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.
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.
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
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