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Dissolution Rate Test Equipment
Dissolution Rate Test Equipment

Dissolution Rate Test Equipment

Dissolution Rate Test Equipment Specification

  • Operate Method
  • Microprocessor Controlled
  • Dimension (L*W*H)
  • 600 x 450 x 600 mm
  • Capacity
  • 6+2 Vessels
  • Power
  • 220 W
  • Color
  • White & Blue
  • Classification
  • Laboratory Instrument
  • Weight
  • Approx. 45 kg
  • Material
  • Stainless Steel & Acrylic
  • Usage
  • Pharmaceutical laboratory testing
  • Application
  • Testing dissolution rate of tablets/capsules
  • Product Type
  • Dissolution Rate Test Equipment
  • Voltage
  • 220 V AC, 50 Hz
 

Dissolution Rate Test Equipment Trade Information

  • Payment Terms
  • Cash Advance (CA), Cash in Advance (CID), Cheque, Telegraphic Transfer (T/T), Letter of Credit (L/C)
  • Sample Available
  • Yes
  • Sample Policy
  • Sample costs shipping and taxes has to be paid by the buyer
  • Packaging Details
  • carton box, export quality also available
  • Main Export Market(s)
  • Asia, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
  • Certifications
  • ISO 9001, 14001 ,CE
 

About Dissolution Rate Test Equipment

Dissolution Rate Test Equipment 

Specification of Dissolution Rate Test Equipment

A stainless steel basket is provided to hold samples. The machine works on 220V AC 50Hz single phase. 
  • Single test    
  • Combined unit for 3 tests.
  • Combined unit for 6 tests.



Precision Temperature and Speed Control

The bath temperature is adjustable from ambient levels up to 45C, featuring an impressive control accuracy of 0.5C. Stirring speeds are selectable between 25 and 250 RPM with 1 RPM accuracy, ensuring dependable and reproducible mixing for dissolution testing protocols. Together, these specifications are crucial for high-quality pharmaceutical analysis.


User-Friendly Operation

A microprocessor-controlled system paired with a digital LED display provides clear reading and intuitive control of all functions. The programmable timer supports up to 99 minutes, allowing automation of test cycles and reducing operator workload, making the equipment suitable for high-throughput laboratory environments.

FAQs of Dissolution Rate Test Equipment:


Q: How is the dissolution rate test conducted using this equipment?

A: Place tablets or capsules into each vessel filled with the appropriate dissolution medium, usually up to 1000 ml. Set the desired bath temperature (ambient to 45C), stirring speed, and timer. The microprocessor-controlled system maintains conditions as per USP, IP, and BP standards, recording dissolution rates digitally for precise analysis.

Q: What are the main benefits of using digital LED display for dissolution testing?

A: The digital LED display ensures real-time visibility of test parameters such as temperature, stirring speed, and time. This facilitates accurate monitoring, quick adjustments, and eliminates guesswork, leading to consistent dissolution results and improved workflow efficiency.

Q: When should the additional stirring paddles be used?

A: The two additional stirring paddles can be used when one of the six main paddles needs replacement or if simultaneous testing in all eight vessels is required. This provides flexibility for maintenance or scaling up sample throughput.

Q: Where is this dissolution apparatus typically installed?

A: Designed for benchtop installation, this equipment is ideally placed in pharmaceutical laboratories dedicated to quality control and research. The compact size (600 x 450 x 600 mm) allows for efficient use of workspace.

Q: What is the significance of compliance with USP, IP, and BP standards?

A: Compliance with USP, IP, and BP standards ensures that testing carried out on this instrument meets global regulatory requirements for pharmaceutical dissolution analysis, which is essential for drug approval and quality assurance.

Q: How does the programmable timer enhance the dissolution testing process?

A: The programmable timer allows users to set test durations up to 99 minutes, automating the process and ensuring consistency across multiple experiments. This streamlines workflow and reduces the risk of human error.

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