Rapid response type nucleus targeting nano diagnosis and treatment probe and preparation method and application thereof
A nanoprobe and cell nucleus technology, applied in the fields of nanomaterials and nanobiomedicine, can solve problems such as side effects, and achieve the effect of high repeatability, strong operability and high practical value
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[0032] The embodiment of the present invention also provides a method for preparing a nucleus-targeted multifunctional nanoprobe, the preparation method comprising the following steps:
[0033] Step 1, preparation of polymer micelles loaded with target marker-hypericin complex: mix the DMSO solution of the target marker-hypericin complex with the toluene solution of stearic acid and cholesterol, heat, Purify to obtain intermediate A; add the intermediate A to the Tris-HCl solution of polymer M, stir and purify at 0-40°C to obtain the polymer micelle core;
[0034] Step 2, preparation of the middle porous Au shell layer: grow a porous Au shell layer on the outer layer of the polymer micelle core, filter and purify it with an ultrafiltration membrane, and redisperse it in PBS buffer solution to obtain a polymerized porous Au shell layer. Micellar core;
[0035] Step 3, modification of DNA-apolipoprotein conjugate: Add the Tris-HCl solution of DNA to the NaCl solution to control...
Embodiment 1
[0039] Step 1, preparation of polymer micelles loaded with targeting marker-hypericin complex: mix DMSO solution (concentration of 2.5 mg / mL) of targeting marker-hypericin complex with stearic acid ( Concentration is 1.8mg / mL) and cholesterol (concentration is 5.3mg / mL) toluene solution is mixed evenly, wherein the molar ratio of hypericin and stearic acid is 1:0.02, and the molar ratio of stearic acid and cholesterol is 1 :0.8. The mixture was heated to 40°C, reacted for 2h, then cooled, and freeze-dried at -20°C to obtain intermediate A; intermediate A was added to the Tris-HCl solution of polymer M (concentration: 2.2mmol / mL), Wherein, the mass ratio of the intermediate A to the polymer M is 1:28, stirred and reacted at 4° C. for 24 h, and purified to obtain the polymer micelle core.
[0040]Step 2, preparation of the middle porous Au shell: grow a porous Au shell on the outer layer of the polymer micelle core, and control the reaction conditions so that the pore diameter ...
Embodiment 2
[0043] Step 1, preparation of polymer micelles loaded with targeting marker-hypericin complex: mix DMSO solution (concentration of 3.65 mg / mL) of targeting marker-hypericin complex with stearic acid ( The concentration is 1.98mg / mL) and the toluene solution of cholesterol (concentration is 4.3mg / mL) is mixed evenly, wherein the molar ratio of hypericin and stearic acid is 1:0.02, and the molar ratio of stearic acid and cholesterol is 1 :0.8. The mixture was heated to 40°C, reacted for 2h, then cooled, and freeze-dried at -20°C to obtain intermediate A; intermediate A was added to the Tris-HCl solution of polymer M (concentration: 2.2mmol / mL), Wherein, the mass ratio of the intermediate A to the polymer M is 1:28, stirred and reacted at 4° C. for 24 h, and purified to obtain the polymer micelle core.
[0044] Step 2, preparation of the middle porous Au shell: grow a porous Au shell on the outer layer of the polymer micelle core, and control the reaction conditions so that the ...
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