4.5 Article

Sustainable glycerol terpolycarbonates as temporary bioadhesives

Journal

BIOMATERIALS SCIENCE
Volume 9, Issue 24, Pages 8366-8372

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1bm00995h

Keywords

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Funding

  1. NSF [DMR-1410450, DMR-1507081, CHE-0619339]
  2. NIH [R01CA232708, R01EB017722]

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The synthesis of poly(glycidyl acetate-co-glycidyl butyrate carbonate)s via terpolymerization provides pressure-sensitive adhesives with tunable adherence and benign degradation products, suitable for use as temporary adhesives. One specific polymer showed proper adhesive strength for surgical applications in an ex vivo sheep model.
We describe the synthesis of poly(glycidyl acetate-co-glycidyl butyrate carbonate)s via the terpolymerization of glycidyl acetate (GA), glycidyl butyrate (GB), and CO2 by a cobalt salen complex in high atom economy. These new non-cytotoxic polycarbonates are pressure-sensitive adhesives, and peel testing shows the adhesive strength ranges from Scotch-Tape (R) to hot-melt glues based on glycidyl butyrate content. The tunable adherence, benign degradation products, and facile application and removal suggest their utility as temporary adhesives, such as those used in biomedical applications or medical devices. One polymer, (GA-co-GB)-87, exhibits the proper adhesive strength to sufficiently adhere a collagen buttress to the jaws of a steel surgical stapler and easily release the buttress after firing to successfully cut, close, and implant the buttress into lung tissue in an ex vivo sheep model.

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