Photothermal targeted nano medicament for treating breast cancer and preparation method thereof
A breast cancer and drug technology, applied in the direction of drug combination, pharmaceutical formula, medical preparations containing active ingredients, etc., can solve the problems of low bioavailability, avoid side effects, improve non-specific distribution, and achieve good biophase capacitive effect
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Embodiment 1
[0019] Prepare the fluorescent dye IR783 into 0.5mg / mL~1.5mg / mL aqueous solution, dissolve lapatinib in dimethyl sulfoxide at a concentration of 2.5mg / mL~20mg / mL, and dissolve lapatinib drop by drop under ultrasonic conditions. The dimethyl sulfoxide solution of Tini is added to the IR783 aqueous solution, and then centrifuged at 3,000rpm-7,000rpm for 10 minutes.
[0020] Wash with deionized water for 5 times, and then resuspend with PBS. The average particle size observed under a transmission electron microscope is 80nm-150nm. For details, see figure 1 shown.
Embodiment 2
[0022] The granules prepared in Example 1 were used for killing experiments on breast cancer cells (human breast cancer cells MDA-MB-231, Cell Bank of Chinese Academy of Sciences). The grouping is as follows:
[0023] (1) Control group: no treatment;
[0024] (2) Targeted therapy group: add lapatinib to a final concentration of 2ppm;
[0025] (3) Photothermal group: add IR783 to a final concentration of 10ppm, replace with fresh medium after 4 hours, and irradiate with 1.5W / cm2 808nm laser for 5min;
[0026] (4) Nanomedicine treatment group: add nanomedicine, adjust to an appropriate concentration so that the final system contains lapatinib 2ppm, IR78010ppm, change fresh medium after 4 hours, and use 1.5W / cm 2 808nm laser irradiation for 5min.
[0027] In a 96-well plate, add 100 microliters of 5000 MDA-MB-231 cells per well, and perform the following treatments in each group:
[0028] After culturing for 48 hours, 10 microliters of CCK-8 solution was added to each well. ...
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Abstract
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