Drug Stability Test Chamber LDST-T2030

Introduction

Drug Stability Test Chamber operates efficiently within a temperature range of 5 to 30℃. Temperature-limiting alarm ensures safe operation by auto-stopping during overheat conditions. Dual refrigeration systems alternate automatically for continuous, failure-free performance. Supports 99 programs, each with 30 segments and extended timing capacity. Applicable to pharmaceutical companies for accelerated test, long-term test high humidity test of drugs.

This test equipment is designed to meet the rigorous requirements of modern laboratory operations, ensuring high precision, reliability, and ease of use for various experimental applications.

Applications

Our Drug Stability Test Chamber is widely used in pharmaceutical companies for accelerated test, long-term test, high humidity test and strong light irradiation test of drugs and new drugs.

Specifications

Chamber Volume	375L
Temperature Range	0 to 60℃
Temperature Fluctuation	±0.5℃
Temperature Uniformity	±2℃
Operating Temperature	5 to 30℃
Humidity Range	30 to 95% RH
Humidity Stability	±3% RH
Timing Range	1 to 99 hours/period
Shelves (Std/Max)	3/10
Power Consumption	2700W
Power Supply	AC 220V±10%, 50HZ
Chamber Size	590mm x 550mm x 1160mm
Exterior Size	780mm x 870mm x 1915mm
Net Weight	680kg
Gross Weight	780kg

Features

Data Logging

Integrated Data Printer

Fan System

UV Sterilization

Leakage Protection System

FAQs

1. What are the core functions of the Drug Stability Test Chamber ?

The Drug Stability Test Chamber is specifically designed to simulate and maintain stable environmental conditions for drug stability testing. It allows precise control over temperature and humidity, supporting various testing protocols such as accelerated stability tests, long-term storage studies, and high-humidity testing. Its robust design, dual refrigeration system, and multi-programmable controller make it ideal for pharmaceutical companies engaged in R&D, quality control, and regulatory compliance testing.

2. How does the dual refrigeration system enhance the Drug Stability Test Chamber performance?

Drug Stability Test Chamber is equipped with a dual refrigeration system that operates on an alternating cycle. This system ensures uninterrupted operation even in the event of a compressor malfunction, reducing downtime and protecting critical samples. It’s particularly beneficial for long-duration tests, where continuous environmental control is essential for obtaining accurate, reliable results.

3. How many programs can be stored, and what is the timing capacity of the Drug Stability Test Chamber ?

Drug Stability Test Chamber supports up to 99 independent user-defined programs, each capable of holding up to 30 segments. Each segment can be customized with specific temperature, humidity, and timing parameters, and the timing range extends up to 99 hours per period. This flexibility allows researchers to conduct complex stability studies across varied environmental conditions, fully compliant with guidelines.

4. What safety features are integrated into the Drug Stability Test Chamber ?

To ensure safe and reliable operation, the Drug Stability Test Chamber includes a temperature-limiting alarm that automatically halts the process if overheating occurs. A leakage protection system is also integrated to prevent electrical hazards. These features are critical in maintaining sample integrity and preventing equipment failure or operational accidents, especially in sensitive pharmaceutical environments.

5. What pharmaceutical tests is the Drug Stability Test Chamber suitable for?

Drug Stability Test Chamber is ideal for a range of stability studies including accelerated testing, long-term storage testing, high-humidity exposure, and strong light irradiation tests. It is used to evaluate the physical, chemical, and microbiological stability of new and existing drug formulations over time. This helps pharmaceutical companies ensure the efficacy and safety of products before market release.