Wagenknecht D M, Baaske D M, Alam A S, Carter J E, Shah J
Am J Hosp Pharm. 1984 Sep;41(9):1807-11.
The stability of nitroglycerin in concentrations of 200 and 400 micrograms/ml in eight common intravenous solutions was studied. Two containers of each solution at each concentration, one glass and one polyolefin, were stored under each of the following conditions: intense light (1400-2000 foot-candles) and ambient room temperature (18-27 degrees C), normal light and ambient room temperature, dark and 40 degrees C, and dark and 5 degrees C. All samples were tested at 0 and 24 hours. Room temperature and refrigerated samples were also tested at 48 hours, 7 days, and 1 month. Testing included measurement for optical density at 400 and 600 nm, pH, and nitroglycerin content as determined by HPLC. The admixtures remained clear and colorless, and no appreciable changes in pH were observed. HPLC assays showed no significant changes in nitroglycerin concentrations. There were no differences in the stability of the admixtures stored in the glass and polyolefin containers. Nitroglycerin is compatible with each of the common intravenous solutions tested under the storage conditions and in the containers used for this study.
研究了硝酸甘油在八种常见静脉输液中浓度为200和400微克/毫升时的稳定性。每种浓度的每种溶液各有两个容器,一个玻璃容器和一个聚烯烃容器,分别在以下条件下储存:强光(1400 - 2000英尺烛光)和室温(18 - 27摄氏度)、正常光照和室温、黑暗和40摄氏度、黑暗和5摄氏度。所有样品在0小时和24小时进行检测。室温及冷藏样品还在48小时、7天和1个月时进行检测。检测包括在400和600纳米处测量光密度、pH值以及通过高效液相色谱法测定硝酸甘油含量。混合液保持澄清无色,未观察到pH值有明显变化。高效液相色谱分析表明硝酸甘油浓度无显著变化。储存在玻璃和聚烯烃容器中的混合液稳定性没有差异。在本研究使用的储存条件和容器中,硝酸甘油与所测试的每种常见静脉输液都具有相容性。