Search results
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 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...
Disintegration Test. This test determines whether dosage forms such as tablets, capsules, boluses pessaries and suppositories disintegrate within a prescribed time when placed in a liquid medium under the prescribed experimental conditions.
Feb 20, 2019 · Since its inception in the 1930s, disintegration testing has become an important quality control (QC) test in pharmaceutical industry, and disintegration test procedures for various dosage forms have been described by the different pharmacopoeias.
Disintegration of Tablets and Capsules, JP 6.09 Disintegration Test, and USP <701> Disintegration can be used as interchangeable in the ICH regions subject to the conditions detailed below. Testing conditions for specific dosage forms are outside the scope of the harmonization of this chapter.
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.
This test is provided to determine whether tablets or capsules disintegrate within the prescribed time when placed in a liquid medium at the experimen-tal conditions presented below. FCompliance.
Mar 1, 2017 · The disintegration process is specifically critical for immediate-release dosage forms. Its mechanisms and the factors impacting disintegration are discussed and methods used to study the disintegration in-situ are presented.
Since its inception in the 1930s, disintegration testing has become an important quality control (QC) test in pharmaceutical industry, and disintegration test procedures for various dosage forms have been described by the different pharmacopoeias, with harmonization among them still not quite complete.
Jun 10, 2004 · The revision to the harmonized standard for disintegration testing of pharmaceutical dosage forms has been approved by the Pharmacopeial Discussion Group (PDG) as described in the PDG sign-off cover sheet.
