Difference between revisions of "Dissolution testing"

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Latest revision as of 19:31, 6 August 2014

In the pharmaceutical industry, drug dissolution testing is routinely used to provide critical in vitro drug release information for both quality control purposes, i.e., to assess batch-to-batch consistency of solid oral dosage forms such as tablets, and drug development, i.e., to predict in vivo drug release profiles.[1]

References

  1. Ge Bai, Yimin Wang and Piero M. Armenante (17 January 2011). "Velocity profiles and shear strain rate variability in the USP Dissolution Testing Apparatus 2 at Different Impeller Agitation Speeds". International Journal of Pharmaceutics 403 (1–2): 1–14. doi:10.1016/j.ijpharm.2010.09.022.