An Unbiased View of disintegration test apparatus

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This SOP is relevant for Procedure and calibration of disintegration test apparatus (Electrolab make), that will be utilized for finding disintegration time of capsules or tablets in good quality Manage Office.

Agilent provides disintegration instruments that meet the United States Pharmacopeia (USP) requirements for disintegration of tablets, capsules, and granules. The Agilent one hundred automated disintegration apparatus is a fully programmable Remedy delivering responsible disintegration testing benefits.

Record the temperature demonstrated from the instrument and calculated by a calibrated thermometer in the record guide.

Verify the diameter of wire chosen at least just one amount from the many tubes and document the observation.

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During the disintegration test, the tablet or capsule is put in a disintegration apparatus that simulates the physiological circumstances on the gastrointestinal tract.

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PROCEDURE:- Area just one dosage unit in Each individual on the six tubes of the basket and when specified include a disc. Run the apparatus employing drinking water as the immersion fluid Unless of course A different liquid is specified and manage its temperature at 35–39 °C. At the end of the desired time elevate the basket with the fluid and observe the dosage units, every one of the dosage models have disintegrated entirely.

This procedure is applicable to disintegration test apparatus, set up in the standard Manage Section.

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Join the main supply, heater connector, and external probe into their respective sockets furnished within the rear ideal-hand side of the instrument.

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