Biodegradable Polymers in Clinical Use and Clinical Development 2011
DOI: 10.1002/9781118015810.ch12
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Medicinal Applications of Cyanoacrylate

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Cited by 5 publications
(2 citation statements)
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“…During application, the CA is exposed to anionic initiators (eg, hydroxyl groups or lone pairs of electrons on pendant NH 2 groups) on the surfaces being glued, inducing polymerization. 9,10 The polymer that forms has unique properties that better lend themselves to particular applications (Figure). The utility of the various CAs in the backcountry is directly related to their physical properties.…”
Section: Properties Of Cyanoacrylate Gluesmentioning
confidence: 99%
“…During application, the CA is exposed to anionic initiators (eg, hydroxyl groups or lone pairs of electrons on pendant NH 2 groups) on the surfaces being glued, inducing polymerization. 9,10 The polymer that forms has unique properties that better lend themselves to particular applications (Figure). The utility of the various CAs in the backcountry is directly related to their physical properties.…”
Section: Properties Of Cyanoacrylate Gluesmentioning
confidence: 99%
“…Alkyl cyanoacrylates are solvent free liquids that polymerize and cure rapidly in the presence of nucleophiles (including moisture from the air) to form adhesive, glue, and films. , These alkyl cyanoacrylates have long been used for bonding nonporous materials in biomedical fields such as tissue adhesives, for drug delivery, in the automobile and electronics industries, and in forensic laboratories for fingerprint development. , Earlier generations of cyanoacrylates (methyl, ethyl) had significant performance limitations such as poor thermal stability, peel strength, and high tissue reaction. Continued research on cyanoacrylates resulted in the development of new alkyl cyanoacrylates to overcome these limitations.…”
Section: Introductionmentioning
confidence: 99%