About Tablet Dissolution
Dissolution rate consists of water bath of 30.5 cm long 20.5cm wide and 23cm high fitted with a thermostatic control maintains the temperature of water at 47C with 0.5 variation convered vessal 100 ml made of coring glass variable speed motor ctlinder basket and shaft with blades of stainless steel.
| A | Single Test |
| B | DoubleTest |
| C | Three Test |
| D | Six Test |
Accurate and Efficient Tablet Dissolution TestingThis dissolution tester is engineered to deliver reliable results in pharmaceutical analysis. With multiple stirring positions, programmable controls, and precise temperature regulation, it provides consistently accurate dissolution rates. Its microprocessor-based system enables tight control of key parameters, making it an essential tool for laboratories requiring high-throughput, repeatable results.
Flexible Design and User-Friendly FeaturesEquipped with a digital LCD display, automatic/manual sample withdrawal, preset programmable timer, and easy-to-clean components, the TDX-Series caters to varied testing needs. The stainless steel and acrylic construction, coupled with a secure vessel made from borosilicate glass, ensures safety, easy maintenance, and resistance to chemicals commonly found in pharmaceutical applications.
FAQs of Tablet Dissolution:
Q: How does the tablet dissolution tester ensure accurate and consistent results?
A: The TDX-Series tester utilizes a microprocessor-controlled water bath to maintain precise temperature (0.2C) and features adjustable stirring speeds (25200 RPM). These controls, alongside programmable settings and user-friendly calibration, ensure each test adheres to strict pharmaceutical standards for accuracy and consistency.
Q: What is the process for conducting a dissolution test using this equipment?
A: To conduct a test, pharmaceutical tablets or capsules are placed into borosilicate glass vessels. The chosen stirring speed and temperature are set via the digital LCD display, and samples can be withdrawn automatically or manually. Data is logged and managed efficiently, thanks to the printer interface and digital timer.
Q: When should calibration and validation be performed on the tester?
A: Calibration and validation should be performed before initial use, after routine maintenance, and at regular scheduled intervals to ensure ongoing accuracy. The user-friendly interface guides operators through quick and efficient calibration, supporting compliance with industry regulations.
Q: Where is this dissolution tester best utilized?
A: This tester is ideally suited for use in pharmaceutical manufacturing facilities, quality control laboratories, and research and development centers. Its robust design and versatile features support a wide range of dissolution testing needs in both small and large operations.
Q: How does the automatic sample withdrawal system work?
A: The automatic withdrawal function allows samples to be collected at programmable intervals without manual intervention, reducing the risk of human error and ensuring uniformity in data collection. Users can also opt for manual withdrawal when required.
Q: What are the key benefits of using the TDX-Series Tablet Dissolution Tester?
A: Key benefits include precise dissolution measurement, high-throughput testing with options for 6, 8, or 12 stations, automated sample handling, easy calibration and cleaning, safety features like audio-visual alarms and safety lock, and a user-friendly digital interface.
Q: What materials are used in the construction of this equipment, and how does this benefit the user?
A: The equipment is constructed from stainless steel (SS-316), acrylic, and borosilicate glass, ensuring durability, chemical resistance, and ease of cleaning. These materials protect both the operator and the integrity of testing samples, offering long-term reliability.