A kind of nickel-titanium alloy drug-loaded material and preparation method thereof
A nickel-titanium alloy and drug-loading technology, which is applied in metal material coating technology, pharmaceutical formulations, drug delivery, etc., can solve the problems of low drug loading, infection, and uncontrollable drug release, so as to improve sensitivity and promote absorption , Excellent biocompatibility effect
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Embodiment 1
[0034] A nickel-titanium disc with a diameter of 12 mm and a thickness of 1 mm was cleaned with alcohol, deionized water and ultrasonic cleaning in sequence, each time for 15 minutes. The hydrothermal treatment was carried out with 5mol / L sodium hydroxide as the medium, the hydrothermal temperature was 120°C, and the time was 8h. After hot water, rinse with a large amount of deionized water, and then carry out acid treatment and boiling water bath successively. During acid treatment, soak the sample in 0.1mol / L dilute hydrochloric acid, the amount of dilute hydrochloric acid is 5mL dilute hydrochloric acid for each sample. Soaking time is 2h. The boiling water bath time is 1h;
[0035] figure 1 (HT) is the low-power and high-power scanning electron microscope pictures of the nickel-titanium surface topography obtained through the modification of the present embodiment. As can be seen from the figure, the surface after treatment presents a sheet-like nanostructure, the lengt...
Embodiment 2
[0037] The sample treated in Example 1 was immersed in a sodium polystyrene sulfonate solution containing 6mmol / L sodium chloride, and the concentration of sodium polystyrene sulfonate was 2g / L. The reaction temperature is 60°C, and the treatment time is 48h;
[0038] figure 1 (HT / PSS) is the SEM picture of the sample after the treatment in Example 2. It can be seen from the figure that a network structure composed of polystyrene sodium sulfonate nanowires appears on the layered double hydroxide nanosheets on the surface of the material.
Embodiment 3
[0040] The sample prepared in Example 2 was placed in 1 mL with a concentration of 1×10 -4 mol / L doxorubicin hydrochloride solution, let stand at 37°C for 24h. figure 1 (LDH / PSS / Dox) is the SEM picture of the sample after the treatment in this embodiment. It can be seen from the figure that the morphology of the material does not change after loading the drug, indicating that the drug molecules are not aggregated and are evenly distributed on the surface of the material.
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