静脉输液袋中稀释的维多珠单抗的物理化学和生物学稳定性。

IF 1.6 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Tine C J Hendrickx, Kevin D H Balcaen, Marielle Baert, Jurgen Haustraete, Bart N Lambrecht
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引用次数: 0

摘要

简介静脉注射韦多珠单抗是一种广泛用于炎症性肠病患者的单克隆抗体。药物配制在给药当天进行,但耗费时间,造成不必要的院内患者延误,配制和分发的物流效率低下。储存韦多珠单抗即用型输液并通过气动气管配送可简化门诊环境中的物流。本研究旨在测试含有维多珠单抗的即用型静脉输液袋的保质期和稳定性:为了评估使用中的保质期,我们在无菌条件下将重组产品(300 毫克固定剂量)在 0.9% 氯化钠中稀释至 1.2 毫克/毫升的浓度,并在分析前将其储存在 2-8°C的聚烯烃输液袋中。我们使用十二烷基硫酸钠聚丙烯酰胺凝胶电泳法、尺寸排阻色谱法和多角度激光光散射法测定了重复样品的浓度、物理和化学稳定性,并使用生物层干涉测定法研究了目标参与的生物活性,以及评估微生物稳定性的内毒素含量。通过气管系统运输后,还对即用型维多珠单抗的稳定性进行了评估。在 30 天的观察期内,在不同的时间点对四个重复样本进行取样:就所有评估参数而言,韦多珠单抗的即用溶液在至少 30 天内保持稳定。没有出现蛋白质聚集、化学性质不稳定或抗体失去与α4β7整合素靶点结合的迹象。随着时间的推移,内毒素浓度没有增加。通过气管系统运输前后的样品在抗体结构稳定性和蛋白质聚集方面没有明显差异:结论:在无菌条件下配制溶解的即用型维多珠单抗输液袋可长期储存于 2-8°C,并通过气动管道运输,不会出现抗体稳定性或结合活性的明显降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Physicochemical and biological stability of diluted vedolizumab in intravenous infusion bags.

Introduction: Intravenous vedolizumab is a widely used monoclonal antibody for outpatients with inflammatory bowel disease. Drug preparation is performed on the day of administration, but is time consuming, causing unnecessary in-hospital patient delay and inefficient logistics for preparation and distribution. Storage of vedolizumab ready-to-administer infusions and distribution via pneumatic air tubes could streamline logistics in the outpatient setting. The aim of this study was to test the shelf life and stability of ready-to-administer intravenous infusion bags containing vedolizumab.

Methods: For assessing in-use shelf life, the reconstituted product (300 mg fixed dose) was diluted to a concentration of 1.2 mg/mL in 0.9% NaCl under aseptic conditions, and stored in polyolefin infusion bags at 2-8°C prior to analysis. On replicate samples, we measured concentration, physical and chemical stability using sodium dodecyl sulphate polyacrylamide gel electrophoresis, size exclusion chromatography, and multi-angle laser light scattering, as well as biological activity using a biolayer interferometry assay to study target engagement, and endotoxin content to assess microbiological stability. Stability of ready-to-use vedolizumab was assessed also after transportation via pneumatic tube system. Samples were taken at different time points over an observation period of 30 days on four replicate samples.

Results: For all parameters assessed, the ready-to-use solution of vedolizumab remained stable over a period of at least 30 days. There were no signs of protein aggregation, chemical instability, or loss of binding of the antibody to the α4β7 integrin target. There was no increase in endotoxin concentration over time. No significant difference was seen in antibody structural stability and protein aggregation between samples before and after transportation via pneumatic tube system.

Conclusion: When prepared under aseptic conditions, dissolved ready-to-administer vedolizumab infusion bags can be stored long term at 2-8°C and transported via pneumatic air tube, without observable loss of antibody stability or binding activity.

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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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