Application of carbon quantum dots/cuprous oxide (CQDs/Cu2O) compound to preparation of cancer treating medicines
A technology of cuprous oxide and carbon quantum dots is applied in the application field of medicine, which can solve the problem of unreported anti-tumor activity, and achieve the effects of inhibiting cell migration, inhibiting cell proliferation and high toxicity.
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Embodiment 1
[0037] Example 1 CQDs / Cu 2 Preparation of O and CQDs
[0038] Weigh 6g NaOH and 3.74g copper sulfate and dissolve them in 150mL deionized water respectively, add the NaOH solution to 0.1mol·L -1 In the copper sulfate solution, a flocculent suspension is formed, and ultrasonic (150W, 40KH) is used for 15 minutes. Weigh 1 g of polyvinylpyrrolidone, dissolve it in deionized water, and add it to the above mixture. Then weigh 18g of glucose and dissolve it in 100mL (1mol·L -1 ) deionized water was added to the mixture, and ultrasonic treatment was performed for 60 minutes. After standing for 16 hours, it was washed three times with deionized water and absolute ethanol, and dried in an oven at 60°C for 6 hours to obtain CQDs / Cu 2 O composite materials.
[0039] Weigh 18g of glucose and dissolve it in deionized water, add 1mol·L -1 The NaOH solution was ultrasonically treated for 5 h to adjust the pH to 7.0, and CQDs were obtained after purification with ethanol and magnesium s...
Embodiment 2
[0046] This example studies the CQDs / Cu in depth 2 Effects of O on the migration, apoptosis, cell cycle, expression of F-actin, matrix metalloproteinase MMP-2, and angiogenesis of SKOV3 cells.
[0047] cell culture
[0048] Cells use low-glucose medium (DMEM) containing 10% fetal bovine serum; BABL-3T3 cells use high-glucose medium containing 15% fetal bovine serum; HUVEC cells are extracted from human umbilical cord with 0.01% collagenase; %BI culture medium. All the cells were cultured in a 37°C, 5% carbon dioxide incubator, and subcultured when the cell confluency reached more than 80%.
[0049] Cell digestion, passaging
[0050] When the cell growth reaches more than 80%, remove the original culture medium in the culture flask, wash once with preheated PBS buffer, digest with preheated 0.25% trypsin for 3-5min, add 10mL DMEM culture medium (containing fetal bovine serum) ), centrifuge for 5min, remove the cells, add 10mL of fresh culture medium, and put them into the i...
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