Is “Slow Inhalation” Always Suitable for Pressurized Metered Dose Inhaler?

被引:0
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作者
Daiki Hira
Tomoyuki Okuda
Ayano Mizutani
Nao Tomida
Megumi Mizuno
Satoshi Ueshima
Mikio Kakumoto
Tomonobu Okano
Hirokazu Okamoto
机构
[1] Meijo University,Faculty of Pharmacy
[2] Ritsumeikan University,College of Pharmaceutical Sciences
[3] Shiga University of Medical Science Hospital,Department of Pharmacy
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关键词
Pressurized metered dose inhaler; Inhalation flow pattern; Particle diameter; Aerosol;
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摘要
To achieve adequate inhalation therapy, a proper inhalation technique is needed in clinical practice. However, there is limited information on proper inhalation flow patterns of commercial inhalers. Here, we quantitatively estimated airway deposition of two commercial pressurized metered dose inhalers (pMDIs) to determine their optimal inhalation patterns. Sultanol® inhaler (drug particles suspended in a propellant, suspension-pMDI) and QVAR™ (drug dissolved in a propellant with ethanol, solution-pMDI) were used as model pMDIs. Aerodynamic properties of the two pMDIs were determined using an Andersen cascade impactor with human inhalation flow simulator developed by our laboratory. As indices of peripheral-airway drug deposition, fine particle fractions (FPFPA) at different inhalation flow rates were calculated. The time-dependent particle diameters of sprayed drug particles were determined by laser diffraction. On aerodynamic testing, FPFPA of suspension-pMDI significantly decreased depending on the increasing inhalation flow rate, while solution-pMDI achieved higher and constant FPFPA in the range of the tested inhalation flow rates. The particle diameter of solution-pMDI markedly decreased from 5 to 3 μm in a time-dependent manner. Conversely, that of suspension-pMDI remained at 4 μm during the spraying time. Although “slow inhalation” is recommended for pMDIs, airway drug deposition via solution-pMDI (extra-fine particles) is independent of patients’ inhalation flow pattern. Clinical studies should be performed to validate instruction for use of pMDIs for each inhaler for the optimization of inhalation therapy.
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