Preparation method and application of sustained-release BIO/IGF (6-bromoindirubin-3'-oxime/insulin-like growth factor) composite hydrogel
A composite hydrogel and hydrogel technology, applied in the direction of medical preparations containing active ingredients, pharmaceutical formulas, drug combinations, etc., to achieve the effect of facilitating cell absorption and individual uniformity
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specific Embodiment approach 1
[0013] Specific embodiment 1: The preparation method of the composite hydrogel of sustained-release BIO / IGF in this embodiment is carried out according to the following steps: 1. At 50°C, add the mixed solution composed of BIO and IGF to a mass concentration of 4% In ~6% gelatin solution, stir at 5000~6000r / min, add acetone dropwise at the same time, then add glutaraldehyde, and then centrifuge at 5000~7000r / min for 5~8h to obtain nanomicroparticles coated with BIO and IGF. 2. Add sodium periodate to the sodium alginate solution with a mass concentration of 0.5mg / mL under the condition of avoiding light. The volume ratio of sodium periodate to sodium alginate solution is 1:350-450, dissolve Then place it on a shaker at 4°C and shake it for 5-8 hours to obtain solution A, add ethylene glycol to solution A, the volume ratio of ethylene glycol to solution A is 1:150-250, and then shake it on a shaker 2 to 3 hours to obtain solution B, add sodium chloride to solution B, the volume...
specific Embodiment approach 2
[0016] Embodiment 2: The difference between this embodiment and Embodiment 1 is that in Step 1, the volume ratio of the mixture composed of BIO and IGF to the gelatin solution is 1:1000. Others are the same as in the first embodiment.
specific Embodiment approach 3
[0017] Embodiment 3: The difference between this embodiment and Embodiment 1 or 2 is that the volume ratio of gelatin solution to glutaraldehyde in step 1 is 5:1. Others are the same as in the first or second embodiment.
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