3PC-058 Physicochemical stability of meropenem in polypropylene syringes at 41.7 mg/mL for intensive care units

G. Loeuille, J. Vigneron, E. D’huart, A. Charmillon, B. Demoré
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Abstract

Background and importance Meropenem is a broad spectrum antibiotic used to treat severe infectious. The maximum dose recommended is 6 g/day. A stability not exceeding 24 hours has been demonstrated by many research teams in different publications. Only two studies were performed at 40 mg/mL in polypropylene syringes with conflicting stability results: 4 hours and 8 hours. Meropenem is a time dependent antibiotic; its continuous administration improves its efficiency. Aim and objectives The objective of this work was to study the stability of meropenem solutions at 41.7 mg/mL (2 g in 48 mL), diluted in 0.9% sodium chloride (0.9% NaCl) or dextrose 5% (D5W), in polypropylene syringes not protected from light, after preparation and after 4 and 8 hours at 20–25°C. Material and methods Three syringes for each condition were prepared. At the time of analysis, one sample from each preparation was analysed by high performance liquid chromatography coupled to a photodiode array detector at 297 nm. The method was validated according to the ICH Q2 (R1). Physical stability was evaluated by visual and subvisual inspection (turbidimetry by UV spectrophotometry at 350, 410 and 550 nm, as recommended by the European Consensus Conference). pH values were measured. Results The method was validated with an r² of 0.9999. The coefficients of variation on repeatability and intermediate precision were Conclusion and relevance In D5W, meropenem was unstable, with chemical and physical instability. Meropenem was stable at 41.7 mg/mL in polypropylene syringes diluted in NaCl 0.9% for 8 hours. This new stability data allows continuous administration. References and/or acknowledgements Curti C, et al. Stability studies of antipyocyanic beta-lactam antibiotics used in continuous infusion. Pharmazie 2019. Carlier M, et al. Stability of generic brands of meropenem reconstituted in isotonic saline. Minerva Anestesiologica 2014. Conflict of interest No conflict of interest
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重症监护病房用41.7 mg/mL聚丙烯注射器中美罗培南的理化稳定性
背景和重要性美罗培南是一种用于治疗严重感染性疾病的广谱抗生素。建议最大剂量为6克/天。许多研究小组在不同的出版物中证明了不超过24小时的稳定性。只有两项研究在聚丙烯注射器中以40 mg/mL进行,稳定性结果相互冲突:4小时和8小时。美罗培南是一种时间依赖性抗生素;它的持续管理提高了它的效率。目的:研究41.7 mg/mL (2 g/ 48ml)的美罗培南溶液,用0.9%氯化钠(0.9% NaCl)或5%葡萄糖(D5W)稀释后,在不避光的聚丙烯注射器中制备后,在20-25℃下放置4和8小时的稳定性。材料与方法每种条件制备3支注射器。在分析时,每种制剂中的一个样品通过高效液相色谱耦合到297 nm的光电二极管阵列检测器进行分析。方法按照ICH Q2 (R1)进行验证。通过目视和亚目视检查评估物理稳定性(根据欧洲共识会议的建议,采用350、410和550 nm的紫外分光光度法进行浊度测定)。测量pH值。结果该方法有效,r²= 0.9999。在D5W中,美罗培南不稳定,存在化学不稳定性和物理不稳定性。在氯化钠0.9%稀释的聚丙烯注射器中,美罗培南稳定浓度为41.7 mg/mL,维持8小时。这个新的稳定性数据允许连续管理。Curti C等。持续输注抗脓毒酸-内酰胺类抗生素的稳定性研究。Pharmazie 2019。Carlier M等。仿制药美罗培南在等渗盐水中复配的稳定性。麻醉学杂志2014。利益冲突无利益冲突
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