Shea B F, Souney P F
Department of Pharmacy Services L-2, Brigham and Women's Hospital, Boston, MA 02115.
DICP. 1990 Mar;24(3):232-5. doi: 10.1177/106002809002400302.
The stability of famotidine in a 3-in-1 total nutrient admixture stored at room temperature (24 degrees C) was evaluated over 24 hours. Famotidine injection was diluted to a theoretical concentration of 20 mg/L in a total nutrient admixture containing 5% amino acid injection, 25% dextrose injection, and 2.25% intravenous fat emulsion. Admixtures were prepared in 2-L ethylene-vinyl acetate bags using conventional techniques and stored at room temperature. At 0, 4, 8, 12, and 24 hours, the admixtures were visually inspected for color change, creaming, or phase separation, and samples were obtained for assay with a stability-indicating method of HPLC, using samples obtained at time zero as controls. Two-way analysis of variance was used for data evaluation. There was no evidence of color change, creaming, or phase separation before quantitative analysis was performed, nor was there significant change in observed famotidine concentration over 24 hours. Based upon our data, famotidine intravenous solution 20 mg/L in the solution tested is stable at room temperature for 24 hours.
在室温(24℃)下,对法莫替丁在三合一全营养混合液中的稳定性进行了24小时的评估。将法莫替丁注射液在含有5%氨基酸注射液、25%葡萄糖注射液和2.25%静脉脂肪乳剂的全营养混合液中稀释至理论浓度20mg/L。使用常规技术在2L乙烯-醋酸乙烯酯袋中制备混合液,并在室温下储存。在0、4、8、12和24小时时,对混合液进行外观检查,查看颜色变化、乳析或分层情况,并使用高效液相色谱法这种稳定性指示方法取样进行分析,以零时取样作为对照。采用双向方差分析进行数据评估。在进行定量分析之前,没有颜色变化、乳析或分层的迹象,并且在24小时内观察到的法莫替丁浓度也没有显著变化。根据我们的数据,在测试溶液中浓度为20mg/L的法莫替丁静脉溶液在室温下24小时稳定。