Fabricating electrospun cellulose nanofibre adsorbents for ion-exchange chromatography

Dods, SR, Hardick, O, Stevens, B ORCID: https://orcid.org/0000-0002-3270-4040 and Bracewell, DG, 2015. Fabricating electrospun cellulose nanofibre adsorbents for ion-exchange chromatography. Journal of Chromatography A, 1376, pp. 74-83. ISSN 0021-9673

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Abstract

Protein separation is an integral step in biopharmaceutical manufacture with diffusion-limited packed bed chromatography remaining the default choice for industry. Rapid bind-elute separation using convective mass transfer media offers advantages in productivity by operating at high flowrates. Electrospun nanofibre adsorbents are a non-woven fibre matrix of high surface area and porosity previously investigated as a bioseparation medium. The effects of compression and bed layers, and subsequent heat treatment after electrospinning cellulose acetate nanofibres were investigated using diethylaminoethyl (DEAE) or carboxylate (COO) functionalisations. Transbed pressures were measured and compared by compression load, COO adsorbents were 30%, 70% and 90% higher than DEAE for compressions 1, 5 and 10 MPa, respectively, which was attributed to the swelling effect of hydrophilic COO groups. Dynamic binding capacities (DBCs) at 10% breakthrough were measured between 2000 and 12,000 CV/h (2 s and 0.3 s residence times) under normal binding conditions, and DBCs increased with reactant concentration from 4 to 12 mg BSA/mL for DEAE and from 10 to 21 mg lysozyme/mL for COO adsorbents. Comparing capacities of compression loads applied after electrospinning showed that the lowest load tested, 1 MPa, yielded the highest DBCs for DEAE and COO adsorbents at 20 mg BSA/mL and 27 mg lysozyme/mL, respectively. At 1 MPa, DBCs were the highest for the lowest flowrate tested but stabilised for flowrates above 2000 CV/h. For compression loads of 5 MPa and 10 MPa, adsorbents recorded lower DBCs than 1 MPa as a result of nanofibre packing and reduced surface area. Increasing the number of bed layers from 4 to 12 showed decreasing DBCs for both adsorbents. Tensile strengths were recorded to indicate the mechanical robustness of the adsorbent and be related to packing the nanofibre adsorbents in large scale configurations such as pleated cartridges. Compared with an uncompressed adsorbent, compressions of 1, 5 and 10 MPa showed increases of 30%, 110% and 110%, respectively, for both functionalisations. The data presented show that capacity and mechanical strength can be balanced through compression after electrospinning and is particular to different functionalisations. This trade-off is critical to the development of nanofibre adsorbents into different packing configurations for application and scale up in bioseparation.

Item Type:	Journal article
Publication Title:	Journal of Chromatography A
Creators:	Dods, S.R., Hardick, O., Stevens, B. and Bracewell, D.G.
Publisher:	Elsevier
Date:	9 January 2015
Volume:	1376
ISSN:	0021-9673
Identifiers:	Number Type 10.1016/j.chroma.2014.12.010 DOI
Rights:	© 2014 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
Divisions:	Schools > School of Science and Technology
Record created by:	Jill Tomkinson
Date Added:	19 Apr 2016 09:45
Last Modified:	13 Oct 2017 08:56
URI:	https://irep.ntu.ac.uk/id/eprint/27648

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