Boehringer Ingelheim Pharma GmbH & Co. KG, Corporate Division Biopharmaceuticals, Process Science, Protein Science, Biberach an der Riss, Germany.
Center for Theoretical Chemistry, Faculty of Chemistry and Biochemistry, Ruhr-University Bochum, Bochum, Germany.
Eur J Pharm Biopharm. 2017 Oct;119:353-360. doi: 10.1016/j.ejpb.2017.06.029. Epub 2017 Jul 6.
High-concentration protein formulation (HCPF) is a term that is used to describe protein formulations, mostly monoclonal antibody (mAb) drugs, at high protein concentration. The concentration is rarely defined, with typical ranges varying between 50 and 150mg/ml for mAbs. The term HCPF is meant to include and express specific solution properties of formulations that are prone to appear at high protein concentrations such as high viscosity, high opalescence, phase separation, gel formation or the increased propensity for protein particle formation. Thus the term HCPF can be understood as a descriptor of protein formulations, usually at high protein (monoclonal antibody) concentrations, which have specific solution, stability and colloidal properties that differ from formulations at low protein concentration (e.g. at 10mg/ml). The current paper highlights in brief the development challenges that might occur for high-concentration protein/monoclonal antibody formulations. In particular, the maximum concentration regimes achievable in HCPF remained unclear. Based on geometrical considerations involving packing of monoclonal antibodies in a lattice we map out a maximum concentration range that might be theoretically achievable. Different geometrical assumptions and packing models are compared and their relevance is critically discussed, in particular concerning the influence of the physicochemical properties of the monoclonal antibodies on their solubility, which is neglected in the simple geometrical model. According to our estimates, monoclonal antibody concentration above 500mg/ml will be very challenging to achieve. Our results have implications for setting up realistic drug product development strategies and for preparing convincing drug target product profiles for development.
高浓度蛋白质制剂(HCPF)是一个术语,用于描述蛋白质制剂,主要是单克隆抗体(mAb)药物,在高蛋白质浓度下。浓度很少被定义,典型范围在 50 至 150mg/ml 之间,适用于 mAb。HCPF 这个术语旨在包括和表达制剂的特定溶液性质,这些性质容易在高蛋白质浓度下出现,如高粘度、高乳光、相分离、凝胶形成或增加蛋白质颗粒形成的倾向。因此,HCPF 这个术语可以被理解为蛋白质制剂的一个描述符,通常在高蛋白质(单克隆抗体)浓度下,具有与低蛋白质浓度(例如 10mg/ml)下的制剂不同的特定溶液、稳定性和胶体性质。本文简要强调了高浓度蛋白质/单克隆抗体制剂可能出现的开发挑战。特别是,在 HCPF 中可实现的最大浓度范围仍不清楚。基于涉及单克隆抗体在晶格中堆积的几何考虑,我们绘制出了一个可能在理论上实现的最大浓度范围。比较了不同的几何假设和堆积模型,并对其相关性进行了批判性讨论,特别是关于单克隆抗体的物理化学性质对其溶解度的影响,这在简单的几何模型中被忽略了。根据我们的估计,单克隆抗体浓度超过 500mg/ml 将非常具有挑战性。我们的结果对制定现实的药物产品开发策略和为开发准备有说服力的药物目标产品概况具有重要意义。