کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5135238 | 1493428 | 2017 | 10 صفحه PDF | دانلود رایگان |

- The kinetic performance of sub-3 μm SEC columns is studied.
- Total and external porosity and calibration curves were characterized.
- Possible secondary interactions were measured.
- Several examples for biopharmaceutical separations are provided.
The aim of this study was to evaluate the practical possibilities and limitations of several recently introduced size exclusion chromatographic (SEC) columns of 150 Ã 4.6 mm, sub-3 μm (Agilent AdvanceBioSEC 2.7 μm, Tosoh TSKgel UP-SW3000 2.0 μm, Phenomenex Yarra SEC X-150 1.8 μm and Waters Acquity BEH200 1.7 μm) for the separation of biopharmaceutical proteins. For this purpose, some model proteins were tested, as well as several commercial therapeutic monoclonal antibodies (mAbs) and antibody-drug-conjugates (ADCs). Calibration curves were drawn to highlight the applicability of these new SEC columns for the separation of mAbs, ADCs and their aggregates, despite some differences in their nominal pore diameter (vary from 150 to 300 à ). The kinetic performance (van Deemter curves and kinetic pots) was evaluated. Columns packed with 1.7-2.0 μm particles improved the plate count by a factor of 1.5-2 compared to 2.7 μm particles, which is in agreement with theoretical expectations. Finally, possible secondary hydrophobic and/or electrostatic interactions between the SEC stationary phases and biopharmaceutical proteins were systematically studied. Significant differences in nonspecific interactions were observed, with hydrophobic interactions generally exerting more influence than electrostatic interactions. The use of a novel bond chemistry with the AdvanceBioSEC column was found highly effective to limit non-specific interactions and pave the way to further improvements for column provider. At the end, the average resolutions achieved on the four sub-3 μm SEC columns between monomer and dimer structures were comparable for ten approved mAbs products.
Journal: Journal of Chromatography A - Volume 1498, 19 May 2017, Pages 80-89