Various alkyl 2-bromoacrylates were synthesized in high purity and yield. They were characterized by spectroscopic techniques. The monomers were then formulated into aerobic adhesive compositions and their adhesive bond strengths between various surfaces were evaluated. D-~ COOR' 1 Br 2 Br /~ COOR'
Synthesis and bioevaluation of alkyl 2-cyanoacryloyl glycolates as potential soft tissue adhesives
β Scribed by Jaffe, H. ;Wade, C. W. R. ;Hegyeli, A. F. ;Rice, R. ;Hodge, J.
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 423 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0021-9304
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β¦ Synopsis
A series of alkyl 2-cyanoacryloyl glycolate tissue adhesives were synthesized and characterized by NMR. Physical properties and bond strengths are presented. Within the series, bond strength decreased with increasing molecular weight. Corresponding polymers were evaluated by in vitro and in vivo techniques for biocompatibility. In general, in vitro biocompatibility increased with molecular weight. Based on in vitro and in vivo results, the isobutyl and isoamyl derivatives gave polymers that were most biocompatible, however, the entire series was found to be less reactive than poly(methyl 2-cyanoacrylate) and only the isopropyl derivative polymers more reactive than poly(isobutyl 2-cyanoacrylate). Approximately one-third of the isobutyl polymer biodegraded in vivo after 6 weeks.
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## Abstract A convenient method for the synthesis of previously unknown oxaziridines having unsaturated substituents at the 3βposition (3aβk) is based on the selective oxidation of the imino group of Ξ±,Ξ²βunsaturated aldimines 2 with __m__βchloroperbenzoic acid. The title compounds and 2β__tert__βbu