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戊巴比妥钠在0.9%氯化钠注射液中复溶后于玻璃注射器和聚丙烯注射器中重新包装后的稳定性。

Stability of pentobarbital sodium after reconstitution in 0.9% sodium chloride injection and repackaging in glass and polypropylene syringes.

作者信息

Gupta V D

机构信息

University of Houston, Houston, TX.

出版信息

Int J Pharm Compd. 2001 Nov-Dec;5(6):482-4.

Abstract

The stability of pentobarbital sodium (10 mg/mL) in 0.9% sodium chloride injection and pentobarbital sodium (50 mg/mL) after repackaging in glass and polypropylene syringes has been studied at 25 deg C by means of a stability-indicating high-performance liquid chromatography assay method. The concentrations of the drug were directly related to peak heights, and the percent relative standard deviation based on 5 injections was 1.7. The pH value of the sample, which was prepared by diluting the injection (50 mg/mL) to 10 mg/mL with 0.9% sodium chloride injection, decreased from 9.2 to 8.2. At this pH, the free base began to crystallize out in less than 24 hours. After the undiluted commercial injection was repackaged in glass or polypropylene syringes, there was no significant loss of potency after 31 days of storage at 25 deg C. The pH value of the injection remained constant at 9.2.The pentobarbital sodium in injection appears to be very stable, because the loss in potency was only about 6.2% after it was boiled in water for 1.5 hours.

摘要

采用一种稳定性指示高效液相色谱测定法,在25℃下研究了戊巴比妥钠(10mg/mL)在0.9%氯化钠注射液中的稳定性,以及戊巴比妥钠(50mg/mL)在玻璃和聚丙烯注射器中重新包装后的稳定性。药物浓度与峰高直接相关,基于5次进样的相对标准偏差百分比为1.7。用0.9%氯化钠注射液将注射液(50mg/mL)稀释至10mg/mL制备的样品,其pH值从9.2降至8.2。在此pH值下,游离碱在不到24小时内开始结晶析出。将未稀释的市售注射液重新包装在玻璃或聚丙烯注射器中后,在25℃下储存31天后效力无显著损失。注射液的pH值保持在9.2不变。注射液中的戊巴比妥钠似乎非常稳定,因为在水中煮沸1.5小时后效力损失仅约6.2%。

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