The Relationship Between the Permeability and the Performance of Carrier-Based Dry Powder Inhalation Mixtures: New Insights and Practical Guidance

AAPS PharmSciTech. 2018 Feb;19(2):912-922. doi: 10.1208/s12249-017-0898-7. Epub 2017 Oct 23.

Abstract

The permeability of a powder bed reflects its particle size distribution, shape, packing, porosity, cohesivity, and tensile strength in a manner relevant to powder fluidization. The relationship between the permeability and the performance of carrier-based dry powder inhalation (DPI) mixtures has, however, aroused controversy. The current study sought to gain new insights into the relationship and to explore its potential applications. We studied eight lactose materials as DPI carriers. The carriers covered a broad permeability range of 0.42-13.53 D and moreover differed in particle size distribution, particle shape, crystal form, and/or porosity. We evaluated the performance of inhalation mixtures of each of these carriers and fluticasone propionate after aerosolization from an Aerolizer®, a model turbulent-shear inhaler, at a flow rate of 60 L/min. Starting from the high permeability side, the inhalation mixture performance increased as the carrier permeability decreased until optimum performance was reached at permeability of ~ 3.2 D. Increased resistance to air flow strengthens aerodynamic dispersion forces. The inhalation mixture performance then decreased as the carrier permeability further decreased. Very high resistance to air flow restricts powder dispersion. The permeability accounted for effects of carrier size, shape, and macroporosity on the performance. We confirmed the relationship by analysis of two literature permeability-performance datasets, representing measurements that differ from ours in terms of carrier grades, drug, technique used to determine permeability, turbulent-shear inhaler, and/or aerosolization flow rate. Permeability provides useful information that can aid development of DPI mixtures for turbulent-shear inhalers. A practical guidance is provided.

Keywords: Aerolizer®; mercury intrusion porosimetry; permeability; pulmonary drug delivery; turbulent-shear dry powder inhaler.

MeSH terms

  • Administration, Inhalation
  • Aerosols / chemistry
  • Aerosols / metabolism
  • Drug Carriers / chemistry
  • Drug Carriers / metabolism*
  • Dry Powder Inhalers / methods*
  • Fluticasone / chemistry
  • Fluticasone / metabolism
  • Lactose / chemistry
  • Lactose / metabolism*
  • Particle Size
  • Permeability
  • Porosity
  • Powders

Substances

  • Aerosols
  • Drug Carriers
  • Powders
  • Fluticasone
  • Lactose