ADENOSINE
dc.subject Asthma
dc.subject Adenosine Monophosphate
dc.subject Disease Models, Animal
dc.subject INTRATRACHEAL INSTILLATION
dc.subject ASTHMA
dc.subject Original Article
dc.subject Powders
dc.subject LUNG
dc.subject.fos 03 medical and health sciences
dc.subject.fos 0302 clinical medicine
dc.subject.sdg 3. Good health
dc.title A novel method for studying airway hyperresponsiveness in allergic guinea pigs in vivo using the PreciseInhale system for delivery of dry powder aerosols
dc.type publication

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