Double-targeted-mediated chemotherapy-photothermal combined cancer therapy compound system, preparation method and application of compound system
A combination therapy and dual-targeting technology, applied in the directions of non-active ingredient medical preparations, medical preparations containing active ingredients, drug combinations, etc., to improve treatment efficiency, synergistic high-efficiency photothermal treatment ability, and high drug-loading capacity Effect
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Embodiment 1
[0044] Preparation of Polypyrrole Nanoparticles (PPy NPs)
[0045] Add ferric chloride hexahydrate (1.3g) to an aqueous solution (20mL) of polyvinyl alcohol (1.5g) and stir at 500rpm for 2.5h, and then add pyrrole monomer (150μL, 0.1mol / L) to continue stirring under the same conditions for 5h, centrifuge (13000rpm, 30min), and wash with water for 5 times to obtain PPy NPs, which were then redispersed in 20mL DMF for use. The concentration is 30mg / mL.
Embodiment 2
[0047] Preparation of PPy-MOFs hybrid materials
[0048] Get PPy NPs solution 1mL among the embodiment 1, zirconium tetrachloride (23.15mg) and 2-aminoterephthalic acid (18.16mg) are dissolved in DMF (4mL) to obtain MOFs precursor solution, PPy NPs solution and MOFs The precursor solutions were mixed, and the resulting mixture was transferred to a pressure-resistant tube at 100°C for 12 h of reaction. After the reaction was completed, the sample was cooled to room temperature, centrifuged, washed with DMF and ethanol three times, and dried to obtain the PPy-MOFs material (PU NPs), the mass is 40mg.
Embodiment 3
[0050] Preparation of Linker Molecule 1-(6-Bromohexane)pyridine Bromide (Py)
[0051] Add 5 mL of 1,6-bromohexane to 50 mL of CH 2 Cl 2 0.5 mL of pyridine was slowly added dropwise to the above mixture, refluxed at 70°C for 36 h, cooled, distilled under reduced pressure, and dried to obtain Py molecule with a mass of 500 mg.
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