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Graft-Then-Shrink: Simultaneous Generation of Antifouling Polymeric Interfaces and Localized Surface Plasmon Resonance Biosensors

Antifouling polymer coatings that are simple to manufacture are crucial for the performance of medical devices such as biosensors. “Grafting-to”, a simple technique where presynthesized polymers are immobilized onto surfaces, is commonly employed but suffers from nonideal polymer packing leading to...

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Bibliographic Details
Published in:ACS applied materials & interfaces 2021-11, Vol.13 (44), p.52362-52373
Main Authors: Jesmer, Alexander H, Huynh, Vincent, Marple, April S.T, Ding, Xiuping, Moran-Mirabal, Jose M, Wylie, Ryan G
Format: Article
Language:English
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Summary:Antifouling polymer coatings that are simple to manufacture are crucial for the performance of medical devices such as biosensors. “Grafting-to”, a simple technique where presynthesized polymers are immobilized onto surfaces, is commonly employed but suffers from nonideal polymer packing leading to increased biofouling. Herein, we present a material prepared via the grafting-to method with improved antifouling surface properties and intrinsic localized surface plasmon resonance (LSPR) sensor capabilities. A new substrate shrinking fabrication method, Graft-then-Shrink, improved the antifouling properties of polymer-coated Au surfaces by altering graft-to polymer packing while simultaneously generating wrinkled Au structures for LSPR biosensing. Thiol-terminated, antifouling, hydrophilic polymers were grafted to Au-coated prestressed polystyrene (PS) followed by shrinking upon heating above the PS glass transition temperature. Interestingly, the polymer molecular weight and hydration influenced Au wrinkling patterns. Compared to Shrink-then-Graft controls, where polymers are immobilized post shrinking, Graft-then-Shrink increased the polymer content by 76% in defined footprints and improved the antifouling properties as demonstrated by 84 and 72% reduction in macrophage adhesion and protein adsorption, respectively. Wrinkled Au LSPR sensors had sensitivities of ∼200–1000 Δλ/ΔRIU, comparing favorably to commercial LSPR sensors, and detected biotin–avidin and desthiobiotin–avidin complexation in a concentration-dependent manner using a standard plate reader and a 96-well format.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.1c14930