HTLP Basket Type Tablet Disintegration Machine HTLP-074

The HTLP Basket Type Tablet Disintegration Machine HTLP-074 is a crucial instrument used in pharmaceutical quality control laboratories to assess the disintegration time of tablets and capsules. Disintegration testing is essential to ensure that oral dosage forms break down properly in the gastrointestinal tract, allowing for efficient drug absorption.

This machine employs a basket method, where tablets or capsules are placed in individual mesh baskets immersed in a dissolution medium, typically water or a simulated gastric fluid. The baskets are then oscillated up and down at a constant rate, simulating the mechanical forces encountered in the digestive system. The disintegration process is monitored visually, with the operator observing when each tablet or capsule disintegrates, signified by the absence of remaining particles or fragments.

The HTLP-074 disintegration machine is designed for accuracy, reliability, and ease of use. It features precise temperature control to maintain the dissolution medium at the required temperature, ensuring consistency in testing conditions. The oscillation mechanism operates smoothly and consistently, facilitating uniform disintegration testing across multiple samples.

Furthermore, the machine offers adjustable parameters, such as oscillation speed and temperature, allowing users to customize testing conditions according to pharmacopeial standards or specific product requirements. This flexibility ensures compliance with regulatory guidelines and facilitates optimization of testing protocols for different formulations.

The HTLP-074 disintegration machine also incorporates safety features to protect both operators and samples during testing. These may include automatic shut-off mechanisms in case of malfunction or overheating, as well as protective enclosures to prevent accidental contact with moving parts.

Overall, the HTLP Basket Type Tablet Disintegration Machine HTLP-074 plays a crucial role in pharmaceutical quality assurance, enabling manufacturers to evaluate the performance of oral dosage forms accurately. Its precision, reliability, and user-friendly design make it an indispensable tool for ensuring the safety, efficacy, and consistency of pharmaceutical products.