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Journal ArticleDOI

Critical characteristics for corticosteroid solution metered dose inhaler bioequivalence.

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TLDR
The cell culture dissolution-absorption model revealed the net effect of the particle formed on drug disposition and was predictive of human systemic absorption of BDP delivered by the test inhalers, illustrating the potential of the technique to detect the effect of formulation on the performance of aerosolized particles and contribute to assessment of bioequivalence.
Abstract
Determining bioequivalence for solution pressurized metered dose inhalers (pMDI) is difficult because the critical characteristics of such products are poorly defined. The aim of this study was to elucidate the non-aerodynamic properties of the emitted aerosol particles from two solution pMDI products that determine their biopharmaceutical differences after deposition. Novel particle capture and analysis techniques were employed to characterize the physicochemical and biopharmaceutical properties of two beclomethasone dipropionate (BDP) products: QVAR and Sanasthmax. The BDP particles emitted from the Sanasthmax inhaler were discernibly different those emitted from QVAR in terms of size (50% larger, less porous), solid state (less crystalline) and dissolution (20-fold slower). When deposited onto the surface of respiratory epithelial cell layers, QVAR delivered ∼50% more BDP across the cell layer in 60 min than Sanasthmax. Biopharmaceutical performance was not attributable to individual particle propertie...

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Citations
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Journal ArticleDOI

Advances in Metered Dose Inhaler Technology: Formulation Development

TL;DR: This review presents a survey of challenges associated with formulating MDIs as solution or suspension products with one or more drugs, while considering the physicochemical properties of various excipients and how the addition of theseexcipients may impact overall product performance of the MDI.
Journal ArticleDOI

Pharmaceutical applications of the Calu-3 lung epithelia cell line

TL;DR: The use of the Calu-3 cell line provides a basic research tool that enables the development of safer and more effective inhaled therapeutics and helps to generate a better understanding of determinants that influences pulmonary drug dissolution, absorption, metabolism and efficacy.
Journal ArticleDOI

Advances in experimental and mechanistic computational models to understand pulmonary exposure to inhaled drugs.

TL;DR: This work provides a comprehensive review of the state of the art with respect to multiscale computer models designed to provide a mechanistic prediction of local and systemic drug exposure following inhalation.
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Across the pulmonary epithelial barrier: Integration of physicochemical properties and human cell models to study pulmonary drug formulations

TL;DR: Pulmonary permeability assessment of drugs may provide insights that will allow formulations to be developed with optimised therapeutic outcomes, and the integration of these physicochemical characteristics with the biological factors to provide a better understanding of the fate of microparticles after deposition on the epithelial cells.
References
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Journal ArticleDOI

Large Porous Particles for Pulmonary Drug Delivery

TL;DR: A new type of inhalation aerosol, characterized by particles of small mass density and large size, permitted the highly efficient delivery of inhaled therapeutics into the systemic circulation.
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Regional lung deposition and bronchodilator response as a function of beta2-agonist particle size.

TL;DR: Regional targeting of inhaled beta2-agonist to the proximal airways is more important than distal alveolar deposition for bronchodilation and can appreciably enhance inhaled drug therapy and may have implications for developing future inhaled treatments.
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Aerosol drug delivery: developments in device design and clinical use.

TL;DR: Recent developments in the design and clinical use of aerosol devices over the past 10-15 years are discussed with an emphasis on the treatment of respiratory disorders.
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Culture of Calu-3 cells at the air interface provides a representative model of the airway epithelial barrier.

TL;DR: Cells grown via AIC generate a model more morphologically representative of the airway epithelium than cells cultured using LCC, and transport rates of flu-Na and FITC-dex were inversely proportional to molecular weight, and were significantly lower in cell layers grown using L CC than AIC.
Journal ArticleDOI

Lung Deposition of Hydrofluoroalkane-134a Beclomethasone Is Greater Than That of Chlorofluorocarbon Fluticasone and Chlorofluorocarbon Beclomethasone: A Cross-over Study in Healthy Volunteers

TL;DR: Deposition values appeared to be related to the particle size distribution of each inhaler, with the smaller particles of HFA-BDP providing the greatest lung deposition and least oropharyngeal deposition.
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