Sericin nerve conduit and its preparation method and application
A technology of sericin and nerve guide, applied in the field of medical biomaterials, can solve problems such as unsatisfactory structure and function recovery, difficult to adjust degradation performance, poor mechanical processing performance, etc., to achieve product quality control and large-scale production , promotion of migration and alignment, good mechanical properties
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Embodiment 1
[0062] The preparation of embodiment 1 sericin nerve guide
[0063] 1. Selection of silkworm cocoons:
[0064] Silkworm cocoons of silkworm silk fibroin-deficient mutant varieties were selected (purchased from the Sericulture Research Institute of the Chinese Academy of Agricultural Sciences, and the silkworm silk fibroin-deficient mutant varieties were preserved in the National Silkworm Resource Preservation Center of the Sericulture Research Institute of the Chinese Academy of Agricultural Sciences, preservation number (or commodity number) 185Nd -s, 140Nd-s, 139Nd-s) as raw materials, the main chemical composition is: sericin.
[0065] 2. Extraction and separation of sericin
[0066] Figure 14 It is a schematic flow chart of preparing a sericin nerve guide according to an embodiment of the present invention, and the specific steps are:
[0067] 1) Weigh 1 g of cocoons of silkworm silk fibroin-deficient mutant varieties and cut them into 1 mm 2 Left and right fragments ...
Embodiment 2
[0089] Example 2 Performance analysis of sericin nerve guide
[0090] The following performance analysis is carried out to the sericin nerve guide (sample D1) prepared in embodiment 1, specifically:
[0091] 1. Macro structure
[0092] Using the selected mold, the obtained sericin nerve conduit was prepared into a hollow conduit structure with an inner diameter of 1.5 mm, a wall thickness of 0.75 mm, and a length of 20 mm.
[0093] 2. Microstructure.
[0094] Sericin nerve conduits were observed under a scanning electron microscope (ULTRA PLUS-43-13, Zeiss, Germany). like Figure 5 As shown, A and B are SEM images of the cross-section of the sericin nerve conduit, the scales are 500 microns and 100 microns respectively, the interior of the conduit is a multi-void structure with an average pore size of 42.24 μm, which can well support cell growth and promote exchange of nutrients and metabolites; Figure 5 Among them, C and D are the SEM images of the surface of the serici...
Embodiment 3
[0108] Example 3 Evaluation of Sericin Supporting Nerve Cell Survival and Proliferation Ability
[0109] Experimental group: use the aseptic sericin protein aqueous solution extracted in Example 1 to directly add to the cell well plate, freeze at -80°C for 4 hours, and then freeze-dry in a vacuum freeze dryer to obtain freeze-dried sericin Protein scaffold: Rat Schwann cells (RSC96) collected from cell culture flasks were suspended, blown apart, and planted on cell culture plates covered with freeze-dried sericin scaffolds. The medium used for cell culture was DMEM (Dulbecco's Modified Eagle's Medium) medium, and the cells were placed in a cell culture incubator (37°C, CO 2 The concentration is 5%, and the humidity is 100%).
[0110] In the control group, the cells were directly planted on ordinary well plates.
[0111] like Figure 8 As shown, after planting, the CCK-8 method was used to detect the proliferation of cells 1, 3, 5 and 7 days after planting. Depend on Figu...
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