Biorelevant intrinsic dissolution profiling in early drug development: Fundamental, methodological, and industrial

Christel A S Bergström1, Karl Box2, René Holm3

  • 1Department of Pharmacy, Uppsala University, Uppsala Biomedical Center, P.O. Box 580, SE-75123 Uppsala, Sweden.

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The acceptance criteria for dissolution profile data are anchored in Q values, representing the percentage of drug dissolved within a specified period. This assessment unfolds in three stages:First Stage: The test passes if all six drug dosage units are equal to or greater than Q plus 5%; otherwise, the sample proceeds to the second stage.Second Stage: The average of twelve units must be equal to or greater than Q, with no unit falling below Q - 15% to pass; if not, it progresses to the final...
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