3.8 Article

Polyphenol-Assisted Chemical Crosslinking: A New Strategy to Achieve Highly Crosslinked, Antioxidative, and Antibacterial Ultrahigh-Molecular-Weight Polyethylene for Total Joint Replacement

Journal

ACS BIOMATERIALS SCIENCE & ENGINEERING
Volume 7, Issue 1, Pages 373-381

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.0c01437

Keywords

tea polyphenol; crosslinking; antioxidant; antibacterial; UHMWPE; joint replacement

Funding

  1. National Natural Science Foundation of China [51761145112, 51773136, 51533004, 81672214]
  2. State Key Laboratory of Polymer Materials Engineering [sklpme2018-2-07]
  3. Sichuan Department of Science and Technology [2018JZ0055]

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A novel strategy of polyphenol-assisted chemical crosslinking was proposed to enhance the oxidation stability and antibacterial performance of highly crosslinked UHMWPE, by increasing the efficiency of crosslinking through higher tea polyphenol content. The study showed promising prospects in clinical applications.
Highly crosslinked ultrahigh-molecular-weight polyethylene (UHMWPE) bearings are wear-resistant to reduce aseptic loosening but are susceptible to oxidize in vivo/in vitro, as reported in clinical studies. Despite widespread acceptance of antioxidants in preventing oxidation, the crosslinking efficiency of UHMWPE is severely impacted by antioxidants, the use of which was trapped in a trace amount. Herein, we proposed a new strategy of polyphenol-assisted chemical crosslinking to facilitate the formation of a crosslinking network in high-loaded tea polyphenol/UHMWPE blends. Epigallocatechin gallate (EGCG), a representative of tea polyphenol, was mixed with UHMWPE and peroxide. Multiple reactive phenolic hydroxyl groups of tea polyphenol coupled with the nearby free radicals to form extra crosslinking sites. The crosslinking efficiency was remarkably enhanced with increasing tea polyphenol content, even at a concentration of 8 wt %. Given by the hydrogen donation principle, the high-loaded tea polyphenol also enhanced the oxidation stability of the crosslinked UHMWPE. The antioxidative performance was preserved even after tea polyphenol elution. Moreover, superior antibacterial performance was achieved by the in situ tea polyphenol release from the interconnected pathways in the present design. The strategy of polyphenol-assisted chemical crosslinking is applicable for producing highly crosslinked, antioxidative, and antibacterial UHMWPE, which has promising prospects in clinical applications.

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