Advancements in High Throughput Biophysical Technologies: Applications for Characterization and Screening during Early Formulation Development of Monoclonal Antibodies

被引:53
作者
Samra, Hardeep S. [1 ]
He, Feng [2 ]
机构
[1] MedImmune, Dept Formulat Sci, Gaithersburg, MD 20878 USA
[2] Amgen Inc, Drug Prod Dev, Seattle, WA 98119 USA
关键词
high throughput; biophysical technology; monoclonal antibody; formulation development; DYNAMIC LIGHT-SCATTERING; SIZE-EXCLUSION CHROMATOGRAPHY; DIFFERENTIAL SCANNING CALORIMETRY; 2ND VIRIAL-COEFFICIENT; HUMAN-IMMUNOGLOBULIN-G; SELF-INTERACTION CHROMATOGRAPHY; PROMOTE PROTEIN STABILITY; THERMAL SHIFT ASSAYS; FLUORESCENCE POLARIZATION; THERAPEUTIC PROTEINS;
D O I
10.1021/mp200404c
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
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 G's (IgG's) 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.
引用
收藏
页码:696 / 707
页数:12
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