A kind of water-soluble conjugated polymer/graphyne nanoparticle and its preparation method and application
A conjugated polymer and nanoparticle technology, used in wave energy or particle radiation treatment materials, drug combinations, pharmaceutical formulations, etc., can solve the problem that photodynamic therapy cannot provide active oxygen, the release efficiency requires multiple injections, and gas therapy limit and other issues
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[0073] Embodiment 1, preparation water-soluble conjugated polymer / graphyne nanoparticle
[0074] 1. Preparation
[0075] according to figure 2 The flow chart shown prepares water-soluble conjugated polymer / graphyne nanoparticles, and the specific steps are as follows:
[0076] (1) Disperse 3 mg of graphdiyne powder in 1 mL of deionized water and sonicate for 4 h, add 0.75 mL of CPs DMSO solution (PBF or PFP, 4 mg / mL) and continue sonicating for 1 h. The interacting polymers were removed by ultrafiltration and centrifugation and washed three times with deionized water to obtain CPs@GDY.
[0077] (2) Add 15 mL of DSPE-PEG2000 (20 mg / mL) aqueous solution and sonicate for 4 h, remove excess DSPE-PEG2000 by ultrafiltration and centrifugation and wash with deionized water three times, and the purified CPs@GDY / DSPE-PEG is concentrated to 6mL, the concentration of CPs@GDY / DSPE-PEG is 0.5mg / mL.
[0078] 2. Representation
[0079] (1) Absorption and fluorescence spectra of conjuga...
Embodiment 2、 application example
[0093] 4T1 cells were purchased from the Cell Resource Center, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, catalog number 3131C0001000800032.
[0094] RPMI 1640 culture medium was purchased from thermalfisher, product number 22400105.
[0095] 1. Intracellular ATP content level test
[0096] Take 8×10 4 / mL 4T1 cells were seeded in a six-well plate and cultured for 24 hours to allow the cells to adhere to the wall (4T1 cells were cultured in RPMI 1640 medium containing 10% FBS in 5% CO 2 , in a cell culture incubator at 37 °C. The cells were digested with 0.25% trypsin for 2 minutes and subcultured at a ratio of 1:4. ). Discard the supernatant medium and replace it with a cell culture medium containing 5 μg / mL CPs@GDY / DSPE-PEG and 1 mM TEOA and incubate overnight. Discard the supernatant, wash three times with PBS, replace with cell culture medium containing 1 mM TEOA, and place the cells in 5% CO 2 , 1%O 2 , and continue to incubate for 6 ...
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