Intelligent gel three-dimensional scaffold material for cell culture
A smart gel and three-dimensional scaffold technology, which is applied in tissue culture, biochemical equipment and methods, microorganisms, etc., can solve the problems of lack of biological interaction, difficult purification of toxic compounds, weak water absorption and swelling ability, etc. It is easy to achieve industrialization , low cost, fast degradation effect
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[0037] The preparation method of the supramolecular gel factor adopted in the present invention is as follows: first synthesize a hydrophobic benzene ring as the core, and insert amino acids such as phenylalanine symmetrically at the 1 and 4 positions of the benzene ring, and have functions such as ethylene glycol. group, the general structure of which is shown in the following formula:
[0038]
[0039] Among them, R 1 Be the structure shown in formula (II), formula (III) or formula (IV):
[0040]
[0041] R 2 Be the structure shown in formula (V), formula (VI), formula (VII) or formula (VIII):
[0042]
Embodiment 1
[0057] Embodiment 1, preparation smart gel support material
[0058] This type of smart gel scaffold material can be prepared by adjusting the temperature of the solvent. The preparation process is as follows: figure 2 shown.
[0059] Firstly, sodium hyaluronate was dissolved in water to prepare a 1wt% sodium hyaluronate solution, and then the aforementioned supramolecular gel factor A was added to the above sodium hyaluronate solution at a concentration of 2.5 mg / ml. Heat (heating temperature 80°C, heating time 5min) the sample until the gel factor is completely dissolved to form a mixed solution, then cool to room temperature, cooling time is 10min, the gel is formed. The gel is dried (drying temperature is 65° C., time is 12 hours) until the moisture is completely evaporated to form a transparent film-xerogel, which is the intelligent gel scaffold material.
[0060] The nanofibers that make up the gel were characterized separately by scanning microscopy, as image 3 s...
Embodiment 2
[0063] Embodiment 2, two-dimensional cell culture experiment
[0064] First, a mixed gel solution containing 0.05wt% gelatin factor A and 0.2wt% natural polysaccharide (the sample was prepared by dissolving the gelatin factor by heating in an aqueous solution of natural polysaccharide and then cooling to 20°C for 30 minutes) was added to the 24-well polystyrene Place the ethylene cell culture plate in an ethanol-sterilized vacuum oven at 70°C and dry for 12 hours to obtain a cell culture plate with a surface modified by the mixed gel. Use DMEM medium (containing 10% fetal bovine serum in the medium) to cultivate human skin fibroblasts (NHSF), under the condition of 37 ℃, feed carbon dioxide so that the volume concentration of carbon dioxide in the culture environment is 5%, and cultivate for 3 days. It was found that the above cells observed the cell morphology in 24 hours, all adhered and spread on the surface of the material, and the growth morphology was good ( Figure 5...
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