Medical polyurethane material containing lactone group, preparation method thereof, and medical catheter

A technology of polyurethane materials and medical catheters, applied in medical science, surgery, etc., can solve the problems of reduced inner diameter of catheters, reduced input flow rate of medicinal liquid, lack of thermoplastic processability, etc., to achieve compression load reduction, increase hydrophilicity, Effect of Rigidity Reduction

Active Publication Date: 2019-10-15
CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
View PDF11 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The disadvantage of this type of catheter is that the inner diameter of the catheter is significantly reduced after absorbing water, resulting in a decrease in the input flow rate of the liquid medicine, which is not conducive to the rapid treatment of diseases, and the melt extrusion process of polyurethane materials is extremely sensitive to water, and the introduction of hydrophilic groups , increasing the difficulty of the drying process of polyurethane materials
The U.S. patent with the publication number US5281677 and the Chinese patent with the authorization number ZL201310302169.8 respectively propose methods for preparing medical interventional catheters using polyurethane blends. They adopt different technical routes. After the prepared blends are processed into catheters, When placed at room temperature, it has rigidity that is conducive to puncture. After entering the human body, the elastic modulus can be reduced by 70-88%, and there will be no water swelling phenomenon, thereby significantly reducing the degree of mechanical stimulation of the catheter to the tissue. However, this Method does not soften enough in vivo relative to hydrophilic polyurethane materials
Publication No. US4156067 uses six-carbon saccharide to prepare alkali water-soluble polyurethane material, but the six-carbon saccharactone in this material contains more than two hydroxyl groups, and the resulting polyurethane material has a cross-linked structure , no thermoplastic processability

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
  • Medical polyurethane material containing lactone group, preparation method thereof, and medical catheter

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0032] The present invention provides a kind of preparation method of medical polyurethane material described in above-mentioned technical scheme, comprises the following steps:

[0033] Mix 4,4`-diphenylmethane diisocyanate, butanediol, polytetrahydrofuran, substances containing butyrolactone groups and lubricants, and then extrude and granulate to obtain medical polyurethane containing butyrolactone groups Material;

[0034] In the present invention, the lubricant is selected from ethylene bisstearamide.

[0035] In the present invention, a twin-screw extruder with an aspect ratio of 44 / 1 is preferably used for extrusion granulation. In the present invention, the extrusion granulation temperature is preferably 200-220°C, more preferably 205-215°C; in a specific embodiment, the extrusion granulation temperature is 210°C.

[0036] The present invention provides a medical catheter, which is produced by extruding the medical polyurethane material described in the above technical...

Embodiment 1

[0042] Slowly add 0.5 mol (51.0 g) of 3-hydroxybutyrolactone to 0.5 mol (125.1 g) of 4,4'-diphenylmethane diisocyanate (MDI) at 80°C, and react for 2 hours. 0.5 mol (45.5 g) of 3-amino-1,2-propanediol (APD) was slowly added dropwise thereto, and the reaction was continued for 2 h to obtain 0.5 mol (221.6 g) of lactone polyol. In a reaction kettle at 100°C, 10mol (2502.4g) of MDI was reacted with 2mol (2000g) of polytetrahydrofuran (PTMO) with a molecular weight of 1000g / mol for 20min, and then 7.5mol (675.5g) was added thereto under vigorous stirring. The mixed solution of butanediol and the lactone polyol of 0.5mol (221.6g), and 16.2g ethylene bisstearamide, pass through the twin-screw extruder that length-diameter ratio is 44 / 1 after fast mixing uniformly at 210 Extrusion granulation at ℃. A medical polyurethane material with a lactone content of 9.2 mmol / g and a hard segment content of 57.5 wt % was obtained. Press the polyurethane material into a sheet with a thickness o...

Embodiment 2

[0045] Slowly add 0.7 mol (71.4 g) of 3-hydroxybutyrolactone to 0.7 mol (175.1 g) of 4,4'-diphenylmethane diisocyanate (MDI) at 80°C, and react for 2 hours. 0.7 mol (63.7 g) of 3-amino-1,2-propanediol (APD) was slowly added dropwise thereto, and the reaction was continued for 2 h to obtain 1.0 mol (310.2 g) of lactone polyol. In a reaction kettle at 100°C, 10mol (2502.4g) of MDI was reacted with 2.5mol (2500g) of polytetrahydrofuran (PTMO) with a molecular weight of 1000g / mol for 20 minutes, and then 6.8mol (612.8g) was added to it under vigorous stirring. ) of butanediol and 0.7mol (310.2g) of the lactone polyol mixed solution, and 16.2g ethylene bisstearamide, after rapid mixing, the length-to-diameter ratio is 44 / 1 through the twin-screw extruder Extruded and granulated at 210° C., a medical polyurethane material with a lactone content of 11.8 mmol / g and a hard segment content of 52.4 wt % was obtained. Press the polyurethane material into a sheet with a thickness of 0.45m...

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

PropertyMeasurementUnit
Outer diameteraaaaaaaaaa
Wall thicknessaaaaaaaaaa
Elastic modulusaaaaaaaaaa
Login to view more

Abstract

The present invention provides a medical polyurethane material containing a lactone group, and a medical catheter prepared therefrom. The medical polyurethane material is prepared by polycondensing 4,4'-diphenylmethane diisocyanate, butanediol, polytetrahydrofuran and a butyrolactone group-containing substance; and the butyrolactone group-containing substance contains at least two hydroxyl groups,and the molar concentration of the butyrolactone group in the medical polyurethane material is 5-20 mmol / g. The lactone group is in a closed-loop state when the medical polyurethane material is in adry state, and can maintain the hydrophobicity of the polyurethane and does not affect the extrusion molding of the polyurethane material, and the lactone group undergoes a hydrolysis ring-opening reaction in an aqueous environment or in the human body to increase the hydrophilicity of the polyurethane material and significantly reduce the elastic modulus of the polyurethane material, so the medical catheter prepared from the material has a high rigidity in vitro, and the softness is significantly increased after entering human blood vessels.

Description

technical field [0001] The invention belongs to the technical field of biomedical polyurethane materials, and in particular relates to a medical polyurethane material containing lactone groups, a preparation method thereof and a medical catheter. Background technique [0002] Medical catheters refer to high-end precision medical devices used to transport gases, liquids and solids into the body during disease treatment. After decades of development, medical interventional catheters play a role in the treatment of various diseases in the medical field today. more and more important. In addition to having good biocompatibility, raw materials for medical catheters must also have special mechanical properties. [0003] Taking intravenous indwelling needle catheter as an example, in order to reduce the intensity of mechanical stimulation of the catheter tip to human tissue and reduce the incidence of complications such as inflammation, pain, thrombus, and drug penetration at the ...

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): C08G18/66C08G18/48C08G18/32C08L75/08A61L31/06A61L31/14
CPCA61L31/06A61L31/14C08G18/3221C08G18/4854C08G18/6674C08L75/08C08L2203/02C08L2203/18
Inventor 杨华伟栾世方殷敬华石恒冲宋凌杰
Owner CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products