Jump to main content
Jump to site search


Synthesis and Adhesion Control of Glucose-based Bioadhesive via Strain-Promoted Azide-Alkyne Cycloaddition

Abstract

A glucose-based bioadhesive, poly(2-methacrylamido glucopyranose-co-N-methacryloyl-3,4-dihydroxyl-l-phenylalanine-co-8-azidooctyl methacrylate) [poly(MG-co-MDOPA-co-AOM)], has been synthesized by thermally-initiated free radical polymerization. The new bioadhesive is composed of three modules: a hydrophilic glycopolymer segment, a mussels-inspired catechol segment, and a crosslinking azide segment. Poly(ethylene glycol) (PEG)-based crosslinker, (1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl PEG (BCN-PEG) was synthesized separately. Bulk adhesion properties of the terpolymer were enhanced by covalent bond forming crosslinking via strain-promoted azide-alkyne cycloaddition (SPAAC). The occurrence of SPAAC was confirmed by 1H NMR and FT-IR. After moistening the adhesive and the crosslinker, BCN-PEG with water, adhesion properties were examined by a lap shear strength test on porcine skins. The control of adhesion was studied under various crosslinker concentrations, crosslinking durations, and crosslinker lengths. Even without crosslinking, the new terpolymer adhesive demonstrated 20-fold higher adhesion strength (115 kPa) compared to a commercial rubber cement (5.8 kPa). The most significant factor to control for adhesion was crosslinker length. BCN-PEG was prepared with 134 and 43 repeating units of PEG. Crosslinking with the long crosslinker, BCN-PEG (PEG repeating units: 134), did not enhance adhesion strength meaningfully. However, crosslinking the short crosslinker BCN-PEG (repeating units: 43) showed significant improvement in work of adhesion (150% higher than uncrosslinked). The overall revealed features of strong adhesion on biological surfaces, structural similarity to natural carbohydrate, water compatibility, control lability of adhesion strength, and non-toxic adhesion enhancement principle via SPAAC crosslinking, suggest that the new glucose-based bioadhesive can be successfully used for biomedical applications.

Back to tab navigation

Supplementary files

Publication details

The article was received on 28 Feb 2018, accepted on 04 Jun 2018 and first published on 13 Jun 2018


Article type: Paper
DOI: 10.1039/C8PY00339D
Citation: Polym. Chem., 2018, Accepted Manuscript
  •   Request permissions

    Synthesis and Adhesion Control of Glucose-based Bioadhesive via Strain-Promoted Azide-Alkyne Cycloaddition

    I. Pramudya, C. Kim and H. Chung, Polym. Chem., 2018, Accepted Manuscript , DOI: 10.1039/C8PY00339D

Search articles by author

Spotlight

Advertisements