Contrast medium for improving nuclear magnetic resonance detection accuracy, preparation method and application
A technology of nuclear magnetic resonance and contrast agent, which is applied in preparations for in vivo tests, pharmaceutical formulas, emulsion delivery, etc., to achieve good water solubility, high relaxation performance, and the effect of saving medical expenses
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[0042] Preparation method of contrast agent
[0043] In this example, the following steps are used to prepare a contrast agent for improving the accuracy of nuclear magnetic resonance detection. For the preparation process of Fe-Dy NPs, see figure 1 :
Embodiment 1
[0044] Embodiment 1: the preparation method of Fe-Dy NPs with a particle size of 18 nm
[0045] Add 0.1 g of iron and 0.1 g of dysprosium into 6 mM oleic acid and 6 mM oleylamine, and dissolve in 20 g of 1-octadecene. The mixture was heated to 300 ºC for 3 hours, and the obtained black precipitate was naturally cooled to room temperature, and Fe-Dy NPs could be obtained by precipitation with alcohol. Dissolve 2 mg of Fe-Dy NPs in cyclohexane, add 10 mL of dimethylformamide, add 100 mg of NOBF4, stir vigorously, and react at room temperature for 2.5 hours. 10 mL of toluene was added to obtain NPs without oleic acid coating, and the resulting precipitate was dissolved in 7.5 mL of cyclohexane, and PAA (concentration: 20 mg / mL) was added, and the reaction was stirred for more than 20 hours. Add 10 mL of acetone to precipitate PAA-coated NPs. NPs were dissolved in 5 mL of water and sonicated until completely dissolved. Water-soluble NPs were filtered at 2 µM and stored at 4 º...
Embodiment 2
[0046] Embodiment 2: the preparation method of Fe-Dy NPs with a particle size of 10 nm
[0047] Add 0.1 g iron and 0.125 g dysprosium to 6 mM oleic acid and 6 mM oleylamine, and dissolve in 20 g 1-octadecene. The mixture was heated to 300 ºC for 3 hours, and the obtained black precipitate was naturally cooled to room temperature, and Fe-Dy NPs could be obtained by precipitation with alcohol. Dissolve 2 mg of Fe-Dy NPs in cyclohexane, add 10 mL of dimethylformamide, add 100 mg of NOBF4, stir vigorously, and react at room temperature for 2.5 hours. 10 mL of toluene was added to obtain NPs without oleic acid coating, and the resulting precipitate was dissolved in 7.5 mL of cyclohexane, and PAA (concentration: 20 mg / mL) was added, and the reaction was stirred for more than 20 hours. Add 10 mL of acetone to precipitate PAA-coated NPs. NPs were dissolved in 5 mL of water and sonicated until completely dissolved. Water-soluble NPs were filtered at 2 µM and stored at 4 ºC.
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