SYSTEM ADR III-7 automated release rate sampling system is suitable for USP apparatus 3 and USP apparatus 7 drug release rate testing. It contains a DISSO III-7 release rate tester, a DSC-800 system controller, a SYP–8L–10mL and a SCR-DL sample collector.

Application:

USP apparatus 3 is used for dissolution testing for control-release drugs, enteric soluble drugs, soft capsules, and chewable drugs.

USP apparatus 7 is used for dissolution testing for transdermal patches, implants, stents, stem and balloons.

Features:

• Switchable between USP apparatus 3 and USP apparatus 7 drug release rate testing
• Unique vessel covers design to prevent evaporation and media contamination
• Automated sampling system for increased efficiency
• Multiple sampling intervals and adjustable dip speed for flexible dissolution methods
• Media replacement as standard configuration to ensure sink condition
• One piece molded clear water bath for easy observation
• Adjustable stroke length suitable for dissolution studies
• Data audit tracking function available and it complies to FDA 21 CFR Part 11 requirements

Extended functions: 

• Compatible with camera system to record drug release process
• SYSTEM ADR III-7 is compatible with UV or HPLC. It can perform online dissolution analysis
• Compatible with PERMETRO system to distinguish the permeation between generic drugs and original drugs, which can exist as a pre-BE study