Exosome preparation suitable for mucosa and having similar needle-free injection effect and preparation method of exosome preparation
A needle-free injection, exosome technology, applied in the field of biomedicine, can solve the problems of reducing the expected curative effect, drug loss, reducing the contact time between drugs and vaginal mucosa, etc., achieving good pertinence and adaptability, regulating menstruation, and increasing penetration. The effect of the skin effect
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Embodiment 1
[0048] An exosome preparation suitable for mucosal injection with a needle-free injection effect, prepared according to the following steps:
[0049] Step 1, co-culture of stem cells and lactic acid bacteria
[0050] 1) Preparation of lactic acid bacteria-sodium alginate gel balls
[0051] Prepare a sodium alginate solution with a mass concentration of 5% and a CaCl solution with a mass concentration of 4% 2 solution. The two solutions were sterilized at 121°C for 20 minutes under high temperature and high pressure, and then placed in a sterile operating table to cool to room temperature.
[0052] Weigh an appropriate amount of lactic acid bacteria, put them into a sterilized beaker, mix evenly with sodium alginate solution, the final wet weight concentration of lactic acid bacteria is 1% (w / w), draw the mixed solution with a syringe or pipette, and drop evenly to CaCl 2 In solution, the surface of the droplet calcifies into balls with a diameter of 1-3 mm, see figure 1 . ...
Embodiment 2
[0073] A method for preparing an exosome preparation with a needle-free injection effect suitable for mucosa, comprising the following steps:
[0074] Step 1, co-culture of stem cells and lactic acid bacteria
[0075] 1) Preparation of lactic acid bacteria-sodium alginate gel balls
[0076] Prepare a sodium alginate solution with a mass concentration of 3% and a CaCl solution with a mass concentration of 2% 2 solution. The two solutions were sterilized at 121°C for 20 minutes under high temperature and high pressure, and then placed in a sterile operating table to cool to room temperature.
[0077] Refer to Example 1 for the remaining operations of step 1, wherein the crosslinking time is changed to 12h.
[0078] 2) Stem cell inoculation
[0079] The P3 passage umbilical cord mesenchymal stem cells were cultured in 4×10 4 Cells / mL were inoculated in the culture container; or, the P6 generation umbilical cord mesenchymal stem cells were inoculated at 7×10 4 Inoculate the ...
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