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What is a disintegration test?
This test determines whether dosage forms such as tablets, capsules, boluses pessaries and suppositories disintegrate within a prescribed time (disintegration time) when placed in a liquid medium under the prescribed experimental conditions.

Disintegration Test and Apparatus : Pharmaguideline

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What is complete disintegration?
Complete disintegration is defined as that state in which any residue of the unit, except fragments of insoluble coating or cap-sule shell, remaining on the screen of the test appa-ratus or adhering to the lower surface of the disk, if used, is a soft mass having no palpably firm core.

DISINTEGRATION - USP–NF

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What are the types of disintegration test apparatus?
Disintegration test apparatus are mainly of two types, Type A and Type B: Type A: It consists of 6 tube assembly mainly used for tablets of size less than 80 mm in length. Type B: It consists of a 3-tube assembly used for tablets of size more than 80 mm in length. DT apparatus assembly Consists of the following parts: 1. Rigid Baskets:

Disintegration Test Apparatus: Diagram, Principle, Types, Procedure

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What is Agilent disintegration testing?
Fast and Simple Disintegration Testing for Reliable, Compliant Results Agilent offers disintegration instruments that meet the United States Pharmacopeia (USP) requirements for disintegration of tablets, capsules, and granules.

Disintegration Testing | Agilent

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pharmaguddu.com › disintegration-test-apparatusDisintegration Test Apparatus: Diagram, Principle, Types ...

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Feb 2, 2024 · Learn how to perform disintegration test for tablets and capsules using Type A or B apparatus. Find out the diagram, principle, limit, assembly and calibration of the apparatus.
www.pharmaguideline.com › 2011 › 06Disintegration Test and Apparatus : Pharmaguideline

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Jun 3, 2023 · Learn how to perform disintegration test for tablets, capsules, enteric-coated tablets, pessaries and suppositories using different apparatus and methods. Find specifications, procedures and examples for each type of dosage form.
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www.ipc.gov.in › images › pdf2.5.1. Disintegration Test - Indian Pharmacopoeia Commission

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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
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www.uspnf.com › sites › defaultDISINTEGRATION - USP–NF

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1. APPARATUS. 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.
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www.agilent.com › disintegration-apparatusDisintegration Testing | Agilent

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The Agilent 100 automated disintegration apparatus is a fully programmable solution delivering reliable disintegration testing results. Our disintegration testing systems are compact and easy to manage, featuring precise temperature control and meeting regulatory compliance requirements.
www.usp.org › pdg › general-methodsDisintegration | USP

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Jun 10, 2004 · This revised standard provides information on the dimensional description of the apparatus in standard format and corrects the description of the disks used in disintegration testing. The revision to <701> Disintegration General Chapter will be incorporated into and become official with USP 43-NF 38.
www.ncbi.nlm.nih.gov › pmc › articlesA Review of Disintegration Mechanisms and Measurement ...

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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.