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盐酸维拉帕米注射液在常用大容量注射剂中的配伍稳定性

Compatibility of verapamil hydrochloride injection in commonly used large-volume parenterals.

作者信息

Cutie M R, Lordi N G

出版信息

Am J Hosp Pharm. 1980 May;37(5):675-6.

PMID:7386476
Abstract

The visual and chemical compatibilities of verapamil hydrochloride injection in 10 commonly used large-volume solutions packaged in glass, polyolefin, or polyvinyl chloride containers were studied. The mixtures, each containing 40 mg/liter of verapamil hydrochloride, were stored away from light for up to 48 hours at 25 degrees C. The solutions were examined visually for haze, precipitate formation, color change, and evolution of gas immediately after mixing and at 0.25, 1, 3, 8, 24, and 48 hours. Spectrophotometry and thin-layer chromatography were used to test for drug decomposition or chemical incompatibilities. All test methods used showed that no significant degradation of verapamil hydrochloride had taken place in the solutions or through contact with the containers. Slightly higher spectrophotometric readings for dextrose-containing solutions, though within experimental error, could have indicated the presence of dextrose degradation products. Evidence from this study suggests that verapamil hydrocholoride is compatible with the large-volume parenterals studied.

摘要

研究了盐酸维拉帕米注射液在玻璃、聚烯烃或聚氯乙烯容器包装的10种常用大容量溶液中的视觉和化学相容性。每种混合物含有40毫克/升盐酸维拉帕米,在25℃避光储存长达48小时。混合后立即以及在0.25、1、3、8、24和48小时对溶液进行外观检查,观察是否有浑浊、沉淀形成、颜色变化和气体产生。采用分光光度法和薄层色谱法检测药物分解或化学不相容性。所有使用的测试方法均表明,溶液中或与容器接触后,盐酸维拉帕米未发生明显降解。含葡萄糖溶液的分光光度读数略高,尽管在实验误差范围内,但可能表明存在葡萄糖降解产物。该研究的证据表明,盐酸维拉帕米与所研究的大容量胃肠外营养液相容。

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