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心脏保护剂ICRF-187在输液中的化学稳定性。

Chemical stability of the cardioprotective agent ICRF-187 in infusion fluids.

作者信息

Beijnen J H, van Gijn R

机构信息

Department of Pharmacy, Slotervaart Hospital/Netherlands Cancer Institute, Amsterdam.

出版信息

J Parenter Sci Technol. 1993 Jul-Aug;47(4):166-71.

PMID:8410562
Abstract

The chemical stability of the cardioprotective agent ICRF-187 in 0.9% sodium chloride and 5% dextrose infusion fluids has been investigated. The admixtures (concentration: 10 mg/mL and 1 mg/mL) were stored in glass bottles or polyvinyl chloride containers at 4 degrees C in the dark and at room temperature (20-22 degrees C) both protected from light and under normal room fluorescent light conditions in a day-night rhythm. Samples withdrawn immediately after preparation and after 6 hours, 1, 2, 3 and 6 days were analyzed using high performance liquid chromatography with ultraviolet detection. Samples were also inspected for visual changes and tested for changes in pH. Chemical stability of ICRF-187 was also investigated as a function of pH (range 1-12) at room temperature. It is concluded that ICRF-187 is slightly more stable in 5% dextrose than in 0.9% sodium chloride infusion fluids. The stability of the drug is not influenced by normal room fluorescent light nor by the type of container material used. Precipitation occurred in both 5% dextrose and 0.9% sodium chloride with a drug concentration of 10 mg/mL and storage in the refrigerator at 4 degrees C. The chemical stability of ICRF-187 in aqueous solution is mainly a function of pH. At pH 1, no decomposition is detected within 24 hours, at pH 7, 35% decomposition occurs in 21 hours, while at pH 12 it degrades completely within 20.5 hours.

摘要

已对心脏保护剂ICRF - 187在0.9%氯化钠注射液和5%葡萄糖注射液中的化学稳定性进行了研究。将混合液(浓度:10 mg/mL和1 mg/mL)分别储存在玻璃瓶或聚氯乙烯容器中,于4℃黑暗条件下、室温(20 - 22℃)有光照防护和正常室内荧光灯下以昼夜节律储存。制备后立即以及6小时、1天、2天、3天和6天后取出的样品,采用带紫外检测的高效液相色谱法进行分析。还对样品进行了外观变化检查和pH值变化测试。在室温下,也研究了ICRF - 187的化学稳定性与pH值(范围1 - 12)的关系。得出的结论是,ICRF - 187在5%葡萄糖注射液中比在0.9%氯化钠注射液中稍稳定。药物的稳定性不受正常室内荧光灯以及所用容器材料类型的影响。药物浓度为10 mg/mL且储存在4℃冰箱中的5%葡萄糖注射液和0.9%氯化钠注射液中均出现了沉淀。ICRF - 187在水溶液中的化学稳定性主要取决于pH值。在pH 1时,24小时内未检测到分解;在pH 7时,21小时内发生35%的分解;而在pH 12时,20.5小时内完全降解。

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