Tannic acid curcumin nanoparticles and preparation method and use thereof
A nanoparticle and tannic acid technology, which is applied in the direction of pharmaceutical formulations, medical preparations with non-active ingredients, non-effective ingredients of polymer compounds, etc., can solve problems such as toxicity, and achieve improvement of colitis, good adhesion, and particle size evenly distributed effect
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Embodiment 1
[0057] Embodiment 1, the preparation of tannic acid curcumin nanoparticles of the present invention
[0058] The present invention mainly adopts oil-in-water (O / W) single emulsion-solvent evaporation technology to prepare tannic acid curcumin nanoparticles (TA / CUR-NPs), and the specific method is as follows:
[0059] (1) Preparation of curcumin nanoparticles: 100mg human serum albumin (HSA) was dissolved in 50mL deionized water to prepare HSA solution; meanwhile, 20mg genipin (Gnp) and 5mg curcumin (CUR) were completely dissolved in 1mL of acetone to obtain the organic phase; the above two organic phases were dropped into the HSA solution under constant magnetic stirring; then the mixture was placed in an ice bath and ultrasonically treated with a probe sonicator at 70% amplitude power for 6 minutes. Forms an oil-in-water emulsion. The emulsion was further stirred at room temperature at 400 rpm for 6 hours to eliminate residual acetone. The emulsion was then introduced into ...
Embodiment 2
[0062] Embodiment 2, the preparation of emodin tannic acid nanoparticles of the present invention
[0063] The present invention mainly adopts oil-in-water (O / W) single emulsion-solvent evaporation technology to prepare emodin tannic acid nanoparticles (TA / EM-NPs), and the specific method is as follows:
[0064] (1) Preparation of emodin nanoparticles: 100 mg of human serum albumin (HSA) was dissolved in 50 mL of deionized water to prepare HSA solution; meanwhile, 20 mg of genipin (Gnp) and 10 mg of emodin (EM) were completely dissolved in 1mL of acetone to obtain the organic phase; the above two organic phases were dropped into the HSA solution under constant magnetic stirring; then the mixture was placed in an ice bath and ultrasonically treated with a probe sonicator at 70% amplitude power for 6 minutes. Forms an oil-in-water emulsion. The emulsion was further stirred at room temperature at 400 rpm for 6 hours to eliminate residual acetone. The emulsion was then introduce...
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