Accuracy of float testing for metered-dose inhaler canisters

Tina Penick Brock1, Andrea M Wessell, Dennis M Williams

  • 1School of Pharmacy, University of North Carolina-Chapel Hill, 27599-7560, USA. tbrock@unc.edu

Journal of the American Pharmaceutical Association (Washington, D.C. : 1996)
|August 2, 2002
PubMed
Abstract

Insights

Metered-dose inhaler (MDI) float tests are unreliable for determining remaining medication. Canister floating patterns vary by product and are not a consistent indicator of inhaler contents.

Area of Science:

  • Pharmaceutical Technology
  • Respiratory Medicine

Background:

  • Metered-dose inhalers (MDIs) are crucial for delivering respiratory medications.
  • Accurate assessment of remaining medication in MDIs is essential for effective asthma management.
  • Current methods for assessing MDI contents may lack reliability.

Purpose of the Study:

  • To characterize and evaluate the floating patterns of commercially available metered-dose inhaler (MDI) canisters.
  • To determine if MDI canister floating behavior can reliably indicate the amount of medication remaining.

Main Methods:

  • Four canisters each of three different asthma medications were tested.
  • Canisters were actuated and weighed to determine remaining medication levels (100% down to 0%).
  • Canister positions and submersion percentages were recorded while floating in water.

Main Results:

  • Significant differences in floating behavior were observed among MDI products.
  • Canisters were fully submerged nozzle-up when two-thirds full or more.
  • Canisters inverted to float nozzle-down when less than half full, with variable positions.

Conclusions:

  • MDI canister float characteristics are product-specific, influenced by canister size, design, and contents.
  • The float test is not a reliable method for patients or clinicians to assess remaining MDI medication.
  • The National Asthma Education and Prevention Program recommends tracking used actuations for accurate dose counting.

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