Walker S E, Paton T W, Fabian T M, Liu C C, Coates P E
Am J Hosp Pharm. 1981 Jun;38(6):881-3.
The stability and sterility of cimetidine hydrochloride admixtures after freezing for extended periods were investigated. Cimetidine hydrochloride, 300 mg, was added to each of six 50-ml minibags containing 5% dextrose injection. The cimetidine concentration was determined and the bags were frozen for up to 30 days. After freezing for the appropriate length of time, the bags were thawed. Cimetidine concentrations were determined by high-pressure liquid chromatography immediately and then daily for eight days while the admixtures were refrigerated. Sterility tests were carried out throughout the study. Data were analyzed by least-squares linear regression to test for trends. The cimetidine hydrochloride admixtures were stable while frozen for up to 30 days and for at least eight days following thawing when kept under refrigeration. Sterility of the admixture was maintained throughout the study period.
研究了盐酸西咪替丁混合物长时间冷冻后的稳定性和无菌性。将300mg盐酸西咪替丁加入到六个装有5%葡萄糖注射液的50ml小袋中。测定西咪替丁浓度,将袋子冷冻长达30天。在冷冻适当时间后,将袋子解冻。立即通过高压液相色谱法测定西咪替丁浓度,然后在混合物冷藏期间每天测定一次,持续八天。在整个研究过程中进行无菌试验。通过最小二乘线性回归分析数据以检验趋势。盐酸西咪替丁混合物在冷冻长达30天以及解冻后冷藏至少八天期间是稳定 的。在整个研究期间,混合物的无菌性得以保持。