A 68ga-labeled exenatide-like compound and its preparation method and application
A technology for exenatide and compounds, which is applied in the field of exenatide-like compounds and their preparation, can solve the problems of high production and maintenance costs, cumbersome synthesis process, etc., and achieve low toxic and side effects, high sensitivity, and low liver uptake Effect
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Embodiment 168
[0035] Example 1 68 Ga-NOTA-MAL-Cys 39 -Preparation of exendin-4
[0036] The present invention relates to experimental instruments and materials: 68 Ge / 68 Ga generator (German ABX company), 2480WIZARD2 automatic gamma counter (U.S. PerkinElmer company), high performance liquid chromatograph LC-20AT (Japan Shimadzu company); 30% Ultrapure hydrochloric acid (Germany Merck Gmbh), sodium acetate (U.S. Sigma), Sep-Pack C18 cartridge (Waters, USA), Physiological Saline (China Otsuka Pharmaceutical Co., Ltd.), NOTA-MAL-Cys 39 -exendin-4(> 98%, provided by Jiangsu Institute of Atomic Medicine, you can also refer to the document "Preliminary evaluation of[ 18 F]AlF-NOTA-MAL-Cys 39 -exendin-4in insulinoma with PET" preparation; absolute ethanol (Merck KGaA, Germany), micro-PET / CT (Siemens, Germany).
[0037] Use a 5ml syringe to extract 4mL of 0.05M HCl to rinse the germanium-gallium generator at a flow rate of 1mL / min while collecting the effluent; take 1ml of sodium acetate (0.25M) buffer...
Embodiment 268
[0040] Example 2 68 Ga-NOTA-MAL-Cys 39 -exendin-4 micro-PET / CT imaging in tumor-bearing mice
[0041] (1) Immunocytochemical staining
[0042] Insulinoma cells (INS-1 cells) press 5×10 5 / Well density is spread on a 24-well plate, placed in an incubator and incubated overnight. The next day, use a pipette to remove the culture medium in the wells, and fix the cells with 95% ethanol for 30 minutes after rinsing with PBS, and then rinse with PBS. After adding hydrogen peroxide to react at room temperature for 5 minutes, rinse with PBS, and then add the primary antibody (1:200 mouse anti-human GLP-1). In the negative control group, PBS was used instead of the primary antibody and placed at 37℃ for 1 hour. After rinsing with PBS, add secondary antibody (rabbit anti-rat IgG-HRP) at 37°C for 15 minutes. After PBS rinsing, diaminobenzidine (DAB) was added for color development, reacted for 3 minutes, washed with PBS, stained with hematoxylin, washed, and inspected under microscope. Aft...
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