1998

Anionic polymerization of 2-propynyl methacrylate (1), 3-trimethylsilyl-2-propynyl methacrylate (2), 2-butynyl methacrylate (3), and 3-pentynyl methacrylate (4) was carried out in tetrahydrofuran at −78°C for 1 h. The employed initiator systems were (diphenylmethyl)potassium/diethylzinc (Et2Zn) and 1,1-bis(4′-trimethylsilyphenyl)-3-methylpentyllithium/lithium chloride (LiCl).

The tacticity assignments from the literature for the 13C-NMR signals of the side-chain methylene group of poly(ethyl cyanoacrylate) are reversed, and new assignments of the main-chain methylene group are proposed. The assignments were made possible by a combination of DEPT and HETCOR NMR experiments on samples of varying microstructure distributions. The polymer tends toward syndiotacticity, not isotacticity as previously reported. The distribution of stereoisomers fits well to a Bernoulian statistical model.

Octyl-2-cyanoacrylate is a long carbon chain cyanoacrylate derivative that is stronger and more pliable than its shorter chain derivatives. One hundred and eleven patients underwent elective surgical procedures by the same surgeon using either octyl-2-cyanoacrylate or sutures for skin closure at the University of Illinois at Chicago. Most patients underwent excision of benign skin lesions with a mean wound size of 112 mm3. Patients were randomized into either control (vertical mattress suture closure) or test groups (closure with octyl-2-cyanoacrylate).

 

BACKGROUND AND AIMS OF THE STUDY:

Although small lacerations of the myocardium may be repaired easily using conventional methods, larger tears or ruptures, especially if they occur in infarcted myocardial tissue, may create formidable technical challenges. Described is a method for applying sutureless pericardial patches for control of hemorrhage.

METHODS:

A sutureless pericardial patch was glued to the myocardium with commercially available household cyanoacrylate (Krazy Glue) in seven patients.

US5807563

Disclosed are methods for draping a surgical incision site prior to surgery. Specifically, the methods of this invention involve the in situ formation of a cyanoacrylate polymeric drape over the skin surface at the surgical incision site. An incision is then made through this surface and the surgery is then conducted through the incision