Pharmaceutical Testing
Disintegration
Background: Disintegration Testing Before the active ingredient(s) of an oral solid dose drug product can be absorbed into the body, the tablet or capsule in which they are contained must first disintegrate into smaller particles. Chapters Ph. Eur. 2.9.1 and USP <701> and <2040> describe reproducible and standardised methods for quantifying the disintegration behaviour of solid dosage forms.
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