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Antimicrobial PDMS Surfaces Prepared through Fast and Oxygen-Tolerant SI-SARA-ATRP, Using Na2SO3 as a Reducing Agent
Christian Andersen1, Libor Zverina1, Koosha Ehtiati2
1Danish Polymer Centre, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Søltofts Plads Building 229, 2800 Kgs. Lyngby, Denmark.
ACS Omega
|June 14, 2021
Summary
A new method creates antimicrobial poly(dimethylsiloxane) (PDMS) surfaces for biomedical devices. This approach enhances PDMS
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Surface Science
Background:
- Poly(dimethylsiloxane) (PDMS) is widely used in biomedical devices due to its favorable properties.
- The inherent hydrophobicity of PDMS leads to microbial colonization, necessitating antimicrobial surfaces.
- Existing surface modification methods for PDMS are limited in scope and scalability.
Purpose of the Study:
- To develop a simple, scalable method for creating antimicrobial PDMS surfaces.
- To functionalize PDMS surfaces with poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) brushes.
- To investigate the antimicrobial properties of the modified surfaces based on charge density and amphiphilicity.
Main Methods:
- Grafting of a novel atom transfer radical polymerization (ATRP) initiator onto the PDMS surface.
- Surface-initiated supplemental activator and reducing agent ATRP (SI-SARA-ATRP) using sodium sulfite.
- Quaternization of the grafted PDMAEMA brushes with alkyl halides.
Main Results:
- Successful grafting of PDMAEMA brushes onto PDMS surfaces with fast and linear polymer growth (400 nm in 120 min).
- The SI-SARA-ATRP method demonstrated high oxygen tolerance and robustness.
- Antimicrobial activity was significantly influenced by the charge density and amphiphilicity of the quaternized surfaces.
Conclusions:
- The developed method provides a facile and scalable route to antimicrobial PDMS surfaces.
- The functionalized PDMS surfaces exhibit tunable antimicrobial properties.
- This advancement facilitates the broader application of PDMS in infection-prone biomedical devices.

