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in the vessel of the specified apparatus given in the individ-ual monograph , assemble the apparatus, equilibrate the Dissolution Medium to 37±0.5°, and remove the thermome-ter. Place 1 dosage unit in the apparatus, taking care to exclude air bubbles from the surface of the dosage unit, and immediately operate the apparatus at the specified rate
The test is intended for a capsule or tablet. This test is provided to determine compliance with the dissolution requirements for solid dosage forms administered orally. In this chapter, a dosage unit is defined as 1 tablet or 1 capsule or the amount specified. (As per BP) Use Apparatus 1 unless otherwise directed.
May 14, 2014 · The review will also focus on modernization of dissolution process and dissolution testing apparatuses including automation in dissolution testing and adoption of fiber optic technology.
The review will also focus on modernization of dissolution process and dissolution testing apparatuses including automation in dissolution testing and adoption of fiber optic technology.
The dissolution procedure requires an apparatus, a dissolution medium, and test conditions that provide a method that is discriminating yet sufficiently rugged and reproducible for day-to-day operation and capable of being transferred between laboratories.
Apparatus: The basic unit for the in-vitro performance testing of dosage units. The apparatus consists of a container (vessel) for the dosage unit and dissolution medium, a device for promoting agitation of the dissolution medium (stirring element), temperature control and support to hold the vessel and stirring element in a fixed orientation.
Apparatus 4, large cell for tablets and capsulesform dissolution testing must include conformance to the (top), tablet holder for the large cell (bottom). (All meas-dimensions and tolerances of the apparatus as given above.
