Pharmacopeial methodologies for determining aerodynamic mass distributions of ultra-high dose inhaler medicines

William Wong, John Crapper, Hak-Kim Chan, Daniela Traini, Paul M. Young

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)


Three different impactor methodologies, the Andersen cascade impactor (ACI), next-generation impactor (NGI) and multistage-liquid impinger (MSLI) were studied to determine their performance when testing ultra-high dose dry powder formulations. Cumulative doses of spray-dried mannitol (Aridol™) were delivered to each impactor at a flow rate of 60 L min−1 (up to a max dose of 800 mg delivering 20 sequential 40 mg capsules). In general, total drug collected in both the ACI and NGI falls below the range 85–115% of label claim criteria recommended by the United States of America Food and Drug Administration (FDA) at nominal mannitol doses exceeding 20 mg and 200 mg, respectively. In comparison analysis of the MSLI data, over a 5–800 mg cumulative dosing range, indicated that the percentage of nominal dose recovered from the MSLI was within the ±15% limits set in this study. Furthermore all samples, apart from the 5 mg and 10 mg analysis were within 5% of the nominal cumulative dose. While the MSLI is not routinely used for regulatory submission, the use of this impinger when studying ultra-high dose formulations should be considered as a complementary and comparative source of aerosol deposition data.
Original languageEnglish
Pages (from-to)853-857
Number of pages5
JournalJournal of Pharmaceutical and Biomedical Analysis
Issue number4
Publication statusPublished - 2010
Externally publishedYes


  • MSLI
  • ACI
  • NGI
  • Dry powder inhaler
  • Impactor efficiency


Dive into the research topics of 'Pharmacopeial methodologies for determining aerodynamic mass distributions of ultra-high dose inhaler medicines'. Together they form a unique fingerprint.

Cite this