Belliveau P P, Shea B F, Scavone J M
Department of Pharmacy Services, Hartford Hospital, CT 06115.
Am J Hosp Pharm. 1993 May;50(5):950-2.
The stability of metoprolol tartrate 0.40 mg/mL in 5% dextrose injection or 0.9% sodium chloride injection in polyvinyl chloride (PVC) bags stored at 24.0 +/- 2.4 degrees C was studied. Triplicate admixtures of each solution were prepared. A stability-indicating high-performance liquid chromatographic assay was used to determine metoprolol tartrate concentrations. At 0, 6, 12, 24, and 36 hours, samples were visually assessed then assayed in duplicate. Stability was defined as a < 10% decline in metoprolol tartrate concentration from the time 0 determination. No notable color changes or precipitation was observed in any sample. All samples demonstrated a < 7% reduction in metoprolol tartrate concentration over 36 hours. Metoprolol tartrate 0.40 mg/mL admixed in 5% dextrose injection or 0.9% sodium chloride injection in PVC bags and stored at 24.0 +/- 2.4 degrees C was stable for 36 hours.
研究了酒石酸美托洛尔0.40mg/mL在24.0±2.4℃下于聚氯乙烯(PVC)袋中5%葡萄糖注射液或0.9%氯化钠注射液中的稳定性。制备了每种溶液的三份混合液。采用一种稳定性指示高效液相色谱法测定酒石酸美托洛尔浓度。在0、6、12、24和36小时时,对样品进行外观评估,然后进行双份测定。稳定性定义为酒石酸美托洛尔浓度相对于0小时测定值下降<10%。在任何样品中均未观察到明显的颜色变化或沉淀。所有样品在36小时内酒石酸美托洛尔浓度降低<7%。酒石酸美托洛尔0.40mg/mL在PVC袋中与5%葡萄糖注射液或0.9%氯化钠注射液混合并在24.0±2.4℃下储存36小时是稳定的。