Johnson C E, Jacobson P A, Pillen H A, Woycik C L
College of Pharmacy, University of Michigan, Ann Arbor 48109-1065.
Am J Hosp Pharm. 1993 Apr;50(4):703-6.
The stability of aminophylline and fluconazole in intravenous admixtures containing both drugs was studied. Admixtures containing aminophylline 2.0 or 1.0 mg/mL and fluconazole 1.5 or 0.5 mg/mL in 5% dextrose injection or 0.9% sodium chloride injection were prepared. Each admixture was prepared in triplicate in glass containers and kept at 24 degrees C. Immediately after preparation and at one, two, and three hours, samples were visually inspected, tested for pH, and assayed in duplicate by high-performance liquid chromatography for theophylline concentration and fluconazole concentration. More than 98% of the initial aminophylline and fluconazole concentrations remained at each test interval. There was no visible evidence of precipitation, gas formation, or color change. No appreciable change in pH occurred during the study period. Aminophylline 1.0-2.0 mg/mL and fluconazole 0.5-1.5 mg/mL admixed in 5% dextrose injection or 0.9% sodium chloride injection were stable and compatible for up to three hours at 24 degrees C.
研究了氨茶碱和氟康唑在含有这两种药物的静脉混合液中的稳定性。制备了在5%葡萄糖注射液或0.9%氯化钠注射液中含有2.0或1.0mg/mL氨茶碱以及1.5或0.5mg/mL氟康唑的混合液。每种混合液在玻璃容器中一式三份制备,并保持在24℃。制备后立即以及在1、2和3小时时,对样品进行外观检查、pH测试,并通过高效液相色谱法对茶碱浓度和氟康唑浓度进行一式两份测定。在每个测试间隔,初始氨茶碱和氟康唑浓度的98%以上得以保留。没有明显的沉淀、气体形成或颜色变化迹象。在研究期间pH没有明显变化。在24℃下,在5%葡萄糖注射液或0.9%氯化钠注射液中混合的1.0 - 2.0mg/mL氨茶碱和0.5 - 1.5mg/mL氟康唑在长达三小时内是稳定且相容的。