Magnetically enhanced centrifugation for continuous biopharmaceutical processing

Effective separation and purification of biopharmaceutical products from the media in which they are produced continues to be a challenging task. Such processes usually involve multiple steps and the overall product loss can be significant. As an integrative technique, high gradient magnetic separation (HGMS), together with the application of functional magnetic particles, provides many advantages over traditional techniques. However, HGMS has a number of drawbacks; and its application is limited because it is inherently a batch process and it is difficult to recycle the magnetic nanoparticles. This thesis explores the development of a new type of continuous magnetic separation process, called magnetically enhanced centrifugation (MEC), which exploits the interactions of magnetic particles with magnetic field gradients, forced convective flows and large centrifugal forces. Magnetically susceptible wires in a uniform magnetic field facilitate the capture and aggregation of magnetic particles on wires, and a centrifugal force perpendicular to the magnetic force conveys the particle sludge parallel to the wires in a continuous mode. The primary focus of this thesis is multi-scale modeling and simulation to understand the underlying physics of MEC processes. The potential of MEC as an effective unit operation for biopharmaceutical downstream processing has been demonstrated. Unlike traditional batch-mode HGMS, MEC has a great advantage in that it can be operated continuously as magnetic particles captured on wire surface are constantly removed.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Chemical Engineering.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2009

Author dc:creator

• Chen, Fei, Ph. D. Massachusetts Institute of Technology

Advisor dc:contributor.advisor

• T. Alan Hatton and Kenneth A. Smith.

• Chemical Engineering.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/51565

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/51565