A kind of pharmaceutical composition for anti-cervical cancer combined with photodynamic therapy
A technology for photodynamic therapy and cervical cancer, applied in the field of medicine, can solve the problem of not finding the biological activity of erythritol against cancer, and achieve the effect of improving targeted killing effect, reducing toxicity and side effects
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Embodiment 1
[0013] Example 1 Study on the Proliferation Inhibitory Rate of Erythritol in Different Concentrations of Human Cervical Cancer Siha and H8 Cells
[0014] Human cervical cancer cell lines Siha and H8 were cultured in RPMI-1640 medium containing 100mL / L calf serum, placed in 37°C, 50mL / L CO 2 , in an incubator with saturated humidity, routinely subcultured with 2.5g / L trypsin. Take the Siha and H8 cells in the logarithmic growth phase, and add erythritol diluted with serum-free RPMI-1640 culture solution after culturing for 24 hours, so that the final concentrations are 1, 5, 10, 20, 40mmol / L respectively . A blank control group with separate culture medium was set up, and each group had 3 replicate wells. Incubate in the incubator in the dark for 24 hours, then discard the culture medium, add 180 μL of fresh serum-free RPMI-1640 culture medium and 20 μL of MTT solution with a concentration of 5 mg / mL to each well, and incubate at 37°C in the dark for 4 hours. Carefully disca...
Embodiment 2
[0019] Example 2 Study on the Proliferation Inhibitory Rate of Erythritol Combined with Photodynamic Therapy on Human Cervical Cancer Siha and H8 Cells
[0020] After the red light (wavelength 630nm, power 300mW) of the photodynamic laser therapy instrument is drawn out through the optical fiber, it irradiates the cells vertically. The experiment was divided into simple erythritol treatment group (ME), simple photodynamic therapy group (PDT), combined erythritol and photodynamic therapy group (ME-PDT).
[0021] Human cervical cancer cell lines Siha and H8 were cultured in RPMI-1640 medium containing 100mL / L calf serum, placed in 37°C, 50mL / L CO 2 , in an incubator with saturated humidity, routinely subcultured with 2.5g / L trypsin. Siha and H8 cells in the logarithmic growth phase of the ME-PDT group were cultured for 24 hours and then added with erythritol diluted with serum-free RPMI-1640 medium to make the final concentrations 10mmol / L respectively. Incubate in the incubat...
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