Raineri D L, Cwik M J, Rodvold K A, Deyo K L, Scaros L P, Fischer J H
Clinical Pharmacokinetics Laboratory, University of Illinois, College of Pharmacy, Chicago 60612.
Am J Hosp Pharm. 1988 Jul;45(7):1523-9.
The stability of nizatidine in commonly used i.v. fluids stored in glass and plastic containers was studied. Stock solutions of nizatidine 0.75, 1.5, and 3.0 mg/mL in 15 i.v. fluids were prepared using nizatidine injection 25 mg/mL. Six 50-mL aliquots of each solution were transferred to separate glass infusion bottles and stored at room temperature or under refrigeration. Twenty-one 40-mL aliquots of additional stock solutions of nizatidine 0.75 and 3.0 mg/mL in 0.9% sodium chloride injection or 5% dextrose injection were transferred to polyvinyl chloride (PVC) bags and stored at room or refrigerated temperature; some of these solutions were frozen, thawed, and refrigerated before analysis. Samples of each admixture were analyzed after 0.5, 1, 2, 3, and 7 days of storage for nizatidine concentration using a stability-indicating high-performance liquid chromatographic assay and also for visible changes and pH. The concentration of nizatidine in each admixture remained within 92%-106% of actual initial storage concentration throughout the study period, with the exception of nizatidine 3.0 mg/mL in 8.5% amino acid injection. The stability of nizatidine in admixtures stored in polyvinyl chloride bags was similar to that of admixtures stored in glass bottles. In the i.v. fluids, concentrations, and containers studied, nizatidine admixtures are stable for at least 7 days at either room or refrigerated temperature and 30 days when stored frozen in polyvinyl chloride bags. Admixtures of nizatidine 3.0 mg/mL in 8.5% amino acid injection should not be stored at room temperature for longer than four days.
研究了尼扎替丁在储存在玻璃和塑料容器中的常用静脉输液中的稳定性。使用25mg/mL的尼扎替丁注射液,在15种静脉输液中制备了浓度为0.75、1.5和3.0mg/mL的尼扎替丁储备溶液。将每种溶液的6个50mL等分试样转移到单独的玻璃输液瓶中,并在室温或冷藏条件下储存。将另外21个40mL等分试样的0.75和3.0mg/mL尼扎替丁储备溶液分别转移到0.9%氯化钠注射液或5%葡萄糖注射液中,再转移到聚氯乙烯(PVC)袋中,并在室温或冷藏温度下储存;其中一些溶液在分析前进行冷冻、解冻和冷藏。在储存0.5、1、2、3和7天后,使用稳定性指示高效液相色谱法分析每种混合物的样品,测定尼扎替丁浓度,同时观察外观变化和pH值。在整个研究期间,每种混合物中尼扎替丁的浓度保持在实际初始储存浓度的92%-106%范围内,但8.5%氨基酸注射液中3.0mg/mL的尼扎替丁除外。尼扎替丁在储存在聚氯乙烯袋中的混合物中的稳定性与储存在玻璃瓶中的混合物相似。在所研究的静脉输液、浓度和容器中,尼扎替丁混合物在室温或冷藏温度下至少稳定7天,在聚氯乙烯袋中冷冻储存时稳定30天。8.5%氨基酸注射液中3.0mg/mL的尼扎替丁混合物在室温下储存不应超过4天。