Riley C M, Junkin P
Department of Pharmaceutical Chemistry and Pharmacy Practice, University of Kansas (UK), Lawrence 66045.
Am J Hosp Pharm. 1991 Jun;48(6):1245-52.
The stability of amrinone and digoxin, procainamide hydrochloride, propranolol hydrochloride, sodium bicarbonate, potassium chloride, or verapamil hydrochloride in intravenous admixtures was studied. Admixtures of amrinone and digoxin were studied at one concentration. Amrinone admixtures with propranolol hydrochloride, sodium bicarbonate, potassium chloride, and verapamil hydrochloride were studied at two concentrations. In general, 0.45% sodium chloride injection was used as the diluent; 5% dextrose injection was also used for the procainamide hydrochloride experiments. Duplicate solutions of each test admixture and single-drug control admixture were prepared and stored for four hours at 22-23 degrees C under fluorescent light. Samples were analyzed by visual inspection, tested for pH, and assayed by high-performance liquid chromatography. Admixtures containing amrinone 1.25 or 2.5 mg/mL (as the lactate salt) and sodium bicarbonate 37.5 mg/mL precipitated immediately or within 10 minutes. No changes in pH or visual appearance were noted for amrinone admixtures with procainamide hydrochloride, digoxin, propranolol hydrochloride, potassium chloride, and verapamil hydrochloride. Appreciable degradation of both amrinone and procainamide was observed after four hours when the two were mixed in 5% dextrose. No degradation of amrinone or procainamide was seen when the 5% dextrose was replaced by 0.45% sodium chloride. Amrinone and sodium bicarbonate were incompatible in intravenous admixtures. Amrinone was compatible with digoxin, propranolol hydrochloride, potassium chloride, and verapamil hydrochloride. Amrinone and procainamide were compatible in 0.45% sodium chloride injection but not in 5% dextrose injection.
研究了氨力农与地高辛、盐酸普鲁卡因胺、盐酸普萘洛尔、碳酸氢钠、氯化钾或盐酸维拉帕米在静脉混合液中的稳定性。对氨力农与地高辛的混合液研究了一种浓度。氨力农与盐酸普萘洛尔、碳酸氢钠、氯化钾和盐酸维拉帕米的混合液研究了两种浓度。一般而言,使用0.45%氯化钠注射液作为稀释剂;5%葡萄糖注射液也用于盐酸普鲁卡因胺的实验。制备每种测试混合液和单药对照混合液的双份溶液,并在22 - 23摄氏度的荧光灯下储存4小时。通过目视检查分析样品,测试pH值,并采用高效液相色谱法进行测定。含有1.25或2.5mg/mL氨力农(乳酸盐)和37.5mg/mL碳酸氢钠的混合液立即或在10分钟内出现沉淀。氨力农与盐酸普鲁卡因胺、地高辛、盐酸普萘洛尔、氯化钾和盐酸维拉帕米的混合液在pH值或外观上没有变化。当氨力农和盐酸普鲁卡因胺在5%葡萄糖中混合时,4小时后观察到两者均有明显降解。当5%葡萄糖被0.45%氯化钠取代时,未观察到氨力农或盐酸普鲁卡因胺的降解。氨力农与碳酸氢钠在静脉混合液中不相容。氨力农与地高辛、盐酸普萘洛尔、氯化钾和盐酸维拉帕米相容。氨力农与盐酸普鲁卡因胺在0.45%氯化钠注射液中相容,但在5%葡萄糖注射液中不相容。