Lee D K, Wang D P, Lee A
Department of Pharmacy, Kaoshung Veterans General Hospital, Taipei, Taiwan, Republic of China.
Am J Hosp Pharm. 1991 Jan;48(1):111-3.
The compatibility of cimetidine hydrochloride and cefoperazone sodium in 5% dextrose injection stored at two temperatures was studied. Cimetidine hydrochloride and cefoperazone sodium were reconstituted or diluted with 5% dextrose injection to form an admixture with a cimetidine concentration of 2 mg/mL and a cefoperazone concentration of 5 mg/mL. The admixture was stored in 100-mL vented i.v. containers in the dark at 4 and 25 degrees C; three containers were stored at each temperature. A 2-mL sample was taken from each container after 0.5, 0.75, 1, 6, 12, 24, and 48 hours of storage and visually inspected, tested for pH, and assayed by a stability-indicating high-performance liquid chromatographic method. Triplicate studies were done for each storage condition. At both temperatures, drug concentrations varied by less than 5% during the study period. No color change, precipitation, or cloudiness was observed for any of the solutions under any of the storage conditions. Cefoperazone sodium 5.0 mg/mL and cimetidine hydrochloride 2.0 mg/mL in admixtures in 5% dextrose injection are stable for 48 hours at 4 and 25 degrees C.
研究了盐酸西咪替丁与头孢哌酮钠在5%葡萄糖注射液中于两种温度下储存时的相容性。将盐酸西咪替丁和头孢哌酮钠用5%葡萄糖注射液复溶或稀释,配制成西咪替丁浓度为2mg/mL、头孢哌酮浓度为5mg/mL的混合液。混合液置于100mL带通气孔的静脉输液容器中,在4℃和25℃的暗处储存;每个温度下储存三个容器。储存0.5、0.75、1、6、12、24和48小时后,从每个容器中取出2mL样品,进行外观检查、pH值检测,并采用稳定性指示高效液相色谱法进行测定。每种储存条件下均进行了三次重复研究。在两个温度下,研究期间药物浓度变化均小于5%。在任何储存条件下,任何溶液均未观察到颜色变化、沉淀或浑浊。5%葡萄糖注射液中含5.0mg/mL头孢哌酮钠和2.0mg/mL盐酸西咪替丁的混合液在4℃和25℃下48小时内稳定。