Transcription of 2.9. PHARMACEUTICAL TECHNICAL PROCEDURES
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2.9. PHARMACEUTICAL TECHNICAL PROCEDURES
EUROPEAN PHARMACOPOEIA disintegration of tablets and PHARMACEUTICALTECHNICAL PROCEDURES01/2008 disintegration OF TABLETSAND CAPSULESThis test is provided to determine whether tablets or capsulesdisintegrate within the prescribed time when placed in aliquid medium under the experimental conditions the purposes of this test, disintegration does notimply complete dissolution of the unit or even of its activeconstituent. Complete disintegration is defined as thatstate in which any residue of the unit, except fragments ofinsoluble coating or capsule shell, remaining on the screenof the test apparatus or adhering to the lower surface of thediscs, if used, is a soft mass having no palpably firm apparatus A for tablets and capsules that are notgreater than 18 mm long.
2.9.1. Disintegration of tablets and capsules EUROPEAN PHARMACOPOEIA 6.0 thesurfaceoftheliquid.Asuitabledevicemaintainsthe temperature of the liquid at 35-39 °C. The design of the basket-rack assembly may be varied
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