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Stability of Nafcillin Sodium Solutions in the Accufuser? Elastomeric Infusion Device

机译:Nafcillin钠溶液在使用者体内的稳定性?弹性输液器

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The aim of this study was to investigate the stabilities of two kinds of solutions of nafcillin sodium (2.5 mg/mL) in 0.9% sodium chloride solution (NS, normal saline) and in injectable 5% dextrose water (D5W) in the intravenous elastomeric infusion device (Accufuser?) based on recommended solutions and storage periods. The injectable nafcillin solutions (NS- and D5W-nafcillin) in the Accufuser??device were stored and evaluated at controlled temperatures (room temperature, RT, 5℃ ± 2℃ and cold temperature, CT, 4℃ ± 2℃) during 6 weeks. Effects of the periods of storage (from 0 to 6 weeks) and the temperatures of storage (RT and CT) on the physicochemical appearances and concentrations of active compounds were determined. The visual clarity, pH, and concentrations of nafcillin sodium were determined by stability-indicating high-performance liquid chromatography (HPLC)-ultraviolet (UV) detection. The results showed that in NS and D5W solutions, the amount of nafcillin slightly changed and remained 92.66% and 97.30% of their initial amounts at CT during 6 weeks, respectively. On the other hand, in NS and D5W solutions at RT, the amount significantly decreased with time and reached 27.66% and 31.97% of their initial amounts during 4 weeks, respectively. Slight decrement of pH was observed in CT storage while significant change was observed in the RT storage. Moreover, in CT, no significant changes in physical appearances and colors of the solutions were observed during the study. However, the solutions changed into yellowish color and some particles were detected in both kinds of nafcillin solutions (NS and D5W) after 1.5 weeks in RT conditions. To sum up, under CT two kinds of nafcillin sodium solutions (NS and D5W) were stable with time in Accufuser??without any significant physical changes and retained almost all of the initial concentrations up to 6 weeks. However, the solutions were not stable in RT storage. We suggest that nafcillin sodium solutions in an Accufuser??should be preferentially diluted in NS and D5W while storing in CT condition.
机译:这项研究的目的是研究那夫西林钠(2.5 mg / mL)的两种溶液在0.9%氯化钠溶液(NS,生理盐水)和注射用5%葡萄糖水(D5W)中的稳定性。静脉注射弹性体输液器(Accufuser?)基于建议的解决方案和储存时间。将Accufuser™装置中的可注射萘夫西林溶液(NS-和D5W-萘夫西林)储存并在控制温度(室温,室温,5℃±2℃和冷温度,CT,4℃±2℃)下进行6次评估周。确定了储存时间(0至6周)和储存温度(RT和CT)对理化外观和活性化合物浓度的影响。通过稳定性指示高效液相色谱(HPLC)-紫外线(UV)检测来确定纳夫西林钠的视觉清晰度,pH和浓度。结果表明,在NS和D5W溶液中,纳非西林的量在6周内略有变化,分别在CT时分别保持其初始量的92.66%和97.30%。另一方面,在室温下的NS和D5W溶液中,该量随时间显着下降,在4周内分别达到其初始量的27.66%和31.97%。在CT存储器中观察到pH值略有下降,而在RT存储器中观察到显着变化。此外,在CT中,在研究过程中未观察到溶液的物理外观和颜色发生明显变化。然而,在室温条件下1.5周后,两种萘夫西林溶液(NS和D5W)中的溶液均变为淡黄色,并检测到一些颗粒。综上所述,在CT下,两种Nafcillin钠溶液(NS和D5W)在Accufuser中随时间变化是稳定的,没有任何明显的物理变化,并且几乎保留了最初的所有浓度直至6周。但是,该解决方案在RT存储中不稳定。我们建议在存放于CT条件下时,应优先将Nafcillin钠溶液置于Accufuser®中,并先在NS和D5W中稀释。

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