Porous material precursor composition, porous material and preparation method
A technology of porous materials and precursors, which is applied in the field of porous materials and their preparation, and precursor compositions of porous materials, can solve the problems of difficult operation, limited pore-forming effect, long time consumption, etc., and achieves broad application prospects and good biocompatibility. sexual effect
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Embodiment 1
[0057] Hydrogel precursor polymer, porogen, photoinitiator, photofoaming agent are dropped into 10mL deionized water according to the material and material amount of each group in Example 1 in Table 1 (the weight and volume percentage in Table 1 is based on Calculated based on the volume of deionized water), heat and stir at 50°C in the dark to dissolve; freeze-dry the above hydrogel precursor solution; heat and stir the freeze-dried hydrogel precursor in 10mL PBS at 37°C in the dark , dissolved into a hydrogel precursor solution, filtered and sterilized, and digested and centrifuged MC3T3-E1 cells (in terms of the volume of the gel obtained, the final planting density was 5*10 6 / mL) were mixed evenly to prepare a cell-containing hydrogel precursor solution, which was injected into a culture vessel and irradiated with a 405nm light source to obtain scaffolds 1-5 (obtained according to the material ratio of 1-5 groups) and scaffolds 1- 18+5 (obtained according to the material ...
Embodiment 2
[0061] According to the materials and material ratios of each group in Example 2 in Table 1, referring to the steps in Example 1, respectively prepare support 2-5, support 2-14+5, support 2-14+5+3;
[0062] Cultivate according to the method of Example 1, and use an optical inverted microscope to take pictures on the 1st and 4th days;
[0063] Such as figure 2 As shown, the scaffolds obtained by the 2-14+5 group and the 2-14+5+3 group showed obvious stretching on the 1st day, while the stretching of the scaffold 2-5 (only adding 5wt% GelMA and photoinitiator) was less; On the 4th day, all the three groups proliferated and stretched, and the 2-14+5+3 scaffold obtained in the 2-14+5+3 group was the most obvious, because the porous structure promotes nutrient transmission and waste discharge, so compared with the untreated Cells proliferate and expand in the porous GelMA (scaffold 2-14+5+3) prepared by phase separation combined with foaming method when adding porogen and photofo...
Embodiment 3
[0065] According to the materials and material ratios of each group in Example 3 in Table 1, referring to the steps in Example 1, respectively prepare support 3-5, support 3-8+5+3, support 3-14+5+3;
[0066] According to the culture method of Example 1, CCK-8 detection was performed on the scaffolds cultivated to 1, 4, and 7 days, and the absorbance of the CCK-8 working solution was measured with a microplate reader to quantitatively analyze the proliferation of cells on the scaffolds. For the proliferation of cells on the 4th and 7th day, see image 3 .
[0067] Depend on image 3 It can be seen that on the 4th day of culture, the 5wt% group (that is, the scaffolds 3-5 obtained from the 3-5 group) proliferated slightly, and the other two groups all proliferated more obviously. When cultured to the 7th day, the scaffold 3-8+5+3 obtained by the 3-8+5+3 group was higher than that of the blank hydrogel group (ie, the 3-5 group), and the 3-14+5+3 group The obtained scaffold 3-1...
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