摘要
药品稳定性试验箱作为一种为药品稳定性研究提供温度、湿度、光线照射等环境试验条件的箱体,应用十分广泛。由于连续工作时间较长、单台设备功率较大,导致药品稳定性试验箱在使用过程中消耗的能源较多。本文根据药品稳定性试验条件,确定了能效测试时环境温湿度和箱体内温湿度的典型状态,通过试验数据,得出了制热工况和制冷工况的试验模型,并提出了完整的、切实可行的能效测试方法。
As a kind of chamber which provides temperature, humidity, light and other environmental test conditions for drug stability research, drug stability test chamber is widely used. Due to long continuous working time and large power of single equipment, more energy is consumed in the use of drug stability test chamber. According to the drug stability test conditions, the paper determines the typical state of environmental temperature and humidity and the temperature and humidity in the chamber during the energy efficiency test, obtains the test models of heating and cooling conditions through the test data, and puts forward a complete and feasible energy efficiency test method.
作者
唐力华
Tang Lihua(Guangdong Testing Institute of Product Quality Supervision,Guangzhou 510670)
出处
《仪器仪表标准化与计量》
2021年第2期26-27,30,共3页
Instrument Standardization & Metrology
关键词
药品稳定性试验箱
能效
测试方法
Drug Stability Test Chamber
Energy Efficiency
Test Method