医院药品生产研究。(七)根据临床需要修改1%亚甲蓝注射液说明书。

Moemi Saito, Machiko Watanabe, H. Ogata, K. Edo
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引用次数: 2

摘要

我院药房配制的1%亚甲基蓝(MB)注射液,浓度分别为0.05%和0.25%,用于治疗高铁血红蛋白血症和感染性休克。为了提供更多关于我们自1996年以来一直在制作的“包装说明书”的信息,我们使用1% MB注射剂进行了pH变化测试,并使用0.05%和0.25% MB注射剂进行了稳定性测试。紫外分光光度法监测MB吸光度的变化。在室温和40°C 1000 Lux荧光灯下,在0.05%或0.25% MB注射条件下,在黑暗中48小时,均未观察到MB吸光度的显著变化。基于这些结果,我们能够在包装说明书上增加有关pH变化测试和稳定性测试的信息量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies on Hospital Pharmaceutical Manufacturing. (VII). The Revision of Package Insert of 1%Methylene Blue Injection on the Basis of Clinical Need.
One percentage Methylene Blue (MB) injection prepared in our hospital pharmacy has been used at concentrations of 0.05% and 0.25% for the treatment for methemoglobinemia and septic shock. In order to provide more information on “the package insert” which we have been making since 1996, we performed a pH variation test using a 1% MB injection and a stability test for 0.05% and 0.25% MB injections.The changes in MB absorbance were monitored by the UV spectrometry method. No significant changes in MB absorbance were observed either at room temperature and 40°C at 1000 Lux fluorescent light or in darkness for 48 hours, under 0.05% or 0.25% MB injection conditions. Based on these results, we were able to increase the amount of information regarding the pH variation tests and stability tests on our package insert.
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