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Labmate Rotational Cylinder Dissolution Tester LMRDT A102

Labmate Rotational Cylinder Dissolution Tester LMRDT A102

Discover unparalleled precision with the Labmate Rotational Cylinder Dissolution Tester LMRDT A102, now available through winselluma. As an authorized distributor, winselluma ensures unmatched quality and customer support for all your laboratory needs. This advanced tester offers dependable performance for accurate dissolution testing, making it an invaluable asset for any pharmaceutical lab. Experience reliable, consistent results and enhance your research capabilities with the LMRDT A102 from Labmate. Trust winselluma to provide the best in laboratory equipment and service excellence.
  • Product Info

    Labmate Rotational Cylinder Dissolution Tester LMRDT A102

    Product Overview

    The Labmate LMRDT A102 is a high‑throughput dissolution tester designed for pharmaceutical laboratories. Featuring a six‑vessel rotational configuration, it allows simultaneous testing of multiple samples with precise agitation and thermal control, ensuring reproducible drug release profiling for tablets, capsules, and other solid dosage forms.

    Key Features

    • Six‑Vessel Rotational Design: Six dissolution vessels and poles arranged in a single horizontal row for efficient batch testing.

    • Wide Speed Range: Adjustable agitation speed between 20 – 200 rpm for accurate dissolution conditions.

    • Microprocessor Control: Digital system manages temperature, rotation speed, and timing with an intuitive LED interface.

    • Magnetic Pump Heating System: Provides uniform water bath temperature for stable and reproducible results.

    • Manual Head Rotation: Simplifies setup and vessel handling.

    • Automation Functions: Includes auto‑set, auto‑diagnosis, and alarm features for safety and efficiency.

    • Corrosion‑Resistant Components: Stainless steel paddles and baskets ensure durability and low maintenance.

    Technical Specifications

    Specification Detail
    Number of Vessels 6
    Number of Poles 6
    Configuration Single horizontal row
    Speed Range 20 – 200 rpm
    Speed Accuracy ±2 rpm
    Temperature Range Room temperature – 45 °C
    Temperature Stability ±0.3 °C
    Timer Range 1 – 999 minutes
    Preset Timing Points 9
    Time Accuracy ±0.1 minute
    Paddle Radial Run‑Out ±0.5 mm
    Basket Radial Run‑Out ±1.0 mm
    Heating System Magnetic pump‑driven circulating water
    Control System Microprocessor
    Display Type LED
    Power Consumption 1200 W
    Power Supply 110 V / 220 V (50/60 Hz)
    Dimensions (W×D×H) 960 × 320 × 480 mm
    Net Weight ~45 kg

    Standard Accessories

    • Six stainless steel dissolution vessels

    • Six paddle assemblies

    • Six basket assemblies

    • LED control panel

    • Water bath and circulation system

    • Safety alarm and automation control functions

    Optional Accessories

    • Replacement paddle and basket units for specific dosage forms

    • Calibration weights or verification certificates

    • Alternative vessel support configurations

    Applications

    The LMRDT A102 is ideal for pharmaceutical and analytical laboratories performing dissolution tests on solid oral dosage forms, including:

    • Tablets

    • Capsules

    • Pellets

    • Other solid formulations

    It is particularly suitable for:

    • Formulation development and comparative studies

    • Quality control and batch release testing

    • Regulatory compliance and method validation

    • High‑volume research workflows requiring parallel sample testing

    Selection Guide

    Choose the LMRDT A102 when your laboratory requires:

    • High throughput testing with six simultaneous samples

    • Accurate and reproducible control of speed, temperature, and timing

    • Uniform heating for consistent dissolution results

    • Automated features and alarms for efficiency and safety

    • Durable, corrosion‑resistant components for long-term reliability

    This model is ideal for labs that need consistent, parallel dissolution analysis in formulation development and quality control environments.

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