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Advancements in high throughput biophysical technologies: Applications for characterization and screening during early formulation development of monoclonal antibodies

机译:高通量生物物理技术的进展:单克隆抗体早期制剂开发过程中的表征和筛选应用

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摘要

The formulation development of monoclonal antibodies is extremely challenging, due to the diversity and complexity contained within this class of molecules. The physical and chemical properties of a monoclonal antibody dictate the behavior of the protein drug during manufacturing, storage and clinical administration. In the past few years, the use of high throughput technologies has been widely adapted to delineate unique properties of individual immunoglobulin Gs (IgGs) important for their development. Numerous screening techniques have been designed to reveal physical and chemical characteristics of a protein relevant to stability under production, formulation and delivery conditions. In addition, protein stability under accelerated stresses has been utilized to predict long-term storage behavior for monoclonal antibodies in the formulation. In this review, we summarize the recent advancements in the field of biophysical technology, with a specific focus on the techniques that can be directly applied to the formulation development of monoclonal antibodies. Several case studies are also presented here to provide examples of combining existing biophysical methods with high throughput screening technology in the formulation development of monoclonal antibody drugs.
机译:由于这类分子中所包含的多样性和复杂性,单克隆抗体的制剂开发极具挑战性。单克隆抗体的物理和化学性质决定了蛋白药物在生产,储存和临床给药过程中的行为。在过去的几年中,高通量技术的使用已广泛适应于描述对它们的发展很重要的单个免疫球蛋白G(IgG)的独特特性。已经设计了许多筛选技术以揭示与在生产,配制和递送条件下的稳定性有关的蛋白质的物理和化学特征。另外,在加速应激下的蛋白质稳定性已被用于预测制剂中单克隆抗体的长期储存行为。在这篇综述中,我们总结了生物物理技术领域的最新进展,特别关注可以直接应用于单克隆抗体制剂开发的技术。本文还提供了一些案例研究,以提供在单克隆抗体药物制剂开发中将现有生物物理方法与高通量筛选技术相结合的实例。

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