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Feb 2, 2024 · Disintegration test apparatus is widely used in pharmaceuticals to identify the disintegration properties of various types of tablets and capsules. The DT apparatus decides whether or not tablets or capsules disintegrate within a recommended time once placed in a liquid medium.
Jun 3, 2023 · Disintegration Test Apparatus and Disintegration Test procedure for tablets and capsules and enteric-coated tablets using basket rack assembly.
Disintegration is defined as that state in which no residue of the unit under test remains on the screen of the apparatus or, if a residue remains, it consists of fragments of disintegrated parts of tablets component parts such as insoluble coating of the tablets or of capsule shells, or of any melted fatty substance from the pessary or supposit...
This test is provided to determine whether tablets or capsules disintegrate within the prescribed time when placed in a liquid medium under the experimental conditions presented below. For the purposes of this test disintegration does not imply complete dissolution of the unit or even of its active constituent.
The apparatus consists of a basket-rack assem-bly, a 1000-mL, low-form beaker, 138 to 160 mm in height and having an inside diameter of 97 to 115 mm for the immersion fluid, a thermostatic ar-rangement for heating the fluid between 35 and.
This test is provided to determine whether tablets, capsules, or granules USP 1-Aug-2019 disintegrate within the prescribed time when placed in a liquid medium at the experimental conditions presented below.
Feb 20, 2019 · In 1948, the British Pharmacopoeia (BP) adopted a disintegration test for tablets based on observing the disintegration behavior in test tubes. The basket-rack assembly apparatus, first adopted by the United States Pharmacopoeia (USP) in 1950.
