NMR contrast agent and preparation method thereof
A nuclear magnetic resonance imaging and contrast agent technology, which is applied in the direction of nuclear magnetic resonance/magnetic resonance imaging contrast agent, etc., can solve the problems of not easy to externally modify groups or targeting reagents, limiting the application of carbon-coated nanomaterials, and unfavorable practical applications.
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Embodiment 1
[0017] Example 1: at room temperature, 40 mg of ferric nitrate as an iron source is dissolved in 10 ml ethanol to form a solution with a mass percentage of 0.5%; 45 mg of decachloropyrene as a carbon source is dissolved in 1 ml toluene to form a mass percentage of 5% solution. Use ammonia water to adjust the pH value of the ethanol solution of ferric nitrate to 8, then mix it with the toluene solution of decachloropyrene, and dilute to 25ml with water. Pour the mixed solution into a polytetrafluoroethylene reactor and seal it in a stainless steel reactor. The reactor was heated to 200°C and kept for 48h. After cooling, the solution in the reactor is poured out, the insolubles are collected, washed and dried to obtain nanoscale carbon-coated iron oxide particles (such as figure 1 ). figure 2 It is the X-ray diffraction spectrum figure of product, proves that product is ferric oxide; Figure 4 is the Raman spectrum of the product, which proves that the carbon shell is compo...
Embodiment 2
[0018] Example 2: 40 mg of ferric sulfate as an iron source was dissolved in 5 ml of methanol to form a solution of 2.5% by mass; 225 mg of hexachlorobenzene as a carbon source was dissolved in 2 ml of benzene to form a solution of 2% by mass; Adjust the pH value of the iron source solution to 10, and react at 250° C. for 24 hours. All the other are with embodiment 1, product result is with embodiment 1.
Embodiment 3
[0019] Embodiment 3: Similar to Embodiment 1. The difference is that 40 mg of ferric chloride as an iron source is dissolved in 1 ml of propanol to form a solution of 5% by mass; 450 mg of hexabromobenzene as a carbon source is dissolved in 10 ml of xylene to form a 5% solution by mass solution; adjust the pH of the iron source solution to 12. Heated to 100°C and kept for 72h. Product result is with embodiment 1.
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