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辅料无法保护液体制剂免受跌落降解的影响。

Secondary Packages cannot Protect Liquid Biopharmaceutical Formulations from Dropping-Induced Degradation.

机构信息

Institute of Drug Metabolism and Pharmaceutical Analysis, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, 310058, China.

Hangzhou Institute of Innovative Medicine, Zhejiang University, Hangzhou, 310016, China.

出版信息

Pharm Res. 2021 Aug;38(8):1397-1404. doi: 10.1007/s11095-021-03073-1. Epub 2021 Jul 19.

Abstract

PURPOSES

Liquid protein-based biopharmaceutical formulations have been reported to form aggregation and protein sub-visible particles (SbVPs) during dropping (Randolph et al., J Pharm Sci 2015, 104, 602). However, effects of secondary package on liquid biopharmaceutical formulation stability during dropping are overlooked and have not been reported so far. This study reports the first real-world evaluation on effects of secondary package on liquid biopharmaceutical formulation stability during dropping, using two monoclonal antibodies (mAb-1 and mAb-2) and one fusion protein (FP-1) as model biopharmaceuticals.

METHODS

The potential protective effects of secondary package and formulation composition on liquid biopharmaceutical formulations during dropping were evaluated with micro-flow imaging (MFI) and dynamic light scattering (DLS).

RESULTS

The dropping-induced degradation could be detected with the two sensitive particle analyzing techniques MFI and DLS. Formulation compositions have dramatic impact on biopharmaceutical stability during dropping. Surprisingly, unlike the primary packages that have been reported to impact liquid biopharmaceutical stability, the secondary packaging system as described in our current preliminary design has little or no protective effect during dropping.

CONCLUSIONS

Our study is the first real-world data showing that the secondary package system has little to no effect on the liquid biopharmaceutical formulation quality during dropping. On the contrary, the stability of liquid biopharmaceutical formulations during dropping is more relevant to formulation compositions and primary packages.

摘要

目的

据报道,液体制剂型生物制药制剂在滴注过程中会形成聚集和蛋白亚可见颗粒(SbVPs)(Randolph 等人,J Pharm Sci 2015, 104, 602)。然而,滴注过程中次级包装对液体制剂型生物制药制剂稳定性的影响尚未得到重视,迄今为止尚未有相关报道。本研究首次报道了次级包装对液体制剂型生物制药制剂在滴注过程中稳定性的实际影响,使用两种单克隆抗体(mAb-1 和 mAb-2)和一种融合蛋白(FP-1)作为模型生物制药进行评估。

方法

使用微流成像(MFI)和动态光散射(DLS)评估次级包装和制剂成分对液体制剂型生物制药制剂在滴注过程中的潜在保护作用。

结果

两种敏感的颗粒分析技术 MFI 和 DLS 均可检测到滴注引起的降解。制剂成分对滴注过程中的生物制药稳定性有显著影响。令人惊讶的是,与已报道的对液体制剂型生物制药稳定性有影响的初级包装不同,我们目前初步设计中描述的次级包装系统在滴注过程中几乎没有或没有保护作用。

结论

我们的研究首次表明,次级包装系统对液体制剂型生物制药制剂在滴注过程中的质量几乎没有影响。相反,液体制剂型生物制药制剂在滴注过程中的稳定性与制剂成分和初级包装更相关。

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