Physico-chemical stability of busulfan in injectable solutions in various administration packages.

Mélanie Houot, Vianney Poinsignon, Lionel Mercier, Cyril Valade, Romain Desmaris, François Lemare, Angelo Paci
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引用次数: 15

Abstract

Background and objectives: Busulfan is used as part of a conditioning regimen prior to hematopoietic stem cell transplantation for the treatment of certain cancers and immune deficiency syndromes. Due to its instability in aqueous preparations, busulfan for infusion is prepared from a concentrate and has a relatively short shelf life once prepared. The purpose of this study was to identify the most suitable storage container and temperature to maximize the shelf life of busulfan therapeutic infusions prepared from Busilvex(®).

Methods: Busilvex(®) 6 mg/mL was diluted to 0.55 mg/mL with 0.9 % NaCl and aliquots dispensed into polypropylene syringes, polyvinyl chloride bags, and glass bottles. Three storage temperatures were evaluated: 2-8 °C, 13-15 °C (thermostatically controlled chamber), and room temperature (20 ± 5 °C). At set time points, samples were analysed for busulfan content, using a high-performance liquid chromatography (HPLC) system with ultraviolet detection. The change in pH and osmolarity on storage was also determined, and solutions were inspected visually for formation of a precipitate or colour change. To determine the contribution of precipitation to loss of busulfan content on storage, samples from one time series were treated with the solvent dimethylacetamide prior to HPLC separation and quantitation of busulfan.

Results: The results of the active substance content monitoring study over a 48-h period demonstrate that busulfan solution is stable at a 5 % threshold, at 2-8 °C for 16 h in syringes, 14 h in glass bottles, and 6 h in bags. In addition, the period of stability decreases as the temperature increases (4 h at 20 ± 5 °C). The solution is considered to be stable, subject to precipitation liable to be observed regardless of the temperature.

Conclusion: The best stability was observed for busulfan solutions placed at 2-8 °C in syringes. This study demonstrated that precipitation, in addition to hydrolysis, has a significant influence on the busulfan content.

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不同给药包装中注射溶液中丁硫丹的物理化学稳定性。
背景和目的:Busulfan被用作造血干细胞移植前调理方案的一部分,用于治疗某些癌症和免疫缺陷综合征。由于其在水制剂中的不稳定性,输注用丁硫丹是由浓缩物制备的,一旦制备,其保质期相对较短。本研究的目的是确定最合适的储存容器和温度,以最大限度地延长由Busilvex(®)制备的busulfan治疗性输液的保质期。方法:将6 mg/mL的Busilvex(®)用0.9% NaCl稀释至0.55 mg/mL,等分装于聚丙烯注射器、聚氯乙烯袋和玻璃瓶中。评估了三种储存温度:2-8°C、13-15°C(恒温控制室)和室温(20±5°C)。在设定的时间点,使用紫外检测的高效液相色谱(HPLC)系统分析样品的硫丹含量。还测定了储存时pH值和渗透压的变化,并目测了溶液是否形成沉淀物或颜色变化。为了确定沉淀对储存中丁硫丹含量损失的贡献,在HPLC分离和定量丁硫丹之前,对一个时间序列的样品进行了二甲乙酰胺溶剂处理。结果:在48小时内的活性物质含量监测研究结果表明,在5%的阈值下,在2-8°C下,在注射器中16小时,在玻璃瓶中14小时,在袋中6小时,busulfan溶液是稳定的。此外,随着温度的升高,稳定时间缩短(20±5℃时为4 h)。溶液被认为是稳定的,无论温度如何,都容易发生沉淀。结论:在2-8°C的温度下,磺胺磺胺在注射器中的稳定性最好。本研究表明,除水解外,沉淀对粗硫丹含量也有显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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