Bionic in-situ regeneration repair nano sticking patch and preparation method and application thereof

An in-situ regeneration and patch technology, applied in the field of nano-patch, can solve the problems of too short degradation time in vivo, insufficient mechanical strength, poor tissue attachment performance, etc., and achieve the effect of avoiding toxic side effects and strengthening mechanical properties

Active Publication Date: 2010-10-06
SUZHOU BOCHUANG TONGKANG PHARM TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there are many defects in its products that affect the performance of its functions. For example, the thickness of collagen sponge or membrane products ranges from 0.5mm to 5mm, resulting in soft products and poor tissue adhesion. Tensile strength makes it inconvenient for clinical surgeons to operate. In order to obtain certain mechanical properties, cross-linking agents such as glutaraldehyde must be added. In addition to certain tissue toxicity, cross-linking agents can easily lead to calcification; animal-derived proteins These products have relatively large safety risks (such as viruses, pathogenic microorganisms, etc.) and adverse reactions such as human allergies caused by protein macromolecules; the mechanical strength of carboxymethyl cellulose and chitosan products is not enough, and the degradation time in vivo is either too short or too long. long; and the degradation of polylactic acid products produces acidic products, etc.; therefore, the development of an innovative product that overcomes the defects of existing membrane products has very important clinical application value

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] Embodiment 1. Prepare a 12 centimeters diameter petri dish, built-in a same diameter macromolecule material film (through washing, sterilization and depyrogenation treatment), dry; Prepare the A solution (1mg / ml) of material with cationic group respectively Chitosan, 0.1mol / L acetic acid, 0.2mol / LNaCl, pH=4) and B liquid with anionic group material (1mg / ml carboxymethyl chitosan, 0.15mol / LNaCl, pH=6); take Add functional polypeptide (1×10 -4 mg / ml) into liquid C, the amino acid sequence of the functional polypeptide is: lysine-lysine-cysteine-serine-arginine-glycine-aspartic acid-serine-cysteine-lysine Acid-lysine: fill the above solutions into the high-pressure instantaneous spraying equipment respectively, first spray liquid C into the petri dish with high pressure instantaneously, and dry it to form a film; then spray liquid A with high pressure instantaneously, rinse with water for injection; then spray high-pressure instantaneously Liquid B, rinse with water for i...

Embodiment 2

[0027] Embodiment 2. prepare a 12 centimeters diameter petri dish, built-in a same diameter macromolecule material film (through washing, sterilization and depyrogenation treatment), dry; prepare respectively the A solution (2mg / ml) of material with cationic group Chitosan, 0.1mol / L acetic acid, 0.2mol / LNaCl, pH=4) and B solution with anionic group material (2mg / ml alginic acid, 0.15mol / LNaCl, pH=6) referred to as B solution; take Part B solution was prepared by adding epidermal growth factor (EGF) (0.01mg / ml) to make C solution; the above solutions were respectively filled into high-pressure instantaneous spraying equipment, firstly high-pressure instantaneous spray C liquid into the culture dish, and dried to form a film; then Spray liquid A with high pressure instantaneously, rinse with water for injection; then spray liquid B with high pressure instantaneously, rinse with water for injection, spray A liquid, B liquid, and rinse alternately in this way, repeat the operation ...

Embodiment 3

[0028] Embodiment 3. prepare a 12 centimeter diameter petri dish, built-in a same diameter macromolecular material membrane (through washing and sterilization depyrogenation treatment), rinse and dry with water for injection; prepare respectively the material with cationic group (1mg / ml collagen , 0.1mol / L acetic acid, 0.2mol / LNaCl, pH=3.5) and liquid B with anionic group materials (1mg / ml hyaluronic acid, 0.15mol / LNaCl, pH=6); fill the above solutions into In the high-pressure instantaneous spraying equipment, first spray liquid A with high pressure in the petri dish, dry it, then spray liquid B with high pressure instantaneously, rinse with water for injection, and repeat the operation 500 times by spraying liquid A, liquid B and rinsing alternately in this way; Instantly spray liquid A, rinse with water for injection, dry, peel off the film, rinse with water for injection on the veneer, and dry to obtain a finished product.

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PUM

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Abstract

The invention relates to a bionic in-situ regeneration repair nano sticking patch, which is formed by overlapping an layer A with a cationic group material and a layer B with an anionic group material sequentially, wherein the sticking patch comprises 20 to 80 percent by mass of the A layer with the cationic group material and the balance of the layer B with the anionic group material; layer A with the cationic group material comprises at least one of polysaccharide with a cationic group, protein with the cationic group or opypeptide (polypeptide) with the cationic group; layer B with the anionic group material comprises at least one of polysaccharide with an anionic group, protein with the anionic group or opypeptide (polypeptide) with the anionic group; and the sticking patch comprises not more than 10 percent by mass of added functional factors and/or functional polypeptide. The raw materials used by the invention are materials which can be degraded in vitro and have biocompatibility. The sticking patch is flexible, has good tissue adhesivity, is suitable for concave-convex surfaces of visceral organs, has strong stretching resistance and air pressure resistance, is suitable for application of sticking, sealing, leak stoppage, hemostasia, isolation, repair, adhesion prevention and artificial meninges of defect tissues and can also be used as a slowly-releasing carrier of a medicament and a nano-grade tissue engineering support material.

Description

technical field [0001] The invention belongs to the technical field of biomedicine, and specifically relates to a nano-patch composed of a material with anion groups, a functional factor and / or a functional polypeptide, and a material with a cationic group. It also provides the preparation method of the nanopatch and its application in the sticking, sealing, plugging, hemostasis, isolation, repair, prevention of adhesion, anti-infection and artificial meninges of defective tissue in surgical operations, and it can also be used as a sustained release of drugs. Carriers and nanoscale tissue engineering scaffold materials. Background technique [0002] In surgical operations, it is often necessary to seal, repair and prevent adhesion of defects and damaged tissues. The existing products include film and gel products of carboxymethylcellulose, chitosan, polylactic acid, collagen and fibrin glue. To a certain extent, the product has played a positive role in the sealing, repairi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61B17/03A61M31/00A61L31/12A61K47/42
Inventor 吴昌琳
Owner SUZHOU BOCHUANG TONGKANG PHARM TECH CO LTD
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