In vivo tumor imaging target molecule and specific probe thereof
A technology of target molecules and probes, applied in the field of in vivo tumor imaging target molecules and their specific probes, can solve the problems of no biological function of proteins, limited expression and distribution, etc.
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Embodiment 1
[0055]Example 1 Preparation of anti-sperm protein 17 monoclonal antibody (anti-Sp17 mAb)
[0056] 1. Anti-Sp17mAb preparation: inject liquid paraffin (0.5ml / mouse) into the peritoneal cavity of mice, and inject hybridoma cells (0.5ml / mouse) with the preservation number CGMCC No.1434 into the peritoneal cavity of mice 14 days later. When the abdomen of the mice was obviously enlarged, the ascites of the mice was extracted with a No. 8 needle, and the ascites was extracted in the same way every 4 days until the mice died. Centrifuge the ascites at 3000rpm for 10 minutes, discard the upper layer of fat and insoluble matter and various cells and insoluble matter in the lower layer, absorb the light yellow supernatant, add an equal volume of glycerol (containing 20g / L Na 2 HPO 4 ), and stored in a -20°C refrigerator after aliquoting.
[0057] 2. Purification of anti-Sp17mAb
[0058] 1) Ammonium sulfate salting out: Add 500g of ammonium sulfate into 500ml of distilled water, heat...
Embodiment 2
[0062] Example 2 Establishment of tumor animal models
[0063] BALB / C nude mice (male or female, 4-6 weeks old, 20-25 g). Ovarian cancer cell line HO8910 or liver cancer cell line SMMC-7721 overexpressing Sp17 were cultured in RPMI1640 medium. When the cells cover more than 80% of the bottom of the bottle, digest the cells with 0.25% trypsin-0.02% EDTA for 1 min, stop the reaction with RPMI1640 culture medium containing 10% calf serum, blow and beat to disperse the cells, centrifuge at 1000rpm for 5 min, discard the supernatant, and use PBS to adjust the number of cells, 2 × 10 6 / 0.2ml, the cells were inoculated subcutaneously in the shoulders or buttocks of 20-25g nude mice. After about 10-20 days, the tumors gradually grew.
Embodiment 3
[0064] Example 3 Preparation of Immunomagnetic Nanoprobes (IMNPs)
[0065] Using chemical coupling agent EDC / NHS (1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide / N-hydroxysuccinimide N-hydroxysuccinimide), the two Magnetic nanoparticles with different surface modifications (nanoscale γ-Fe 2 o 3 Particles, prepared by the School of Biological Science and Medical Engineering of Southeast University by co-precipitation method) were coupled with anti-Sp17mAb to prepare immunomagnetic nanoprobes (anti-Sp17IMNPs, hereinafter referred to as IMNPs), and compared the targeting effect of the two on tumors.
[0066] 1. Anti-Sp17-Silane@MNPs probe preparation: Take 0.2 mg of silane-modified magnetic nanoparticles (Silane@MNPs), add 100 μg of anti-Sp17 mAb activated by EDC / NHS, mix well, and shake at room temperature for 2 hours. Then the mixture was magnetically separated and washed with PBS buffer three times to remove free antibodies, and finally the precipitate was suspended in PBS (0...
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