Pharmaceutical laboratories frequently face the challenge of inconsistent drug release profiles, cross-contamination risks, and tedious manual sampling during active pharmaceutical ingredient evaluations. These workflow bottlenecks drastically delay critical batch releases and compromise strict pharmacopeia compliance. Implementing an advanced automated Tablet Dissolution Tester laboratory platform directly resolves these analytical hurdles by combining high-precision robotic sampling with an exceptionally stable thermodynamic water bath environment.

Technical Specifications

• Model Number: MSMDS2014DSSWISS

• Product Part Number: 2014DS-SWISS

• Dissolution Vessel Capacity: 14 independent vessels available in 1000 mL or 250 mL specifications

• Water Bath Heating Range: Room temperature to 45.0 °C

• Temperature Control Accuracy: ± 0.2 °C utilizing advanced PID and fuzzy logic control

• Stirring Speed Range: 25.0 to 250.0 RPM

• Rotational Speed Accuracy: ± 0.5 RPM ensuring strict mechanical repetition

• Temperature Monitoring: 8 independent temperature probes for real-time solvent tracking

• Sampling Volume Range: 0.2 to 15 mL for single and 0.4 to 30 mL for double operations

• Sampling Accuracy: Less than or equal to 0.8 percent for a 10 mL sample volume

• User Interface: 10 inch high resolution color touch screen

• Data Management: Internal storage for up to 100 experimental methods with global audit trail

• Main Unit Power Requirements: AC 220V ± 10 percent consuming 1300W

• Main Unit Dimensions: 670 by 565 by 640 millimeters weighing 65 kilograms

• Sampler Dimensions: 515 by 660 by 460 millimeters weighing 35 kilograms

Key Benefits and Solving Lab Challenges

Quality assurance technicians often lose critical time executing manual solvent sampling or navigating complex equipment interfaces that lack proper security protocols. This system completely eliminates these operational pain points. By utilizing a high precision Tablet Dissolution Tester sampling mechanism, operators can leverage a fully automated syringe pump that flawlessly handles rinsing, filling, dispensing, and exact dilution without human intervention. This guarantees drastically faster, highly accurate measurements while minimizing the risk of accidental cross-contamination through a one-click automatic pipeline cleaning protocol.

Regulatory compliance and data integrity are major vulnerabilities for any facility aiming to meet strict international standards. This instrument actively prevents compliance failures through a comprehensive three-level administrative access control system that strictly satisfies global audit trail requirements. The comprehensive capabilities of the device allow users to safely track every action, completely securing the testing history from unauthorized modifications.

Core Operational Features

Every unit is engineered to maximize testing throughput, improve data accuracy, and minimize the need for constant manual observation during extended drug release cycles.

• Intelligent Automated Dosing: Prevents sticky pharmaceutical formulations from adhering to the vessel walls, allowing for perfectly synchronized simultaneous or sequential capsule drops.

• Advanced Photosensitive Environment: Integrates specialized low actinic red vessels and a dedicated lighting system, acting as a secure Tablet Dissolution Tester for photosensitive substances to prevent sample degradation during analysis.

• Seamless Hardware Maintenance: Features a highly durable segmented 316L stainless steel propeller shaft that allows for immediate replacement without requiring full system disassembly.

• Integrated Thermal Printing: A built-in printer immediately generates real-time experimental data and operation logs, ensuring physical traceability is effortlessly maintained on the laboratory floor.

Upgrade Your Quality Control Workflow

Modern pharmaceutical manufacturing demands instruments that deliver uncompromising accuracy, rapid sample processing, and absolute regulatory compliance. Integrating a top-tier Tablet Dissolution Tester into your standard quality control regimen ensures your facility remains highly efficient and your final dosage forms are perfectly safe for consumer use. Invest in state-of-the-art dissolution analysis technology today to streamline your complex evaluation protocols, eliminate costly operational downtime, and achieve absolute confidence in every single drug release profile.