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Agilent 708-DS Dissolution Apparatus System with Integrated 850-DS Automated Sampling Station
Product Description
The Agilent 708-DS Dissolution Apparatus System combined with the 850-DS Sampling Station offers a fully integrated USP-compliant platform designed for precise pharmaceutical dissolution testing in quality control and R&D laboratories. Engineered for regulated pharmaceutical environments, this system supports high-throughput dissolution analysis with critical control over paddle or basket rotation speed, bath temperature uniformity, and programmable multi-timepoint sampling.
Key technical features include:
- An 8-position dissolution bath ensuring uniform temperature control and consistent hydrodynamics for reproducible kinetics across vessels.
- The 850-DS sampling station with integrated peristaltic pumping, automated filter handling, and an integrated sample tray for automated, repeatable sample collection.
- Touchscreen control panel enabling comprehensive monitoring and programming of test parameters and sampling schedules.
- Electrical specifications supporting global operation (100–240 V, 50/60 Hz, 300 W power consumption).
- Built-in automation capabilities ideal for applications such as finished dosage testing, method development, stability studies, and routine pharmaceutical QC workflows requiring accuracy, traceability, and repeatability.
This dissolution system is widely adopted for molecular diagnostics, biopharmaceutical production pipelines, and bioprocessing workflows where dissolution profiling is a critical analytical step. Its automated sampling functionality enhances throughput and data reliability, making it essential for regulated biotechnological and pharmaceutical laboratories aiming to optimize drug release studies and formulation assessments.
Accessories include sample trays, tubing, connectors, spare filters, capsules, power cables, and software documentation. Dimensions approximately 48” L × 24” W × 30” H, weight around 150 lbs. Manufactured in 2023, this system integrates seamlessly into advanced laboratory environments conducting biotechnology-driven drug release analyses and synthetic biology related biopharmaceutical validation.
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