Automated Disso Rate Tester USP Apparatus 3,7

DISSO III-7 release rate tester is suitable for USP apparatus 3 and USP apparatus 7 drug release rate testing. USP apparatus 3 is used for testing controlled-release drugs, enteric soluble drugs, soft gel, and chewable tablets. USP apparatus 7 is used for testing transdermal patches and implants, stents and balloons, hip stems etc.

Features:

• Switchable between USP apparatus 3 and USP apparatus 7 drug release rate testing
• Unique vessel covers designed to prevent evaporation and media contamination
• Multiple sampling intervals and adjustable dip speed for flexible dissolution methods
• One-piece-molded clear water bath for easy observation
• Adjustable stroke length suitable for dissolution studies
• Data audit tracking function available that complies with FDA 21 CFR Part 11 requirements

Extended functions:

• Capable of upgrading to an automated sampling system to increase efficiency
• Compatible with camera systems to record the drug release process
• DISSO III-7 is compatible with UV or HPLC. It can perform online dissolution analysis
• Compatible with PERMETRO system to distinguish between the permeation of generic drugs and original drugs, which can exist as a pre-BE study