Preparation method of cellular reticular alginate porous material used as artificial skin

Abstract

The invention discloses a preparation method of a cellular reticular alginate porous material used as an artificial skin. The preparation method comprises: by taking sodium alginate or oxidized sodium alginate of which the relative molecular mass is more than or equal to 100000 as a solute, and deionized water, distilled water, normal saline, injection water or ringer's solution as a solvent, performing freeze forming by forming a vertical temperature gradient in a special forming mold, and performing crosslinking reaction to obtain a porous material, wherein the inside of the porous material is cellular, the porous material comprises a plurality of pores, the pore diameters of the pores change from big to small in gradient from the lower surface to the upper surface, the pore diameters of the pores on the upper surface are 5-70 mu m, the pore diameters of the pores on the lower surface are 50-200 mu m, and every two adjacent pores are communicated with each other and have skin bionic structures. The preparation method disclosed by the invention is simple, is easy to control and is low in manufacturing cost, and the prepared product is good and stable in quality, has a skin bionic structure, and has good hygroscopicity, biodegradability and biocompatibility.

Description

technical field [0001] The invention relates to a preparation method of a medical porous material, in particular to a preparation method of a honeycomb mesh alginate porous material used as an artificial skin. Background technique [0002] The choice of biomaterial determines the biocompatibility of the constructed porous scaffold material. Sodium alginate is a natural material extracted from seaweed plants, and is one of the natural biomaterials approved by the US Food and Drug Administration (FDA) for use in medical fields such as tissue engineering. [0003] Sodium alginate, a polysaccharide, has a structure similar to that of the skin dermal matrix component: aminoglycan, and has good biocompatibility. Skin fibroblasts, liver cells, chondrocytes, and osteoblasts are easily absorbed in alginate porous materials. It survives and forms an extracellular matrix. At the same time, sodium alginate also has good film-forming, gelling, hygroscopicity, and barrier bacteria proper...

AI Technical Summary

Problems solved by technology

Since the temperature conduction in the low-temperature refrigerator is along the axis of the pre-freezing model, the pore diameters of porous materials are different along this direction, but the pore size of the longitudinal section is the same. Preparation and performance research of calcium acid-based interpenetrating network membrane materials" studied the alginate solution with a concentration of 2% and pre-frozen in a low-temperature refrigerator at -5°C. The pores in the longitudinal section were uniform and the pore diameter was 100-300 μm. , but due to the single pore size, it is not suitable for the cultivation of full-thickness skin, and it is easy to cause scars when used clinically

Studies have shown that gradient tissue engineering scaffolds with biomimetic skin structures are more conducive to skin regeneration. For skin tissue engineering scaffolds with biomimetic skin structures, research reports are mostly prepared by double-layer or multi-layer composite methods or other methods. It is more time-consuming. For example, Harley and Oh et al. studied the use of rotation/centrifugation technology combined with freeze-drying technology to construct a porous scaffold with a gradient pore structure in the radial direction. The pore size of the scaffold can be adjusted by the rotation speed, but this technology is generally only applicable to the preparation of blood vessels. Tubular scaffold materials are not suitable for constructing other scaffold materials (Harley, B.A., Hastings, A.Z., Yannas, I.V. & Sannino, A. Fabricating tubular scaffolds with a radial pore size gradient by a spinning technique. Biomaterials 27, 866-874, doi: 10.1016 /j.biomaterials.2005.07.012(2006); Oh,S.H.,Park,I.K