• Login
    View Item 
    •   Home
    • UA Graduate and Undergraduate Research
    • UA Theses and Dissertations
    • Honors Theses
    • View Item
    •   Home
    • UA Graduate and Undergraduate Research
    • UA Theses and Dissertations
    • Honors Theses
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Browse

    All of UA Campus RepositoryCommunitiesTitleAuthorsIssue DateSubmit DateSubjectsPublisherJournalThis CollectionTitleAuthorsIssue DateSubmit DateSubjectsPublisherJournal

    My Account

    LoginRegister

    About

    AboutUA Faculty PublicationsUA DissertationsUA Master's ThesesUA Honors ThesesUA PressUA YearbooksUA CatalogsUA Libraries

    Statistics

    Most Popular ItemsStatistics by CountryMost Popular Authors

    MONOCLONAL ANTIBODY PRODUCTION FOR CANCER IMMUNOTHERAPY

    • CSV
    • RefMan
    • EndNote
    • BibTex
    • RefWorks
    Thumbnail
    Name:
    azu_etd_hr_2018_0180_sip1_m.pdf
    Size:
    978.3Kb
    Format:
    PDF
    Download
    Author
    Slosky, Sara Elizabeth
    Issue Date
    2018
    Advisor
    Ogden, Kim
    
    Metadata
    Show full item record
    Publisher
    The University of Arizona.
    Rights
    Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
    Abstract
    The goal of the proposed plant is to produce 8760 g of bevacizumab at a concentration of 25 mg/mL which yields 349 L of product per year. Bevacizumab is a monoclonal antibody that is used to treat six different types of cancer. It acts by binding to the growth factor which essentially starves the cancerous tumor. To mass produce the antibody, recombinant Chinese Hamster Ovary cells that produce the desired humanized antibody are grown in a cascade of bioreactors. The cell solution then goes through a series of purification steps to isolate the desired antibody. A centrifuge is used to remove cell mass and chromatography columns are used to rid the solution of the undesired proteins. Filtration removes the buffer salts and then the final product is freeze dried. While the startup cost of the proposed plant is high, the pharmaceutical market is very lucrative and the facility is expected to make a profit within the first year. After seven years the investment has an estimated net present value of over $120 million. Due to the high economic return, the proposed plant design should move on to further development and implementation.
    Type
    text
    Electronic Thesis
    Degree Name
    B.S.
    Degree Level
    bachelors
    Degree Program
    Honors College
    Chemical and Environmental Engineering
    Collections
    Honors Theses

    entitlement

     
    The University of Arizona Libraries | 1510 E. University Blvd. | Tucson, AZ 85721-0055
    Tel 520-621-6442 | repository@u.library.arizona.edu
    DSpace software copyright © 2002-2017  DuraSpace
    Quick Guide | Contact Us | Send Feedback
    Open Repository is a service operated by 
    Atmire NV
     

    Export search results

    The export option will allow you to export the current search results of the entered query to a file. Different formats are available for download. To export the items, click on the button corresponding with the preferred download format.

    By default, clicking on the export buttons will result in a download of the allowed maximum amount of items.

    To select a subset of the search results, click "Selective Export" button and make a selection of the items you want to export. The amount of items that can be exported at once is similarly restricted as the full export.

    After making a selection, click one of the export format buttons. The amount of items that will be exported is indicated in the bubble next to export format.