Analytical

Tablet Dissolution Test Apparatus DS 14000 with Peristaltic Pump

DISSOLUTION TEST APPARATUS

Dissolution Tests are conducted to determine the drug release patterns, physiological availability and bioavailability of formulated 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 interface, temperature, and solvent composition.

LABINDIA 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 12+2 (6+1 & 6+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.

• Tablet dispenser - drops 12 dosage form at single instance.

• Low Evaporation Lids:

» The conical shape low evaporation recover y lids reduces media loss during long run.

» Integrated pre-centered lids; no manual removal or positioning of lids. This ensures automatic vessel centering and precise positioning of paddle/basket with shaft without any special tool as per pharmacopeia requirements.

• State-of-the-art design:

» Easy placement and locking of vessels, the Easealign system allows the vessels to simply slide into the place (Bionet Locking).

Once placed, vessels do not float even when empty.

» Facility to monitor Vessel temp., with DTS Technology (Digital Temperature Sensor)

 

REGULATORY COMPLIANCE:

• DS 14000 meets all requirements relating to validation, qualification and calibration.

• Appropriate qualification documents (I.Q. / O.Q.) can be supplied with the instrument.

 

INTELLIGENT SAMPLING SYSTEM

• Automated sampling as per USP Specifications. Sampling tubes are lowered in the media only at the time of sampling and withdrawn

immediately after sampling, thus no part of the assembly contributes motion, agitation or vibration.

• Sampling tubes are accurately moved to the USP sampling position i.e. a zone mid way between the sur face of media and the top of

paddle/basket parameters, not less than 1 cm from the vessels wall as selected in the method.

• 12 bowls temperature monitoring system automatically measures and records the temperature of individual vessel at specified sample points.

 

PERISTALTIC PUMP

• Imported Pump with click-n-go Cassette design for volume accuracy.

• Fixed length pump tubings with stopper for sampling volume accuracy.

• Volume calibration through sof tware.

• Tygon pump tubings for SLS Compatibility with long life.

• Imported Pump with Planetary drive for very accurate pumping.

• High repeatability on all Channels.

• 24 actively driven stainless steel rollers.

 

SAMPLE COLLECTION

• 12 X 6 X 2 sets of samples can be collected. For more sampling interval, 24 X 6 collection trays are available.

• Option of 1.5ml & 2ml HPLC vials is available.

• Over Head Design for electronic safety and fail safe operation.

• Sensor to locate proper position of tray with alarm facility for collection of sample

• Wide mouth vial to minimise SLS spillover problem due to foaming characteristics

• Easy positioning with respect to vials or test tube tray for easy changeover

 

ADDITIONAL FEATURES

• Facility to RINSE the entire sampling path in between sampling time points to reduce contamination & carryover

• Specially developed cleaning system to clean the entire sampling path after each run.

• Facilities to perform the dissolution test using two buffers (Buffer changing) to cater the application of enteric coating tablets.

• Recovery Test facility to study 100% Drug Dissolution.

• Split & on-time interval

 

TYPICAL SPECIFICATIONS

• Control: Micro controller based (Advanced version of microprocessor).

• Display: 40 x 2 line back lighted liquid cr ystal display (LCD)

• Keyboard: Alphanumeric splash waterproof polyester sof t keys.

• Method Storage: 15 programs with parameters.

• Data Storage: Available with Non-Volatile memory.

• Water Bath: 29 litres capacity with built-in water level sensor.

• Bath Circulation: External vibration free water circulator

• Temperature Range: 20°C to 55°C

• Temperature Resolution: 0.1° C

• Temperature Accuracy: up to 45°C ±0.1°C & >45°C up to 55°C ±0.2°C

Temperature Sensor: DTS - Digital Temperature Sensor

• Paddle / Basket Shaft Speed: Range 20 to 250 RPM ± 1%.

• Dissolution Vessel: Polycarbonate / Glass Vessels (clear, amber, peak vessels, 250, 150 & 100 ml. dissolution vessels available)

• Sampling Time Selectivity: Fixed / Programmable (varying intervals).

• Time Interval Selectivity: In steps of 1 minute.

• Sampling Volume Range: 0.5 - 25.5

• Replenishing mode selectivity: User selectable.

• Rinsing Functionality: Optional.

• Maximum Number of Intervals: 30

• Dissolution Process Time: 1 min. to 720 hours.

• 6 Channel Temperature Reader: Built-In

Report Format: a) GLP & Pharmacopeia compliant b) Program parameter repor t

Output:

a) Printer: Compatible for deskjet, inject and dot matrix printer

b) RS232C: For PC Connectivity

c) 21 CFR Part 11 compliance software available (Optional)

• Power: 210-230 V AC ± 10%, 50 Hz. - 60 Hz.

• Environmental Operating Conditions: a) Operation: Indoor. b) Temperature: Ambient to 45° C. c) Humidity: 5 to 90% non-condensing.

• Dimensions: 115 x 60 x 70.5 cms. (W x D x H)

• Weight: 140 kgs. approx.

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