Chemical Stability of Epinephrine 10 mcg/mL Diluted in 0.9% Sodium Chloride and Stored in Polypropylene Syringes at 4 degrees C and 25 degrees C.

Q4 Medicine
Roxanne Hook, Ashleigh Neault, Devan Scharrer, Shirley Law, Scott E Walker, Nathan H Ma, Vera Riss
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Abstract

Studies have evaluated epinephrine stability in higher concentrations and shorter durations than we require. The objective of this study was to evaluate the chemical stability of epinephrine in syringes at concentrations of 10 mcg/mL in 0.9% sodium chloride at 4°C and 25°C. Solutions of 10 mcg/mL epinephrine in 0.9% sodium chloride were prepared and stored in 10-mL Becton, Dickinson and Company syringes. Three units of each container were stored at 4°C and 25°C. Concentration analysis was completed on study days 0, 2, 7, 14, 21, 28, 42, 56, 72, and 91 using a validated stability-indicating liquid chromatographic method with ultraviolet detection. Chemical stability was based on the intersection of the lower limit of the 95% confidence interval of the observed degradation rate and the time to achieve 90% of the initial concentration (T-90). The analytical method separated degradation products from epinephrine to measure concentration specifically, accurately, and reproducibly. During the study period, all solutions at 4°C retained more than 89.62% of the initial concentration for 91 days. Solutions stored at 25°C retained more than 90% for 21 days. Multiple linear regression revealed significant differences in percent remaining due to study day (P<0.001) and temperature (P=0.002). The calculated T-90, with 95% confidence, was 71.40 days for solutions stored at 4°C but only 12.77 days for solutions stored at 25°C. We conclude that 10 mcg/mL epinephrine solution diluted in 0.9% sodium chloride stored at 4°C is chemically and physically stable for 64 days, with 95% confidence. The syringe may be held at room temperature for up to 24 hours during this period and still retain more than 90% of the initial concentration.

肾上腺素10 mcg/mL在0.9%氯化钠中稀释并在4摄氏度和25摄氏度下储存在聚丙烯注射器中的化学稳定性。
研究已经评估了肾上腺素在比我们要求的更高浓度和更短时间内的稳定性。本研究的目的是评估肾上腺素在0.9%氯化钠中浓度为10 mcg/mL的注射器中在4°C和25°C下的化学稳定性。制备10mcg/mL肾上腺素在0.9%氯化钠中的溶液,并将其储存在10mL Becton,Dickinson and Company注射器中。每个容器的三个单元分别储存在4°C和25°C下。在研究第0天、第2天、第7天、第14天、第21天、第28天、第42天、第56天、第72天和第91天,使用经验证的稳定性指示液相色谱法和紫外检测法完成浓度分析。化学稳定性基于观察到的降解率的95%置信区间下限与达到初始浓度90%的时间(T-90)的交集。该分析方法从肾上腺素中分离出降解产物,以专门、准确和可重复地测量浓度。在研究期间,所有4°C的溶液在91天内保持了超过89.62%的初始浓度。在25°C下储存的溶液在21天内保留了90%以上。多元线性回归显示,研究日剩余百分比存在显著差异(P
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
62
期刊介绍: The International Journal of Pharmaceutical Compounding (IJPC) is a bi-monthly, scientific and professional journal emphasizing quality pharmaceutical compounding. IJPC is the only publication that covers pharmaceutical compounding topics relevant and necessary to empower pharmacists to meet the needs of today"s patients. No other publication features hands-on, how-to compounding techniques or the information that contemporary pharmacists need to provide individualized care.
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