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A preparation method of a thermosetting elastomer tissue engineering scaffold with a multi-level pore structure

A tissue engineering scaffold and pore structure technology, applied in tissue regeneration, prosthesis, additive processing, etc., can solve the problems of destroying the original structure, no FDM printing PGS elastomer scaffold, and inability to process PGS elastomer, etc., to achieve The effect of simple method and good application prospect

Active Publication Date: 2020-05-29
DONGHUA UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

FDM printing technology has been used and researched as a thermoplastic material processing method because of its fusion forming principle, and it is difficult to apply to the above-mentioned thermosetting elastomer materials
Taking PGS as an example, the main difficulty is: first, the prepolymer is a thermoplastic material that can withstand plastic processing and has printability, and then needs further high temperature and vacuum environment for crosslinking and curing
However, in the second step, since the prepolymer itself is sensitive to heat, the heat can greatly increase its fluidity, and it will deform before cross-linking and curing to destroy the original structure. In the end, it is impossible to process PGS by 3D printing. cross-linked elastomer
Due to the incompatibility between the above-mentioned properties of thermosetting materials and the principle of FDM thermoplastic processing, there have been no reports of using FDM to print thermosetting bioscaffolds, let alone FDM printing of PGS elastomeric scaffolds.

Method used

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  • A preparation method of a thermosetting elastomer tissue engineering scaffold with a multi-level pore structure
  • A preparation method of a thermosetting elastomer tissue engineering scaffold with a multi-level pore structure
  • A preparation method of a thermosetting elastomer tissue engineering scaffold with a multi-level pore structure

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Experimental program
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Effect test

Embodiment 1

[0036] 1. Printing material preparation

[0037] The mixing parameters of PGS prepolymer (Pre-PGS) and salt particles directly determine the extrudability, initial shape stability, high-temperature curing shape retention and pore structure of the scaffold during printing, which indirectly determine the performance of the scaffold. Including mechanical properties and biodegradability. The parameters that need to be studied in the mixing process include the mixing method, the mixing ratio and the diameter of the salt particles.

[0038] 1.1 Mixing method

[0039] Pre-PGS is viscous and has a high viscosity at room temperature. As the proportion of mixed salt increases, the viscosity of the mixture gradually increases, which is easy to cause uneven mixing. Therefore, it is necessary to consider reducing the viscosity of the mixture. There are two commonly used methods to reduce viscosity: solvent method and heating method. Therefore, two methods are used to mix materials, and ...

Embodiment 2

[0118] Prepare the PCLU stent, the method is the same as in Example 1. Using polycaprolactone diol and HDI trimer as raw materials, mixed with salt particles, printed and then solidified, the prepolymer synthesis step is omitted, and the raw material unit is reacted and solidified under heating conditions on the 3D formed structure.

[0119] Such as Figure 11 As shown, this method is also suitable for the printing and molding of PCLU, which can prepare bioscaffolds and other irregular shapes. This thermosetting PCLU is also an elastic body, which can still recover quickly after repeated folding (a-d). The electron microscopy test of the scaffold shows that the fiber units are clearly and regularly arranged and stacked, the fiber cross-section is circular, no obvious fiber collapse is found, and it has good curing shape retention. At the same time, there are a large number of micropores distributed on the surface and inside of the fiber. The whole has a multi-level pore struc...

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Abstract

The invention relates to a preparation method of a thermosetting elastomer tissue engineering scaffold with a multi-level porous structure. The preparation method comprises the following steps of: (1) mixing a thermosetting material with a filling material to obtain a mixed material; establishing a model of a cuboid netty structure by means of CAD (Computer Aided Design) software; and then adding the mixed material into a heating cavity of a 3D printer and performing 3D printing to obtain an initial scaffold; and (2) performing thermal crosslinking or optical crosslinking on the initial scaffold in the step (1) to obtain the thermosetting elastomer tissue engineering scaffold; and finally, removing the filling material to obtain the thermosetting elastomer tissue engineering scaffold with the multi-level porous structure. The invention solves the fundamental problem of directly printing thermosetting material by thermoplastic FDM (Fused Deposition Modeling), and the prepared tissue engineering scaffold has the multi-level porous structure which is controllable in precision in structure. The method is simple and convenient and suitable for various biological materials and has a good application prospect.

Description

technical field [0001] The invention belongs to the field of tissue engineering scaffolds, in particular to a method for preparing a thermosetting elastomer tissue engineering scaffold with a multi-level pore structure. Background technique [0002] Tissue and organ damage is one of the major diseases that seriously threaten human health. Traditionally, it is mainly treated through clinical organ transplantation and other means. Professor Yuan-Cheng Fung, a pioneer of bioengineering in the 1980s, first coined the term tissue engineering, whose purpose is to generate replaceable tissues or organs with three-dimensional structures in vivo or in vitro to repair, regenerate damaged or lost Human tissues and organs, so as to break through the limitations of existing clinical medical methods on the treatment of damaged tissues or organs, including the limited number of donated organs, allogeneic rejection, potential virus infection, autologous "repairing trauma with trauma" second...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61L27/56A61L27/58A61L27/50A61L27/18A61L27/02B33Y10/00B33Y70/00
CPCA61L27/025A61L27/18A61L27/50A61L27/56A61L27/58A61L2400/08A61L2400/16A61L2430/06A61L2430/20B33Y10/00B33Y70/00C08L67/00C08L67/04
Inventor 游正伟雷东
Owner DONGHUA UNIV
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