About ConXport Tablet Dissolution Test Apparatus
ProductDescription
With avision to be a pioneer in our domain and establish ourselves as a brand, we areengaged in manufacturing and supplying excellent quality Table Dissolution Test Apparatus. Itconsists of 6 stages water bath with 2kvv heater covered with 1000 ml vesselmade from borosilicate glass. The temperature of the both is maintained at 37cwith an accuracy of 1c a cylindrical glass vessel of 1000 ml capacitywith slightly concave bottom has a flanged edge at the top. Table Dissolution Test Apparatus isduly checked on well defined quality parameters prior to dispatch.
Features:
Long lastingmaintenance free life
Rugged and sturdyconstruction
Reliable Dissolution TestingThis apparatus offers laboratory professionals dependable results with its microprocessor-based temperature bath and precisely controlled stirring mechanism. Designed for accuracy, the system ensures compliance with USP, IP, and BP pharmacopoeia standards, making it ideal for pharmaceutical quality control and research purposes.
User-Friendly and Efficient OperationUsing the ConXport device is straightforward thanks to its digital step-less control, programmable timer (up to 99 hours, 59 minutes), and LCD display. The robust construction, manual sampling system, and included paddles and baskets make it adaptable for a variety of dissolution analysis scenarios.
Advanced Safety and ConstructionThe apparatus features over-temperature protection and is built from high-quality stainless steel and borosilicate glass, offering durability and resistance to corrosion. Its rectangular design and integrated control panel facilitate easy handling and maintenance in any lab setting.
FAQs of ConXport Tablet Dissolution Test Apparatus:
Q: How do I operate the ConXport Tablet Dissolution Test Apparatus for tablet testing?
A: To operate the apparatus, fill the borosilicate glass vessels with the dissolution medium, load your tablet or capsule, select the appropriate paddle or basket, and set the required temperature and RPM via the digital controls. Start the test and use the manual sampling feature as needed. Detailed instructions are provided in the operational manual.
Q: What makes this apparatus suitable for pharmaceutical and academic laboratories?
A: The devices semi-automatic functions, precision controls, and conformity with USP, IP, and BP standards ensure credible analytical results. Its also durable, easy to use, and versatile, making it highly suitable for quality control, research, and teaching purposes in various lab environments.
Q: When should the programmable timer be used during dissolution analysis?
A: The programmable timer should be set at the start of the test to automate run duration, up to 99 hours and 59 minutes. This helps maintain consistency and reliability in time-sensitive dissolution tests, crucial for both QC and R&D workflows.
Q: Where can I find user support or technical assistance for this apparatus?
A: Full user support, including operational guidance and technical assistance, is available through the supplier, manufacturer, or exporter. Additionally, the operational manual included with the unit provides setup, maintenance, and troubleshooting information.
Q: What safety features are integrated into the ConXport Dissolution Test Apparatus?
A: The unit is equipped with over-temperature protection, ensuring that the bath heater will automatically disengage if the set temperature is exceeded, thereby preventing sample degradation or equipment damage.
Q: How does the apparatus maintain accuracy in RPM and temperature during testing?
A: The microprocessor-controlled bath and PT-100 sensor deliver temperature accuracy within 0.2C, while the digital speed control provides stirrer speed accuracy within 1 RPM. These features ensure reliable and reproducible test conditions.
Q: What are the key benefits of using this dissolution test apparatus in routine analysis?
A: Key benefits include easy digital operation, corrosion-resistant construction, accurate control of dissolution parameters, compliance with international standards, and adaptability for both routine quality control and research applications.