Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for preparing medical adhesive from alpha-alkyl cyanoacrylate monomer

A technology of alkyl cyanoacrylate and monomer, which is applied in the field of preparing medical adhesive from α-alkyl cyanoacrylate monomer, can solve the problem of reducing the bonding ability of α-alkyl cyanoacrylate and medical , reduce the reaction speed of the reagents, etc., to achieve the effect of increasing the reaction rate, improving the thermal conductivity, and improving the efficiency

Inactive Publication Date: 2020-09-29
秦皇岛市科峰医疗器械有限公司
View PDF3 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In order to make up for the deficiencies in the prior art, the technical problem to be solved by the present invention is to provide a method for preparing medical glue from α-alkyl cyanoacrylate monomer. Due to the poor compatibility between the reagents, the reaction speed of the reagents is slow, and the bonding ability of the medical ones is not strong. At the same time, during the distillation of the stock solution in the there-necked flask, due to the Methyl silicone oil is evenly heated. During the process of distilling and conducting heat conduction to the three-necked flask with methyl silicone oil, the stock solution in the three-necked flask will be heated unevenly, which will lead to stratification of the stock solution in the three-necked flask. layer, which will reduce the reaction speed of various reagents in the stock solution, thereby reducing the process problem of the exchange reaction of α-alkyl cyanoacrylate

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for preparing medical adhesive from alpha-alkyl cyanoacrylate monomer
  • Method for preparing medical adhesive from alpha-alkyl cyanoacrylate monomer
  • Method for preparing medical adhesive from alpha-alkyl cyanoacrylate monomer

Examples

Experimental program
Comparison scheme
Effect test

Embodiment approach

[0047] As an embodiment of the present invention, an arc-shaped bag 27 is fixedly connected to the inner surface of the oil bath bin 2 in the cavity of the oil bath bin 2, and the arc-shaped bag 27 is made of heat-conducting silica gel material; the arc-shaped bag 27 Design of the third through hole 23 of the wrapping part; uniformly arranged spray holes 28 are opened in the inner wall of the arc-shaped bag 27;

[0048] During work, since the arc-shaped layer partly wrapped on the inner surface of the oil bath warehouse 2 is designed to wrap the third through-hole 23, the oil flowing out in the third through-hole 23 can flow into the arc-shaped bag 27, when the oil in the arc-shaped bag 27 When the oil increases, it will expand, and when the arc-shaped bag 27 expands, it can be attached to the outer surface of the three-necked flask 21. In this process, the three-necked flask 21 can be heated evenly, and at the same time, the diffusion of the stock solution in the three-necked ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention belongs to the field of biological materials, and specifically relates to a method for preparing a medical adhesive from an alpha-alkyl cyanoacrylate monomer. According to the invention,the medical adhesive prepared from the alpha-alkyl cyanoacrylate monomer, formaldehyde, a catalyst, namely piperidine, lauryl sodium sulfate, a basic catalyst, namely phosphoric acid, purified water,a plasticizer, namely tricresyl phosphate, a polymerization inhibitor, namely hydroquinone, ethyl cyanoacetate, isobutyl alcohol, phthalate and an acid catalyst has the following advantages: the compatibility of the medical adhesive can be improved; and the bonding capacity of the medical adhesive can be reduced at the same time. The medical adhesive provided by the invention is mainly used for solving the problems of low reaction speed of reagents and poor medical bonding capacity due to poor compatibility among the reagents in the preparation process of a conventional medical adhesive, andthe problem of layering of a stock solution in a three-neck flask due to the facts that methyl silicone oil in an oil pan is uniformly heated and the stock solution in the three-neck flask is heated unevenly in the process that the three-neck flask is subjected to distillation heat conduction by the methyl silicone oil.

Description

technical field [0001] The invention belongs to the field of biological materials, in particular to a method for preparing medical glue from an alpha-cyanoacrylate alkyl ester monomer. Background technique [0002] α-isobutyl cyanoacrylate, n-butyl α-cyanoacrylate, and n-octyl α-cyanoacrylate are three α-cyanoacrylate alkyl ester monomers, due to the presence of cyano [-CN] and carbonyl [ -C=O] Two electron-withdrawing groups, which can react with anionic groups such as carbonyl [-OH] and amino groups [-NH2] in trace moisture on the skin surface and body fluids, and can quickly trigger isobutyl α-cyanoacrylate The monomer polymerizes, and after 5-15 seconds, a protective film is formed on the skin surface, which can tightly adhere the skin and isolate the tissue from bacteria. The bonding strength of the adhesive film is greater than the natural tension of the wound, which can tightly bond the skin, and play the role of immediate hemostasis and coagulation under the action ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): A61L24/06C07C253/30C07C255/22C07C253/34C07C255/23
CPCA61L24/06A61L2400/04C07C253/30C07C253/34C07C255/22C07C255/23C08L33/08
Inventor 李永太
Owner 秦皇岛市科峰医疗器械有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products