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预填充硅化注射器中聚集体和硅油计数的评估:一项表征整个亚可见尺寸范围的正交研究。

Evaluation of aggregate and silicone-oil counts in pre-filled siliconized syringes: An orthogonal study characterising the entire subvisible size range.

作者信息

Shah Maryam, Rattray Zahra, Day Katie, Uddin Shahid, Curtis Robin, van der Walle Christopher F, Pluen Alain

机构信息

Division of Pharmacy and Optometry, School of Health Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

MedImmune Ltd, Formulation Sciences, Granta Park, Cambridge, UK.

出版信息

Int J Pharm. 2017 Mar 15;519(1-2):58-66. doi: 10.1016/j.ijpharm.2017.01.015. Epub 2017 Jan 9.

Abstract

Characterisation of particulates in therapeutic monoclonal antibody (mAb) formulations is routinely extended to the sub-visible size-range (0.1-10μm). Additionally, with the increased use of pre-filled syringes (PFS), particle differentiation is required between proteinaceous and non-proteinaceous particles such as silicone-oil droplets. Here, three orthogonal techniques: Raster Image Correlation Spectroscopy (RICS), Resonance Mass Measurements (RMM) and Micro-Flow Imaging (MFI), were evaluated with respect to their sub-visible particle measurement and characterisation capabilities. Particle formation in mAb PFS solutions was evaluated with increasing polysorbate-20 (PS-20) concentrations. All three techniques provided complementary but distinct information on protein aggregate and silicone-oil droplet presence. PS-20 limited the generation of mAb aggregates during agitation, while increasing the number of silicone-oil droplets (PS-20 concentration dependant). MFI and RMM revealed PS-20 lead to the formation of larger micron-sized droplets, with RICS revealing an increase in smaller sub-micron droplets. Subtle differences in data sets complicate the apparent correlation between silicone-oil sloughing and mAb aggregates' generation. RICS (though the use of a specific dye) demonstrates an improved selectivity for mAb aggregates, a broader measurement size-range and smaller sample volume requirement. Thus, RICS is proposed to add value to the currently available particle measurement techniques and enable informed decisions during mAb formulation development.

摘要

治疗性单克隆抗体(mAb)制剂中颗粒的表征通常会扩展到亚可见尺寸范围(0.1 - 10μm)。此外,随着预填充注射器(PFS)使用的增加,需要区分蛋白质颗粒和非蛋白质颗粒,如硅油滴。在此,对三种正交技术:光栅图像相关光谱法(RICS)、共振质量测量法(RMM)和微流成像法(MFI)在亚可见颗粒测量和表征能力方面进行了评估。随着聚山梨酯 - 20(PS - 20)浓度的增加,评估了mAb PFS溶液中的颗粒形成情况。所有这三种技术都提供了关于蛋白质聚集体和硅油滴存在的互补但不同的信息。PS - 20在搅拌过程中限制了mAb聚集体的产生,同时增加了硅油滴的数量(取决于PS - 20浓度)。MFI和RMM显示PS - 20导致形成更大的微米级液滴,而RICS显示较小的亚微米级液滴数量增加。数据集中的细微差异使硅油脱落与mAb聚集体产生之间的明显相关性变得复杂。RICS(通过使用特定染料)对mAb聚集体表现出更高的选择性、更宽的测量尺寸范围和更小的样品体积要求。因此,建议RICS为当前可用的颗粒测量技术增添价值,并在mAb制剂开发过程中做出明智的决策。

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