Long-term stability of esketamine in polypropylene syringes at 5 ± 3°C.

IF 1.6 4区 医学 Q3 PHARMACOLOGY & PHARMACY European journal of hospital pharmacy : science and practice Pub Date : 2024-07-31 DOI:10.1136/ejhpharm-2024-004227
Amélie Kinet-Poleur, Marie-Lise Colsoul, Emilie Catry, Benoît P Bihin, Barbara E Sneyers, Justine Hubert, Jacques Jamart, Laura Soumoy, Laurence M Galanti, Jean-Daniel Hecq, Mélanie Closset
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Abstract

Objective: Esketamine (Vesierra) is a molecule, used alone or in combination, to induce and maintain general anaesthesia and to relieve pain in emergency medicine. The aim of this study is to evaluate the long-term physicochemical stability of a 1 mg/mL solution of esketamine diluted in 0.9% sodium chloride (NaCl) and stored in polypropylene syringes at 5±3°C during 65 days (64+1 day at 22±3°C) and 72 hours at 22±3°C (room temperature), in order to centralise preparation under aseptic conditions in hospital pharmacy.

Methods: Ten syringes were prepared under aseptic conditions. Five syringes were stored at 22±3°C for 3 days, and the five others were stored at 5±3°C for 64 days (+ 1 day at room temperature). The stability was periodically investigated. Particle appearance or colour changes were checked by visual inspection. A research of crystals was performed under the microscope. pH was followed to assess its stability. The turbidity of the solutions was estimated by a measure of optical densities at 350, 410 and 550 nm. The molecule concentrations were measured by ultra-high performance liquid chromatography (UHPLC) coupled with a photodiode array detection (PDA), using a newly developed method.

Results: Based on microscopic examination, no crystals were observed, during the observation period. pH and absorbances at 350, 410 and 550 nm were also stable. Macroscopically, there was no change in colour and appearance of opacity, turbidity or precipitation. Statistical analysis indicates that 1 mg/mL esketamine solutions were chemically stable under these conditions, given that less than 5% of the solutions have lost more than 10% of their initial content during the study based on the prediction interval.

Conclusions: One mg/mL solutions of esketamine hydrochloride are physically and chemically stable after production, for at least 72 hours at 22±3°C and 64 days at 5±3°C (+ 1 day at room temperature).

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聚丙烯注射器中的埃克他敏在 5 ± 3°C 下的长期稳定性。
目的:艾司卡胺(Vesierra)是一种分子,可单独或联合使用,用于诱导和维持全身麻醉,并在急诊医学中缓解疼痛。本研究旨在评估用 0.9% 氯化钠(NaCl)稀释的 1 mg/mL 埃斯可他敏溶液在 5±3°C 下保存 65 天(22±3°C 下保存 64+1 天)和 22±3°C 下保存 72 小时(室温)的长期理化稳定性,以便医院药房在无菌条件下集中配制:在无菌条件下配制 10 支注射器。方法:在无菌条件下配制了 10 支注射器,其中 5 支在 22±3°C 下存放 3 天,其余 5 支在 5±3°C 下存放 64 天(+ 1 天室温)。定期检查稳定性。通过目测检查颗粒外观或颜色变化。在显微镜下对晶体进行研究,并跟踪 pH 值以评估其稳定性。通过测量 350、410 和 550 纳米波长下的光密度来估计溶液的浊度。分子浓度的测量采用新开发的超高效液相色谱法(UHPLC)和光电二极管阵列检测法(PDA):根据显微镜检查,在观察期间没有观察到晶体,pH 值和 350、410 和 550 纳米波长处的吸光度也很稳定。从宏观上看,颜色没有变化,也没有出现不透明、浑浊或沉淀。统计分析表明,在这些条件下,1 毫克/毫升埃斯卡敏溶液的化学性质是稳定的,因为在研究期间,根据预测间隔,只有不到 5%的溶液损失了 10%以上的初始含量:1毫克/毫升的盐酸埃司氯胺酮溶液在生产后的物理和化学性质稳定,在22±3°C条件下至少可保持72小时,在5±3°C条件下可保持64天(+室温下1天)。
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来源期刊
CiteScore
3.40
自引率
5.90%
发文量
104
审稿时长
6-12 weeks
期刊介绍: European Journal of Hospital Pharmacy (EJHP) offers a high quality, peer-reviewed platform for the publication of practical and innovative research which aims to strengthen the profile and professional status of hospital pharmacists. EJHP is committed to being the leading journal on all aspects of hospital pharmacy, thereby advancing the science, practice and profession of hospital pharmacy. The journal aims to become a major source for education and inspiration to improve practice and the standard of patient care in hospitals and related institutions worldwide. EJHP is the only official journal of the European Association of Hospital Pharmacists.
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