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Extended Stability of Epinephrine Hydrochloride Injection in Polyvinyl Chloride Bags Stored in Amber Ultraviolet Light–Blocking Bags

机译:琥珀色紫外线阻隔袋中储存的聚氯乙烯袋中盐酸肾上腺素注射液的扩展稳定性

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摘要

>Objective: The objective of this study was to evaluate the stability of epinephrine hydrochloride in 0.9% sodium chloride in polyvinyl chloride bags for up to 60 days. >Methods: Dilutions of epinephrine hydrochloride to concentrations of 16 and 64 µg/mL were performed under aseptic conditions. The bags were then placed into ultraviolet light–blocking bags and stored at room temperature (23°C-25°C) or under refrigeration (3°C-5°C). Three samples of each preparation and storage environment were analyzed on days 0, 30, 45, and 60. Physical stability was performed by visual examination. The pH was assessed at baseline and upon final degradation evaluation. Sterility of the samples was not assessed. Chemical stability of epinephrine hydrochloride was evaluated using high-performance liquid chromatography. To determine the stability-indicating nature of the assay, degradation 12 months following preparation was evaluated. Samples were considered stable if there was less than 10% degradation of the initial concentration. >Results: Epinephrine hydrochloride diluted to 16 and 64 µg/mL with 0.9% sodium chloride injection and stored in amber ultraviolet light–blocking bags was physically stable throughout the study. No precipitation was observed. At days 30 and 45, all bags had less than 10% degradation. At day 60, all refrigerated bags had less than 10% degradation. Overall, the mean concentration of all measurements demonstrated less than 10% degradation at 60 days at room temperature and under refrigeration. >Conclusion: Epinephrine hydrochloride diluted to 16 and 64 µg/mL with 0.9% sodium chloride injection in polyvinyl chloride bags stored in amber ultraviolet light–blocking bags was stable up to 45 days at room temperature and up to 60 days under refrigeration.
机译:>目的:该研究的目的是评估盐酸肾上腺素在聚氯乙烯袋中的0.9%氯化钠中的稳定性,最长可达60天。 >方法:在无菌条件下将盐酸肾上腺素稀释至16和64 µg / mL的浓度。然后将袋子放入防紫外线的袋子中,并在室温(23°C-25°C)或冷藏(3°C-5°C)下存储。在第0、30、45和60天对每种制备和储存环境的三个样品进行了分析。物理稳定性通过目测进行。在基线和最终降解评估时评估pH。没有评估样品的无菌性。使用高效液相色谱法评估盐酸肾上腺素的化学稳定性。为了确定测定的稳定性指示性质,评估了制备后12个月的降解。如果初始浓度的降解小于10%,则认为样品稳定。 >结果:在整个研究过程中,用0.9%氯化钠注射液将肾上腺素盐酸盐稀释至16和64 µg / mL,并保存在琥珀色的紫外线阻隔袋中。没有观察到沉淀。在第30和45天,所有袋子的降解率均不到10%。在第60天,所有冷藏袋的降解率均不到10%。总的来说,所有测量的平均浓度在室温和冷藏下于60天时显示不到10%的降解。 >结论:盐酸肾上腺素在0.9%氯化钠注射液中稀释至16和64 µg / mL,在琥珀色紫外线阻隔袋中储存的聚氯乙烯袋中在室温下最多可稳定45天,在60天内稳定。天在冷藏下。

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