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

    Browse

    All of TUScholarShareCommunitiesDateAuthorsTitlesSubjectsGenresThis CollectionDateAuthorsTitlesSubjectsGenres

    My Account

    LoginRegister

    Help

    AboutPeoplePoliciesHelp for DepositorsData DepositFAQs

    Statistics

    Most Popular ItemsStatistics by CountryMost Popular Authors

    Antibiotic Movement through Heterogeneous Biofilms

    • CSV
    • RefMan
    • EndNote
    • BibTex
    • RefWorks
    Thumbnail
    Name:
    Henry_temple_0225E_15885.pdf
    Size:
    27.66Mb
    Format:
    PDF
    Download
    Genre
    Thesis/Dissertation
    Date
    2024-08
    Author
    Henry, Brandi
    Advisor
    Queisser, Gillian
    Committee member
    Seibold, Benjamin
    Klapper, Isaac
    Buttaro, Bettina A.
    Department
    Mathematics
    Subject
    Applied mathematics
    Antibiotic resistance
    Biofilms
    Mathematical modeling
    Numerical simulations
    Partial differential equations
    Permanent link to this record
    http://hdl.handle.net/20.500.12613/10718
    
    Metadata
    Show full item record
    DOI
    http://dx.doi.org/10.34944/dspace/10680
    Abstract
    Biofilms are communities of microorganisms that can form in the human microbiome and on medical implants among other locations. These communities provide greater protection for their member cells resulting in an increase in resistance to antibiotic treatment and persistent infections. There are several factors that may contribute to antibiotic resistance of biofilms. These studies were done concurrently with biological experiments to test the hypothesis that dense, rigid structures within the biofilm may be an additional mechanism for protection from antibiotics. A computational tool and workflow was developed to analyze bead movement for the characterization of biofilm biomaterial properties including rigidity. With this tool, the analysis revealed that the amyloid, curli, confers rigidity in biofilms, thereby restricting bead movement. Greater movement of the beads is seen in biofilms lacking curli and biofilms that produced complex heterogeneous rigid structures. A new model was also developed that uses microscopy imaging data to simulate diffusion-reaction of antibiotics within heterogeneous biofilms. This model was used to investigate the effect of the dense, rigid structures on antibiotic treatment through test simulations and simulations using biological imaging data. These studies reveal various properties about the dense, rigid structures that confer protection.
    ADA compliance
    For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact [email protected]
    Collections
    Theses and Dissertations

    entitlement

     

    Show Statistical Information

    DSpace software (copyright © 2002 - 2024)  DuraSpace
    Temple University Libraries | 1900 N. 13th Street | Philadelphia, PA 19122
    (215) 204-8212 | [email protected]
    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.