Photothermal therapy and chemical therapy combined targeted medicine delivery system and synthesis method
A chemotherapy and drug delivery system technology, applied in the medical field, can solve the problems of limited curative effect, poor targeting of head and neck squamous cell carcinoma, and the combination of photothermal therapy and chemotherapy, so as to reduce damage, improve therapeutic effect, and be well received The effect of cellular uptake
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[0036] Such as figure 1 As shown, according to an embodiment of the present invention, a synthesis method for targeted drug delivery combining photothermal and chemotherapy is also provided, including the following steps:
[0037] S101, combined with doxorubicin:
[0038] Take 1 mL of PEGylated AuNPs (2.46 mg / mL), centrifuge at 15,000 rpm for 10 min, remove the supernatant, add EDC / NHS solution and shake for 2 h, after washing, add doxorubicin (0.1 mg / mL) in PBS solution, shake overnight, PEG end The carboxyl group of doxorubicin reacts with the amino group of doxorubicin to form a DOX-AuNPs complex;
[0039] S103, Conjugate Podoplanin Antibody:
[0040] Add DOX-AuNPs complex to EDC / NHS solution and shake at 37°C for 2 hours. After washing, add 40 μL Podoplanin antibody, ultrasonically shake for 10 seconds, shake for 7 hours, wash with PBS, add 5% BSA+0.05% Tween in PBS solution and shake overnight to synthesize Podoplanin- AuNPs-DOX complexes.
[0041] Further, both the E...
specific Embodiment approach : Embodiment 1
[0043] Specific embodiments: Example 1: drug release detection
[0044] The synthetic material Podoplanin-AuNPs-DOX was dissolved in 1 mL of LPBS and sealed in a dialysis bag. The dialysis bag was placed in a 10 mL medium, shaken at 37°C and 120 rpm, and the release of DOX (doxorubicin) was recorded at different times.
Embodiment 2
[0045] Example 2: 293T cytotoxicity detection
[0046] The non-tumor cell 293T was selected to detect the toxicity of PEGylated gold nanoparticles (hereinafter referred to as AuNPs). The 293T cells were seeded in a 96-well plate, and 5×103 cells were added to each well. Cultured in DMEM+10% fetal bovine serum+1% penicillin-streptomycin medium for 24 hours, then sucked off the medium, washed 3 times with PBS, added / mL, 200 μL / well) culture medium of AuNPs for 48h, and then use the MTT kit to test the cell activity (cell proliferation and cytotoxicity detection kit). After AuNPs were treated for 48 hours, the cell viability was still high, which proved that AuNPs had low toxicity.
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