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Diosna MiniLab XP Laboratory High-Efficiency Tablet Coater

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Brand Diosna
Origin Germany
Model MiniLab XP
Batch Capacity 50–1,000 g (expandable to 3 kg)
Inlet Air Temperature Range Up to 100 °C (digital display)
Temperature Monitoring Inlet & outlet air
Spray System Dual-fluid high-pressure nozzle with adjustable atomization and fan-air pressure
Power Supply 380 V / 50 Hz, 7.5 kW
Dimensions (W×D×H) 1290 × 890 × 1100 mm
Weight 200 kg
Construction 316L stainless steel contact parts, 304 stainless steel non-contact structural components
Control System Siemens PLC with HMI touchscreen interface
Compliance Designed to support GMP, ISO 9001, and FDA 21 CFR Part 11–ready data integrity workflows

Overview

The Diosna MiniLab XP Laboratory High-Efficiency Tablet Coater is a precision-engineered, benchtop-scale coating system designed for pharmaceutical and nutraceutical R&D laboratories requiring full process scalability, reproducible film formation, and strict adherence to regulatory design principles. Based on Diosna’s proven fluidized-bed and pan-coating architecture, the MiniLab XP operates on the bottom-spray Wurster principle—optimized for uniform suspension, controlled droplet deposition, and rapid solvent evaporation under negative-pressure airflow. Thermal energy is introduced tangentially at the upper right quadrant of the coating drum and exhausted from the lower left, establishing a consistent, laminar thermal gradient across the tablet bed. This configuration ensures homogeneous heat transfer, minimizes thermal stress on thermolabile actives, and supports robust film integrity for aqueous, organic, enteric, sustained-release, and taste-masking formulations. The system is not a scaled-down production unit but a purpose-built development platform engineered for method transfer to Diosna’s PilotLab and production-scale systems (e.g., P10, P30), enabling seamless progression from formulation screening to clinical batch manufacturing.

Key Features

  • Modular drum design with quick-release mounting system—enables tool-free interchange of coating pans (standard 1 L, optional 3 L) in under 90 seconds without recalibration.
  • Dual-fluid spray nozzle with independent pressure regulation for atomizing air and shaping air—permits precise control over droplet size distribution (Sauter mean diameter adjustable between 30–120 µm) and spray pattern geometry.
  • Integrated temperature monitoring at both inlet and exhaust ducts, with PID-controlled heating and real-time thermal profiling—ensures compliance with ICH Q5C stability requirements during process development.
  • Full-view borosilicate glass viewport with anti-fog heating element—provides unobstructed visual assessment of tablet motion, film uniformity, and agglomeration behavior without interrupting operation.
  • Siemens SIMATIC S7-1200 PLC with 10.1″ capacitive touchscreen HMI—supports recipe management, parameter logging, alarm history, and audit-trail-enabled user access levels per ALCOA+ principles.
  • GMP-compliant construction: All product-contact surfaces fabricated from electropolished ASTM A276 Type 316L stainless steel (Ra ≤ 0.4 µm); non-contact frame from 304 stainless steel; IP54-rated enclosure for laboratory environments.

Sample Compatibility & Compliance

The MiniLab XP accommodates tablets (round, oval, biconvex), pellets, granules, and mini-tablets ranging from 2 mm to 12 mm in diameter. It supports all major coating excipients—including hydroxypropyl methylcellulose (HPMC), ethylcellulose, Eudragit® series (L100, S100, RL/RS), shellac, and polyvinyl alcohol—under both aqueous and organic solvent systems. Process validation documentation aligns with ASTM E2500-22 (Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems) and supports qualification protocols per EU Annex 15 and USP . Data integrity features include electronic signatures, time-stamped event logs, and exportable CSV/Excel reports compatible with LIMS integration. The system meets mechanical safety standards per EN 61000-6-2/6-4 and is CE-marked for use in Class D cleanrooms when installed with appropriate HVAC interfaces.

Software & Data Management

The embedded control software provides real-time visualization of critical process parameters—including drum rotation speed (0.5–20 rpm), inlet/exhaust temperature (±0.3 °C accuracy), spray rate (0.5–15 g/min, gravimetrically verified), and relative humidity (optional sensor). All parameters are logged at 1-second intervals and stored with cryptographic hash integrity. Export functions support raw .csv, PDF summary reports, and XML-formatted data packages compliant with FDA 21 CFR Part 11 Annex 11 requirements. Optional OPC UA server enables bidirectional communication with MES platforms (e.g., Siemens Opcenter, Werum PAS-X) for centralized batch record compilation and deviation tracking.

Applications

  • Early-phase formulation screening for immediate-release, delayed-release, and extended-release solid oral dosage forms.
  • Process parameter optimization (e.g., spray rate vs. inlet temperature vs. drum speed) using Design of Experiments (DoE) frameworks.
  • Stability-indicating coating studies under accelerated conditions (40 °C/75% RH) per ICH Q1A(R2).
  • Excipient compatibility testing with APIs prone to hydrolysis or oxidation during film application.
  • GMP-compliant clinical trial material (CTM) manufacturing up to Phase IIb scale.
  • Training platform for operator qualification in cGMP coating operations.

FAQ

What is the minimum batch size supported for reliable coating uniformity?
The validated lower limit is 50 g of tablets (≥6 mm diameter) with coefficient of variation (CV) for weight gain ≤3.5% across three replicate runs.
Can the MiniLab XP be integrated into an existing facility’s SCADA system?
Yes—via standard Ethernet/IP or Modbus TCP protocols; optional Siemens S7-PLCSIM Advanced license enables virtual commissioning prior to physical installation.
Is cleaning validation support provided?
Diosna supplies a comprehensive CIP/SIP protocol package including swab recovery studies, rinse water analysis templates, and residue acceptance criteria aligned with EMA CHMP/Q5C guidance.
Does the system support nitrogen inerting for oxygen-sensitive formulations?
An optional nitrogen purge module (with O₂ sensor feedback loop and automatic flow modulation) is available as a factory-installed add-on.
What documentation is included for regulatory submissions?
IQ/OQ/PQ protocols, FAT/SAT reports, material traceability dossiers, and 21 CFR Part 11 compliance evidence are delivered with each system.

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