Use of microcalorimetry and its correlation with size exclusion chromatography for rapid screening of the physical stability of large pharmaceutical proteins in solution

被引:16
作者
Burton, Lori
Gandhi, Rajesh
Duke, Gerald
Paborji, Mehdi
机构
[1] Bristol Myers Squibb Co, New Brunswick, NJ 08903 USA
[2] Bristol Myers Squibb Co, Princeton, NJ USA
[3] Thera Vida, Irvine, CA USA
关键词
proteins; pH stability; aggregation; excipients; microcalorimetry; size exclusion chromatography;
D O I
10.1080/10837450701212610
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The utility of microcalorimetry as a rapid screening tool for assessing the solution stability of high molecular weight pharmaceutical proteins was evaluated by using model recombinant antibodies, Protein I and Protein II. Changes in the transition midpoint, T-m, were monitored as a function of pH and/or in the presence of excipients, and results were compared with traditional accelerated stability data from samples that were analyzed by size exclusion chromatography (SEC). The data from microcalorimetry were well correlated with those from SEC for predicting both optimal solution pH as well as excipient effects on solution stability. These results indicate that microcalorimetry can be an efficient screening tool useful in identifying optimal pH conditions and excipients to stabilize pharmaceutical proteins in solution formulations.
引用
收藏
页码:265 / 273
页数:9
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