Customization: | Available |
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After-sales Service: | Online Support, video Technical Support |
Application: | Pharmaceutical Industry |
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The design of the dissolution meter complies with the national pharmacopoeia regulations, and laboratory operations should follow good manufacturing practices (GMP). The dissolution meter and sampler can be applied to different types of samples such as tablets, capsules, semi-solids, transdermal patches, microspheres, implants, etc.
Model | LMDS-2008 |
Instrument performance index | Water bath heating range: room temperature -45. 0 ºC |
Temperature Resolution: 0.1 ºC | |
Temperature control accuracy: ±0.2 ºC | |
Stirring speed range: 10.0-300.0 RPM | |
Speed Resolution: 0.1 RPM | |
Speed Accuracy: ±0.5 RPM | |
Instrument mechanical indicators | Basket (paddle) shaft swing amplitude: ≤0.5mm |
Basket swing range: ≤ 1.0 mm | |
rotating shaft and the dissolution vessel shaft: ≤ ± 1.5mm | |
Dissolution apparatus horizontality: 0.2° | |
Basket (paddle) axis verticality: 90±0.5° | |
Instrument function | Compatible with basket method, paddle method, small cup method, paddle butterfly method, rotating drum method |
Number of dissolution vessels: 6/8 cups | |
Segmented shaft design, no need to manually re-adjust the height of the positioning basket (paddle) when the dissolution method is switched. | |
Automatic simultaneous dosing/sequential dosing | |
Photosensitive lighting: white light/red light three-level lighting | |
Can store 100 experimental methods, and can import and export USB | |
It can store 39 login accounts and passwords, and the operation authority can be controlled in 3 levels | |
With operation record printing and log recording function, and can audit trail | |
input power | 220Vac ± 10% 1300W |
Overall size | 670*565*640mm(W×D×H) |
Total Weight | 65kg |
Operating temperature | (10~30) ºC |
storage temperature | (-20~60) ºC |
Working humidity | (20 ~ 80) % RH |
Storage humidity | (5~95) % RH |
Performance parameters | Single sampling volume: 0.1-15mL (single); 0.2-30mL (double) |
Sampling times: 1-16 times (single); 1-8 times (double) | |
Sampling accuracy: ≤0.8% (10mL sampling) | |
Instrument function | Fully automatic rinsing, filling, dripping, sampling, replenishment, dilution, emptying, cleaning |
Precise sampling by syringe pump, suction and stop time can be set | |
input power | 220Vac ± 10% 200W |
Overall size | 515*660*460mm(W×D×H) |
Total Weight | 53Kg |
Operating temperature | (10~30) ºC |
storage temperature | (-20~60) ºC |
Working humidity | (20~80) % RH |
Storage humidity | (5~95) % RH |
Q1: Can the dissolution tester accommodate different types of samples?
A1: Absolutely, the RC-8 dissolution tester is designed to detect the dissolution velocity and extent from various forms such as tablets and capsules, providing flexibility for different sample types.
Q2: How accurate is the temperature control in the dissolution tester?
A2: The dissolution tester utilizes an MPU for automatic temperature control, ensuring precise and consistent temperature regulation throughout the testing process. This guarantees reliable and reproducible results.
Q3: Is the dissolution tester easy to operate?
A3: Yes, the dissolution tester can be conveniently operated via keystroke, and the measurement results are displayed on the LED screen. Additionally, it offers automation features such as auto-test, auto-diagnose, and auto-alarm, simplifying the testing process.
Q4: Can the dissolution parameters be preset and adjusted according to our specific requirements?
A4: Certainly, parameters such as temperature, rotational speed, and time can be preset at any time to meet the specific testing needs of our customers. This flexibility ensures that the dissolution tester can adapt to various testing protocols.
Q5: How reliable is the alarm system in case of any issues during testing?
A5: The dissolution tester is equipped with a robust alarm system that automatically alerts users in case of any anomalies or faults during testing. Additionally, it features auto-diagnosis functionality to identify and address potential issues promptly, ensuring the reliability of the testing process.