Development of a Material Sparing Bulk Density Test Comparable to a Standard USP Method for Use in Early Development of API’s
- 216 Downloads
Bulk density can be a key indicator of performance, and may influence choice of formulation route of materials in pharmaceutical development. During early development, the cost of API’s can be expensive and the availability of material for powder property analysis is limited. The aim of this work was to investigate a suitable small-scale, low material requirement, bulk density test which would provide comparable data to the recommended large volume USP test. Materials with a range of morphological characteristics typically seen in the pharmaceutical industry were assessed to ensure that methods were suitably robust. It was found that the USP II “low volume” test does not give equivalent results to other tests in the USP, across the range of materials. An alternative test based on the FT4 powder rheometer at a scale of 25 mL gave results equivalent to the large volume USP I standard test. The use of smaller 10-mL methods was also found to give acceptable results for materials that were considered well-behaved but were more variable with difficult to handle materials with low bulk density.
KEY WORDSactive pharmaceutical ingredient (API) bulk density compressibility index excipients pharmaceuticals
The team is grateful for the help of Peter Timmins, Venkatramana Rao, and Joanne Kelleher in executing this work.
- 3.United States Pharmacopeia and National Formulary. USP 36-NF 31. Rockville: United States Pharmacopeia Convention; 2013. p. 265–7.Google Scholar
- 7.Rawle AF. Particle morphology and characterization in preformulation. In: Adeyeye MC, Brittain HG, editors. Preformulation in solid dosage form development: Informa Healthcare; 2008. p. 145–84.Google Scholar