Application of carbon nanotube-chitosan-phycocyanin complex in the preparation of antitumor drugs
An anti-tumor drug, phycocyanin technology, applied in anti-tumor drugs, drug combinations, peptide/protein components, etc., can solve the problems of cytotoxicity, cell damage, death, etc., and achieve good growth inhibition and inhibition enhanced effect
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Embodiment 1
[0031] Example 1 Preparation of carbon nanotube-chitosan-phycocyanin composite (MWCNT-CS-PC)
[0032] (1) Weigh 40mg of carboxylated carbon nanotube powder with a diameter of 10nm (carboxylation rate 1wt%), add it to 150ml 5mM PBS solution, ultrasonically disperse for 60 minutes, then add 170mg water-soluble chitosan CS, and continue ultrasonic oscillation After 60 minutes, the mixed solution was magnetically stirred for 1 hour after sonication. After standing and stratifying for 6 hours, take the upper layer liquid and centrifuge at a high speed of 10000r / min. The upper layer liquid after centrifugation is the intermediate sample: chitosan-modified water-soluble multi-walled carbon nanotube homogeneous solution (MWCNT-CS) . Use a 30kD ultrafiltration tube to remove excess CS in MWCNT-CS, and freeze-dry the resulting filter cake as a sample for characterization analysis;
[0033] (2) Add 70 mg of carbodiimide hydrochloride (EDC-HCl) and 160 mg of N-hydroxysuccinimide (NHS) t...
Embodiment 2
[0038] (1) Tumor cell growth inhibition
[0039] The growth inhibitory effect of the complex on tumor cells was analyzed by MTT colorimetry.
[0040] The revived breast cancer MCF-7 cells and liver cancer HepG2 cell lines were placed in DMEM complete culture medium containing 10% fetal bovine serum, at 37°C, 5% CO 2 Subculture in an incubator under saturated humidity conditions. Cell concentration 3×10 3 / 100μL Inoculate two kinds of cancer cells in a 96-well culture plate, 200μl per well. At 37°C, 5% CO 2 Culture in the incubator for 24 hours to remove the original medium, then add 100 μL of fresh high-sugar DMEM complete medium without calf serum, and then add the MWCNT-CS-PC prepared in Example 1, the concentrations of which are respectively 30, 60, 90, 120, 150 (μg / mL), the medium wells without MWCNT-CS-PC were used as the negative control group, cultured for 24 hours, washed with phosphate buffer saline (PBS) for two time; then add 20μL 5mg.mL -1 MTT solution, cont...
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