A core-shell nano-medicine for in situ visualized treatment of tumors and its preparation method
A nano-drug and core-shell technology, which is applied in the direction of nano-drugs, anti-tumor drugs, preparations for in vivo experiments, etc., can solve problems such as long intervals, side effects superposition, and delayed treatment timing
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Embodiment 1
[0071] A core-shell nanomedicine for in situ visualization therapy of tumors, such as figure 1 As shown, it is characterized in that: a core-shell nano-medicine for in situ visualized treatment of tumors, characterized in that: the core of the core-shell nano-medicine includes: polycationic compound, and the polycationic compound passes through The immune adjuvant oligonucleotides combined by electrostatic attraction, the immune adjuvant oligonucleotides are labeled with fluorescent probes; the shell of the core-shell nano-medicine includes: a hydrophilic shell, and a hydrophilic shell An MRI imaging contrast agent chelated on the surface of the shell, the hydrophilic shell includes a negatively charged phototherapy drug modified by polydopamine, and the phototherapy drug is formed by copolymerization of aminated graphene quantum dots and a carboxyl-containing photosensitizer ; The core-shell structure is formed by electrostatic assembly between polycationic compounds and poly...
Embodiment 2
[0088] Stability experiment of nanomedicine:
[0089] Such as Figure 5 As shown, figure (a) is the different incubation time of nano-medicine of the present invention and DNase I enzyme, and figure (b) is the protective effect of different nanoparticles on CpG, wherein M is Maker, 1 is free CpG, and 2 is CpG+DNase I Enzyme, 3 is P / C+DNase I enzyme+heparin sodium, 4 is P / C+heparin sodium+DNase I enzyme, 5 is P / C@GCpD(Gd)+DNase I enzyme+heparin sodium, 6 is P / C @GCpD(Gd) + sodium heparin + DNase I enzyme.
[0090] Through agarose gel electrophoresis experiments, it was shown that the P / C@GCpD(Gd) nanoparticles of the present invention can protect CpG from being degraded by enzymes. Compared with free CpG, the P / C@GCpD(Gd) particles of the present invention can Improve the circulation time of CpG in the body to a certain extent.
[0091] Such as Image 6 As shown, figure (a) and figure (b) are respectively the change figure of particle size and PDI of P / C@GCpD (Gd) of the pr...
Embodiment 3
[0093] In vitro photothermal and photodynamic properties experiments of nanomedicine:
[0094] Such as Figure 7 As shown, under 660nm laser excitation (1W / cm 2 , 10 minutes), the nanomedicine P / C@GCpD(Gd) of the present invention has a good photothermal heating effect measured by an infrared thermal imager and a thermocouple; P / C@GCpD(Gd) was measured by a singlet oxygen probe SOSG ( Gd) has a high singlet oxygen yield and can be used in photodynamic experiments.
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