Overview

Drug Dissolution Tester LMDDT-B100 accommodates 6 high-quality vessels for reliable testing of tablet and capsule dissolution. Equipped with HD touch screen and intuitive interface, enabling seamless performance control. Incorporates access control, audit trail, data system, plus USB export for simplified monitoring. Integrates rapid heating, energy-efficient design, along automated fault detection and temperature protection. Our Tester is ideal for pharmaceutical labs, research institutes, and quality control departments seeking efficient drug release evaluation.

Features :

Bidirectional rotation

Self-diagnosis system

Real-time temperature control

Energy-efficient design

Specifications :

Vessel Number	6 pieces
Stirring Paddle Swing Amplitude	Greater than or equal to 0.5 mm
Basket Swing Range	Greater than or equal to 1mm
Deviation Between Rotating Rod And Vessel Axis	Greater than or equal to 2mm
Speed Setting Range	10 to 300 rpm
Rotation Direction	Clockwise/Counterclockwise
Steady Speed Error	Greater than or equal to 1 rpm/min
Temperature Range	Room Temperature to 45°C
Temperature Resolution	0.1°C
Temperature Control Accuracy	Greater than or equal to 0.3°C
Sampling Points	Greater than or equal to 100 pieces
Sampling Countdown Time	Greater than or equal to 999 hours 59 minutes 59 seconds
Number Of Paddles And Baskets	6 pieces for each
Dissolution Cup Height	185mm
Dissolution Cup Volume	1000ml
Power Supply	AC220V±10%, 50Hz
Dimensions	58× 54× 54 cm³
Weight	46 kg

Applications :

Drug Dissolution Tester LMDDT-B100 is designed for pharmaceutical labs, quality control, and regulatory testing, ensuring consistent drug release analysis.

Selection Guide :

Drug Dissolution Tester LMDDT-B100 is a reliable instrument designed for pharmaceutical research, quality control, and formulation development. With six vessels, it is suitable for routine testing and method validation. Its technical features, such as a stirring paddle swing amplitude of ≥0.5 mm, basket swing range of ≥1 mm, and deviation between the rotating rod and vessel axis of ≥2 mm, ensure uniform mixing and accurate dissolution results. This model is widely used in studies involving drug release profiles, bioequivalence testing, and formulation stability. Compliant with pharmacopeial standards like USP and EP, it is suitable for customers seeking precision, consistency, and regulatory compliance in drug dissolution experiments.