A kind of medical titanium-based material with drug-loaded layered double hydroxide film and its preparation method and application
A technology of hydroxide and layered double, which is applied in metal material coating technology, coating, medical science, etc., can solve the problems of local loading and release of unsuitable drugs, complicated process, etc., achieve large drug loading capacity and simple process , evenly distributed effect
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Embodiment 1
[0038] In this embodiment, nickel-titanium alloy among titanium alloys is selected as the substrate, and a nickel-titanium alloy disc with a diameter of 12 mm and a thickness of 1 mm is cleaned with alcohol, deionized water and ultrasonic cleaning in sequence, each time for 15 minutes. With (a) 6mM divalent metal M 1 Soluble salt of NiCl 2 (b) 2mM tetravalent metal M 2 Soluble salt of TiCl 4 (c) A mixed solution of 6.5g / L urea (d) 6mM sodium butyrate was used as a hydrothermal medium for hydrothermal treatment. The hydrothermal temperature was 120°C for 24 hours. The filling degree of the hydrothermal kettle is 35%. Rinse with plenty of deionized water after hydrothermal treatment.
[0039] figure 1 It is the low-magnification and high-magnification scanning electron microscope pictures of the surface morphology of the sample obtained through the modification treatment of this embodiment. It can be seen from the figure that the prepared drug-loaded film presents a sheet-...
Embodiment 2
[0041] Soak the sample treated in Example 1 in phosphate buffer solution (PBS, pH=7.4), take out the extract at regular intervals, and measure the concentration of the model drug sodium butyrate in the extract by an ultraviolet spectrophotometer. After soaking for a certain period of time, 125 μM hydrogen peroxide was added to PBS, and the release amount of sodium butyrate was measured immediately, so as to detect the effect of hydrogen peroxide on drug release. Figure 4 The situation of drug release is given, and it can be seen that before hydrogen peroxide is added, the drug release is at a low level, and after hydrogen peroxide is added, the drug release increases sharply. After removing the hydrogen peroxide in the environment, the drug release returned to a lower level. This shows that the concentration of hydrogen peroxide in the environment can be used as a "switch" to initiate drug release, which can effectively regulate the amount of drug release.
Embodiment 3
[0043] Human cholangiocarcinoma cells RBE and normal intrahepatic bile duct epithelial cells HIBEpiC were cultured in vitro to evaluate the effect of the drug-loaded layered double hydroxide film prepared in Example 1 on the viability of cancer cells and normal cells, using untreated nickel-titanium alloy As a control sample (marked as NiTi) using Alamar Blue (AlamarBlue TM , AbD serotec Ltd, UK) kit to detect the proliferation of cells on the material surface. Methods as below:
[0044] 1) Put the sample sterilized with 75% ethanol into a 24-well culture plate, add 1 mL dropwise to each well with a density of 5×10 4 cell / mL cell suspension;
[0045] 2) Put the cell culture plate into 5% CO 2 Incubate at 36.5°C for 18 hours in a cell culture incubator with saturated humidity;
[0046] 3) Aspirate the cell culture medium, wash the surface of the sample with PBS, transfer the sample to a new 24-well plate, and put it in an incubator to continue culturing;
[0047] 4) After ...
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