Amino-Acid-Incorporating Nonionic Surfactants for Stabilization of Protein Pharmaceuticals

被引:20
|
作者
Katz, Joshua S. [1 ]
Tan, Yujing [2 ]
Kuppannan, Krishna [2 ]
Song, Yang [3 ,4 ]
Brennan, David J. [4 ]
Young, Timothy [4 ]
Yao, Lu [1 ]
Jordan, Susan [1 ]
机构
[1] Dow Chem Co USA, Core R&D, Formulat Sci, 400 Arcola Rd, Collegeville, PA 19426 USA
[2] Dow Chem Co USA, Core R&D, Analyt Sci, 1897 Bldg, Midland, MI 48674 USA
[3] Univ Illinois, Dept Chem, 405 North Matthews Ave, Urbana, IL 61801 USA
[4] Dow Chem Co USA, Core R&D, Formulat Sci, 1712 Bldg, Midland, MI 48674 USA
来源
关键词
biopharmaceutical; aggregation; surfactant; stabilization; AGGREGATION; FORMULATION; POLYSORBATE-80; ADSORPTION; SURFACES;
D O I
10.1021/acsbiomaterials.6b00245
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
With the rapid development of protein-based pharmaceutical products over the past decade, one of the biggest challenges in product development is maintaining the structural stability of proteins during purification, processing, and storage. In this work, the design of a new class of surfactants, polyether-modified N-acyl amino acids, is presented. One surfactant from this series, containing a phenylalanine moiety, demonstrated remarkable stabilization against aggregation of several model protein drugs. Dynamic light scattering, size exclusion chromatography, and circular dichroism all show the rate of thermally accelerated protein aggregation slowed. IgG aggregation was reduced by 3-fold compared to polysorbate controls. Testing of Orencia, a prescription biologic drug for rheumatoid arthritis, demonstrated a 36% improvement in monomer retention upon heat-aging.
引用
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页码:1093 / 1096
页数:4
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