Preparation method of micro RNA nano microsphere and application of micro RNA nano microsphere in anti-tumor aspects
A nano-microsphere and tiny technology, applied in the field of tumor molecular biology, can solve the problems of difficult to confirm the effect, poor stability, difficult to apply to tumor patients, etc., to achieve the effect of inhibiting metastasis, solving preservation problems, and enhancing stability.
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Embodiment 1
[0024] Example 1. Preparation scheme of tiny nano-microspheres
[0025] Dissolve miR-125b-AS (synthetic miR-125b-AS sample purchased from Shanghai Gemma Biopharmaceutical Company) in 10 times the volume of distilled water to prepare an RNA aqueous solution, and add the RNA aqueous solution to the protective oil layer (soybean oil at a volume ratio of 3:2 ), place the ultrasonic probe at the water-oil interface (≈150 W / cm 2 ), the reaction temperature was set at 20 °C, and the ultrasonic time was 3 Min. A 20kDa ultrafiltration membrane is used to separate the nano-microspheres. After the nano-microspheres are separated, their size and particle size distribution are analyzed by DLS and SME methods. The 125b-AS-RNs nanoparticles were fixed with glutaraldehyde and analyzed by scanning electron microscopy. The results of the implementation are shown in the appendix figure 1 Shown, scale bar: 500nm. The results show that the method can be used to prepare nano-RNA microspheres w...
Embodiment 2
[0026] Example 2. In vitro stability detection of microRNA nanospheres
[0027] In order to test the in vitro stability of microRNA nanospheres, the purchased miR-125b-AS samples synthesized by Shanghai Gemma Biopharmaceutical Company and the nanosphere mi125b-AS-RNs samples prepared by the present invention were respectively heated at 25°C. The UV absorbance of RNA was monitored at 260 nanometers with a UV spectrometer for 0-7 days. The results showed that after miR-125b-AS was placed for 7 days, the absorbance decreased significantly, but the absorbance of miR-125b-AS decreased significantly. There was no change, indicating that the stability of microRNA was significantly increased after being prepared as nanospheres.
[0028] Further, we used formaldehyde-denatured PAGE gel electrophoresis to detect the integrity of RNA to evaluate the storage time of microRNA nanospheres at room temperature. The implementation results are attached figure 2 , the results show that micr...
Embodiment 3
[0029] Example 3. Effect of miR-125b antisense nucleotide nanoparticles on growth and apoptosis of malignant glioma cells
[0030] cells by 10 3Each well was inoculated in a 96-well plate, cultured for 24 hours, and 87 cells were transfected with negative control miRNA (NC-AS) and miR-125b antisense strand (miR-125b-AS, marked as 125b-AS in the figure) , the transfection reagent lipofectamine 2000 from Invitrogen Company was used; the transfection reagent lipofectamine 2000 from Invitrogen Company was used; the nanospheres of miR-125b-AS (125b-AS-RNs) were directly transfected without the transfection reagent lipofectamin2000, and finally The concentration is 100nM / L. After 72 hours of culture, the cells were collected and 24 hours after transfection, the cells were collected to detect cell apoptosis by TUNEL assay and flow cytometry AV / FITC double staining. The results showed that both miR-125b-AS and its nanospheres could induce glial Tumor cell apoptosis, indicating tha...
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