2014
DOI: 10.7569/raa.2014.097306
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Cyanoacrylate Adhesives in Surgical Applications

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Cited by 40 publications
(32 citation statements)
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“…A number of review papers on medical applications of cyanoacrylate adhesives have been published (118)(119)(120). More recently, a review of cyanoacrylate adhesives in surgical applications has been published and which gives an overview of the chemistry and clinical applications of medical-grade cyanoacrylate adhesives over the past 50 years (121).…”
Section: Cyanoacrylates In Medical Applicationsmentioning
confidence: 99%
See 1 more Smart Citation
“…A number of review papers on medical applications of cyanoacrylate adhesives have been published (118)(119)(120). More recently, a review of cyanoacrylate adhesives in surgical applications has been published and which gives an overview of the chemistry and clinical applications of medical-grade cyanoacrylate adhesives over the past 50 years (121).…”
Section: Cyanoacrylates In Medical Applicationsmentioning
confidence: 99%
“…The FDA granted approval of Dermabond for external clinical use in 1998 (124). Other adhesives such as Indermil, Trufill, LiquiBand Optima, Flexifuze, and Surgiseal (Adhezion Biomedical) have all subsequently been granted regulatory approval in many regions around the world for topical wound closure applications (121).…”
Section: Cyanoacrylates In Medical Applicationsmentioning
confidence: 99%
“…Among fluid adhesives available for medical use, cyanoacrylate glues are extremely adhesive to tissues even in wet conditions. However, when applied as a glue, they show non-elastic adhesion with risk of damage due to traction 20 and its application in intrauterine environment is complex due to its non-solid condition. Previous studies have investigated the use of mussel-like glues as an alternative to cyanoacrylate 15 , since they are based on a catechol side chain of 3,4-dihydroxyphenylalanine (DOPA) amino acid that theoretically secures strong adhesion to almost any surface even underwater 15 , 15 .…”
Section: Discussionmentioning
confidence: 99%
“…Research showed that the longer the hydrocarbon group at the –R position, the slower the rate of polymerization, the less heat released during polymerization, and the lower the histotoxicity. 7 In addition, longer chain esters degrade much slower, allowing more efficient metabolism of the degradation products and reducing the inflammatory response. 8 2-octyl-cyanoacrylate was developed to address toxicity concern and to reduce skin irritation and allergic response, improving properties for medical applications.…”
Section: Discussionmentioning
confidence: 99%