Drug Stability Chamber With Illumination LDST-T2021

Introduction

Drug Stability Chamber with Illumination delivers 475L internal space for efficient sample accommodation. Equipped with UV sterilization to maintain a contamination-free chamber environment. Features tempered glass inner door for visibility and magnetic outer door for sealing. microprocessor ensures accurate temperature and humidity control with stability. Widely used for photostability testing, shelf-life evaluation and degradation profile analysis.

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

Specifications

Volume	475L
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)	3/12
Light Intensity	0 to 6000 LX (step control)
Power Consumption	2900W
Power Supply	AC 220V±10%, 50HZ
Chamber Size	700mm x 550mm x 1250mm
Exterior Size	880mm x 870mm x 1995mm

Features

Over temperature protection

Compressor overload safeguard 

Water shortage alert 

Heater overheats protection 

Audible-visual alarm system

FAQs

1. What is the storage capacity and structural design of the Drug Stability Chamber with Illumination ?

The Drug Stability Chamber with Illumination offers a generous 475-liter internal chamber, designed to accommodate large volumes of test samples efficiently. It includes three standard shelves, expandable up to 12, providing ample space and flexibility for organizing samples. The inner door is made of tempered glass, allowing easy visibility during tests, while the outer magnetic-seal door ensures an airtight, insulated environment. This combination enhances usability, cleanliness, and sample integrity during long-term or light-sensitive testing processes.

2. How does the Drug Stability Chamber with Illumination maintain temperature and humidity stability during testing?

Drug Stability Chamber with Illumination uses a microprocessor control system to deliver precise temperature and humidity regulation. It supports a temperature range of 10 to 60 with light and 4 to 60 without light, with a fluctuation of ±0.5 and uniformity of ±2. The humidity range extends from 30% to 95% RH, with a stability of ±3% RH. These parameters make the ideal for accurate simulation of real-world environmental conditions in pharmaceutical and biotech testing.

3. What are the key applications of the Drug Stability Chamber with Illumination ?

Drug Stability Chamber with Illumination is commonly used in the pharmaceutical and biotechnology industries for critical stability studies. It is ideal for photostability testing, shelf-life evaluation, and degradation profile analysis of drugs and formulations. The chamber’s ability to simulate precise environmental conditions, including controlled light exposure and humidity, allows manufacturers to assess how products behave over time under various storage and transit conditions.

4. How is light intensity managed for photostability testing in the Drug Stability Chamber with Illumination ?

Drug Stability Chamber with Illumination supports step-controlled light intensity from 0 to 6000 LX, enabling users to simulate a range of light exposure conditions for compliance with Q1B photostability guidelines. This feature is essential for determining the light-induced degradation of drugs, packaging, and raw materials. The adjustable light intensity helps tailor testing to specific regulatory or internal protocols for pharmaceutical product validation.

5. What features ensure a contamination-free and safe testing environment?

To maintain sample integrity, the Drug Stability Chamber with Illumination is equipped with UV sterilization, which minimizes the risk of microbial contamination inside the chamber. The anti-corrosive chamber materials extend durability, while the airtight magnetic-seal door enhances environmental control. These features work together to ensure that the internal conditions remain clean and consistent throughout the testing period, protecting both the product and the data.