Overview

Drug Dissolution Tester LMDDT-B101 supports up to 8 vessels for simultaneous multiple drug sample testing. Equipped with advanced circuit design for reliable measurement and control. Integrated synchronous water circulation system enhances temperature stability and simplifies maintenance. Incorporated real-time control ensures fast heating, minimal drift, and over-temperature protection. Our Tester is extensively applied in pharmaceutical manufacturing, research, and quality control for dependable analysis of drug formulations. 

Features :

Easy Data Export

Energy-Efficient

Customizable Settings

Quick Setup

Specifications :

Number Of Vessels	8
Number Of Paddles/Baskets	8
Vessel Height	185 mm
Paddle Swing Amplitude	Greater than or equal to 0.5 mm
Basket Swing Range	Greater than or equal to 1 mm
Speed Range	10 to 300 RPM
Speed Accuracy	Greater than or equal to 1 RPM
Temperature Range	Room Temp to 45°C
Temperature Resolution	0.1°C
Temperature Accuracy	Greater than or equal to 0.3°C
Sampling Times	Greater than or equal to 100 times
Countdown Timer	Greater than or equal to 999 hours 59 minutes 59 seconds
Display	High-definition touchscreen
Water Circulation	Integrated synchronous system
Temperature Control	Real-time with over-temperature protection
Data Management	USB data export, audit trail, user access rights
Power Supply	AC 220V ±10%, 50Hz
Dimensions	66 × 55 × 57 cm³
Weight	62 kg

Applications :

Drug Dissolution Tester LMDDT-B101 is designed for testing tablets and capsules, supporting pharma R&D, manufacturing, and QC to ensure consistent drug release and meet regulatory standards.

Selection Guide :

Drug Dissolution Tester LMDDT-B101 is designed to meet the precision requirements of pharmaceutical research, quality control, and dissolution studies. With 8 vessels and 8 paddles or baskets, it provides flexibility for testing multiple samples simultaneously, making it suitable for laboratories conducting medium to high throughput dissolution experiments. The vessel height of 185 mm ensures adequate sample volume for various dosage forms, including tablets and capsules. A paddle swing amplitude of ≥ 0.5 mm confirms mechanical precision in line with pharmacopoeia standards (USP, IP, or BP), ensuring consistent and reproducible results. Customers seeking a reliable instrument for formulation development, bioequivalence studies, or batch release testing will find this model suitable. Its specifications support compliance with regulatory certifications, making it a strong candidate for both academic research and industrial pharmaceutical labs.