NMR contrast agent and preparation method thereof
A technology of nuclear magnetic resonance imaging and contrast agent, which can be applied in the direction of nuclear magnetic resonance/magnetic resonance imaging contrast agent, etc., can solve the problems of limiting the application of carbon-coated nanomaterials, unfavorable practical application, and difficult to externally externally modify groups or targeting reagents, etc.
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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, pour out the solution in the reactor, collect the insoluble matter, wash and dry to obtain nano-scale carbon-coated iron oxide particles (as shown in Figure 1). Fig. 2 is the X-ray diffraction spectrogram of product, proves that product is ferric oxide; Fig. 4 is the Raman spectrogram of product, proves that carbon shell layer is made of graphitic carbon and p...
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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