Natural nano-vesicle and preparation method and applications thereof
A nanovesicle, a natural technology, applied in animal cells, digestive system, medical raw materials derived from mammals, etc., can solve problems such as unclear roles and invasion
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Embodiment 1
[0028] The application of the natural nanovesicle of the present invention in the preparation of inhibitors for regulating cell transfer and TGF-β signaling pathway.
[0029] The application of the natural nanovesicle of the present invention in the preparation of various acute and chronic liver diseases or liver damage drugs or inhibitors caused by acute and chronic liver diseases.
[0030] The application of a natural nanovesicle of the present invention in the preparation of drugs or inhibitors of HCC primary liver cancer.
[0031] The cells are exosomes derived from HCC primary liver cancer cells.
[0032] The exosomes derived from HCC primary liver cancer cells promote the invasion and metastasis of HCC in vivo.
[0033] The exosomes derived from HCC primary liver cancer cells can activate recipient cells by transporting fibroblast growth factor FGF, vascular endothelial growth factor VEGF and epidermal growth factor EGF to affect cell growth and migration.
[0034] The...
Embodiment 2
[0043] The difference between embodiment 2 and embodiment 1 is:
[0044] The preparation method of the natural nanovesicles of the present invention comprises the following steps: (1) extraction of exosomes: the extraction of exosomes in patient serum adopts ExoquickTM Kit (System Biosciences, USA) method; ExoquickTM Kit (System Biosciences , USA) The steps of the method are as follows: 50 μl of serum was centrifuged at 5000 g for 20 minutes to remove cells and debris, the supernatant was transferred to another clean and sterilized tube, 20 μl of Exoquick TM Kit reagent was added and mixed up and down, incubated at 4 °C, centrifuged at 1500 g for 20 Minutes, an off-white precipitate can be seen at the bottom of the tube, remove the supernatant and centrifuge again at 1500g for 20 minutes, carefully remove the supernatant, and resuspend the pellet with PBS buffer or RNA lysate according to the subsequent use. The extracted precipitate was observed by transmission electron micro...
Embodiment 3
[0049] The difference between embodiment 3 and embodiment 1 is:
[0050] The preparation method of the natural nanovesicles of the present invention comprises the following steps: (1) extraction of exosomes: the extraction of exosomes in patient serum adopts ExoquickTM Kit (System Biosciences, USA) method; ExoquickTM Kit (System Biosciences , USA) The steps of the method are as follows: 300 μl of serum was centrifuged at 4000g for 10 minutes to remove cells and debris, the supernatant was transferred to another clean sterile tube, 100 μl of Exoquick™ Kit reagent was added and mixed upside down, incubated at 4°C, centrifuged at 1500g for 10 Minutes, an off-white precipitate can be seen at the bottom of the tube, remove the supernatant and centrifuge again at 1500g for 30 minutes, carefully remove the supernatant, and resuspend the pellet with PBS buffer or RNA lysate according to the subsequent use. The extracted precipitate was observed by transmission electron microscope acco...
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