Agilent | 400-DS Apparatus 7

Integrated features within a small footprint

The Agilent 400-DS Dissolution Apparatus for small volume sets the performance standard for drug-release testing of medical devices. It is the first dissolution apparatus built specifically for small-volume dissolution testing of combination drug products that meets all compendial requirements for USP Apparatus 7. The 400-DS complies with 21 CFR Part 11 guidelines and brings an unprecedented level of convenience, throughput, and efficiency to your quality control and R&D operations.

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Features

Small-Volume Dissolution Testing. The 400-DS can perform automated dissolution testing using as little as 3 mL media volume in either 5 or 10 mL vessels
Bathless Design eliminates sample losses while providing direct and efficient heating
Integrated and Efficient Autosampling directly into HPLC vials up to 36 time points. Conveniently removable trays make transportation to the HPLC easy
Unique Dissolution Cell Design. Each unit of the 400-DS is capable of testing up to 13 samples in the dissolution cells
Reciprocating Holders. Agilent’s patent-pending magnetically-driven reciprocation mechanism is capable of providing dip rates between 5 and 35 DPM, controlled through the software
Automated Media Replacement and liquid handling capabilities
Low Evaporation Rates. Completely sealed dissolution vessel
Software. 21 CFR Part 11 compliant software and a single PC can independently control up to four 400-DS systems

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