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Intravenous Suitability Studies of Commonly Used Oxacillin Sodium Solutions in the ACCUFUSER? Infusion Device

机译:ACCUFUSER中常用奥沙西林钠溶液的静脉内适应性研究?输液器

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Our study compares two commonly used solutions of oxacillin sodium, 5.0 mg/mL in either 0.9% sodium chloride (NS) or 5% dextrose water (D5W), for their continued suitability for IV usage, and stability of active compound over time, when stored at two different controlled temperatures for six weeks. Both solutions were stored in an intravenous infusion device commercially available as Accufuser? and kept at a continuously maintained temperature of either 4 ± 2?C (CT) or 25 ± 2?C (RT). Suitability for IV administration was assessed by measuring changes in macrographical transparency and pH over time, and drug stability was assessed by measuring changes in oxacillin concentration over time using high-performance liquid chromatography (HPLC). After 6 weeks, concentrations of oxacillin were unchanged in the CT solutions, while both RT solutions showed significant decreases in the concentration of oxacillin after only two weeks. Final concentration compared to starting concentrations after 6 weeks at RT, were 36.57% in NS, while virtually no oxacillin was detectable in D5W. Also pH measurements showed a slight decrement at 2 weeks with RT, and at 6 weeks, there was a significant change in pH in both NS and D5W at RT. There was no significant change in color, transparency or appearance after 6 weeks in any of the oxacillin solutions stored in the Accufuser? infusion device. In summary, two commonly used IV solutions for oxacillin administration(5 mg/mL in NS or D5W) stored ready to use in the Accufuser? showed significant changes over time when maintained at RT, that would make the solutions inappropriate for therapeutic use. Both solutions when maintained in CT were not significantly altered and continued to be appropriate in pH and drug concentration for IV therapy. This suggests that ready-to-use solutions of oxacillin sodium in the Accufuser? infusion device can be kept at CT for up to 6 weeks safely but should not be stored at RT due to loss of potency and changes in pH.
机译:我们的研究比较了两种常用的0.9%氯化钠(NS)或5%葡萄糖水(D5W)中5.0 mg / mL的奥沙西林钠溶液的持续适应性和活性化合物随时间的稳定性在两个不同的控制温度下保存六个星期。两种溶液均储存在静脉输液器中,可作为Accufuser?购买。并保持在4±2?C(CT)或25±2?C(RT)的连续温度下。通过测量宏观透明度和pH随时间的变化来评估IV给药的适用性,并使用高效液相色谱(HPLC)通过测量奥沙西林浓度随时间的变化来评估药物的稳定性。 6周后,CT溶液中的奥沙西林浓度未发生变化,而两种RT溶液仅两周后均显示出奥沙西林浓度显着下降。在室温下6周后,最终浓度与起始浓度相比在NS中为36.57%,而在D5W中几乎未检测到奥沙西林。同样,pH测量显示在室温下2周时略有下降,在6周时,在室温下NS和D5W的pH值都有明显变化。 6周后,Accufuser®中储存的任何奥沙西林溶液的颜色,透明度或外观都没有显着变化。输液装置。总之,已将两种常用的用于奥沙西林给药的IV溶液(在NS或D5W中为5 mg / mL)储存起来,准备在Accufuser中使用?在室温下显示出随时间变化的显着变化,这将使溶液不适用于治疗。两种溶液均保持在CT上并没有明显改变,并且继续在pH和药物浓度上适合进行IV治疗。这表明Accufuser中的奥沙西林钠即用型溶液?输液器可以在CT上安全保存长达6周,但由于效能下降和pH值变化,不应在RT下保存。

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