TY - JOUR
T1 - Drug distribution transients in solution and suspension-based pressurised metered dose inhaler sprays
AU - Duke, Daniel J.
AU - Scott, Harry N.
AU - Kusangaya, Anesu J.
AU - Kastengren, Alan L.
AU - Matusik, Katarzyna
AU - Young, Paul
AU - Lewis, David
AU - Honnery, Damon
PY - 2019/7/20
Y1 - 2019/7/20
N2 - This paper presents in situ time-resolved drug mass fraction measurements in pressurised metered dose inhaler (PMDI) sprays, using a novel combination of synchrotron X-ray fluorescence and scattering. Equivalent suspension and solution formulations of ipratropium bromide in HFA-134a propellant were considered. Measurements were made both inside the expansion chamber behind the nozzle orifice, and in the first few millimeters of the spray where droplet and particle formation occur. We observed a consistent spike in drug mass fraction at the beginning of the spray when the first fluid exits the nozzle orifice. Approximately 20% of the total delivered dose exits the nozzle in the first 0.1 s of the spray. The drug mass fraction in the droplets immediately upon exiting the nozzle peaked at approximately 50% of the canister mass fraction, asymptoting to approximately 20% of the canister concentration. The effect is due to a change in the drug mass fraction inside the droplets, rather than changes in droplet size or distribution. The transient was found to originate inside the expansion chamber. We propose that this effect may be a major contributor to low delivery efficiency in PMDIs, and have important implications for oropharyngeal deposition and inhalation technique. This highlights the importance of expansion chamber and nozzle design on the structure of PMDI sprays, and indicates areas of focus that may lead to improvement in drug delivery outcomes.
AB - This paper presents in situ time-resolved drug mass fraction measurements in pressurised metered dose inhaler (PMDI) sprays, using a novel combination of synchrotron X-ray fluorescence and scattering. Equivalent suspension and solution formulations of ipratropium bromide in HFA-134a propellant were considered. Measurements were made both inside the expansion chamber behind the nozzle orifice, and in the first few millimeters of the spray where droplet and particle formation occur. We observed a consistent spike in drug mass fraction at the beginning of the spray when the first fluid exits the nozzle orifice. Approximately 20% of the total delivered dose exits the nozzle in the first 0.1 s of the spray. The drug mass fraction in the droplets immediately upon exiting the nozzle peaked at approximately 50% of the canister mass fraction, asymptoting to approximately 20% of the canister concentration. The effect is due to a change in the drug mass fraction inside the droplets, rather than changes in droplet size or distribution. The transient was found to originate inside the expansion chamber. We propose that this effect may be a major contributor to low delivery efficiency in PMDIs, and have important implications for oropharyngeal deposition and inhalation technique. This highlights the importance of expansion chamber and nozzle design on the structure of PMDI sprays, and indicates areas of focus that may lead to improvement in drug delivery outcomes.
KW - MDI
KW - X-ray
KW - Ipratropium bromide
UR - http://www.scopus.com/inward/record.url?scp=85066936450&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/arc/DE170100018
UR - http://purl.org/au-research/grants/arc/LP160101845
U2 - 10.1016/j.ijpharm.2019.05.067
DO - 10.1016/j.ijpharm.2019.05.067
M3 - Article
C2 - 31173800
SN - 0378-5173
VL - 566
SP - 463
EP - 475
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
ER -