Evidence map›Paper›PMID 29468423›Full record

ArticleDrug delivery and translational research2018

A novel method for studying airway hyperresponsiveness in allergic guinea pigs in vivo using the PreciseInhale system for delivery of dry powder aerosols.

A J Lexmond, S Keir, W Terakosolphan, C P Page, B Forbes

Open access · hybridAbstract read
In one paragraph

Article in Drug delivery and translational research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

A J LexmondInstitute of Pharmaceutical Science, King's College London, London, SE1 9NH, UK. a.j.lexmond@rug.nl.
S KeirInstitute of Pharmaceutical Science, King's College London, London, SE1 9NH, UK.
W TerakosolphanInstitute of Pharmaceutical Science, King's College London, London, SE1 9NH, UK.
C P PageInstitute of Pharmaceutical Science, King's College London, London, SE1 9NH, UK.
B ForbesInstitute of Pharmaceutical Science, King's College London, London, SE1 9NH, UK.
King's College London · GB

Funding

National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/C013109/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/C013203/1
6 · The paper itself

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.

Indexed as

Nebulizers and VaporizersAdenosineAdenosine MonophosphateAerosolsAnimalsBronchoconstrictionDisease Models, AnimalGuinea PigsLungMaleParticle SizePowdersPurinergic P1 Receptor AgonistsRespiratory HypersensitivityAdenosineAdenosine MonophosphateAerosolsN(6)-cyclopentyladenosinePowdersPurinergic P1 Receptor AgonistsAdenosineAdenosine 5′-monophosphateAsthmaBronchoconstrictionDrug developmentDry powder inhalation

Identifiers

PMID29468423
PMCPMC5937854
OpenAlexW2793624404

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.