Tomar Dheeraj S, Kumar Sandeep, Singh Satish K, Goswami Sumit, Li Li
a Biotherapeutics Pharmaceutical Sciences Research and Development, Pfizer Inc. , 700 Chesterfield Parkway West, Chesterfield , Missouri , 63017 , USA.
b Biotherapeutics Pharmaceutical Sciences Research and Development, Pfizer Inc ., 1 Burtt Road, Andover , Massachusetts , 01810 , USA.
MAbs. 2016;8(2):216-28. doi: 10.1080/19420862.2015.1128606. Epub 2016 Jan 6.
Effective translation of breakthrough discoveries into innovative products in the clinic requires proactive mitigation or elimination of several drug development challenges. These challenges can vary depending upon the type of drug molecule. In the case of therapeutic antibody candidates, a commonly encountered challenge is high viscosity of the concentrated antibody solutions. Concentration-dependent viscosity behaviors of mAbs and other biologic entities may depend on pairwise and higher-order intermolecular interactions, non-native aggregation, and concentration-dependent fluctuations of various antibody regions. This article reviews our current understanding of molecular origins of viscosity behaviors of antibody solutions. We discuss general strategies and guidelines to select low viscosity candidates or optimize lead candidates for lower viscosity at early drug discovery stages. Moreover, strategies for formulation optimization and excipient design are also presented for candidates already in advanced product development stages. Potential future directions for research in this field are also explored.
将突破性发现有效地转化为临床创新产品需要积极缓解或消除若干药物开发挑战。这些挑战会因药物分子类型而异。就治疗性抗体候选药物而言,一个常见的挑战是浓缩抗体溶液的高粘度。单克隆抗体和其他生物实体的浓度依赖性粘度行为可能取决于成对及更高阶的分子间相互作用、非天然聚集以及各种抗体区域的浓度依赖性波动。本文综述了我们目前对抗体溶液粘度行为分子起源的理解。我们讨论了在药物发现早期阶段选择低粘度候选药物或优化先导候选药物以降低粘度的一般策略和指导原则。此外,还针对已处于高级产品开发阶段的候选药物提出了制剂优化和辅料设计策略。还探索了该领域未来潜在的研究方向。