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利奈唑胺在水溶液及常用静脉输液中的稳定性评估。

Evaluation of the stability of linezolid in aqueous solution and commonly used intravenous fluids.

作者信息

Taylor Rachel, Sunderland Bruce, Luna Giuseppe, Czarniak Petra

机构信息

School of Pharmacy, Faculty of Health Sciences, Curtin University, Bentley, WA, Australia.

出版信息

Drug Des Devel Ther. 2017 Jul 10;11:2087-2097. doi: 10.2147/DDDT.S136335. eCollection 2017.

Abstract

PURPOSE

The aim was to evaluate the stability of linezolid in commonly used intravenous fluids and in aqueous solution to determine the kinetics of degradation and shelf-life values at alkaline pH values.

METHODS

Forced degradation studies were performed on linezolid in solution to develop a validated high-performance liquid chromatography analysis. Sodium chloride 0.9%, sodium lactate, and glucose 5% and glucose 10% solution containing 2.0 mg/mL linezolid were stored at 25.0°C (±0.1°C) for 34 days. The effect of temperature on the stability of linezolid in 0.1 M sodium hydroxide solution was investigated to determine the activation energy. The degradation rates of linezolid at selected pH values at 70.0°C and the influence of ionic strength were also examined. Activation energy data were applied to determine the shelf-life values at selected pH values, and a pH rate profile was constructed over the pH range of 8.7-11.4. The stability of intravenous linezolid (Zyvox) solution was evaluated by storing at 70.0°C for 72 hours.

RESULTS

Linezolid was found to maintain >95.0% of its initial concentration after storage at 25.0°C for 34 days in sodium lactate, 0.9% in sodium chloride, and 5% and 10% in glucose solutions. Linezolid was degraded at alkaline pH values by first-order kinetics. Activation energy data showed that temperature, but not ionic strength, influenced the degradation rate significantly. An activation energy of 58.22 kJ/mol was determined for linezolid in 0.1 M sodium hydroxide solution. Linezolid was least stable at high pH values and at elevated temperatures. It was determined that linezolid has adequate stability for the preparation of intravenous fluids for clinical administration.

CONCLUSION

Linezolid was found to have a shelf life of 34 days at 25°C when added to sodium lactate, 0.9% sodium chloride, and 5% and 10% glucose solutions. It was least stable at high pH values and at elevated temperatures.

摘要

目的

评估利奈唑胺在常用静脉输液及水溶液中的稳定性,以确定其在碱性pH值下的降解动力学及保质期数值。

方法

对溶液中的利奈唑胺进行强制降解研究,以建立经过验证的高效液相色谱分析方法。将含有2.0mg/mL利奈唑胺的0.9%氯化钠、乳酸钠以及5%和10%葡萄糖溶液在25.0°C(±0.1°C)下储存34天。研究温度对利奈唑胺在0.1M氢氧化钠溶液中稳定性的影响,以确定活化能。还考察了利奈唑胺在70.0°C下选定pH值时的降解速率以及离子强度的影响。应用活化能数据来确定选定pH值下的保质期数值,并在8.7 - 11.4的pH范围内构建pH速率曲线。通过在70.0°C下储存72小时来评估静脉用利奈唑胺(Zyvox)溶液的稳定性。

结果

发现在乳酸钠溶液中于25.0°C储存34天后、在氯化钠溶液中0.9%、在葡萄糖溶液中5%和10%时,利奈唑胺保持其初始浓度的>95.0%。利奈唑胺在碱性pH值下按一级动力学降解。活化能数据表明,温度而非离子强度对降解速率有显著影响。确定利奈唑胺在0.1M氢氧化钠溶液中的活化能为58.22kJ/mol。利奈唑胺在高pH值和高温下最不稳定。已确定利奈唑胺对于制备临床给药的静脉输液具有足够的稳定性。

结论

当添加到乳酸钠、0.9%氯化钠以及5%和10%葡萄糖溶液中时,利奈唑胺在25°C下的保质期为34天。它在高pH值和高温下最不稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/743b/5513848/3d94cb8a9ffc/dddt-11-2087Fig1.jpg

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