Evidence map›Paper›PMID 39939559›Full record

ArticlePharmaceutical research2025

In-vitro Evaluation of Solution Pressurised Metered Dose Inhaler Sprays with Low-GWP Propellants.

Daniel J Duke, Lingzhe Rao, Benjamin Myatt, Phil Cocks, Stephen Stein, Nirmal Marasini, Hui Xin Ong, Paul Young

Abstract read
In one paragraph

Article in Pharmaceutical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Daniel J DukeDepartment of Mechanical & Aerospace Engineering, Monash University, Clayton, 3168, Victoria, Australia. daniel.duke@monash.edu.ORCID http://orcid.org/0000-0001-8692-6493
Lingzhe RaoDepartment of Mechanical & Aerospace Engineering, Monash University, Clayton, 3168, Victoria, Australia.
Benjamin MyattKindeva Drug Delivery, Loughborough, LE11 5RB, United Kingdom.
Phil CocksKindeva Drug Delivery, Loughborough, LE11 5RB, United Kingdom.
Stephen SteinKindeva Drug Delivery, Woodbury, 55129, Minnesota, United States of America.
Nirmal MarasiniRespiratory Technology, Woolcock Institute of Medical Research, Macquarie Park, 2113, New South Wales, Australia.
Hui Xin OngRespiratory Technology, Woolcock Institute of Medical Research, Macquarie Park, 2113, New South Wales, Australia.
Paul YoungRespiratory Technology, Woolcock Institute of Medical Research, Macquarie Park, 2113, New South Wales, Australia.

Funding

Australian Research Council DP200102016Australian Research Council LP190100938
6 · The paper itself

Abstract

purposeThe transition from high Global Warming Potential (GWP) propellants such as HFA134a to low-GWP alternatives such as HFA152a and HFO1234ze(E) in pressurised metered dose inhalers (pMDIs) poses a number of challenges for inhaled pharmaceutical product development. Changes in chemicophysical properties will alter product performance, impacting in-vitro bioequivalence metrics. This study investigates those differences using equivalent pMDI hardware and formulations.

methodsAerodynamic particle size distribution (APSD) measurements, laser diffraction and high-speed imaging were used to compare the performance of HFA134a, HFA152a and HFO1234ze(E) solution formulations of beclomethasone dipropionate. Propellant-only placebos, cosolvent-free solutions, and ethanol solutions at 8% and 15% w/w were investigated.

resultsHFA152a formulations had increased drug deposition on the actuator and throat while HFO1234ze(E) produced comparable APSD performance to HFA134a formulations. Plumes from HFA152a formulations spread more rapidly and were less stable and repeatable than those from HFA134a. HFO1234ze(E) plumes spread more slowly than HFA134a, but converged with HFA134a ex-mouthpiece. Differences between propellants were moderated by the addition of ethanol.

conclusionPlume stability is a driver of differences between formulations in the near-orifice region. Shot-to-shot repeatability differences are more pronounced ex-mouthpiece, where mixing with ambient air is dominant. Modifications to low-GWP pMDI product actuator orifice and mouthpiece geometries may provide a route to improved in-vitro product bioequivalence relative to current pMDIs. Differences between formulations are modest and may be managed through a combination of formulation, orifice and mouthpiece geometry changes. These generic formulations provide a database of benchmark data against which the performance of low-GWP products may be compared.

Indexed as

Aerosol PropellantsBeclomethasoneHydrocarbons, FluorinatedMetered Dose InhalersAdministration, InhalationAerosolsChemistry, PharmaceuticalFluorocarbonsHumansParticle SizeTherapeutic EquivalencyAerosol PropellantsAerosolsapafluraneBeclomethasoneFluorocarbonsHydrocarbons, FluorinatedHFA152aHFO1234ze(E)low-GWPpMDIpropellant

Identifiers

PMID39939559
PMCPMC11880099

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.