2011
DOI: 10.1111/j.2042-7158.2011.01370.x
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Co-deposition of a triple therapy drug formulation for the treatment of chronic obstructive pulmonary disease using solution-based pressurised metered dose inhalers

Abstract: This study demonstrated the feasibility of formulating a solution-based pMDI containing a triple therapy with identical deposition pattern for the treatment of several respiratory diseases where multi-drug cell targeting is required.

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Cited by 13 publications
(5 citation statements)
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References 47 publications
(46 reference statements)
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“…The mean in vitro lung doses per actuation as measured on the filters at each altitude are listed in Table . The in vitro lung doses were close to reported fine particle doses for inhalers with high performance, that is, 90–100 μg for the budesonide component of Symbicort ® , or slightly larger than the reported fine particle doses for Ventolin ® and Airomir™, as expected. The in vitro lung dose for QVar ® agreed with previously reported mouth–throat deposition using the Alberta Idealized Throat …”
Section: Resultssupporting
confidence: 81%
“…The mean in vitro lung doses per actuation as measured on the filters at each altitude are listed in Table . The in vitro lung doses were close to reported fine particle doses for inhalers with high performance, that is, 90–100 μg for the budesonide component of Symbicort ® , or slightly larger than the reported fine particle doses for Ventolin ® and Airomir™, as expected. The in vitro lung dose for QVar ® agreed with previously reported mouth–throat deposition using the Alberta Idealized Throat …”
Section: Resultssupporting
confidence: 81%
“…The recent approval of tiotropium–olodaterol SMI 62 illustrates that demand for combination therapy is driving device innovation. Cosuspension-based pMDIs, for example, are in development, 89 , 91 , 92 which may facilitate further innovation in fixed-dose combination inhaler products. For example, the US Federal Drug Administration recently approved a novel LAMA/LABA cosuspension-based pMDI (glycopyrrolate and formoterol fumarate) for patients with COPD.…”
Section: Discussionmentioning
confidence: 99%
“…Finally, two or three of the drugs can be formulated in an HFA system as a solution formulation. To formulate ipratropium, formoterol, and budesonide in HFA, the drugs were dissolved in the system using ethanol (161). The resulting formulation delivered 5 μg ipratropium bromide, 2.25 μg fomoterol fumarate, and 80 μg budesonide.…”
Section: Combination Drug MDI Productsmentioning
confidence: 99%