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氨苄西林钠、萘夫西林钠和苯唑西林钠在自动给药输液系统袋中的稳定性。

Stability of Ampicillin Sodium, Nafcillin Sodium, And Oxacillin Sodium in AutoDose Infusion System Bags.

作者信息

Zhang Yanping, Trissel Lawrence A

机构信息

Clinical Pharmaceutics Research, Division of Pharmacy, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.

出版信息

Int J Pharm Compd. 2002 May-Jun;6(3):226-9.

Abstract

The objective of this study was to evaluate the physical and chemical stability of ampicillin sodium 1g/100mL, nafcillin sodium 1g/100mL, and oxacillin sodium 1g/100mL, each of which was admixed in 0.9% sodium chloride injection and packaged in an AutoDose Infusion System bag. Triplicate test samples were prepared by reconstituting the penicillin antibiotics and bringing the required amount of each drug to a final volume of 100 mL with 0.9% sodium chloride injection. The test solutions were packaged in AutoDose Bags, which are ethylene vinyl acetate plastic containers designed for use in the AutoDose Infusion System. Samples were stored protected from light and were evaluated at appropriate intervals for up to 7 days at 23 deg C and up to 30 days at 4 deg C. Physical stability was assessed by means of a multistep evaluation procedure that included both turbidimetric and particulate measurement as well as visual inspection. Chemical stability was assesed with stability-indicating high-perofrmance liquid chromatographic (HPLC) analytical techniques based on the determination of drug concentrations initially and at appropriate intervals over the study periods. All the penicillin admixtures were initially clear when viewed in normal fluorescent room light. When the admixtures were viewed with a Tyndall beam, a trace haze was observed with the ampicillin sodium and nafcillin sodium mixtures but not with the oxacillin sodium mixture. Measured turbidity and particulate content were low and exhibited little change in the ampicillin sodium and oxacillin sodium samples throughout the study. The nafcillin sodium samples stored at room temperature remained clear, but a microprecipitate developed in the refrigerated samples between 14 and 21 days of storage. All samples were essentially colorless throughout the study. HPLC analysis indicated some decomposition in the samples. Ampicillin sodium, which was the least stable, exhibited a 10% loss after 24 hours at 23 deg C. In the samples stored at 4 deg C, ampicillin losses were 6% and 11% after 3 days and 5 days,respecively. Nafcillin sodium exhiibited a 10% loss after 5 days at 23 deg C. Less than 3% loss occurred after 14 days at 4 deg C, but the microprecipitation that developed resulted in the termination of that portion of the study. Oxacillin sodium was the most stable; it exhibited less than a 10% loss after 7 days at 23 deg C and less than a 5% loss after 30 days at 4 deg C. Ampicillin sodium, nafcillin sodium, and oxacillin sodium exhibited physical and chemical stability consistent with previous studies on these drugs. The AutoDose Infusion System bags did not adversely affect the physical and chemical stability of those three penicillin antibiotics.

摘要

本研究的目的是评估1g/100mL氨苄西林钠、1g/100mL萘夫西林钠和1g/100mL苯唑西林钠在0.9%氯化钠注射液中混合并包装于自动给药输液系统袋中的物理和化学稳定性。通过复溶青霉素类抗生素并用0.9%氯化钠注射液将每种药物所需量配制成最终体积为100 mL的溶液,制备三份重复的测试样品。测试溶液包装在自动给药袋中,自动给药袋是设计用于自动给药输液系统的乙烯-醋酸乙烯酯塑料容器。样品避光保存,并在23℃下每隔适当时间进行评估,最长7天,在4℃下最长30天。通过多步骤评估程序评估物理稳定性,该程序包括比浊法和颗粒测量以及目视检查。基于在研究期间初始和适当时间间隔测定药物浓度,采用稳定性指示高效液相色谱(HPLC)分析技术评估化学稳定性。在正常荧光室内光线下观察时,所有青霉素混合液最初均澄清。当用廷德尔光束观察混合液时,氨苄西林钠和萘夫西林钠混合液观察到微量浑浊,但苯唑西林钠混合液未观察到。在整个研究过程中,氨苄西林钠和苯唑西林钠样品的测量浊度和颗粒含量较低且变化不大。室温下保存的萘夫西林钠样品保持澄清,但冷藏样品在储存14至21天之间出现微沉淀。在整个研究过程中,所有样品基本无色。HPLC分析表明样品有一些分解。最不稳定的氨苄西林钠在23℃下24小时后损失10%。在4℃下保存的样品中,氨苄西林在3天和5天后的损失分别为6%和11%。萘夫西林钠在23℃下5天后损失10%。在4℃下14天后损失不到3%,但出现的微沉淀导致该部分研究终止。苯唑西林钠最稳定;在23℃下7天后损失不到10%,在4℃下30天后损失不到5%。氨苄西林钠、萘夫西林钠和苯唑西林钠的物理和化学稳定性与先前对这些药物的研究一致。自动给药输液系统袋对这三种青霉素类抗生素的物理和化学稳定性没有不利影响。

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