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A novel method for studying airway hyperresponsiveness in allergic guinea pigs in vivo using the PreciseInhale system for delivery of dry powder aerosols.
Lexmond, A J; Keir, S; Terakosolphan, W; Page, C P; Forbes, B.
Affiliation
  • Lexmond AJ; Institute of Pharmaceutical Science, King's College London, London, SE1 9NH, UK. a.j.lexmond@rug.nl.
  • Keir S; Sackler Institute of Pulmonary Pharmacology, Institute of Pharmaceutical Science, King's College London, London, SE1 9NH, UK. a.j.lexmond@rug.nl.
  • Terakosolphan W; Department of Pharmaceutical Technology and Biopharmacy, Groningen Research Institute of Pharmacy, University of Groningen, 9713, AV, Groningen, The Netherlands. a.j.lexmond@rug.nl.
  • Page CP; Institute of Pharmaceutical Science, King's College London, London, SE1 9NH, UK.
  • Forbes B; Sackler Institute of Pulmonary Pharmacology, Institute of Pharmaceutical Science, King's College London, London, SE1 9NH, UK.
Drug Deliv Transl Res ; 8(3): 760-769, 2018 06.
Article in En | MEDLINE | ID: mdl-29468423
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Hypersensitivity / Nebulizers and Vaporizers / Adenosine / Adenosine Monophosphate / Purinergic P1 Receptor Agonists Limits: Animals Language: En Journal: Drug Deliv Transl Res Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Hypersensitivity / Nebulizers and Vaporizers / Adenosine / Adenosine Monophosphate / Purinergic P1 Receptor Agonists Limits: Animals Language: En Journal: Drug Deliv Transl Res Year: 2018 Document type: Article