Method for preparing medical polylactic acid melt-spun fiber porous ordered scaffold

A technology of polylactic acid and melt spinning, which is applied in medical science, prosthesis, coating, etc., can solve the problem of difficult control of the number of fibers, and achieve the effect of small thickness, simple process, good pore size and order degree

Active Publication Date: 2016-01-13
ZHEJIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

(3) Degradation products must be non-toxic
It is difficult to control the number of fibers in the ordered scaffold and form a larger-sized scaffold during the preparation of ordered scaffolds by fiber knotting method and pulse heat sealer hot pressing method

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0044] PLA slices with a molecular weight of 170,000 were prepared by melt spinning into PLA melt-spun fibers with an average diameter of 12.41 μm, and a YG086 skein length measuring instrument was used to wind parallel aggregates at a speed of 300 r / min. The circumference is 1000mm, the width is 3.5cm, and the initial tension is 100cN, and PLA ordered fiber bundles are obtained. Weigh 0.5g of PLGA and dissolve it in 10mL of tetrahydrofuran (volume concentration: 5%), stir until completely dissolved to form a uniform PLGA / tetrahydrofuran solution. Brush the PLGA / tetrahydrofuran solution evenly on the front and back of the PLA ordered fiber bundle twice, and then put it in the fume hood for 24 hours to completely volatilize the tetrahydrofuran. After it is completely volatilized, place it in a vacuum desiccator, and dry it at 45°C for 24 hours to obtain a PLGA bonded PLA fiber porous ordered scaffold (see figure 1 , figure 2 ). The pore diameter of the scaffold is 3.65±2.54...

Embodiment 2

[0046] PLA slices with a molecular weight of 170,000 were prepared by melt spinning into PLA melt-spun fibers with an average diameter of 12.41 μm, and a YG086 skein length measuring instrument was used to wind parallel aggregates at a speed of 300 r / min. The circumference is 1000mm, the width is 3.5cm, and the initial tension is 100cN, and PLA ordered fiber bundles are obtained. Weigh 0.5g of PGA and dissolve it in 10mL of tetrahydrofuran (5% volume concentration), stir until completely dissolved to form a uniform PGA / tetrahydrofuran solution. Brush the PGA / tetrahydrofuran solution evenly on the front and back of the ordered PLA fiber bundle twice, and then put it in the fume hood for 24 hours to completely volatilize the tetrahydrofuran. After it volatilized completely, put it in a vacuum desiccator, and dry it at 45°C for 24 hours to obtain a PGA-bonded PLA fiber porous and ordered scaffold (see image 3 , Figure 4 ). The pore diameter of the scaffold is 3.15±1.47 μm, a...

Embodiment 3

[0048] PLA slices with a molecular weight of 170,000 were prepared by melt spinning into PLA melt-spun fibers with an average diameter of 12.41 μm, and a YG086 skein length measuring instrument was used to wind parallel aggregates at a speed of 300 r / min. The circumference is 1000mm, the width is 3.5cm, and the initial tension is 100cN, and PLA ordered fiber bundles are obtained. Weigh 0.5g of PCL and dissolve it in 10mL of tetrahydrofuran (5% volume concentration), stir until completely dissolved to form a uniform PCL / tetrahydrofuran solution. Brush the PCL / tetrahydrofuran solution evenly on the front and back of the PLA ordered fiber bundle twice, and then put it in the fume hood for 24 hours to completely volatilize the tetrahydrofuran. After it is completely volatilized, place it in a vacuum desiccator and dry it at 45°C for 24 hours to obtain a PCL-bonded PLA fiber porous and ordered scaffold (see Figure 5 , Figure 6 ). The pore diameter of the scaffold is 5.89±3.04 ...

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Abstract

The invention discloses a method for preparing a medical polymer melt-spun fiber porous ordered scaffold. The method comprises the following steps: sequentially spinning and winding polylactic acid slices into fiber assemblies in parallel arrangement; forming the loose and parallel polylactic acid fiber assemblies into a stable structure by adopting the solvent cementing method; and performing vacuum drying. The medical polymer melt-spun fiber ordered scaffold prepared by the method is relatively small in thickness and relatively good in aperture and degree of order and can be applied to the aspects of bone tissue engineering and the like.

Description

technical field [0001] The invention relates to a method for preparing medical polylactic acid melt-spun fiber ordered support, in particular to a method for preparing medical polylactic acid melt-spun fiber porous ordered support by solvent bonding. Background technique [0002] When an ideal biomaterial meets the actual clinical application, it needs to meet four performance requirements: (1) Good biocompatibility and degradability, and the scaffold can be replaced by protein synthesis and secretion of implanted cells. (2) The material should have good clinical applicability and reduce inflammation and immune response so that tissue damage can be avoided. (3) Degradation products must be non-toxic. (4) The preparation, purification and processing of materials must be convenient and scalable. According to these four performance requirements, biomaterials that can be applied to tissue engineering scaffolds include natural polymers and synthetic polymers. Among them, nat...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61L27/34A61L27/18A61L27/56A61L27/50
Inventor 高长有冯建永
Owner ZHEJIANG UNIV
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