2016
DOI: 10.1016/j.bjoms.2016.01.035
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Haemostatic property of cyanoacrylate in pedicled flaps

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Cited by 3 publications
(3 citation statements)
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“…In addition, the cyanoacrylate adhesive has been used in free gingival grafting [1921], apicectomy [10], root sectioning [22], and bonding of fractured tooth fragments [23]. Kulkarni et al [24] reported the use of cyanoacrylate in periodontal pockets during surgical procedures involving periodontal flaps in 24 individuals, Ozcan et al [25] used it to promote palatal wound healing after free gingival graft harvesting, and Ranson et al [26] used it for stabilizing pedicle grafts during soft tissue surgeries.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, the cyanoacrylate adhesive has been used in free gingival grafting [1921], apicectomy [10], root sectioning [22], and bonding of fractured tooth fragments [23]. Kulkarni et al [24] reported the use of cyanoacrylate in periodontal pockets during surgical procedures involving periodontal flaps in 24 individuals, Ozcan et al [25] used it to promote palatal wound healing after free gingival graft harvesting, and Ranson et al [26] used it for stabilizing pedicle grafts during soft tissue surgeries.…”
Section: Introductionmentioning
confidence: 99%
“…They are formulated with synthetic polymers as a backbone functionalized with reactive groups and are crosslinked or coated via a non‐natural cross‐linker. The most common synthetic bioadhesives include polyurethane‐, polyethylene glycol (PEG)‐ and cyanoacrylate‐based formulations. Cyanoacrylate‐based adhesives (e.g., Histoacryl®, 20 Dermabond®, 21 Indermil™, and Glubran 2® 22 ) have been on the market for almost four decades now. They contain alkyl‐2‐cyanoacrylate monomers, which polymerize by an exothermic reaction on exposure to nucleophilic species, such as hydroxyl groups (in the exudate), at room temperature (Figure 1A).…”
Section: Bioadhesive Classification and Reaction Mechanismsmentioning
confidence: 99%
“…• Cyanoacrylate-based adhesives (e.g., Histoacryl ® , 20 Dermabond ® , 21 Indermil™, and Glubran 2 ®22 ) have been on the market for almost four decades now. They contain alkyl-2-cyanoacrylate monomers, which polymerize by an exothermic reaction on exposure to nucleophilic species, such as hydroxyl groups (in the exudate), at room temperature (Figure 1A).…”
Section: Synthetic-derived Bioadhesivesmentioning
confidence: 99%