Drug Stability Chamber With Illumination LDST-T2020

Introduction

Drug Stability Chamber with Illumination supports stable operation within a temperature range of 5 to 30℃. Dual refrigeration systems alternate automatically for continuous, failure-free performance. Internal humidity sensor with external water tank ensures minimal deviation. Digital temperature and humidity display with high-precision multi-segment control. Ideally used for high humidity test and strong light irradiation 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 Chamber with Illumination , is ideally used in pharmaceutical companies to carry out humidity tolerance testing of tablets, vaccine testing, high humidity test and strong light irradiation test of drugs.

Specifications

Volume	375L
Temperature Range	10 to 60℃ with light
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
Light Intensity	0 to 6000 LX (step control)
Power Consumption	2700W
Power Supply	AC 220V±10%, 50HZ
Chamber Size	590mm x 550mm x 1160mm
Exterior Size	780mm x 870mm x 1915mm

Features

UV sterilization

temperature control

Anti-corrosive chamber

Optimized air duct design

Adjustable shelves 

FAQs

1. What temperature range does the Drug Stability Chamber with Illumination support for stability testing?

Drug Stability Chamber with Illumination offers flexible temperature control to accommodate various stability testing needs. It operates within a temperature range of 10 to 60°C with illumination and 4 to 60°C without illumination, ensuring suitability for both standard and photostability testing. The chamber maintains a consistent temperature fluctuation of ±0.5°C and uniformity of ±2°C, ideal for precise testing conditions. The system supports a working ambient temperature of 5 to 30°C, making it reliable in controlled lab environments. These features enable the chamber to comply with international pharmaceutical testing standards, such as guidelines.

2. How does the Drug Stability Chamber with Illumination ensure accurate humidity control during testing?

To maintain consistent humidity conditions, the Drug Stability Chamber with Illumination features a high-precision -controlled humidity system. It includes an internal humidity sensor paired with an external water tank to reduce humidity deviations and prevent fluctuations during long-term tests. The chamber supports a humidity range of 30% to 95% RH, with a stability of ±3% RH, making it ideal for humidity tolerance testing of tablets, vaccines, and other pharmaceutical products. The system ensures controlled moisture exposure, which is critical for evaluating product shelf-life and degradation under varying environmental conditions.

3. What makes the Drug Stability Chamber with Illumination suitable for photostability testing of drugs?

Drug Stability Chamber with Illumination is specially designed for photostability and strong light irradiation testing. It offers a controllable light intensity ranging from 0 to 6000 LX through step adjustment. This allows users to simulate various lighting conditions and assess light-induced degradation of pharmaceutical formulations, packaging, and raw materials. The chamber complies with Q1B guidelines for photostability testing. Its UV sterilization feature further ensures that light-sensitive tests are conducted in a sterile and contamination-free environment, improving the reliability of photostability test results.

4. What key features contribute to the chamber’s reliable and contamination-free operation?

Drug Stability Chamber with Illumination integrates several advanced features that enhance performance and operational safety. UV sterilization eliminates microbial contamination, while the anti-corrosive inner chamber extends the equipment’s service life. An optimized air duct design ensures uniform airflow and stable conditions throughout the chamber. Adjustable shelves provide flexible sample placement for various testing volumes. Additionally, the chamber includes a digital display for real-time temperature and humidity monitoring, along with multi-segment programmable control for tailored testing cycles. These features make it suitable for routine pharmaceutical testing and regulatory validation.

5. What are the typical applications of the Drug Stability Chamber ?

Drug Stability Chamber with Illumination is widely used in pharmaceutical laboratories, R&D centers, and quality control departments. It is ideal for performing humidity tolerance tests, vaccine stability evaluations, strong light irradiation testing, and accelerated aging studies of drug products. The chamber supports compliance with global regulatory standards by simulating real-world environmental conditions under controlled laboratory settings. It is also suitable for packaging stability tests and photodegradation analysis of light-sensitive substances, making it a versatile tool in pharmaceutical product development and approval processes.

6. How does the dual refrigeration system enhance operational efficiency of the Drug Stability Chamber with Illumination ?

Drug Stability Chamber with Illumination comes with a dual refrigeration system that operates in an alternating sequence to ensure uninterrupted performance. This setup helps to maintain a stable internal environment, even during long-duration tests, by reducing the workload on each compressor and enhancing cooling efficiency. In case one system requires maintenance or downtime, the other continues to function, ensuring that critical stability studies are not interrupted. This redundancy is especially important in regulated environments where equipment reliability and data integrity are essential.