Dissolution Tester
Standard
- Chinese Pharmacopoeia (2005/2015 Editions): Ensuring compliance with national regulations for pharmaceutical quality control.
- USP (United States Pharmacopoeia): Meeting global benchmarks for dissolution testing in the pharmaceutical industry.
- JJG56-2005 Verification Regulation: Aligning with China’s metrological standards for precision and accuracy.
Product Advantages
- Precision Engineering:
- Speed Control: Adjustable range of 25–250 RPM with ±1% accuracy, ensuring consistent agitation for diverse formulations.
- Temperature Stability: Controlled range of 5.0–45.0°C with ±0.3°C precision, mimicking physiological conditions for accurate in vitro simulations.
- Advanced Automation:
- Pre-set Parameters: Store and recall test protocols (speed, temperature, timing) for repeatability.
- Real-Time Monitoring: LED/LCD displays show preset and actual values simultaneously, with automatic alerts for deviations.
- Durability & Compliance:
- Stainless Steel Components: Baskets, paddles, and vessels made of SUS316L stainless steel resist corrosion and meet pharmacopoeia specifications.
- Multi-Standard Compliance: Suitable for USP, EP, JP, and FDA guidelines, streamlining global product registrations.
- User-Centric Design:
- Ergonomic Interface: Intuitive controls with multi-language support (English/Chinese) for global usability.
- Low Maintenance: Self-diagnostic functions and modular design minimize downtime.
Product Features
- Dual Testing Modes:
- Basket Method: For capsules and granules, with ≤±1mm radial run-out.
- Paddle Method: For tablets, with ≤±0.5mm radial run-out.
- Expanded Capacity:
- 8 vessels/shafts with optional 12-vessel configurations for high-throughput testing.
- Additional vessels for reference standards or sequential testing.
- Smart Temperature Control:
- Embedded digital sensors and software calibration ensure rapid heating and minimal deviation.
- Safety & Protection:
- Over-temperature/speed alarms, automatic shutoff, and fault code display for safe operation.
- Data Integrity:
- USB storage and optional printers for GMP-compliant record-keeping.
Technical Parameters
| Parameter | Specification |
|---|---|
| Speed Range | 25–250 RPM |
| Speed Accuracy | ±1% (25–50 RPM), ±2% (51–250 RPM) |
| Temperature Range | 5.0–45.0°C (Adjustable) |
| Temperature Accuracy | ±0.3°C |
| Vessel Capacity | 1000 mL (6–12 vessels) |
| Timer | 99h59m max, 9–12 programmable intervals |
| Power Supply | AC 220V±10%, 50/60Hz, 1350W |
| Operating Environment | 5–37°C, ≤80% RH |
| Dimensions (W×D×H) | 680×540×480 mm |
| Weight | 75 kg |
Why Choose Our Dissolution Tester?
- Global Compliance: Simplify regulatory approvals with multi-pharmacopoeia alignment.
- Cost Efficiency: Reduce testing cycles by 30% with automated workflows.
- Scalability: Modular design accommodates future upgrades (e.g., automated sampling).
- 24/7 Support: Worldwide service network for installation, training, and maintenance.
Ideal Applications:
- Pharmaceutical R&D (tablets, capsules, pellets)
- Quality control labs (drug release profiling)
- Academic institutions (biopharmaceutical studies)
Contact Us for customized quotations, live demos, or free catalogs. Elevate your dissolution testing with precision, compliance, and reliability.
[Standard Group] – Partnering in Global Health Innovation.