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交联硅胶涂层:一种新型预填充注射器技术,可减少亚可见颗粒并保持与生物制品的兼容性。

Cross-linked silicone coating: a novel prefilled syringe technology that reduces subvisible particles and maintains compatibility with biologics.

作者信息

Depaz Roberto A, Chevolleau Tzvetelina, Jouffray Sébastien, Narwal Roja, Dimitrova Mariana N

机构信息

Formulation Sciences Department, MedImmune, Gaithersburg, Maryland, 20878.

出版信息

J Pharm Sci. 2014 May;103(5):1384-93. doi: 10.1002/jps.23947. Epub 2014 Mar 18.

DOI:10.1002/jps.23947
PMID:24643773
Abstract

Prefilled syringes (PFSs) offer improvements in the delivery of drugs to patients compared with traditional vial presentations and are becoming necessities in an increasingly competitive biologics market. However, the development of a product in a PFS must take into account potential incompatibilities between the drug and the components of the syringe. One such component is silicone oil, which has previously been suggested to promote protein aggregation, loss of soluble protein, and an increase in the particulate content of injectable formulations. This study evaluated the particulate content in a model buffer system (polysorbate 80/phosphate-buffered saline) after agitation in glass syringes with a novel cross-linked silicone coating. We also evaluated the compatibility of two monoclonal antibodies with these syringes. We report that syringes with this novel coating, compared with standard siliconized syringes, exhibited reduced particle content and enhanced integrity of the lubricant layer as determined by reflectometry, optical microscopy, and time-of-flight secondary ion mass spectrometry measurements, while maintaining the desired functional properties of the syringe and the antibodies' stability profiles as determined by high-performance size-exclusion chromatography. Enhanced integrity of the lubricant coating led to significantly fewer subvisible particles in the liquid formulations, particularly after agitation stresses introduced by shipping of the syringes.

摘要

与传统的瓶装剂型相比,预填充注射器(PFS)在向患者给药方面有改进,并且在竞争日益激烈的生物制品市场中正成为必需品。然而,开发PFS剂型的产品必须考虑药物与注射器组件之间的潜在不相容性。硅油就是这样一种组件,此前有人认为它会促进蛋白质聚集、可溶性蛋白质损失以及注射剂颗粒含量增加。本研究评估了在带有新型交联硅涂层的玻璃注射器中搅拌后,模型缓冲系统(聚山梨酯80/磷酸盐缓冲盐水)中的颗粒含量。我们还评估了两种单克隆抗体与这些注射器的相容性。我们报告称,与标准硅化注射器相比,带有这种新型涂层的注射器颗粒含量降低,通过反射测量、光学显微镜和飞行时间二次离子质谱测量确定,润滑剂层的完整性增强,同时保持了注射器所需的功能特性以及通过高效尺寸排阻色谱法测定的抗体稳定性。润滑剂涂层完整性的增强导致液体制剂中不可见颗粒显著减少,尤其是在注射器运输引入的搅拌应力之后。

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