Sarin Deepika, Chakraborty Debasmita, Sreenivasan Shravan, Mishra Avinash, Rathore Anurag S
Department of Chemical Engineering, Indian Institute of Technology Delhi, India.
Growdea Technologies Pvt. Ltd., Gurugram, Haryana, India.
J Pharm Sci. 2025 Feb;114(2):1398-1409. doi: 10.1016/j.xphs.2024.12.017. Epub 2025 Jan 10.
Stability of complex biotherapeutics like monoclonal antibodies is paramount for their safe and efficacious use. Excipients are inactive ingredients that are added to the purified product so as to offer it a stable environment. Trehalose dihydrate is a non-reducing sugar that is commonly used as a stabilizing agent in biotherapeutic formulations under liquid and frozen states. The stabilizing effect of trehalose against aggregation in protein formulations is well known. The present study aims to offer insights into the stability effects of higher trehalose concentration (230 mM) on liquid trastuzumab under different forced stress conditions including thermal, light with and without hydrogen peroxide (HO), humidity and extraction stresses. Under thermal stress, while high molecular weight (HMW) accounted for 38.80 % in the trastuzumab sample without trehalose, it was 4.89 % at high trehalose concentration. Similarly, under light stress with HO, the trastuzumab sample without trehalose had >80 % more HMW than at high trehalose concentration. Two other IgG1 mAbs (rituximab and bevacizumab) were also evaluated for stability at higher trehalose concentrations (230 mM). Similar to trastuzumab, stabilization was observed under thermal stress for rituximab and bevacizumab at higher trehalose concentration compared to samples without trehalose (21.90 % and 29.90 % HMW, respectively). Likewise, accelerated (under humidity stress) and extraction stress induced secondary and tertiary structure disruptions were reduced at higher trehalose concentration. An in-silico study between binding interactions of trehalose and trastuzumab Fab region at different concentrations depicted an increase in hydrogen bonding with trastuzumab Fab when the trehalose concentration is increased, thereby reducing aggregation. Overall, mAb stability under forced stress conditions improved significantly at higher trehalose concentrations. While higher trehalose concentration (>200 mM) is used in mAb formulations and is known to minimise aggregation under thermal stress, however, the current study aims to also explore the stability imparted under light (with HO), humidity and extraction stresses for three different mAbs and attempts to explain the underlying mechanisms via in-silico studies.
像单克隆抗体这样的复杂生物治疗药物的稳定性对于其安全有效的使用至关重要。辅料是添加到纯化产品中以提供稳定环境的非活性成分。海藻糖二水合物是一种非还原糖,常用于生物治疗制剂在液态和冷冻状态下的稳定剂。海藻糖对蛋白质制剂中聚集的稳定作用是众所周知的。本研究旨在深入了解较高海藻糖浓度(230 mM)在不同强制应激条件下,包括热、有和没有过氧化氢(HO)的光照、湿度和提取应激,对液态曲妥珠单抗稳定性的影响。在热应激下,不含海藻糖的曲妥珠单抗样品中高分子量(HMW)占38.80%,而在高海藻糖浓度下为4.89%。同样,在有HO的光照应激下,不含海藻糖的曲妥珠单抗样品的HMW比高海藻糖浓度下多80%以上。还评估了另外两种IgG1单克隆抗体(利妥昔单抗和贝伐单抗)在较高海藻糖浓度(230 mM)下的稳定性。与曲妥珠单抗类似,与不含海藻糖的样品相比,在较高海藻糖浓度下,利妥昔单抗和贝伐单抗在热应激下观察到稳定作用(分别为21.90%和29.90%的HMW)。同样,在加速条件下(湿度应激)以及提取应激诱导的二级和三级结构破坏在较高海藻糖浓度下减少。一项关于不同浓度海藻糖与曲妥珠单抗Fab区域结合相互作用的计算机模拟研究表明,当海藻糖浓度增加时,与曲妥珠单抗Fab的氢键增加,从而减少聚集。总体而言,在较高海藻糖浓度下,强制应激条件下单克隆抗体的稳定性显著提高。虽然在单克隆抗体制剂中使用了较高的海藻糖浓度(>200 mM),并且已知其在热应激下可使聚集最小化,然而,当前研究旨在还探索在光照(有HO)、湿度和提取应激下三种不同单克隆抗体的稳定性,并试图通过计算机模拟研究解释其潜在机制。