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Artificial dermal scaffold and production method thereof

A dermal and artificial technology, applied in the field of biomedicine, can solve the problems of stents being easily dissolved, collapsed or degraded in a short period of time, unable to support cells and blood vessels, and poor permeability of dermal stents, etc., to achieve good three-dimensional shape and Strength, good biocompatibility, and no adverse effects

Active Publication Date: 2016-05-11
MEDPRIN REGENERATIVE MEDICAL TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The current artificial dermal scaffold mimics the three-dimensional structure of collagen fibers. Studies have found that the scaffold material with dense pores has good anti-scar effect, but it will limit the rapid arrival of dermal fibroblasts to the wound site, resulting in poor permeability of the dermal scaffold and slow vascularization rate. The anti-infection effect is not good; the scaffold material with loose pores is conducive to the rapid growth of blood vessels and fibroblasts, but the anti-scar effect is poor in the later stage
In addition, it is also very important for the scaffold material to maintain a complete three-dimensional structure and proper degradation time in a wet state. The scaffolds prepared by some processes are easy to dissolve, collapse or degrade in a short period of time in a wet state, making newborns Before the tissue grows in, the scaffold structure does not exist, so it cannot support cells and blood vessels well

Method used

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  • Artificial dermal scaffold and production method thereof
  • Artificial dermal scaffold and production method thereof
  • Artificial dermal scaffold and production method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0053] An artificial dermis support, prepared as follows:

[0054] S1. Slowly add 6 grams of hydroxyethyl cellulose into 200 milliliters of ultrapure water, wherein the pH value of the solution is adjusted to 3 with dilute hydrochloric acid; then add 0.6 grams of calcium chloride and stir evenly;

[0055] S2. Add 0.12 ml of glutaraldehyde with a concentration of 25% to the solution treated in S1. Stir and heat up to 80° C. to allow the cross-linking reaction to proceed. The time for the cross-linking reaction is 60 minutes to obtain a uniform solution;

[0056] S3. Add 1.2 grams of glycerin to the solution after the cross-linking reaction in S2. Mix well and stir for 60 minutes at a stirring speed of 1500r / min. A large number of bubbles will be generated, and the foaming volume will reach twice the volume of the original solution. In a dry dish, the thickness is 0.3cm;

[0057] S4. Immediately place the freeze-drying tray of S3 in a freeze dryer pre-adjusted to -80°C for low-...

Embodiment 2

[0061] An artificial dermis support, prepared as follows:

[0062] S1. Slowly add 5 grams of hydroxypropyl cellulose into 125 milliliters of ultrapure water, wherein the pH value of the solution is adjusted to 2.9 with formic acid; then add 0.25 grams of potassium chloride and stir evenly;

[0063] S2. Add 0.2ml of glutaraldehyde with a concentration of 25% to the solution treated in S1. Stir and heat up to 70°C to allow the crosslinking reaction to proceed. The time for the crosslinking reaction is 40min to obtain a uniform solution;

[0064] S3. Add 0.5 g of glycerin to the solution after the cross-linking reaction in S2, mix well and stir at a stirring speed of 1800r / min, stir for 30min, a large number of bubbles will be generated, and the volume of the foam will reach 3 times the volume of the original solution, pour into frozen In a dry dish, the thickness is 0.4cm;

[0065] S4. Immediately place the freeze-drying tray of S3 in a freeze dryer pre-adjusted to -80°C for lo...

Embodiment 3

[0069] An artificial dermis support, prepared as follows:

[0070] S1. Slowly add 2.5 grams of hydroxypropyl cellulose and 2.5 grams of hydroxyethyl cellulose into 62.5 milliliters of ultrapure water, wherein the pH value of the solution is adjusted to 2.95 with dilute hydrochloric acid; then add 1 gram of sodium chloride and stir Uniform;

[0071] S2. Add 0.25ml of formaldehyde to the solution treated in S1. Stir and heat up to 90°C to allow the crosslinking reaction to proceed. The crosslinking reaction time is 100min to obtain a uniform solution;

[0072] S3. Add 2 grams of glycerin to the solution after the cross-linking reaction in S2. Mix well and stir for 40 minutes at a stirring speed of 1300r / min. A large number of bubbles will be generated, and the volume of foaming will reach twice the volume of the original solution. In a dry dish, the thickness is 0.3cm;

[0073] S4. Immediately place the freeze-drying tray of S3 in a freeze dryer pre-adjusted to -20°C for low-t...

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Abstract

The invention discloses an artificial dermal scaffold and a production method thereof. The artificial dermal scaffold comprises a porous scaffold produced from oxycellulose and a cross-linking agent, the amount of porosity of the porous scaffold is 85-96%, the average aperture is 50-200[mu]m, the water absorption rate is 17-28 times the self weight of the porous scaffold, and the saturated water content is 90-97%. The artificial dermal scaffold is similar to human body skins in softness, can keep good three dimensional form and strength in a wet state, can cling to wounds, has good adhesiveness and breathability, can absorb human body diffusate and has no untoward effects. The artificial dermal scaffold has appropriate aperture size and porosity amount, can effectively promote wound healing, and also can promote generation of granulation tissues and new vessels. The artificial dermal scaffold also has an appropriate degradation time, and can reduce formation of scars.

Description

technical field [0001] The invention relates to the field of biomedicine, and more specifically relates to an artificial dermis support and a preparation method thereof. Background technique [0002] As the largest organ of the human body, the skin has the functions of retaining moisture, ventilating and preventing bacterial invasion. When the skin is damaged by factors such as trauma, burns or diseases, especially when a large area of ​​skin is seriously damaged, it will pose a serious threat to the life safety of the patient. The prior art mostly adopts the method of autologous skin transplantation at present, which not only causes new wound defect in the skin donor area of ​​the patient, but also is often limited by the source of skin donor. Therefore, researchers from various countries are devoted to the research of artificial skin, and only a few developed countries have mastered this technology and realized industrialization, including Integra, Dermagraft, AlloDerm, B...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61L27/60A61L27/20A61L27/56A61L27/54
CPCA61L27/20A61L27/54A61L27/56A61L27/60A61L2300/412C08L1/04
Inventor 李林静李广耀邓坤学袁玉宇
Owner MEDPRIN REGENERATIVE MEDICAL TECH
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