Tablet Dissolution Test Apparatus DS 8000 (Basic)

Dissolution Tests are conducted to determine the drug release patterns, physiological availability and bioavailability of for mulated drug products. It is also used as a quality control tool. The Dissolution rate of a drug from the solid state is defined as the amount of drug substance that goes into solution per unit time under standardised conditions of liquid / solid inter face, temperature, and solvent composition.

It brings to you the State-of-the-art Dissolution Testing Apparatus in elegant design with advanced features, which supports USP 1, 2, 5 & 6. Apparatus for Intrinsic test & stationary basket methods are available.

STANDARD FEATURES

• Advanced, Micro-Controller based: User-friendly, complies with current USP , IP & EP specifications.

• Splash waterproof keyboard: Alphanumeric polyester soft keys for keyboard.

• Moulded water bath with 6+2 (3+1 & 3+1) vessel configuration enables comparative studies.

• External vibration free Water Circulator: for uniform water circulation, with audible, low water level alarm, with indication on display for safety.

• Mono shaft design with automatic adjustment for 25 mm depth setting with easy changeover between Apparatus I & II eliminates routine height validation as per USP.

• Paddles, Baskets and Vessels are laser marked with serial numbers for traceability.