A stem cell tumor targeting system loaded with nano-prodrug and its preparation method
A technology of tumor targeting and stem cells, which is applied in the fields of biomedicine and nanomedicine, can solve the problems that chemotherapy drugs are difficult to guarantee time requirements, reduce targeting and anti-tumor effects, and lose specific targeting effects, so as to prolong the survival of animals , enhance the anti-tumor effect, the method is simple and easy to operate
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Embodiment 1
[0072] Example 1: Toxicity investigation of the original drug and nano-prodrug on MSCs:
[0073] Take the MSCs cells in the logarithmic growth phase, and take 10 4 Each well was inoculated in a 96-well plate, 100 μL per well, and after culturing at 37°C for 24 hours, different concentrations of DOX, PPCD and RGD-PPCD (DOXequiv.) were added, and the culture was continued for 24 hours, and then 0.2 mL containing 0.5 mg / For the serum-free culture solution of mLMTT, continue to incubate for 2 hours, then absorb the culture solution, add 0.1mL DMSO, measure the absorbance value (λ=570nm) with a microplate reader after the dissolution is uniform, and calculate the inhibition of cell viability.
Embodiment 2
[0074] Embodiment 2: the investigation of the time frame of MSCs toxicity by former drug and nano-prodrug:
[0075] With the test method of Example 1, the drug concentrations of DOX and PPCD / RGD-PPCD were fixed, and the incubation time was changed to 36h, 48h, and 60h to obtain the inhibition of MSCs cell viability by drugs at different incubation times.
Embodiment 3
[0076] Embodiment 3: MSCs—(RGD-PPCD) n Investigation of the best incubation time:
[0077] MSCs cells in the logarithmic growth phase were taken and co-incubated with DOX, PPCD and RGD-PPCD in the culture medium at a drug concentration of 50 μg / mL (DOX equiv.), and incubated in a 37°C incubator for 0h, 1h, 2h, 4h, 8h, 24h, 48h, wash and digest with PBS (pH7.4) at 4°C, and measure the average fluorescence intensity with a flow cytometer (Ex488nm; Em550nm).
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