2009
DOI: 10.1590/s0365-05962009000600003
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Adesivos à base de cianoacrilato para síntese de tecido mole

Abstract: Resumo: FUNDAMENTOS -Adesivos teciduais têm sido muito usados para síntese de ferida, em função de ser um método indolor, rápido e de fácil execução. OBJETIVOS -Analisar e comparar compatibilidade dos adesivos, etil-cianoacrilato (Super Bonder) e butilcianoacrilato (Histoacryl), e a reparação de incisões em dorso de ratos entre o fio de sutura e os respectivos adesivos. MÉTODOS -Foram usados 15 ratos. Realizaram-se duas lojas cirúrgicas no dorso. Em cada uma, foi implantado um tubo de polietileno (10mm x 1mm),… Show more

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Cited by 15 publications
(10 citation statements)
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“…Moreover, cyanoacrylates do not exhibit genotoxic activity or systemic toxicity, and they do not cause mucosal irritation or cutaneous sensitivity [4, 8, 10, 43]. Researchers have also reported minimal inflammatory response in regions of use, with zero potential for necrosis [2, 17, 44, 45]. Finally, some authors have reported excellent cosmetic results without dehiscence or allergic reactions [17, 44, 46, 47].…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, cyanoacrylates do not exhibit genotoxic activity or systemic toxicity, and they do not cause mucosal irritation or cutaneous sensitivity [4, 8, 10, 43]. Researchers have also reported minimal inflammatory response in regions of use, with zero potential for necrosis [2, 17, 44, 45]. Finally, some authors have reported excellent cosmetic results without dehiscence or allergic reactions [17, 44, 46, 47].…”
Section: Introductionmentioning
confidence: 99%
“…The synthesis of cyanoacrylates is the result of the reaction of formaldehyde with alkyl cyanoacetate, which makes it possible to obtain many different combinations of cyanoacrylate, such as methyl (CH 3 ), ethyl (C 2 H 5 ), butyl and isobutyl (R = C 4 H 9 ) …”
mentioning
confidence: 99%
“…1 The synthesis of cyanoacrylates is the result of the reaction of formaldehyde with alkyl cyanoacetate, which makes it possible to obtain many different combinations of cyanoacrylate, such as methyl (CH 3 ), ethyl (C 2 H 5 ), 2 butyl and isobutyl (R = C 4 H 9 ). 3,4 Analyzing the biocompatibility of the cyanoacrylate adhesives, it was observed that methyl-cyanoacrylate causes inflammation and tissue necrosis 5,6 and is therefore contraindicated for clinical use. 7 Mehmet and colleagues 8 observed that adhesives based on ethyl-cyanoacrylate showed no inflammatory reaction, and according to Saska and colleagues, 9 both adhesives have hemostatic and bacteriostatic effects.…”
mentioning
confidence: 99%
“…39 Two surgical holes were prepared in the back of 15 rats. A tube of polyethylene was implanted in each hole and filled with the chosen adhesive.…”
Section: Literature Reviewmentioning
confidence: 99%