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Tinware-Inspired Aerobic Surface-Initiated Controlled Radical Polymerization (SI-SnCRP) for Biocompatible Surface Engineering. | LitMetric

Tinware-Inspired Aerobic Surface-Initiated Controlled Radical Polymerization (SI-SnCRP) for Biocompatible Surface Engineering.

ACS Macro Lett

Key Laboratory of Marine Materials and Related Technologies, Zhejiang Key Laboratory of Marine Materials and Protective Technologies, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, China.

Published: January 2023

AI Article Synopsis

  • Surface-initiated controlled radical polymerization (SI-CRP) has gained attention in biomaterials, but the presence of toxic transition metal catalysts has limited its use in biomedical fields.
  • The study introduces a new method using a tin (Sn(0)) catalyst (SI-SnCRP) that operates effectively under normal conditions, allowing for the creation of various functionalized polymer brushes.
  • This method not only ensures high control over the polymer structures but also results in biocompatible brushes that perform better with blood and cells compared to those made using copper-based methods, making it suitable for biological applications.

Article Abstract

Surface anchored polymer brushes prepared by surface-initiated controlled radical polymerization (SI-CRP) have raised considerable interest in biomaterials and bioengineering. However, undesired residues of noxious transition metal catalysts critically restrain their widespread biomedical applications. Herein, we present a robust and biocompatible surface-initiated controlled radical polymerization catalyzed by a Sn(0) sheet (SI-SnCRP) under ambient conditions. Through this approach, microliter volumes of vinyl monomers with diverse functions (heterocyclic, ionic, hydrophilic, and hydrophobic) could be efficiently converted to homogeneous polymer brushes. The excellent controllability of SI-SnCRP strategy is further demonstrated by the exquisite fabrication of predetermined block and patterned polymer brushes through chain extension and photolithography, respectively. Additionally, in virtue of intrinsic biocompatibility of Sn, the resultant polymer brushes present transcendent affinity toward blood and cell, in marked contrast to those of copper-based approaches. This strategy could provide an avenue for the controllable fabrication of biocompatible polymer brushes toward biological applications.

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Source
http://dx.doi.org/10.1021/acsmacrolett.2c00556DOI Listing

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