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盐酸胺碘酮与其他注射用药物混合液的稳定性。

Stability of amiodarone hydrochloride in admixtures with other injectable drugs.

作者信息

Campbell S, Nolan P E, Bliss M, Wood R, Mayersohn M

出版信息

Am J Hosp Pharm. 1986 Apr;43(4):917-21.

PMID:3706337
Abstract

The stability of amiodarone hydrochloride in intravenous admixtures was studied. Amiodarone hydrochloride 900 mg was mixed with 500 mL of either 5% dextrose injection or 0.9% sodium chloride injection in polyvinyl chloride or polyolefin containers; identical solutions were also mixed with either potassium chloride 20 meq, lidocaine hydrochloride 2000 mg, quinidine gluconate 500 mg, procainamide hydrochloride 2000 mg, verapamil hydrochloride 25 mg, or furosemide 100 mg. All admixtures were prepared in triplicate and stored for 24 hours at 24 degrees C. Amiodarone concentrations were determined using a stability-indicating high-performance liquid chromatographic assay immediately after admixture and at intervals during storage. Each solution was visually inspected and tested for pH. Amiodarone concentrations decreased less than 10% in all admixtures except those containing quinidine gluconate in polyvinyl chloride containers. The only visual incompatibility observed was in admixtures containing quinidine gluconate and 5% dextrose injection. In most solutions pH either decreased slightly or remained unchanged. Amiodarone hydrochloride is stable when mixed with either 5% dextrose injection or 0.9% sodium chloride injection in polyvinyl chloride or polyolefin containers alone or with potassium chloride, lidocaine, procainamide, verapamil, or furosemide and stored for 24 hours at 24 degrees C. Amiodarone should not be mixed with quinidine gluconate in polyvinyl chloride containers.

摘要

研究了盐酸胺碘酮在静脉混合液中的稳定性。将900mg盐酸胺碘酮与500mL 5%葡萄糖注射液或0.9%氯化钠注射液在聚氯乙烯或聚烯烃容器中混合;相同的溶液还分别与20meq氯化钾、2000mg盐酸利多卡因、500mg葡萄糖酸奎尼丁、2000mg盐酸普鲁卡因胺、25mg盐酸维拉帕米或100mg呋塞米混合。所有混合液均一式三份制备,并在24℃下储存24小时。混合后立即以及储存期间每隔一段时间,使用稳定性指示高效液相色谱法测定胺碘酮浓度。对每种溶液进行外观检查并测试pH值。除了在聚氯乙烯容器中含有葡萄糖酸奎尼丁的混合液外,所有混合液中胺碘酮浓度下降均小于10%。观察到的唯一外观不相容情况是含有葡萄糖酸奎尼丁和5%葡萄糖注射液的混合液。在大多数溶液中,pH值要么略有下降,要么保持不变。当盐酸胺碘酮单独与5%葡萄糖注射液或0.9%氯化钠注射液在聚氯乙烯或聚烯烃容器中混合,或与氯化钾、利多卡因、普鲁卡因胺、维拉帕米或呋塞米混合,并在24℃下储存24小时时是稳定的。盐酸胺碘酮不应与聚氯乙烯容器中的葡萄糖酸奎尼丁混合。

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