Drug Stability Chamber with Illumination LDST-T2023

Introduction

Drug Stability Chamber with Illumination supports stable operation within a temperature range of 5 to 30℃. Integrated UV sterilization ensures a contamination-free chamber environment. Ensures reliable operation by preventing compressor overcurrent and electrical overload. Features robust stainless-steel chamber offering 1075L internal volume. Ideal for shelf-life evaluation, degradation profile analysis and vaccine testing.

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 ideal for photostability testing, shelf-life evaluation, degradation profile analysis, vaccine testing and other pharmaceutical drug analysis.

Specifications

Volume	1075L
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)	3/15
Light Intensity	0 to 6000 LX (step control)
Power Consumption	4000W
Power Supply	AC 220V±10%, 50HZ
Chamber Size	965mm x 700mm x 1600mm
Exterior Size	1010mm x 900mm x 2340mm

Features

Integrated Data Printer

Optimized Airflow Structure

Double Door Design

Digital Control Interface

Dual Refrigeration System

FAQs

1. What is the primary function of the Drug Stability Chamber with Illumination ?

The Drug Stability Chamber with Illumination is designed to simulate controlled environmental conditions, specifically temperature, humidity, and illumination—for pharmaceutical drug stability testing. It helps evaluate the shelf life, degradation profile, photostability, and humidity tolerance of drugs and vaccines. The chamber complies with guidelines and is ideal for long-term, accelerated, and photostability testing.

2. How does the illumination feature of the Drug Stability Chamber with Illumination benefit pharmaceutical testing?

Drug Stability Chamber with Illumination includes a controllable illumination system (up to 6000 Lux) that enables photostability testing, a critical requirement for drugs sensitive to light exposure. This feature allows pharmaceutical companies to assess light-induced degradation and ensures compliance with Q1B photostability testing standards.

3. What safety features are integrated into the Drug Stability Chamber with Illumination ?

Drug Stability Chamber with Illumination includes several advanced safety mechanisms such as UV sterilization to maintain a contamination-free environment, compressor overcurrent protection, and dual refrigeration systems to prevent operational failures. These features ensure continuous, reliable, and secure testing, even under extended use.

4. What makes the Drug Stability Chamber with Illumination suitable for high-volume pharmaceutical applications?

With a 1075L internal volume and up to 15 adjustable shelves, the Drug Stability Chamber with Illumination is ideal for large-scale stability testing. The spacious stainless-steel chamber accommodates multiple samples efficiently, while the double-door design offers safe, easy access and observation.

5. How is data recorded and monitored during operation in the Drug Stability Chamber with Illumination ?

Drug Stability Chamber with Illumination features a digital control interface for real-time monitoring of temperature and humidity. It is equipped with an integrated data printer that records and prints operational parameters continuously, ensuring traceability and compliance with quality standards.

6. Can the Drug Stability Chamber with Illumination maintain precise environmental conditions?

Yes, Drug Stability Chamber with Illumination maintains a temperature fluctuation of ±0.5 degree Celsius and humidity stability of ±3% RH. Its optimized airflow structure and control system ensure uniform and stable chamber conditions, critical for reproducible testing outcomes.