Gupta Vishnu D
Pharmaceutics Division, University of Houston, Houston, TX.
Int J Pharm Compd. 2002 Sep-Oct;6(5):395-7.
The chemical stability of dexamethasone sodium phosphate (1mg/mL and 0.1 mg/mL) in 0.9% sodium chloride injection was studied at 25 deg C in polypropylene syringes by means of a stability-indicating high-performance liquid chromatographic assay method. The concentrations of the drug were directly related to peak heights, and the percent relative standard deviation based on 5 injections was 1.5. The benzyl alcohol did not interfere with the assay procedure at 278 nm. The products of decomposition separated from the intact drug. At a concentration of 1mg/mL, the loss in potency was 1% after 22 days of storage and less than 3% at a concentration of 0.1mg/mL after storage for 22 days. The pH value of the injection (1mg/mL) decreased from 7.3 to 7.2 after 22 days of storage and from 6.5 to 6.3 in the 0.1-mg/mL sample. The physical appearance of the injection did not change.
采用稳定性指示高效液相色谱分析法,在25℃下于聚丙烯注射器中研究了地塞米松磷酸钠(1mg/mL和0.1mg/mL)在0.9%氯化钠注射液中的化学稳定性。药物浓度与峰高直接相关,基于5次进样的相对标准偏差百分比为1.5。苯甲醇在278nm处不干扰测定过程。分解产物与完整药物分离。浓度为1mg/mL时,储存22天后效价损失1%,浓度为0.1mg/mL时储存22天后效价损失小于3%。注射液(1mg/mL)储存22天后pH值从7.3降至7.2,0.1mg/mL样品的pH值从6.5降至6.3。注射液的外观未发生变化。