Skip navigation
  • Home
  • Browse
    • Communities
      & Collections
    • Browse Items by:
    • Publication Date
    • Author
    • Title
    • Subject
    • Department
  • Sign on to:
    • My MacSphere
    • Receive email
      updates
    • Edit Profile


McMaster University Home Page
  1. MacSphere
  2. Open Access Dissertations and Theses Community
  3. Open Access Dissertations and Theses
Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/29233
Title: CHEMICAL AND TOPOGRAPHICAL SURFACE MODIFICATION OF POLYMERS FOR PROTEIN IMMOBILIZATION
Authors: Li, Jie
Advisor: Sask, Kyla
Department: Biomedical Engineering
Publication Date: 2024
Abstract: When materials contact biological fluids including blood, protein adsorption occurs rapidly and the proteins present at the interface can subsequently influence the biological response, potentially causing undesired reactions and the failure of medical devices. This thesis explores the impact of surface properties on protein attachment to materials, providing crucial insights into material functionality and the response in biological conditions. To address the lack of control of proteins at interfaces, several surface modification strategies were developed including topographical, chemical and biological methods. These approaches aim to enhance the immobilization of specific proteins on polymer surfaces and obtain an improved understanding of the interactions. Bovine serum albumin (BSA), fibrinogen (Fg), fetuin-A (Fet-A) and immunoglobulin G (IgG) served as models to investigate the protein adsorption, competitive surface affinity and immobilization efficiency on modified surfaces. These desired biomolecules were immobilized on polymers using polydopamine (PDA) and newly synthesized diazirine molecules as linkers for surface conjugation with detailed characterization performed. The results indicated that micropatterned surfaces increased protein immobilization on polydimethylsiloxane (PDMS) by providing greater surface area. PDA-modified PDMS exhibited enhanced protein capacity along with good stability and combining micropatterns with PDA improved levels further. Multiple proteins were immobilized and the amounts could be controlled through either simultaneous or sequential methods. The strength of attachment of the proteins was influenced by the surrounding biological environment based on the concentrations of proteins. For diazirine-modified surfaces, activation through thermal and ultraviolet (UV) methods significantly improved both the quantity and stability of proteins immobilized on PDMS and polyurethane (PU). The diazirine conjugation approach is applicable to other substrates and can provide benefits for intricate devices and implants. Overall, this thesis contributes new knowledge to understanding protein-material interactions and provides novel and promising strategies for modifying polymer surfaces to achieve functionalized biomaterials for various medical applications.
URI: http://hdl.handle.net/11375/29233
Appears in Collections:Open Access Dissertations and Theses

Files in This Item:
File Description SizeFormat 
Li_Jie_2023Nov_PhD.pdf
Access is allowed from: 2024-11-26
5.92 MBAdobe PDFView/Open
Show full item record Statistics


Items in MacSphere are protected by copyright, with all rights reserved, unless otherwise indicated.

Sherman Centre for Digital Scholarship     McMaster University Libraries
©2022 McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4L8 | 905-525-9140 | Contact Us | Terms of Use & Privacy Policy | Feedback

Report Accessibility Issue