Biological type highly cross-linked reticular sustained release ECMO coating material, preparation method and application thereof

A coating material, high cross-linking technology, applied in the direction of coating, packaging item types, special packaging items, etc., can solve the problem that the heparin coating technology cannot achieve the ideal biocompatibility, the expected anticoagulation effect, and the coating Material human injury and other problems, to protect platelets and coagulation factors, reduce blood loss and blood bank consumption, and alleviate clinical blood shortage problems.

Inactive Publication Date: 2010-06-16
李彤 +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, the heparin coating methods can be roughly divided into three categories: (1) Ionic bonding method: the ionic bonding method is to introduce positively charged quaternary ammonium groups on the surface of polymer materials by utilizing the property of heparin itself with a large amount of negative charges. Group coupling agents, surfactants or polymers containing cations, and then interact with heparin to form a heparinized layer on the surface of the material by ionic bonds. Due to the instability of ionic bonds, plasma macromolecules such as albumin with affinity Substances can be combined with heparin to cause heparin molecules to fall off, so it can only be used for a short period of time; (2) Covalent bond method: This method generally uses the -CNS group, -NH2 group, -OH group, etc. on the surface of polymer materials The specific active group interacts with the -OH group of the heparin molecule to immobilize heparin, but because heparin has a large number of functional groups, it often binds too firmly with the surface of the material, resulting in the loss of activity of the heparin molecule, so the expected anticoagulation is often not obtained Effect; (3) End point immobilization method: The end point immobilization method first prepares a binding ion complex on the surface of the biological material, and then activates heparin through a controlled nitrous acid, and fixes heparin on the amino group-containing amino acid in a covalent bond. The surface of the material, this kind of fixing method is costly, and the peeling coating material will cause harm to the human body
[0005] In summary, the current heparin coating technology cannot achieve ideal biocompatibility and still has certain limitations. Therefore, the development of a new ECMO coating material is an important problem to be solved at this stage

Method used

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  • Biological type highly cross-linked reticular sustained release ECMO coating material, preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] FeCI at a concentration of 18mM 2 50ml of the solution was injected into a 25cm medical polyvinyl chloride extracorporeal circulation pipeline with one end closed, poured out the remaining solution after 30 minutes in a water bath at 37°C, repeated 3 times, and dried under vacuum at room temperature for later use.

[0035] Prepare 95 ml of 1.6% sodium alginate solution, add heparin to a solution concentration of 0.5 mg / ml, stir for 30 minutes, and place at room temperature overnight.

[0036] will pass through 18mM FeCI 2 One end of the treated 25cm-long medical polyvinyl chloride pipeline is closed, and the other end is injected with 1.6% sodium alginate and 0.5% (pH=1) heparin solution, 100ml in total, and the remaining solution is poured out after 30 minutes in a water bath at 37°C, and repeated 3 times. Dry under vacuum at normal temperature; the remaining solution is used to measure the concentration of heparin, and calculate the content of heparin in the inner coat...

Embodiment 2

[0041] CaCl at a concentration of 16 mM 2 50ml of the solution was injected into a 25cm medical polyvinyl chloride extracorporeal circulation pipeline with one end closed, poured out the remaining solution after 30 minutes in a water bath at 37°C, repeated 3 times, and dried under vacuum at room temperature for later use.

[0042] Prepare 100ml of 1.5% sodium alginate solution, add 5ml of 6% polyvinyl alcohol, stir and cross-link at room temperature and let it stand overnight. After adding heparin, the solution concentration is 0.8mg / ml, stir for 30 minutes, and let stand overnight at room temperature.

[0043] will pass through 16mM CaCl 2 One end of the treated 25cm-long medical polyvinyl chloride pipeline is closed, and the other end is injected with 1.5% sodium alginate-polyvinyl alcohol and 1.2% (pH=1) heparin solution, a total of 100ml, and the remaining solution is poured out after 30 minutes of water bath at 37°C. Repeat 3 times, dry under vacuum at room temperature, ...

Embodiment 3

[0046] ZnCl at a concentration of 17mM 2 50ml of the solution was injected into a 25cm medical polyvinyl chloride extracorporeal circulation pipeline with one end closed, poured out the remaining solution after 30 minutes in a water bath at 37°C, repeated 3 times, and dried under vacuum at room temperature for later use.

[0047] Prepare 90ml of 1.3% sodium alginate solution, and react overnight with electrostatic cross-linking reaction with chitosan oligosaccharide dissolved in 2% HAC. After adding heparin, the solution concentration is 1.5mg / ml, stir for 30 minutes, and stand at room temperature overnight.

[0048] will pass through 17mM ZnCI 2 One end of the 25cm long medical polyvinyl chloride pipeline treated by the solution is sealed, and the other end is injected with 1.3% sodium alginate and 2% HAC-dissolved chitosan oligosaccharide electrostatic cross-linking solution, and 1.8% (pH=1) heparin solution is added to 100ml altogether. After 30 minutes of water bath at 37...

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PUM

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Abstract

The invention relates to a biological type highly cross-linked reticular sustained release ECMO coating material, a preparation method and application thereof. The coating material is a complex mainly formed by combining a natural biological polysaccharide polymer with negative charges and an anticoagulative substance which reaches certain therapeutic concentration, and is prepared by combining the natural biological polysaccharide polymer with the negative charges and the anticoagulative substance in the form of physical blending and physical adsorption. The coating material has broad application prospect in the preparation of membrane lungs, blood pumps, ducts or intubations; and the coating material has important significance in the aspects such as the improvement on blood compatibility of coating ducts, the improvement on combination density of anticoagulative substances such as heparin and the like, the strengthening of the safety, the reduction of medical cost and the like.

Description

technical field [0001] The invention relates to a coating material and its preparation method and application, in particular to a bio-type highly cross-linked slow-release ECMO coating material and its preparation method and application. Background technique [0002] Cardiopulmonary failure is a serious global public health and clinical problem with high morbidity and mortality. The most effective method for end-stage cardiopulmonary disease is heart-lung transplantation, but the lack of donors limits the widespread development of heart-lung transplantation. Many patients die while waiting for heart transplantation or heart-lung transplantation, while others with reversible heart-lung failure are difficult to overcome. Passed a short critical pass and died. [0003] With the emergence of extracorporeal membrane oxygenation (ECMO) technology, the treatment rate of critically ill cardiopulmonary patients has been greatly improved. Extracorporeal membrane oxygenation (ECMO) i...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61L31/08A61L31/16A61L29/08A61L29/16A61L33/10
Inventor 李彤于美丽
Owner 李彤
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