Method for promoting activation and differentiation of cells
A cell and cell therapy technology, applied in biochemical equipment and methods, using electricity/wave energy to treat microorganisms, electricity/wave energy to treat enzymes, etc., can solve problems such as poor test and stimulation effects, and achieve good clinical application prospects, The effect of promoting cell growth and differentiation
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Embodiment 1
[0028] Embodiment 1 The present invention promotes cell activation and differentiation method
[0029] The structure of the instrument for promoting cell activation and differentiation of the present invention—the cell therapy conversion instrument is as follows: figure 1 , 2 As shown, it includes a base, an outer cover 1 and an LED lamp tube 2 located inside the outer cover. There is a syringe inlet 3 on one side of the outer cover 1, a liquid crystal display 4 and an instrument start key 10 are arranged on the surface of the outer cover, and there is a housing needle inside the LED lamp tube 2. The channel 7 of the barrel, the opening of one end of the channel 7 is opposite to the inlet 3 of the syringe, the side of the channel 7 has an LED light source, the inside of the outer cover 1 has a control panel, the liquid crystal display 4, the LED light source and the instrument start key 10 are electrically connected to the control panel, The outer cover 1 is fixedly connected...
experiment example 1
[0039] Experimental example 1 adopts the method of the present invention to process platelet-rich plasma
[0040] 1. Instrument
[0041] The cell therapy conversion instrument described in Example 1 of the present invention.
[0042] 2. Processing method
[0043] Raw materials: Collect 10ml of venous peripheral blood from healthy people in a medical anticoagulant tube, immediately mix it upside down for 5-10 times, and centrifuge using the improved 2-time centrifugation method. The first centrifugation is at room temperature for 10 minutes to collect the supernatant; then the second time is centrifugation at room temperature for 1000g for 10 minutes. , Discard about 2 / 3 of the supernatant, and mix the remaining liquid to obtain 4-6ml of highly concentrated platelet-rich plasma (PRP).
[0044] The experimental groups are: the control group without LED light radiation (no treatment), the instrument LED light radiation group (in step (2), do not open the rotation control key at t...
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