Preparation method and application of nano eye medicine
A drug and ophthalmic technology, applied in the fields of nanomedicine and biomedicine, can solve the problems of no effective effect, decreased curative effect, retinal fibrosis, etc., and achieve the effect of delaying further deterioration and improving the quality of life
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Embodiment 1
[0026] A nanometer ophthalmic drug for pre-intervention of oxidative stress-damaged fundus diseases, the preparation method of which comprises the following steps:
[0027] Mix graphite powder and polypeptide molecules in a mass ratio of 1:2-3:1 and place them in a ball mill jar. Ball mill at room temperature for 2-4 hours at a speed of 300-500 rpm. After ball milling, high-speed centrifugation and deionized water dialysis are used respectively to remove impurities in the precipitate in turn. Finally, the precipitate is dispersed in deionized water to obtain a nitrogen-containing polypeptide-modified graphene nanosystem. from figure 1 As can be seen in the schematic diagram of , the synthesized new nanomedicine enters the cell through the size effect of atomically thick nanosheets, attracts ROS through the large π bond on the surface, and then catalyzes the elimination of ROS through the excellent activity obtained by nitrogen doping.
Embodiment 2
[0029] The nanometer product aqueous phase that embodiment 1 obtains is dispersed in deionized water, as figure 2 As shown in (a), a stable dispersion can be obtained. The dispersion liquid was stored at 4°C for more than 2 weeks, and no change was found in the dispersion liquid, indicating that the nanomedicine has good long-term aqueous phase dispersibility. After co-cultivating the prepared nano-drugs with ARPE-19 cells, a cell line of retinal pigment epithelial (RPE) cells for a certain period of time, it can be found that even after 72 hours of co-cultivation with up to 10 µg / mL of nano-drugs, the cells The survival rate is still as high as 100% ( figure 2 b), which fully demonstrates the good biocompatibility of the prepared nanomedicine.
Embodiment 3
[0031] The aqueous nano-drug dispersion obtained in Example 2 was spot-coated on a mica sheet, and then its morphology was detected by AFM. from image 3 It can be seen that the prepared nitrogen-doped polypeptide-modified graphene exhibits a typical graphene nanosheet structure with a thickness of about 1.4 nm, indicating that its excellent size effect can penetrate the cell membrane and enter the cell.
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