Recent studies have demonstrated that box-shaped or cuboid packed-bed chromatographic devices represent an efficient alternative to conventional cylindrical columns for high-resolution preparative protein separations. This has been attributed to the greater uniformity of flow within these devices. However, for a more complete explanation, it is important to understand how the system hydrodynamics affects band broadening during the transport of proteins through these devices. In this study, we present first principle mathematical models to capture this interplay. These models were validated by flow-through and bind-and-elute experiments carried out using a colored protein as tracer. Control experiments were also carried out using equivalent commercial columns, i.e. having same bed height and cross-sectional area, and packed with same media. The trends observed in the experiments matched those predicted by the models, though there were deviations in the absolute values. These deviations are explained in terms of non-idealities that exist in the experimental set-up, as well as in terms of factors that were not considered in the model. The models discussed in this paper are not only useful for understanding the workings of the cuboid packed-bed device, but are also useful tools for designing, optimizing and scaling-up such devices.
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http://dx.doi.org/10.1016/j.chroma.2019.460764 | DOI Listing |
J Chromatogr A
March 2022
Department of Chemical Engineering, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4L7, Canada.
We describe and discuss a simple dry-compression technique for preparing a flat cuboid chromatography device containing a shallow packed-bed of crystalline hydroxyapatite nanoparticles. We then discuss the use of this device for fast protein separation in the bind-and-elute mode. Such separation could be carried out at quite low pressures, making it possible to use inexpensive low pressure chromatography systems.
View Article and Find Full Text PDFJ Chromatogr A
June 2021
Department of Chemical Engineering, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4L7, Canada. Electronic address:
Simultaneously reducing the bed-height and increasing the area of cross-section, while keeping the bed-volume the same, would substantially reduce the pressure drop across a process chromatography column. This would minimize problems such as resin compaction and non-uniformity in column packing, which are commonly faced when using soft chromatographic media. However, the increase in macroscale convective dispersion due to the increase in column diameter, and the resultant loss in resolution would far outweigh any potential benefit.
View Article and Find Full Text PDFJ Chromatogr A
September 2020
Department of Chemical Engineering, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4L7, Canada. Electronic address:
PEGylated proteins which are a class of protein-synthetic polymer conjugates that have shown significant promise in the area of biotherapeutics are difficult to purify. A cuboid packed-bed device was used to purify a mono-PEGylated therapeutic protein from impurities such as high molecular weight (HMW) species (e.g.
View Article and Find Full Text PDFJ Chromatogr A
May 2020
Department of Chemical Engineering, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada.
We discuss how the efficiency of a chromatography device could be enhanced by incorporating a new feature which ensures flow uniformity. The overall flow of fluid within the device, which has a cuboid shape, could be visualized as a combination of two z patterns. The device is therefore designated as cuboid z.
View Article and Find Full Text PDFJ Chromatogr A
March 2020
Department of Chemical Engineering, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4L7, Canada. Electronic address:
Recent studies have demonstrated that box-shaped or cuboid packed-bed chromatographic devices represent an efficient alternative to conventional cylindrical columns for high-resolution preparative protein separations. This has been attributed to the greater uniformity of flow within these devices. However, for a more complete explanation, it is important to understand how the system hydrodynamics affects band broadening during the transport of proteins through these devices.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!