Using design of experiments to improve a batch chemical process

Thesis (M.B.A.)--Massachusetts Institute of Technology, Sloan School of Management; and, (S.M.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering; in conjunction with the Leaders for Global Operations Program at MIT, 2010. === Cataloged from PDF version of thesis. === Includes bi...

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Main Author: Hill, Andrew, S.M. (Andrew James). Massachusetts Institute of Technology
Other Authors: Roy Welsch and Charles L. Cooney.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2010
Subjects:
Online Access:http://hdl.handle.net/1721.1/59183
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-591832019-05-02T16:10:07Z Using design of experiments to improve a batch chemical process Hill, Andrew, S.M. (Andrew James). Massachusetts Institute of Technology Roy Welsch and Charles L. Cooney. Leaders for Global Operations Program. Sloan School of Management. Massachusetts Institute of Technology. Dept. of Chemical Engineering. Leaders for Global Operations Program. Sloan School of Management. Chemical Engineering. Leaders for Global Operations Program. Thesis (M.B.A.)--Massachusetts Institute of Technology, Sloan School of Management; and, (S.M.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering; in conjunction with the Leaders for Global Operations Program at MIT, 2010. Cataloged from PDF version of thesis. Includes bibliographical references (p. 70-71). Novartis Vaccines and Diagnostics has made a strong commitment to manufacturing seasonal influenza vaccines through their cell culture technology called Optaflu®. The goal of this project is to improve overall process yield by modifying the upstream process. The focus is on using a batch process to generate a high-density cell culture and then infecting said culture. This thesis presents the approach of using a Design of Experiment series to change a manufacturing process. Current vaccine production occurs with a fed-batch process by feeding glucose as a carbon-energy source for the final cell expansion step. This cell culture is diluted, infected, harvested, and purified for use in an influenza vaccine. Primarily, the project aims to increase cell density, using a batch process, at the infection step which should improve overall process yield. The project can therefore be broken into two main steps: batch cell growth and highdensity infection. Experiments for this project were conducted with a small-scale laboratory process that mimics the production process. The planned approach was a Design of Experiment series to screen parameters and partially optimize the cell growth process, a scale-up cell growth experiment, and finally another Design of Experiment series to explore high-density cell infection. While initial small-scale experiments showed extremely positive results, the results were not consistent and could not be replicated at a larger scale. A number of exploratory experiments were run to attempt to identify which factors inhibit high-density cell growth, particularly around scale-up, but no key parameter was identified. Given the process improvement and cost savings implications from the success of the initial small-scale experiments, this project is worth further exploration. by Andrew Hill. S.M. M.B.A. 2010-10-12T18:06:01Z 2010-10-12T18:06:01Z 2010 2010 Thesis http://hdl.handle.net/1721.1/59183 659806756 eng 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. http://dspace.mit.edu/handle/1721.1/7582 71 p. application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Sloan School of Management.
Chemical Engineering.
Leaders for Global Operations Program.
spellingShingle Sloan School of Management.
Chemical Engineering.
Leaders for Global Operations Program.
Hill, Andrew, S.M. (Andrew James). Massachusetts Institute of Technology
Using design of experiments to improve a batch chemical process
description Thesis (M.B.A.)--Massachusetts Institute of Technology, Sloan School of Management; and, (S.M.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering; in conjunction with the Leaders for Global Operations Program at MIT, 2010. === Cataloged from PDF version of thesis. === Includes bibliographical references (p. 70-71). === Novartis Vaccines and Diagnostics has made a strong commitment to manufacturing seasonal influenza vaccines through their cell culture technology called Optaflu®. The goal of this project is to improve overall process yield by modifying the upstream process. The focus is on using a batch process to generate a high-density cell culture and then infecting said culture. This thesis presents the approach of using a Design of Experiment series to change a manufacturing process. Current vaccine production occurs with a fed-batch process by feeding glucose as a carbon-energy source for the final cell expansion step. This cell culture is diluted, infected, harvested, and purified for use in an influenza vaccine. Primarily, the project aims to increase cell density, using a batch process, at the infection step which should improve overall process yield. The project can therefore be broken into two main steps: batch cell growth and highdensity infection. Experiments for this project were conducted with a small-scale laboratory process that mimics the production process. The planned approach was a Design of Experiment series to screen parameters and partially optimize the cell growth process, a scale-up cell growth experiment, and finally another Design of Experiment series to explore high-density cell infection. While initial small-scale experiments showed extremely positive results, the results were not consistent and could not be replicated at a larger scale. A number of exploratory experiments were run to attempt to identify which factors inhibit high-density cell growth, particularly around scale-up, but no key parameter was identified. Given the process improvement and cost savings implications from the success of the initial small-scale experiments, this project is worth further exploration. === by Andrew Hill. === S.M. === M.B.A.
author2 Roy Welsch and Charles L. Cooney.
author_facet Roy Welsch and Charles L. Cooney.
Hill, Andrew, S.M. (Andrew James). Massachusetts Institute of Technology
author Hill, Andrew, S.M. (Andrew James). Massachusetts Institute of Technology
author_sort Hill, Andrew, S.M. (Andrew James). Massachusetts Institute of Technology
title Using design of experiments to improve a batch chemical process
title_short Using design of experiments to improve a batch chemical process
title_full Using design of experiments to improve a batch chemical process
title_fullStr Using design of experiments to improve a batch chemical process
title_full_unstemmed Using design of experiments to improve a batch chemical process
title_sort using design of experiments to improve a batch chemical process
publisher Massachusetts Institute of Technology
publishDate 2010
url http://hdl.handle.net/1721.1/59183
work_keys_str_mv AT hillandrewsmandrewjamesmassachusettsinstituteoftechnology usingdesignofexperimentstoimproveabatchchemicalprocess
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