Dual Zone with Independent Control
Capable of significantly improving drug quality control and
the efficiency of new drug R&D
12 Position Auto-Sampling Dissolution Apparatus
D1200 Pro automated 12-position dissolution sampling apparatus meets the technical requirements in 0931 Methods for Determination of Dissolution Rate and Release of the 2020 edition of the Chinese Pharmacopoeia. Corresponding adapters can be used for switch between dissolution devices for the basket, paddle, small-volume dissolution, paddle-over-disk and rotating cylinder methods. It is applicable to various dosage forms including routine immediate-release, extended-release and controlled-release preparation
Functional
Using the Same Lifting Column as High-End Medical Equipment
With an IP20 rating, it is safe, quiet, firm and stable
Variable Speed Process
With the function of changing speed during the testing process,
and capable of completing extreme endpoint dissolution testing
Accessory Stand
For tidy collection and easy reach
Imaging System
Optional imaging system is capable of recording the testing
process with precision
Secondary Filtering
The convenient secondary filtering system can significantly
improve test efficiency
Drain Pan
Facilitate convenient cleaning
Easy Switch between Accessories
Switch between accessories for the basket and paddle methods and
other methods can be completed without requiring complex operations
Safety Compliance
Compliant with ChP, USP, EP, BP, and JP technical requirements.
Three levels of user rights and operation log management, in compliance with FDA 21 CFR Part 11 requirements, ensure the validity and reliability of electronic data.
Interface for easy connection to the LIMS laboratory information management system to track information and data throughout the experimental process and improve management efficiency.
Multiple alarm modes, including sampling time and temperature overload alarms, are available.
Accuracy and Reliability
The instrument structure is optimized by building a complete mechanical data modelto improve the stability design of the mechanical structure.
Equipped with the three-section synchronous linear lift column of high-end medical equipment(medical certification in compliance with IEC 60601-1), which meets the lP 20 protection level for a safe, quietrobust and stable lifting system.
Highly chemically stable Teflon piping makes every piping channel reliable.
Extensive Functions
Double-zone control is standard, which can signifcantly improve the eficiency of drug quality control and new drug development.
The changeable speed function for dissolution experiments is available to complete the end-point dissolution experiment.
The easy-to-use secondary filtration system greatly improves the efficiency of experiments.
Quickly switch between basket,paddle, and other methods.
Equipped with a dissolution accessory holder and a cleaning tray to facilitate easy storage and cleaning.
Equipped with the same temperature replenishment module as standard to minimize temperature variations after replenishment to guarantee that accurate data can be obtained from the experiment.
With the design of supplemental light, the drug dissolution process can be observed even in poor lighting conditions.
The optional camera system is available to accurately record the dissolution process and the operation status of the instrument.
Technical Specifications
| 12 Position Dissolution Apparatus | Autosampler |
|---|---|
| Temperature control range: room temperature to 50℃ | Test tube/liquid phase vial: 240 positions |
| Temperature control accuracy: ±0.2℃ | Sampling collector size: 450mm×718mm×790mm |
| Main unit size: 910mm×540mm×670mm | Sampling path: 12 ways |
| Dissolution station: 12 positions | Sampling range: 0.5mL ~ 10mL |
| Water tank volume: 46L | Sampling accuracy: ±0.1mL |
| Temperature resolution: 0.1℃ | Maximum sampling times: 20 times |