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Development of a Novel Hydrophilic, Biocompatible AdhesiveDepartments of Chemistry and Biomedical Engineering The University of Akron Akron, OH 44325
Departments of Chemistry and Biomedical Engineering The University of Akron Akron, OH 44325
Department of Physiology and Biophysics School of Medicine Case Western Reserve University Cleveland, OH 44106
Department of Physiology and Biophysics School of Medicine Case Western Reserve University Cleveland, OH 44106 The synthesis of two novel hydrogel adhesive films, poly(butoxy- Entprol) and poly(butoxy/ethylene-Entprol) was accomplished by crosslinking either epoxy end-capped oligomeric-butoxy-Entprol or epoxy end-capped oligo meric-butoxy/ethylene-Entprol with 5-10 mole% diethylenetriamine. The two oligomers with Mn 1700 to 5000 were obtained in a 78-87% yield, by the reac tion of one equivalent of N,N'-bis(2-hydroxypropyl)ethylenediamine with either one equivalent of 1,4-butanediol diglycidyl ether or one equivalent of a 1:1 mole ratio mixture of 1,2,7,8-diepoxyoctane and 1,4-butanediol diglycidyl ether. Peel adhesion to glass for poly(BE) and poly(BEE) gave peel forces of 12.02 and 13.61 N, respectively, as compared to five acrylate adhesives, ranging from 4.90-11.56 N. Poly(BE) had superior adhesion to skin (3.45 N) compared to poly(BEE) (0.97 N) and the acrylate-based adhesives (0.79-2.64 N). In addition, fully hydrated poly(BE) and poly(BEE) have both a high water uptake (971% and 630%, respectively) and equilibrium water content (90% and 86%, respec tively). Both films lose adhesion with progressive hydration. These hydrogels actively support the growth of 3T3 fibroblasts and SCC-13 epithelial cells. These results strongly support the potential of these films as single-layered adhesive hydrogel dressings.
Journal of Bioactive and Compatible Polymers, Vol. 7, No. 4,
324-336 (1992) |
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