In-use stability of ready-to-administer daratumumab subcutaneous injection solution in plastic syringes.

IF 1.6 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Laura Knoll, Judith Thiesen, Martin D Klassen, Lars M H Reinders, Jochen Tuerk, Irene Kraemer
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Abstract

Objective: In multiple myeloma patients, daratumumab is preferably injected subcutaneously. The summary of product characteristics of daratumumab subcutaneous injection solution specifies physicochemical stability for the prepared syringe for 24 hours at 2-8°C protected from light, and another 12 hours at room temperature (15-25°C) in ambient light conditions. The aim of this study was to determine the in-use stability of ready-to-administer daratumumab subcutaneous injection solution in different types of syringe and different conditions over a 28-day period.

Methods: Daratumumab subcutaneous (DARZALEX 1800 mg) injection solution was withdrawn into disposable three-piece Luer-Lock syringes (20 mL, 50 mL), capped, and stored light protected at 2-8°C or at room temperature (22±2°C) over a maximum period of 28 days. Samples were taken immediately after preparation (day 0) and after 2, 7, 14, 21, and 28 days. Physicochemical stability was determined by ion-exchange high-performance liquid chromatography (IE-HPLC) and size-exclusion high-performance liquid chromatography (SE-HPLC) with ultraviolet detection, pH measurement and visual inspection for particles or colour changes.

Results: In the IE-HPLC assay, peak areas and peak-to-peak area ratios remained unchanged over the whole study period, and showed no additional peaks of degraded daratumumab charge variants. In the SE-HPLC assay, neither a formation of aggregates nor of fragments was detected. Daratumumab monomer concentrations exceeded 95% of the initially measured concentrations over the entire test period. pH values remained constant. Test solutions remained clear, and no colour changes or visible particles were detected. All results were independent of storage conditions.

Conclusion: Daratumumab subcutaneous injection solution proved to be physicochemically stable in capped three-piece plastic syringes for at least 28 days when stored light protected at 2-8°C or at room temperature (22±2°C). For microbiological reasons aseptic preparation and refrigerated storage are recommended. In-use stability of ready-to-administer daratumumab subcutaneous syringes prepared under appropriate aseptic conditions is given for 28 days.

在塑料注射器中的daratumumab皮下注射溶液的使用稳定性。
目的:多发性骨髓瘤患者最好皮下注射达拉图单抗。daratumumab皮下注射溶液的产品特性摘要规定了制备的注射器在2-8°C避光条件下24小时的物理化学稳定性,以及在室温(15-25°C)环境光条件下12小时的物理物理化学稳定性。本研究的目的是确定daratumumab皮下注射溶液在不同类型的注射器和不同条件下28天内的使用稳定性。方法:Daratumumab皮下注射(DARZALEX 1800 mg)注射溶液抽出到一次性三件式Luer-Lock注射器(20 mL,50 mL),加盖,并在2-8°C或室温(22±2°C)下避光保存,最长保存28天。在制备后(第0天)以及第2、7、14、21和28天后立即取样。通过离子交换高效液相色谱法(IE-HPLC)和尺寸排阻高效液相色谱仪(SE-HPLC)测定物理化学稳定性,并进行紫外线检测、pH测量和颗粒或颜色变化的目视检查。结果:在IE-HPLC测定中,峰面积和峰面积比在整个研究期间保持不变,并且没有显示降解的daratumumab电荷变体的额外峰值。在SE-HPLC测定中,既没有检测到聚集体的形成,也没有检测到片段的形成。Daratumumab单体浓度在整个试验期间超过了最初测量浓度的95%。pH值保持恒定。试验溶液保持澄清,未检测到颜色变化或可见颗粒。所有结果与储存条件无关。结论:Daratumumab皮下注射溶液在2-8°C或室温(22±2°C)下避光保存,在带帽三件式塑料注射器中物理化学稳定至少28天。出于微生物原因,建议进行无菌制备和冷藏。在适当无菌条件下制备的达拉图单抗皮下注射器的使用稳定性为28天。
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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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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