Abstract

Implantable sensor devices require coatings that efficiently interface with the tissue environment to mediate biochemical analysis. In this regard, bioinspired polymer hydrogels offer an attractive and abundant source of coating materials. However, upon implantation these materials generally elicit inflammation and the foreign body reaction as a consequence of protein fouling on their surface and concomitant poor hemocompatibility. In this report we investigate a strategy to endow chitosan hydrogel coatings with antifouling properties by the grafting of polymer brushes in a "grafting-from" approach. Chitosan coatings were functionalized with polymer brushes of oligo(ethylene glycol) methyl ether methacrylate and 2-hydroxyethyl methacrylate using photoinduced single electron transfer living radical polymerization and the surfaces were thoroughly characterized by XPS, AFM, water contact angle goniometry, and in situ ellipsometry. The antifouling properties of these new bioinspired hydrogel-brush coatings were investigated by surface plasmon resonance. The influence of the modifications to the chitosan on hemocompatibility was assessed by contacting the surfaces with platelets and leukocytes. The coatings were hydrophilic and reached a thickness of up to 180 nm within 30 min of polymerization. The functionalization of the surface with polymer brushes significantly reduced the protein fouling and eliminated platelet activation and leukocyte adhesion. This methodology offers a facile route to functionalizing implantable sensor systems with antifouling coatings that improve hemocompatibility and pave the way for enhanced device integration in tissue.

Highlights

  • Continuous health monitoring using wearable sensors linked to cell phones is rapidly becoming a reality

  • Chitosan coatings were functionalized with polymer brushes of oligo(ethylene glycol) methyl ether methacrylate and 2-hydroxyethyl methacrylate using photoinduced single electron transfer living radical polymerization and the surfaces were thoroughly characterized by X-ray Photoelectron Spectroscopy (XPS), AFM, water contact angle goniometry, and in situ ellipsometry

  • A biocompatible implantable sensor should ideally integrate and interface with surrounding tissue, facilitate the measurement of the target analyte, and maintain the required accuracy over its lifetime.[4−6] Upon implantation of a foreign device inside of the human body, its surface suffers the rapid adsorption of proteins, eliciting cellular and tissue responses that isolate and attempt to degrade the foreign body diverging from natural wound healing process

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Summary

Introduction

Continuous health monitoring using wearable sensors linked to cell phones is rapidly becoming a reality. The first events after device implantation are protein adsorption from blood and interstitial fluids on the surface of the implant and constitution of a provisional blood matrix (thrombus). Chemical messengers such as cytokines, growth factors, and chemoattractants elicit the recruiting of innate immune system cells to the wound, triggering an acute inflammation dominated by neutrophils and lasting up to a few days. Upon resolution of the Received: April 10, 2017 Revised: May 3, 2017 Published: May 5, 2017

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