Nanocomposite for treating malignant tumors as well as preparation method and application thereof
A nanocomposite and malignant tumor technology, applied in the field of nanocomposites for the treatment of malignant tumors and its preparation, can solve the problems that cannot be directly applied to the diagnosis and treatment of malignant tumors, insufficient uptake of acutely toxic tumors, poor water solubility, etc., and achieve excellent Photothermal conversion ability, enhancing the effect of phototherapy and sonodynamic therapy, and the effect of easy degradation
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Embodiment 1
[0037] S1. Disperse 1 g of solid sodium hydroxide in 40 mL of N-methylpyrrolidone, and perform ultrasonic treatment to obtain a saturated sodium hydroxide N-methylpyrrolidone solution. Then 20mg black phosphorus powder was dispersed in the above solution, ultrasonically pulverized in ice water for 8h (3s cycle, 3s intermittent, 400W), then ultrasonically peeled for 10h, and a cooling circulation device was added to maintain the surrounding water temperature below 20 °C. The obtained brown-black suspension was centrifuged at 6000 r / min for 10 min to remove unflaked black phosphorus particles, the supernatant was collected, and then the precipitate was collected by centrifugation at 12000 r / min for 20 min. Washed twice with alcohol and deionized water, and then freeze-dried to obtain black phosphorus nanosheets.
[0038] S2. Preparation of cationic polymer-modified near-infrared dye NH 2 -PEG2000-IR780 and cationic polymer modified tumor targeting molecule NH 2 -PEG-RGD;
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Embodiment 2-10
[0044] The only difference from Example 1 is that the cationic polymer and the near-infrared dye are shown in Table 1.
[0045] Table 1: Example 2-10 cationic polymer, tumor targeting molecule, near-infrared dye raw material selection
[0046] Example Cationic polymer tumor targeting molecule near-infrared dyes Example 2 NH 2 -PEG
[0047] The tumor targeting molecule RGD is a polypeptide whose amino acid sequence arginine, glycine and aspartic acid are arranged in order.
Embodiment 11-20
[0049] The only difference from Example 1 is that the cationic polymers, tumor targeting molecules, and near-infrared dyes are shown in Table 2.
[0050] Table 2: Examples 11-20 cationic polymers, tumor targeting molecules, and selection of raw materials for near-infrared dyes
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