RT710 USP Apparatus 4 Flow-through Dissolution System
The RT806 is structured as a small-sized Vertical Franz Diffusion Cell system that includes heating functionalities with a built-in stirrer module. The device comes with a portable layout that makes it easy to place in any location for convenient operation. The system delivers detailed temperature and speed management needed for reliable transdermal testing. The system meets the performance requirements outlined in USP<1724> for the simulation of in vitro release and permeation procedures. Bubbles are prevented through the filling point design which results in dependable experimental outcomes.
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Download Sheet
- Velocity Range: 1~40mL/min
- Sampling Volume Error: ≤± 2% (closed-loop mode), ≤± 5% (open-loop mode)
- Pump Type: syringe pump
- Number of Channels: 7
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description
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The design and performance of RT7 Flow-Through Cell Dissolution System meet the requirements of the sixth method for determination of dissolution and release in Chinese Pharmacopoeia 2020,USP dissolution apparatus 4 and European Pharmacopoeia dissolution apparatus 4.A single RT7 Flow-Through Cell Dissolution System can simply switch between closed-loop method and open-loop method without replacing the automatic sampling work station, so as to meet the needs of various samples corresponding to different flow-through cell methods.
Features
Dual Flow Rates
7-channel flow cell apparatus that supports testing with 2 flow rates simultaneously.
Integrated Heating
Integrated Water Bath Heating &Stirring Device can meet the experimental requirements of 7 sample medium vessels+1 replenishment medium vessel.
Real-Time Monitoring
7 independent temperature sensors, real-time monitoring of the temperature within each channel.
Pharmacopoeia Compliance
Each of the pharmacopoeia-accepted flow-through cell is available.
Teflon pipe
Teflon pipe with high chemical stability and high adsorption resistance is adopted.Effectively avoid adsorption and residue.
Multifunctional sample holder design
The sample holders suitable for70 ml sample vessel,10 mltesttube and liquid phase vial.
High precision syringe pump application
Utilizing high-precision syringe pumps. Each channel is equipped within dependent over pressure protection and liquid leakage inspection device.
Efficient filtration
Patented multiple filtration device, effectively reducing the back pressure of filtration.
Multi-mode sampling system
The closed-loop and open-loop sampling can be realized in one machine.
Filtration membrane diversity
Can provide filter membranes of different materials and pore sizes.
Cloud technology support
Supports comprehensive dissolution data management through cloud-based systems (automatic backup, automatic synchronization).
Application
Widely used in pharmaceutical research and quality control, drug dissolution testing plays a crucial role in evaluating drug release profiles and ensuring batch consistency. Ideal for applications in R&D labs, manufacturing processes, and regulatory compliance testing.
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Injection
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Ophthalmic preparation
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Soft Capsules
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Powder
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Oral Preparations
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Topical preparations
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Enteric-coated tablets
Specifications
Product Brochure
Flow-Through Cell Dissolution Apparatus
| Length ×Width× Height: ~ 80 cm × 62 cm ×60 cm | Length ×Width× Height: ~ 80 cm × 62 cm ×60 cm |
| Number of channels: 7 | Number of channels: 7 |
| Temperature resolution: 0.1 ℃ | Temperature resolution: 0.1 ℃ |
Medium Conveying Workstation
| Length ×Width× Height: ~ 98cm × 63 cm ×55 cm | Length ×Width× Height: ~ 98cm × 63 cm ×55 cm |
| Stirring speed error: ≤± 10% | Stirring speed error: ≤± 10% |
| Velocity resolution: 0.1mL/min | Velocity resolution: 0.1mL/min |
| Temperature probe error: ≤± 0.5 ℃ | Temperature probe error: ≤± 0.5 ℃ |
Automatic Sampling Workstation
| Length ×Width× Height: ~75cm × 63 cm ×56 cm | Length ×Width× Height: ~75cm × 63 cm ×56 cm |
| Test tube type: 70 ml sample bottle, 10 ml test tube, liquid phase vial | Test tube type: 70 ml sample bottle, 10 ml test tube, liquid phase vial |
| Sampling volume error: ≤± 2% (closed-loop mode), ≤± 5% (open-loop mode ) | Sampling volume error: ≤± 2% (closed-loop mode), ≤± 5% (open-loop mode ) |
Operating System
| *Meet the requirements of FDA21 CFR Part 11 |
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